@article {2497, title = {Acute and Subchronic Toxicity Study of Sampilnorov Wurile}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {203-210}, type = {Original Article}, chapter = {203}, abstract = {

Introduction: Sampilnorov Wurile (SW) is a traditional medicinal preparation containing 29 plant-, mineral-, and animal-derived components. It is used for cerebrovascular ischemia, retinal disorders, cardiovascular diseases, and neurological conditions. This study aimed to evaluate the acute and subchronic toxicities of SW. Methods: Acute toxicity was assessed in C57BL/6 mice based on OECD-423 guidelines, with oral doses ranging from 500 to 6,000 mg/kg body weight. Subchronic toxicity was evaluated in Wistar rats following OECD-407 guidelines, with daily oral doses of 300 and 600 mg/kg of SW daily for 4 weeks. Clinical signs, mortality, body weight, and physical condition were monitored. Hematological, biochemical, and histopathological analyses were conducted on day 29. Results: No mortality or significant clinical signs of toxicity were observed at doses up to 6,000 mg/kg, suggesting an oral median lethal dose exceeding this level. Subchronic toxicity assessment revealed no clinical signs of toxicity or mortality. SW at 300 and 600 mg/kg had no significant effects on serum biochemical parameters or vital organ histology compared to controls. Conclusion: SW exhibited no acute toxicity at doses up to 6,000 mg/kg and showed no adverse effects in a 28-d subchronic toxicity study. These findings support its safety at tested doses.

}, keywords = {Acute and subchronic toxicity; biochemistry; blood test; histopathological analysis; Sampilnorov Wurile}, doi = {10.5530/pj.2025.17.25}, author = {Li ChangSheng and Chimgee Tserendash and Maral-Erdene Gerelt-Od and Batdavaa Batbayar and Uyangamaa Altankhuyag and Mend-Amar Batbaatar and Narankhajid Myadagsuren and Davaadagva Damdinjav and Enkhmaa Gonchig and Yeruult Chultemsuren} } @article {2526, title = {Anti-aging Efficacy and Safety of Topical Application of Two Standardized Fenugreek Seed Extracts on Facial Skin in Women: Randomized, Double-Blind, Placebo-Controlled, Clinical Study}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {August 2025}, pages = {470-479}, type = {Original Article}, chapter = {470}, abstract = {

Introduction: Fenugreek (Trigonella foenum graecum L.) is widely used in culinary and medicinal applications and has recently gained attention for its potential anti-aging properties. Objectives: This randomized, double-blind, placebo-controlled study evaluated the anti-aging efficacy and safety of topical application of flavonoid glycosides-based and eleutheroside-oligosaccharide-based standardized fenugreek seed extract creams, namely INDUS1520 and INDUS1530, respectively. Methods: Seventy-five healthy women aged between 35 and 55 years with mild to moderate facial wrinkles were randomly allocated to receive either INDUS1520, INDUS1530, or a Placebo cream for 60 days. Efficacy outcomes included skin luminescence, color, trans-epidermal water loss, moisture content, gloss, elasticity, firmness, wrinkle depth, surface roughness, and collagen distribution. Safety was assessed using a dermatological assessment and subject-reported intolerance questionnaire for adverse events. Results: INDUS1530 significantly improved skin hydration and wrinkle depth, while INDUS1520 significantly reduced transepidermal water loss compared with Placebo. Both creams showed a trend of decreased skin roughness and increased collagen distribution, although this difference was not statistically significant between the groups. All treatments, including Placebo, increased skin gloss. No adverse events or skin irritation were observed. Conclusions: Both fenugreek seed extract creams were well tolerated and demonstrated potential anti-aging benefits, with INDUS1530 showing more pronounced effects on skin hydration and wrinkle reduction. These findings support the use of standardized fenugreek seed extracts as safe and effective ingredients in anti-aging skin care products.

}, keywords = {Anti-aging, Fenugreek seed extract, Skin elasticity, Skin hydration}, doi = {10.5530/pj.2025.17.60}, author = {Prasad Arvind Thakurdesai and Pallavi Onkar Deshpande and Savita Raju Nimse} } @article {2547, title = {Antioxidant and Neuroprotective Effects of Chuquiraga spinosa Less. and Baccharis genistelloides (Pers.) Lam. in a Rat Model of Transient Cerebral Ischemia-reperfusion}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {September 2025}, pages = {620-631}, type = {Original Article}, chapter = {620}, abstract = {

Background: Cerebral ischemia, a leading cause of disability and mortality, is strongly related to oxidative stress and inflammation, highlighting the need for neuroprotective antioxidant and cytokinemodulating agents. Objective: To characterize the phytochemical profile and evaluate the antioxidant and neuroprotective effects of hydroalcoholic extracts of Chuquiraga spinosa (ChS) and Baccharis genistelloides (BaG), individually and in combination, in a rat model of cerebral ischemia{\textendash}reperfusion. Methodology: Phytochemical screening and GC-MS were performed with antioxidant assays (ABTS{\textbullet}$^{+}$, DPPH{\textbullet}, FRAP). Neurological deficit was assessed (Bederson scale), while histopathology, oxidative stress markers (MDA, GSH, SOD, CAT, NOx), and cytokines (IL-6, TNF-α, IL-1β) were measured. Groups included Normal (no ischemia), Ischemia (oral placebo), Citicoline 300 mg/kg, ChS 500 mg/kg, BaG 500 mg/kg, and the oral combination ChS 500 + BaG 500 mg/kg, all administered for seven days prior to ischemia induction. Results: ChS had higher total phenolic content than BaG (p = 0.0079). GC-MS identified 23 compounds in ChS and 17 in BaG. The combination displayed greater antioxidant activity than either extract. At 24 h, ChS 500 mg/Kg and the combination reduced severe neurological deficit to 17\% (vs. 83\% in ischemia). Histopathology revealed less neuronal damage with the combination, comparable to ChS 500 mg/Kg. All treatments decreased MDA levels; the combination also enhanced GSH and CAT and significantly reduced TNF-α and IL-1β. Conclusion: ChS and BaG extracts exert neuroprotective effects against cerebral ischemia. Their combination shows synergistic antioxidant activity against free radicals and enhances the modulation of inflammatory cytokines, supporting a greater neuroprotective potential.

}, keywords = {Cerebral ischemia; neuroprotection; antioxidants; Chuquiraga spinosa Less.; Baccharis genistelloides (Pers.) Lam}, doi = {10.5530/pj.2025.17.77}, author = {Hugo Jes{\'u}s Justil-Guerrero and Jorge Luis Arroyo-Acevedo and Juan Pedro Rojas-Armas and Miriam Palomino- Pacheco and Carlos Orlando Garcia-Bustamante and Edwin Cesar Cieza-Macedo and Jessica Yolanda Huarcaya-Rojas and Jaime David Torres-L{\'e}vano and Julio Jose Pena-Galindo and Esther Obdulia Franco-Soto and Juana E. Chavez-Flores and Robert Armando Cardenas-Orihuela} } @article {2530, title = {Comparative Phytochemical, Antioxidant, and Antibacterial Study of Different Solvent Extracts of Cissus hastata Leaves}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {August 2025}, pages = {511-519}, type = {Research Article}, chapter = {511}, abstract = {

Introduction: Plants have long been utilized in traditional medicine for treating a variety of diseases. Plant-derived extracts are a rich source of phytochemicals with documented antibacterial and antioxidant properties. Objective: This study aimed to investigate and compare the phytochemical profiles, antioxidant capacities, and antibacterial activities of various crude extracts from the leaves of Cissus hastata. Methods: Leaf extracts of C. hastata were prepared using hexane (Hex), ethyl acetate (EtOAc), 95\% ethanol (EtOH), and 50\% ethanol (AqE). These extracts were analyzed for preliminary phytochemical constituents, total phenolic content (TPC), total flavonoid content (TFC), antioxidant activity (DPPH, ABTS, and FRAP assays), and antibacterial activity against five bacterial strains: Staphylococcus aureus (TISTR 517), methicillin-resistant Staphylococcus aureus (MRSA 142), Bacillus cereus (ATCC 11778), Escherichia coli (ESBL 182), and Salmonella typhimurium (TISTR 292). Results: Phytochemical screening of different solvent extracts of C. hastata leaves revealed the presence of diverse bioactive compounds. The EtOAc and AqE extracts exhibited the highest TPC (65.31 {\textpm} 1.85 and 61.45 {\textpm} 3.34 mg GAE/g extract, respectively) (p \< 0.05). In contrast, the EtOH extract showed the highest TFC (29.92 {\textpm} 3.42 mg QE/g extract) (p \< 0.05). The EtOH and AqE extracts also demonstrated the strongest antioxidant activities in the DPPH (IC50: 307.07 {\textpm} 7.18 μg/mL and 316.86 {\textpm} 11.78 μg/mL), ABTS (IC50: 160.21 {\textpm} 5.43 μg/mL and 208.45 {\textpm} 3.84 μg/ mL) (p \< 0.05), and FRAP (4.69 {\textpm} 0.08 and 4.96 {\textpm} 0.07 mM FeSO4/mg extract) assays. The antibacterial activity was observed exclusively against Gram-positive bacteria. Among all the extracts, the AqE extract at a concentration of 100 mg/mL exhibited significant antibacterial effects against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, and Bacillus cereus, with zones of inhibition measuring 15.43 {\textpm} 0.46 mm, 14.76 {\textpm} 0.58 mm, and 15.66 {\textpm} 1.04 mm, respectively. Conclusion: Ethanol-based extracts of C. hastata leaves demonstrate high antioxidant and antibacterial activities and represent a promising source of bioactive compounds for developing natural therapeutic agents.

}, keywords = {Antibacterial, Antioxidant, Cissus hastata, Leaves, Phytochemical}, doi = {10.5530/pj.2025.17.64}, author = {Patcharin Singdam and Anussara Kamnate and On-Anong Somsap and Ruhainee Tohkayomatee} } @article {2463, title = {Comparison of the Effectiveness of Cream Extracts and VEGF Expression on Incision Wounds in Male Wistar Rats Treated with Ethanol Extracts of Papaya Leaf, Fruit Flesh, and Seeds (Carica Papaya L.)}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {January 2025}, pages = {28-39}, type = {Original Article}, chapter = {28}, abstract = {

Background: Papaya (Carica papaya Linn) is a tropical fruit plant known for its medicinal benefits, including wound healing. Objective: This study aimed to analyze and compare the potential of papaya leaf, fruit, and seed extracts in accelerating incision wound healing in male Wistar rats. Additionally, we compared the flavonoid content and stability of the extracts in cream formulations. Materials and Methods: Creams containing 30\% ethanol extracts of papaya leaf, fruit, and seeds were prepared and applied to the backs of male Wistar rats for two weeks. The wound diameter, epithelial thickness, fibroblast count, macrophage count, collagen density, and VEGF expression were measured after two weeks. Results: Our findings revealed no significant differences between the effects of the papaya leaf, fruit, and seed ethanol extracts on wound diameter, epithelial thickness, fibroblast count, macrophage count, and collagen density (p \> 0.05). There were also no significant differences when compared to the negative control group (p \> 0.05). The highest flavonoid content was found in the ethanol extract of papaya leaves. Application of the ethanol extract creams of leaf, fruit, and seeds had a significant effect on angiogenesis, as evidenced by VEGF expression (p = 0.002). Conclusion: Papaya leaf, fruit, and seed extracts are promising products for wound healing. Further research is recommended to conduct periodic histopathological examinations during the wound healing process and to explore different extract concentrations for optimal results.

}, keywords = {Incision wound; Male Wistar rats; Papaya; VEGF}, doi = {10.5530/pj.2025.17.4}, author = {Ali Napiah Nasution and Juanto Tiojaya and Stephanie and Erny Tandanu and Suandy Suandy and Andre Budi and Masdalena Nasution} } @article {2531, title = {A Comprehensive Review on the Pharmacological Potential of Dioscorea bulbifera and its Potential Hepatotoxicity}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {August 2025}, pages = {520-530}, type = {Review Article}, chapter = {520}, abstract = {

Dioscorea bulbifera, or the air potato has been studied and used in traditional medicine for centuries particularly in countries like China and India. It is loaded in different secondary metabolites such as steroidal saponins, flavonoids, diterpenoids, tannins, and carotenoids, which all play a major role in its pharmacological activities. Researchers have shown that it can be useful in the treatment of inflammation, microbial infections, oxidative stress, cancer, and liver diseases. even with these benefits there remains a shortage of clinical trials, toxicity assessment, and standardized extraction procedures to facilitate its application in herbal drug industry in a safe manner. One of the most striking features of Dioscorea bulbifera is its antimicrobial activity especially in the fight against antibiotic-resistant bacteria. also, studies done on anticancer activity are actively being conducted with some compounds being reported to induce apoptosis in cancer cells and suppress the growth of tumour. However, talking about its drawbacks some diterpenoid compounds such as diosbulbin A have been reported to show hepatotoxicity in humans and hence further studies are required to determine its safety for therapeutic purposes. The other significant challenge to developing this plant as a standard drug is its variability in chemical composition. The bioactive content is dependent on its cultivation, so it is quite a challenge to control for consistent potency. Sophisticated analytical methods such as HPLC and LC-MS could be utilized to overcome this and contemporary drug delivery systems like nano-formulations could enhance its absorption and bioavailability. Bringing together the ancient herbal knowledge and new scientific inquiry might reveal even greater therapeutic applications of the plant constituents. In the future the studies need to penetrate deeply into its safety, carry out extensive clinical trials, and explore sustainable mechanisms for massproducing its major compounds. With additional studies, Dioscorea bulbifera could become a prominent natural medicine, providing solutions for numerous health conditions while maintaining its traditional medicinal significance.

}, keywords = {air potato, Anticancer, Antimicrobial, Bioactive compounds, Dioscorea bulbifera, Medicinal plants}, doi = {10.5530/pj.2025.17.65}, author = {Rudresh Adarkar and Chandrashekar K S and Vasudev Pai and Richard Lobo and Aswatharam H N and Vamshi Krishna Tippavajhala and Ullas Prakash D{\textquoteright}Souza and Rajesh Kaverikana Shankara} } @article {2482, title = {A Detail Study of an Ethnomedicinal Plant Sarcostemma Acidum Voigt}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {188-190}, type = {Original Article}, chapter = {188}, abstract = {

Sarcostemma acidum Voigt is a leafless plant of the family Apocynaceae. Plant is locally known as Somlata. It is a traditional medicinal plant used to prepare Somras. Geographically S.acidum is mainly found in Bihar, West Bengal, Odisha and South India. It is mostly grown in dry rocky places. S.acidum is a shrub , more branched but no leaves. The phytochemicals present in the S.acidum are carbohydrates, glycosides, alkaloids, tannins, flavonoids, proteins, steroids, triterpenoids, fixed oils, mucilage, gums and waxes. Ethnomedicinally the S.acidum was used in otitis, dog bite, snake bite, rabies, emesis, arthritis and leprosy. The juice of this plant having some medicinal value, so used as natural restorative for health. S.acidum stem extract inhibits spermatogenesis and reduce the sperm count. Also the extract of S.acidum shown antipsychotic effect. The result of present pharmacological study shown that the S.acidum possess Analgesic, Antipyretic and Antidiabetic effects.

}, keywords = {Ethnomedicinal uses, Macroscopy, microscopy, Pharmacological Effects, Phytochemicals, Sarcostemma acidum Voigt}, doi = {10.5530/pj.2025.17.23}, author = {Pravanjan Kumar Tripathy and Manas Ranjan Mishra} } @article {2574, title = {Effect of Components of Gamma Oryzanol on Toll-Like Receptor 4: Receptor Structure-Based Pharmacophore, Hit Identification, and In Silico Evidence}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {329-335}, type = {Original Article}, chapter = {329}, abstract = {

Introduction: Polycystic ovarian syndrome is a leading cause of female infertility. Inflammation has a central role in infertility. Persistent activation of Toll-like receptor 4 contributes to inflammation in PCOS. Gamma-oryzanol consists of esters of ferulic acid combined with phytosterols and triterpene alcohol derivatives of rice bran oil, and is known to have anti-inflammatory effects. However, the structural interaction of different gamma-oryzanol compounds with TLR4 remains unknown. Objectives: The study aimed to investigate gamma oryzanol compounds as hit compounds and inhibitors of Toll-like receptor 4 by developing a pharmacophore model through a receptor structure-based approach coupled with molecular docking studies with the Molecular Operating Environment (MOE) software. Methods: A structure-based pharmacophore model was generated from the co-crystalized structure of the TLR4{\textendash} MD2 complex. Gamma-oryzanol derivatives were evaluated against the constructed pharmacophore model to identify potential hit compounds. The potential hit compounds that satisfied essential pharmacophoric features were subjected to molecular docking with TLR4. Results: The pharmacophore consisted of three characteristics: a hydrogen bond donor, a hydrogen bond acceptor, and a hydrophobic. Cycloartenyl ferulate, 24-methylenecycloartenyl ferulate, Campesteryl ferulate, and β-sitosteryl ferulate were found to be the hit compounds against the generated pharmacophore. The docking experiment showed that Cycloartenyl ferulate had the most potent binding interaction with TLR4 (7.9933), followed by 24-methylenecycloartenyl ferulate (-7.8580), Campesteryl ferulate (-6.1675), and β-sitosteryl ferulate (-5.9673). Conclusion: The present pharmacophore modeling and docking findings predict that gammaoryzanol may bind with the TLR4 ligand binding domain, providing structural insights into their therapeutic potential role as a modulator of the TLR4-mediated inflammatory pathway. These findings provide a theoretical foundation for future in vitro and in vivo validation studies aimed at elucidating the mechanistic basis of gamma-oryzanol{\textquoteright}s anti-inflammatory activity in PCOS.

}, keywords = {Anti-inflammatory, Gamma oryzanol, Infertility, Polycystic ovarian syndrome, TLR4 antagonist}, doi = {10.5530/pj.2025.17.103}, author = {Aasia Kanwal and Muhammad Hamdi Mahmood and Mahad Butt and Hidayat Ur Rahman and Norhida Ramli and Saiful Bahri Talip and Showkat Ahmad Bhawani} } @article {2560, title = {The Effectiveness of Beltfish (Trichiurus lepturus) Protein Intake and Physical Activity on Muscle Mass Growth}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {714-717}, type = {Original Article}, chapter = {714}, abstract = {

Malnutrition cases have increased every year. One of the causes is insufficient food intake, marked by a decrease in muscle mass. Preventing malnutrition can be done by increasing muscle mass through providing daily protein intake according to needs and engaging in physical activity. The fish species Trichiurus lepturus is a high-protein source from the sea. The protein content in this fish can help promote muscle mass growth. This study aims to determine the effectiveness of protein intake from Trichiurus lepturus combined with physical activity on increasing muscle mass. The research method is experimental, using test animals (Rattus norvegicus) given protein intake and physical activity for 28 days. The animals were divided into six groups: three control groups and three treatment groups receiving different protein levels. Muscle growth was assessed by observing the enlargement of the cruris muscle using HE (hematoxylin and eosin) staining under a 4x microscope magnification. The data obtained were analyzed using ANOVA with an Bonferroni test. The results showed a significant difference between all groups (p=0.000). The treatment groups receiving protein intake and physical activity had larger muscle sizes compared to the control groups (P<=0.05). The conclusion is that protein intake accompanied by physical activity causes changes in muscle mass. Additionally, the amount of protein intake is directly proportional to the increase in muscle size.

}, keywords = {Malnutrition, Muscle Mass, Physical Activity, Protein Intake, Trichiurus lepturus}, doi = {10.5530/pj.2025.17.89}, author = {Rivan Virlando Suryadinata and Gabriel Tirtawijaya and Sawitri Boengas and Priscilla Keshia Jayasaputri and Henriette Milda Latuputty and Nisa Kirania Dianti Mulyadi and Nawal Fajril Haya} } @article {2580, title = {Free Radical Scavenging and Anticancer Activities of Methanolic Twig Extract of Annonaceae Plant}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {362-365}, type = {Original Article}, chapter = {362}, abstract = {

Introduction: The Annonaceae family represents a promising source of bioactive compounds with potential therapeutic applications. This study aimed to comprehensively evaluate the antioxidant and anticancer potential of methanolic twig extracts from seven Annonaceae species. Methods: Twig specimens from Cananga latifolia, Goniothalamus elegans, Goniothalamus tamirensis, Melodorum fructicosum, Polyalthia dubia, Polyalthia cerasoides, and Uvaria fauveliana were subjected to standardized methanolic extraction. Antioxidant activity was assessed using DPPH radical scavenging assay. Anticancer potential was evaluated through Sulforhodamine B assay against three human cancer cell lines and normal human dermal fibroblasts at 25 μg/mL concentration. Results: Goniothalamus elegans demonstrated exceptional antioxidant activity (IC50 = 5.62 {\textpm} 1.21 μg/mL) comparable to ascorbic acid. In anticancer evaluation, G. elegans exhibited remarkable cytotoxicity against MCF-7 (95.19 {\textpm} 0.62\%) and HeLa (94.46 {\textpm} 1.69\%) cancer cells while demonstrating exceptional selectivity with minimal toxicity toward normal cells (19.72 {\textpm} 1.19\%). Melodorum fructicosum showed highest activity against HT-29 colon cancer cells (75.84 {\textpm} 1.57\%). Conclusions: Goniothalamus elegans demonstrated exceptional dual bioactivity with both potent antioxidant properties and selective anticancer effects. The remarkable selectivity indices and broad-spectrum anticancer activity suggest significant clinical potential. These findings provide scientific validation for traditional medicinal uses of Annonaceae species.

}, keywords = {Annonaceae, Anticancer, antioxidant activity, Cancer cell selectivity, DPPH assay, Goniothalamus elegans}, doi = {10.5530/pj.2025.17s.107}, author = {Sawitree Wongtangtintharn and Sirirath McCloskey and Rungruedee Thiwthong and U-sa Thongpairoj and Surapong Rattana} } @article {2513, title = {In-silico Analysis of Molecular Interaction Between Silk Proteins with BMP-2 Type IA and Type II Receptors}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {June 2025}, pages = {378-383}, type = {Original Article}, chapter = {378}, abstract = {

Background: Alveolar ridge defects are commonly associated with delayed tooth replacement. Natural biomaterial with enhanced regenerative potential is always sought after as a primary choice for ridge reconstruction. Silk, a biopolymer with its constituent proteins (fibroin and sericin) has recently demonstrated promising outcomes in vitro. However, the molecular mechanism by which this occurs remains to be elucidated. Objective: We assessed the molecular interactions between silk proteins bone morphogenetic protein (BMP)-2 type IA and type II receptors using molecular docking. Methodology: The N-terminal domain of silk proteins and structural complex of BMP-2 type IA and type II receptors were considered for protein{\textendash}protein docking using the high ambiguity-driven protein{\textendash}protein docking (HADDOCK) server. HADDOCK scores are a measure of the predicted stability of the protein{\textendash}protein complex, and a lower score indicates a more stable complex and a higher affinity for binding. Results: The HADDOCK scores and root mean square deviation value for interaction between silk proteins with BMP-2 type IA and type II receptors were (-114.2 {\textpm} 25.0 and -143.1 {\textpm} 11.3) and (2.9 {\textpm} 0.4 and 1.9 {\textpm} 0.5), respectively, for fibroin and (-1.8 {\textpm} 15.6 and -9.7 {\textpm} 25.2) and (3.5 {\textpm}0.3 and 0.9 {\textpm} 0.6), respectively, for sericin. Conclusion: The interaction between fibroin and BMP-2 receptors was more stable with higher affinity.

}, keywords = {biopolymer, Fibroin, HADDOCK, RMSD, Sericin}, doi = {10.5530/pj.2025.17.47}, author = {Nandhinee Thiagaraj and Lekha Ashokkumar and Ram Sabarish and Balaji SK} } @article {2528, title = {In-Silico Study of Bioactive Compounds from Moringa oleifera Fruit as Anti Premature Senescence Agents in Cardiac Cells: A Study on the p53 Protein}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {August 2025}, pages = {497-505}, type = {Original Article}, chapter = {497}, abstract = {

Background: Cellular senescence, characterized by irreversible cell cycle arrest, contributes significantly to the pathogenesis of cardiovascular diseases through mechanisms involving oxidative stress and activation of p53-mediated signaling. Moringa oleifera, widely recognized for its antioxidant properties, has demonstrated anti-aging effects; however, the specific bioactive compounds within its fruit and their mechanisms of action remain poorly understood. Objective: This study aimed to investigate the potential of M. oleifera fruit-derived compounds as anti-premature senescence agents targeting the p53 protein using in-silico molecular docking approaches. Methods: Bioactive compounds from M. oleifera fruit were screened via molecular docking against the human p53 protein, with Nutlin-3 used as a positive control. Binding affinities, hydrogen bonding, and hydrophobic interactions were analyzed to determine ligand{\textendash} receptor interactions. Results: Niacin and oxalic acid exhibited stronger binding affinities ({\textendash}5.90 and {\textendash}6.00 kcal/mol, respectively) compared to Nutlin-3 ({\textendash}5.64 kcal/mol). Niacin formed stable hydrogen bonds and hydrophobic interactions with key residues within the p53 active site, suggesting a capacity to modulate p53 activity. Oxalic acid demonstrated the highest binding affinity but lacked hydrogen bonding, indicating potential instability despite strong interaction. These findings support previous studies highlighting M. oleifera{\textquoteright}s role in ROS suppression and p53 modulation, pointing to its therapeutic relevance in mitigating cellular aging. Conclusion: Niacin and oxalic acid from M. oleifera exhibit promising binding characteristics as modulators of the p53 pathway. Their anti-senescence potential warrants further validation through molecular dynamics simulations and biological assays. This study supports the development of natural compound-based therapeutics for age-related cardiac degeneration.

}, keywords = {Antioxidant, cellular senescence, in silico, Molecular docking, Moringa oleifera, p53 protein}, doi = {10.5530/pj.2025.17.62}, author = {Tiwuk Susantiningsih and Ichwan Baihaki and Maria Selvester Thadeaus and Yuni Setyaningsih and Mila Citrawati} } @article {2491, title = {Mucuna Pruriens Seeds Extract Loaded Phytosomal Intranasal Gel for the Effective Treatment of Parkinson{\textquoteright}s Disease}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {129-154}, type = {Original Article}, chapter = {129}, abstract = {

One phytoconstituent derived from Mucuna pruriens (legumes) is levodopa. This medication{\textquoteright}s oral usage is limited by its high first-pass metabolism and low absorption. The goal of the present research was to develop a phytosomal gel filled with levodopa extract for better delivery and brain targeting. Various techniques, including solvent evaporation, salting out anti-solvent precipitation, direct egg yolk, and egg lipids methods, were used to create phytosomal formulations. Scanning electron microscopy, particle size, x-ray diffraction, and other techniques were used to characterize phytosomes. And added into gel formation, the more successful batch was examined for several parameters. The final batch underwent a variety of animal tests, including pharmacokinetic analysis, irritation to the nasal cavity testing. The most effective phytosomes were those made via the antisolvent precipitation approach. In this investigation, a 32-randomized complete factorial design was employed. Batch F4 had an entrapment efficiency of 70\%, a particle size of 15 (μg) and 60\% CDR. The gel-formulated batch F4G3 demonstrated improved results in terms of extrudability (90.82), amount of drug (89.32\%), viscosity (5421 cps at 100 rpm), and spreadability (25.18). Batch F4G3 of the Mucuna pruriens phytosome gel exhibited Higuchi{\textquoteright}s kinetics. According to the findings of the animal study, dopamine levels were significantly elevated. The pharmacokinetic and nasal irritation studies showed notable in vitro penetration of the nasal mucosa without resulting in skin irritation. For improving Parkinson{\textquoteright}s disease treatment, the phytosomal gel formulation delivered via the nasal route would be the ideal option.

}, keywords = {Gel, L-Dopa extract, Mucuna pruriens, Nasal gel, Optimization, Phytosome}, doi = {10.5530/pj.2025.17.18}, author = {Aniruddha Kulkarni and Manoj Tare and Meera Singh} } @article {2495, title = {Phytochemical Screening, Antioxidant Potential, and α-Glucosidase Inhibition of Causonis trifolia Leaf Extracts: A Solvent-Based Comparative Study}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {April 2025}, pages = {164-170}, type = {Original Article}, chapter = {164}, abstract = {

Introduction: Medicinal plants are used in diabetes mellitus due to their proven minimal adverse effects in humans. Causonis trifolia leaves have been used as traditional medicine for various treatments. Objective: The aim of this research was to investigate the phytochemicals, the total flavonoid and phenolic content, and in-vitro antioxidant and antidiabetic activities of the extracts of C. trifolia leaves. Method: The leaves of C. trifolia were sequentially extracted with maceration in hexane, ethyl acetate, ethanol, and 50\% ethanol. Then, the C. trifolia leaf extracts were assessed for antioxidant activity by the DPPH and ABTS radical scavenging and FRAP assay. Total phenolic and flavonoid contents were determined by the Folin- Ciocalteu and aluminum chloride colorimetric methods, respectively. Antidiabetic activity was evaluated by determination of α-glucosidase inhibitory effect. Results: Preliminary phytochemical analysis of ethanol and 50\% ethanol extracts of C. trifolia leaves showed positive results for alkaloids, coumarin, tannins, saponins, cardiac glycosides, terpenoids, and steroids. The 50\% ethanol extract had the best antioxidant activities of the three antioxidant assays (p \< 0.05). The results revealed higher phenolic and flavonoid contents in 50\% ethanol extract than in the other extracts (p \< 0.05). Moreover, the 50\% ethanol extract exhibited the best potential as α-glucosidase inhibitors of all the extracts and acarbose (p \< 0.05). Conclusions: The results conclude that the C. trifolia leaves with 50\% ethanol as the solvent possessed the potential to extract the highest levels of phytochemical content and have potential antioxidant and α-glucosidase inhibitory activities for diabetic therapy.

}, keywords = {Antidiabetic, Antioxidant, Causonis trifolia, α-glucosidase}, doi = {10.5530/pj.2025.17.20}, author = {Patcharin Singdam and Anussara Kamnate and On-Anong Somsap and Ruhainee Tohkayomatee} } @article {2573, title = {Preclinical Safety Assessment of a Polyherbal Formulation: Acute, Subchronic, and Mutagenic Evaluation}, journal = {Pharmacognosy Journal}, volume = {17}, year = {2025}, month = {December 2025}, pages = {322-328}, type = {Original Article}, chapter = {322}, abstract = {

Introduction: Before market approval, novel herbal medicines and bioactive compounds require rigorous genotoxicity and safety evaluations. A polyherbal formulation derived from Dasiphora fruticosa, Cynara scolymus, and Rosa acicularis has previously demonstrated antioxidant and nephroprotective properties. However, comprehensive toxicological and mutagenicity evaluations are needed to support its clinical development. In this study, we aimed to evaluate the acute and subchronic toxicities and mutagenic potential of this polyherbal formulation. Methods: Acute oral toxicity was assessed in C57BL/6 mice using a two-phase protocol based on Lorke{\textquoteright}s method. Subchronic toxicity was evaluated in Wistar rats following OECD guideline 407, with daily oral administration of the polyherbal formulation at doses of 500 and 1,000 mg/kg for 28 days. Mutagenicity was assessed using the Muta-Chromoplate (Ames test) kit according to OECD guideline 471. Results: Acute toxicity evaluation determined that the median lethal dose (LD50) of the polyherbal formulation exceeds 5,000 mg/kg, categorising it as practically nontoxic. The subchronic toxicity assessment revealed that doses of 500 and 1,000 mg/kg had no significant effects on body and organ weight, haematological and biochemical parameters, and histopathological features compared with the controls. Furthermore, the Ames test confirmed that the polyherbal formulation had no mutagenic activity. Conclusions: The polyherbal formulation exhibited no acute toxicity at doses up to 5,000 mg/kg, and no adverse effects were observed in a 28-day subchronic toxicity study. Furthermore, its favourable safety profile was further confirmed by its lack of mutagenic potential. Collectively, these findings provide a robust foundation for continued preclinical and clinical development of the polyherbal formulation

}, keywords = {acute toxicity; mutagenicity; phytochemicals; polyherbal formulation; safety evaluation; subchronic toxicity}, doi = {10.5530/pj.2025.17.102}, author = {Enkhmaa Gonchig and Chimgee Tserendash and Maral-Erdene Gerelt-Od and Batdavaa Batbayar and Mend-Amar Batbaatar and Perleidulam Bunddulam and Enerel Yeruult and Narankhajid Myadagsuren and Otgonbat Altangerel and Yeruult Chultemsuren} } @article {2349, title = {Analysis of Executive and Legislative Behavior in Planning the Stunting Program in Maros District}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {851-859}, type = {Research Article}, chapter = {851}, abstract = {

Objective: Indonesia has quite a serious nutritional problem which is characterized by the large number of cases of malnutrition in children under five, as a result this problem has become the attention of the Indonesian government so that it has become a national protas called stunting, so it must be resolved in an integrated manner across sectors. Unfortunately, this problem has not been resolved so stunting cases are still very high, one of which is Maros district which has the eighth number of stunting cases based on SSGI data for 2022. Method: Qualitative research is carried out in natural settings to seek information from executive and legislative experience based on knowledge, attitudes, actions and interests. We used indepth interviews, assisted by interview guides, and reviewed the rules to answer the research objectives. The researchers carried out a review of the regulations in the form of basic reading of the recommendations and outreach carried out by the relevant government. Results: Interestingly, government planning uses new methods, namely bottom up, participatory and top down. The reason given by the executive is that this method is the most effective method in government organizations because planning is made based on the Maros district government budget calendar. Conclusion: In analyzing the behavior of the Executive and the legislature, not all of them understand stunting program planning so their involvement is lacking and not all of them play an active role in the stunting program, even though they have an interest in improving the level of health in the people of Maros district by trying to achieve zero stunting for the sustainability of regional development in Maros district. Recommendation: Continuing research on the theme of Analysis of Community Behavior towards the Implementation of Stunting Program Planning in Maros Regency, we suggest to the regional government to accelerate the realization of community welfare through improving human resource services and health levels, overcoming poverty.

}, keywords = {Executive, Legislative, Natural conditions, Strategy, Stunting}, doi = {10.5530/pj.2024.16.139}, author = {Andi Yulyana Mulmaharani and Sukri Palutturi and Indar and Darmawansyah and Aminuddin Syam and Yahya Thamrin and Anwar Mallongi} } @article {2210, title = {Analysis of Hepcidin and Interleukin-6 Levels among Transfusion-Dependent Thalassemia Patients With and Without Alloimmunization/Autoimmunization}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {60-66}, type = {Original Article}, chapter = {60}, abstract = {

Background: Transfusion-dependent thalassemia (TDT) necessitates regular transfusions, resulting in complications such as iron overload, hemolytic anemia, and the emergence of alloantibodies/ autoantibodies. This situation poses challenges in obtaining compatible transfusions. Excessive iron and chronic hemolysis impact the elevation of Interleukin-6 (IL-6), initiating an inflammatory process that triggers hepcidin formation and influences antibody development. This study aims to analyze disparities in IL-6 and hepcidin levels and establish the correlation between IL-6 and hepcidin in TDT patients with and without alloimmunization/autoimmunization. Methods: Forty whole blood samples were collected from TDT patients with and without alloimmunization/autoimmunization, centrifuged, and the serum extracted, then stored in a refrigerator at -80{\textdegree}C. IL-6 and hepcidin levels were assessed using the ELISA method. The Mann-Whitney U test was employed to evaluate differences in hepcidin and IL-6 levels between the two groups. In contrast, the Spearman Correlation test was utilized to analyze the correlation between hepcidin and IL-6 levels. Results: IL-6 levels in the TDT group with alloimmunization/autoimmunization (3.64 pg/ mL) were significantly higher compared to the TDT group without alloimmunization/autoimmunization (1.41 pg/mL; p \< 0.05). Hepcidin levels in the TDT group with alloimmunization/autoimmunization (2,950.6 pg/mL) were significantly higher compared to the TDT group without alloimmunization/autoimmunization (1,599.6 pg/mL; p \< 0.05). The Spearman correlation test revealed a significant positive correlation between hepcidin and IL-6 levels in TDT patients with alloimmunization/autoimmunization (r = 0.764; p = 0.000). Additionally, a significant positive correlation was observed between hepcidin and IL-6 levels in TDT patients without alloimmunization/autoimmunization (r = 0.559; p = 0.010). Conclusion: IL-6 and hepcidin levels were elevated in TDT patients with alloimmunization/autoimmunization compared to those without. Interleukin-6 and hepcidin exhibited a positive correlation in both transfusion-dependent thalassemia groups.

}, keywords = {Anemia, Antibodies, Hepcidin, Interleukin-6, Transfusion-Dependent Thalassemia}, doi = {10.5530/pj.2024.16.9}, author = {Widya Firly Novitasari and Jusak Nugraha and Mia Ratwita Andarsini and Betty Agustina Tambunan} } @article {2258, title = {Analysis of the Giving of Mp-Asi Through Food Based on Majene{\textquoteright}s Local Wisdom for Stunting Prevention}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {372-377}, type = {Research Article}, chapter = {372}, abstract = {

Background: Majene Society own tradition and knowledge typical in selecting, processing, and consuming food. Use food local can maintain diversity food and culture local. Food local has proven effective for growth baby optimally. Goals: With do comprehensive analysis to provision of MP-ASI through foodbased wisdom local Majene, expected can an effective and sustainable stunting prevention program was developed. Method: Method research used is study qualitative with design phenomenology. Informant in study This are 103 Baduta mothers who are exclusively breastfed, and live in rural districts Pamboang and District Tameroddo. Data analyzed use content analysis through N-Vivo 12 app. Results: Food tree chief in Tameroddo is rice red Because rice red become plant lots of fields found and easy grows in mountainous areas. Meanwhile in the Coastal Region Pamboang Still consistent with rice white or yams. Typical vegetables is leaf moringa, Langurru {\textquoteright}, and Lallere {\textquoteright}. Government Regency Majene push planting leaf moringa in each home easy get and help in increase continuity food, savings cost, and independence food in Majene. Besides That, leaf moringa of course known known as " tree magic " because mark high nutrition. Majene Society own access and consumption vegetables langngurru {\textquoteright} and lallere {\textquoteright} are just that found in the area mountains Tameroddo. Usually leaf This used as plant medicine, but in this area made as processed vegetables with add mango sour. Side dish typical Majene known with called " Baupapi ". Habit consumption child given Eat with Fish sauce is considered Already enough , even often this fish sauce considered as replacement vegetables , though very easy found various the main fish species in the coastal area Pamboang . Known Pineapple in local language Majene as {\textquotedblleft}Pandeng{\textquotedblright} is easiest fruit found Because grow with flourish in the yards House citizen. Findings food local the has content test nutrition and recipe test so that can used as the proper MP-ASI menu for given to baby for optimal growth. Conclusions and Suggestions: Important For ensure that kids get too consumption of fish or other protein sources as well as nutrition from vegetables and sources food other. Order child get appropriate nutrition through provision of adequate MP-ASI. Recommended to nanny , power health and government regency Majene to encourage provision of local MP-ASI with still notice mark appropriate nutrition , MP -ASI module as research output This can used as guidelines Proper provision of MP-ASI .

}, keywords = {Food based Local, MP-ASI, Stunting Prevention}, doi = {10.5530/pj.2024.16.57}, author = {Evawati and Nurhaedar Jafar and Healthy Hidayanty and Sudirman Natsir and Razak Thaha and Ridwan Amiruddin and Citrakesumasari and Lucy Widiasari and Anwar Mallongi} } @article {2354, title = {Analysis of the Implementation of the Use of Hospital Management Information Systems (Simrs) in Hospitals Kindergarten IV Dr Sumantri Parepare}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {888-894}, type = {Research Article}, chapter = {888}, abstract = {

Background: TK Hospital management information system . IV DR Sumantri Parepare is not yet fully integrated and SIMRS must be developed to meet the criteria. Objective: This research aims to analyze the use of the Hospital Management Information System (SIMRS) at TK Hospital. IV DR. Sumantri Parepare, Parepare City. Method: The type of research used in this research is qualitative research and data collection using interviews, observation, documentation. With key informants and supporting informants using purposive sampling techniques. Results: The research results show that in terms of HR input the number of officers is sufficient and training has been given to officers regarding SIMRS, there are funds available, the availability of computers is not sufficient, SIMRS is not yet integrated , the infrastructure inadequate , inadequate implementation of SOPs and socialization Not yet done. The ability of medical records staff to use SIMRS is not optimal , there is incompleteness in filling out medical resumes and informed consent in SIMRS and reporting is carried out every month, quarterly and annually, but experiences delays. Conclusion: Improvement efforts that can be made include disseminating information about the importance or benefits of SIMRS in backing up and searching for data that is entered routinely.

}, keywords = {Hospital, Management, Reporting, SIMRS}, doi = {10.5530/pj.2024.16.144}, author = {Suparno and Muhammad Alwy Arifin and Sukri Palutturi and Darmawansyah and Yahya Thamrin and Ida Leida} } @article {2203, title = {Androgenic Efficacy and Mechanism of Glycosides-Based Standardized Fenugreek Seeds Extract Through Aromatase And 5-Alpha Reductase Inhibition}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February}, pages = {09-19}, type = {Original Article}, chapter = {09}, abstract = {

Introduction: Fenugreek seeds glycosides content have many health benefits. Objective: To evaluate the androgenic efficacy and probable mechanism of glycosides-based standardized fenugreek seed extract (SFSE-G) in laboratory rats. Methods: Male Wistar rats were administrated with 28-days of once-daily oral administration of SFSE-G (10 or 35 mg/kg) on sexual and orientational behavior with female rats, serum testosterone concentrations, weights of reproductive system-related organs (seminal vesicles, prostate, levator ani), nitric oxide level in penis homogenate, sperm count in the cauda epididymis, and testis histology were evaluated. Separate groups of rats with a positive control (testosterone propionate (10 mg/ kg, s.c. bi-weekly) and vehicle control (distilled water) were maintained. In addition, the safety of acute intravenous administration of SFSE-G (1 mg/kg) on cardiovascular function parameters was evaluated. Moreover, the inhibitory potential of SFSE-G against aromatase and 5-alpha-reductase enzymes was evaluated in vitro. Results: Subacute administration of SFSE-G (35 mg/kg, oral) to male rats showed androgenic efficacy in sexual behavior (increased mounting and intromission latency and rearing), with increased weights of seminal vehicles, prostate and levator ani muscles, serum testosterone levels, sperm count, and penile NO concentration, while preserving the normal architecture of the testes. Acute intravenous administration of SFSE-G to rats increased intracavernous pressure but retained normal cardiovascular parameters, such as blood pressure, heart rate, and corrected QT interval (QTc). SFSE-G showed significant inhibition of aromatase and 5-alpha-reductase in vitro. Conclusion: SFFE-G exhibited significant androgenic and spermatogenic efficacy, mediated through testosterone metabolism inhibition, without affecting the cardiovascular system in laboratory rats.

}, keywords = {Androgenic, Fenugreek extract, Glycosides, Sexual Behavior, Spermatogenic, Testosterone}, doi = {10.5530/pj.2024.16.2}, author = {Urmila M Aswar and Savita R. Nimse and Prasad A. Thakurdesai} } @article {2238, title = {Antibacterial Potential of Durian (Durio zibethinus murr.) Waste as an Alternative Disinfectant in Raw Drinking Water - A Literature Review}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {255-262}, type = {Review Article}, chapter = {255}, abstract = {

Efforts continue to be made to eliminate pathogenic bacteria in drinking water by using safer disinfection materials. The use of local plants as disinfection materials is highly desirable. The durian plant (Durio zibethinus) can be a very promising alternative as a natural disinfection agent to destroy pathogenic bacteria in drinking water. This narrative review comes from three online journal databases that provide free journal articles in PDF format, collected over the last ten years. The main keywords in conducting a literature review through online journals are "Durian, Durio Zibethinus, antibacterial, disinfectant, drinking water". Of the 5,693 journals identified in the three databases, 21 studies remained that met the requirements for inclusion in this review. This included study illustrates that fruit rind, seed, and leaf extracts from the durian plant have antimicrobial properties. Durian plants have antibacterial active compounds such as phenolics, alkaloids, steroids, saponins, tannins, flavonoids and triterpenoids. The antimicrobial potential tested using the diffusion and dilution method indicated that the presence of antimicrobial ingredients in the durian plant extraction was in the strong category. Some pathogenic bacteria in water that can be inhibited or killed are Escherichia coli, Pseudomonas aerugenosa, Bacillus subtilis, Bacillus cereus, Enterococcus faecalis, Staphilococcus aureus, Shigella boydii and Salmonella Typhi. This shows that there is an opportunity for the durian plant to provide a solution and great hope as a safe and economical alternative disinfection material as a replacement for current disinfection materials. Index terms: Durian (Durio zibethinus), antibacterial, disinfectant, drinking water.

}, doi = {10.5530/pj.2024.16.37}, author = {Rahwan Ahmad and Ridwan Amiruddin and A.Arsunan Arsin and Stang Stang and Hasanuddin Ishak and Yahya Thamrin and Anwar Mallongi} } @article {2281, title = {A Case Report: High Dose Systemic Corticosteroids as the Therapy for Severe Case Impetigo Herpetiformis}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {498-502}, type = {Case Report}, chapter = {498}, abstract = {

Introduction: Impetigo herpetiformis (IH) is a rare but life-threatening dermatosis of pregnancy. Early recognition and treatment of IH is important because it may cause maternal and fetal morbidity and mortality. Systemic corticosteroids remain the mainstay of treatment for IH and are considered safe for pregnancy. The purpose of this study was to present successful high-dose corticosteroids as a therapy for severe cases of IH. Case: We reported a 34-year-old pregnant woman in third trimester of pregnancy with a two-week history of reddish patches and pustules spread almost all over her body. She had a history of the same complaint in her latest pregnancy. The diagnosis of severe IH was made based on clinical, laboratory, and histopathology findings. She was prescribed 80 mg/day of oral prednisolone. The eruption and systemic symptoms gradually improved after 12 weeks of treatment. The dose was maintained until delivery before tapered gradually and stopped. The baby was born healthy, and there were not any new lesions. Discussion: Given the possibility of fetal and maternal complications that are potentially lifethreatening, IH needs to be detected and treated right away. The mainstay of treatment for IH is systemic corticosteroids. Steroids control the eruption by preventing polymorphonuclear cells from migrating. Due to its limited placental transmission, prednisolone is regarded to be safe for uses during pregnancy. After 12 weeks of treatment of 80 mg daily prednisolone, the eruptions were resolved and there were not any side effects of steroid observed in both the mother and the baby. Conclusion: Impetigo herpetiformis not only needs early treatment to prevent maternal and fetal complications but also the safety of the treatment chosen. High-dose oral prednisolone is considered effective and safe to control a severe case of IH as it has low placental transmission.

}, keywords = {Impetigo herpetiformis, Prednisolone, Pustular Psoriasis of Pregnancy}, doi = {10.5530/pj.2024.16.80}, author = {Laila Tsaqilah and Annisa Febrieza Zulkarnaen and Hartati Purbo Dharmadji and Risa Miliawati Nurul Hidayah and Erda Avriyanti} } @article {2397, title = {Clinicopathological Analysis of Mucinous Ovarian Tumors at a Single Center in Indonesia, 2019-2023}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1138-1142}, type = {Research Article}, chapter = {1138}, abstract = {

Background: Mucinous ovarian tumors are a rare subtype of epithelial ovarian tumors, accounting for approximately 3\% of all cases. These tumors exhibit unique clinical and pathological characteristics, with a particularly poor prognosis in advanced stages due to low responsiveness to platinum-based chemotherapy. Objective: This study aims to analyze the relationships between clinicopathological characteristics in patients with mucinous ovarian tumors treated at a single center in Indonesia between 2019 and 2023. Materials and Methods: A correlational study from March to June 2024 analyzed patients with confirmed mucinous ovarian tumors in Indonesia, focusing on age, histopathological grade, FIGO stage, CA-125 levels, tumor size, and metastasis presence. Results: A study of 123 mucinous ovarian tumor patients found that 57.7\% were over 40. Histopathological analysis revealed 21.1\% were benign, 26\% borderline, and 52.8\% malignant. Patients over 40 had more malignant tumors, advanced-stage disease, and omental metastasis. A significant correlation was found between malignant histopathology and advanced FIGO stage, as well as between advanced FIGO stage and both lymph node and omental metastasis. Tumor size was associated with elevated CA-125 levels and bilateral tumors. Conclusion: Mucinous ovarian tumors in patients over 40 years old are more likely to be malignant, present at an advanced stage, and involve omental metastasis. Malignant histopathological results are associated with advanced FIGO stages, which in turn are linked to lymph node and omental metastasis. Tumors larger than 10 cm tend to have elevated CA-125 levels.

}, keywords = {Clinicopathological characteristics, Indonesia, Mucinous ovarian tumors, Single center}, doi = {10.5530/pj.2024.16.186}, author = {Bayu Aditya Nugraha and Brahmana Askandar Tjokroprawiro} } @article {2265, title = {Determinants of Adverse Birth Outcomes in Ambon, Indonesia: A Case-Control Study}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {410-414}, type = {Research Article}, chapter = {410}, abstract = {

Background: Globally, adverse birth outcomes were still high, especially in low and middle-income countries like Indonesia. Stillbirth, preterm birth (PTB), low birth weight (LBW), and first-minute birth asphyxia are some of the adverse birth outcomes. The incidence of adverse birth in Ambon is quite high but never been any research about determinants of adverse birth outcomes. Objective: This study aims to examine the determinants of adverse birth outcomes and identify the main modifiable risk factors in Ambon. Method: This retrospective case-control study included all birth outcomes in August and September 2023 in Ambon, Indonesia. A total of 165 birth outcomes (55 cases and 110 controls) with complete information in Puskesmas and Posyandu were included in the analysis. The Chi-square test and regression analyses were applied to evaluate the association between variables. Result: This study showed the impact of pregnant women{\textquoteright}s age, parity, passive smoking, ANC examination, and ANC counseling on birth outcomes. There are differences in maternal age (p=0.006; 95\% CI: 1.22-6.11), parity (p=0.001; 95\% CI: 1.52-8.51), passive smokers (p=0.004; 95\% CI: 1.37-8.99, ANC examination (p=0.02; 95\% CI: 1.08-5.01) and ANC counseling (p=0.002; 95\% CI: 1.44-8.67) between case and control groups. Conclusion: Maternal age (<= 20 and \>35 years old), parity (one and >= 5), passive smokers, ANC examination not according to standard, and ANC counseling without a husband were associated with a high risk of all adverse birth outcomes.

}, doi = {10.5530/pj.2024.16.64}, author = {Magdalena Paunno and Ridwan Amiruddin and Masni and Mardiana Ahmad and Bertha Jean Que and Ridwan Thaha and Sudirman Nasir and Anwar Mallongi} } @article {2416, title = {A Double-blind, Randomized Controlled Study of Triterpenoids based Standardized Gotu Kola Leaves Extract in the Patients with Tension Type Headache}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1238-1251}, type = {Original Article}, chapter = {1238}, abstract = {

Introduction: Triterpenoid-based standardized Centella asiatica leaves extract as nasal solution (INDCANS) has shown potential in animal models of stress-related disorders. Objective: Efficacy and safety evaluation of INDCA-NS in patients with Tension-type headache (TTH). Methods: Ninety-one patients with TTH were randomized and administered INDCA-NS (46 patients) or PLACEBOCA-NS (45 patients) nasal spray (400 μg/day, 100 μg in 100 μL shot/ nostril, twice daily) for 28 days, with a 14-day follow-up. Efficacy (headache duration, frequency, and intensity; 21-item {\textquotedblleft}Depression, Anxiety, and Stress Scale{\textquotedblright} (DASS-21); {\textquotedblleft}Work Productivity and Activity Questionnaire{\textquotedblright} (WPAI: SHP); {\textquotedblleft}World Health Organization Brief{\textquotedblright} (WHOQOL-BREF), cortisol and DHEA levels, rescue medications), and safety outcome measures (including adverse events) were monitored. Results: Subacute administration of INDCA-NS (but not PLACEBOCA-NS) significantly reduced the duration of headache and TTH{\textquoteright}s effect of TTH on WPAI:SHP (Q5) scores, namely productivity in working patients (P \< 0.05, within the groups). The INDCA-NS showed significant difference (P \< 0.05) in headache duration with and without covariate adjustment (vs. PLACEBOCA-NS). Both treatments found safe, well- tolerated, with no treatment-related adverse events, significantly reduced headache frequency, pain intensity, DASS-21 (stress domain), TTH{\textquoteright}s impact on daily activities (Q6 of WPAI:SHP), and improved WHOQOL scores (P \< 0.05, within the group). The other outcome measures were not statistically significant within or between groups. Conclusion: Subacute INDCA-NS reduced headache duration and improved work productivity in TTH patients.

}, keywords = {Centella asiatica leaves; Chronic Stress; Pain; Work productivity}, doi = {10.5530/pj.2024.16.202}, author = {Prasad Thakurdesai and Pallavi Deshpande and Namrata Desai and Prasanna Mathad and Sandhya Rani and Dhananjay Raje} } @article {2403, title = {Effect of Moringa Oleifera Plus Royal Jelly Capsules in The Gestation Age and Placenta Weight of Newborns in Indonesia}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1177-1182}, type = {Research Article}, chapter = {1177}, abstract = {

Background: The incidence of adverse birth outcomes (ABO) in low- and middle-income countries (LIMC) remains significantly elevated. Moringa oleifera (MO), rich nutritional profile, offers to reduce ABO. Therefore, this study aimed to evaluate the impact of MO plus royal jelly capsules on the gestational age and placental weight of newborns in Indonesia. Materials and Methods: A quasi-experimental design setup in the Banggai district, Central Sulawesi Province. The study used a purposive sampling of 80 pregnant women from each sub-district. Moilong District received MRJ, while South Batui District was the Multiple Micronutrient Supplement (MMS) control group. Both groups took one capsule daily for six months. Data analysis using SPSS v28 for Windows, including Chi-square/Fisher{\textquoteright}s exact test, Kolmogorov- Smirnov test, Mann-Whitney test, and ANCOVA, with a significance level of p \< 0.05. Results: The demographic characteristics in both groups were similar (p \> 0.05), except for BMI (p=0.031). Pregnancy outcomes data were also identical (p \> 0.05). The Mann-Whitney test did not show a significant difference (p = 0.696) in the gestational age of delivery between the groups. However, there was a significant difference (p \< 0.05) in the PW variable within the MRJ group, as shown by the Mann-Whitney test. After adjusting for BMI in PW, the ANCOVA test indicated a significant difference (p = 0.001). Conclusions: The study concludes that MRJ and MMS interventions are effective and safe in preventing ABO in newborns based on gestational age and placental weight.

}, keywords = {Adverse Birth Outcomes, Moringa oleifera, Multiple Micronutrient Supplement, Pregnancy outcomes, Pregnant women}, doi = {10.5530/pj.2024.16.192}, author = {Lina Fitriani and Citrakesumasari and Veni Hadju and Sudirman Nasir and Apik Indarty Moedjiono and Masyitha Muis and Nurpudji Astuti Taslim and Sri Sumarni and M.Bambang Uswatul Firdaus} } @article {2334, title = {Effects of ADCES7 Self Care Behavior Application and Acupressure on Changes in Blood Glucose Levels in Obesive, Prediabetic Women}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {744-750}, type = {Original Article}, chapter = {744}, abstract = {

Background: Prediabetes and obesity in women are important health problems today. Appropriate selfmanagement and other methods are needed to overcome this. Objective: To assess the magnitude of the difference in changes in fasting blood glucose levels, before and after carrying out ADCES7 self-care behavior and acupressure. Method: This research is quasi-experimental research. The research design used was the Non-Randomized Pre Test - Post Test Control Group, which gathered obese, prediabetic women in the Kalumata Community Health Center, Siko Community Health Center and Posbindu under the PKK Ternate City through screening by excluding those who had suffered from diabetes mellitus and were pregnant. This group was then divided into the ADCES7 self care behavior intervention group, the acupressure group and the combined ADCES7 self care behavior and acupressure group. Multivariate logistic regression was used to assess changes in fasting blood glucose levels. Results: Respondents in this study were 102 people who were divided into three groups. The results showed that there was an effect of Self Management intervention p(0.016)\<0.05, acupressure intervention p(0.032)\<0.05, and the combination group of Self Management and Acupressure p(0.011)\<0.05 on changes in fasting blood glucose levels in prediabetic obese women. Conclusion: obese prediabetic women who are aware and active in self-management ACDES7 self care behavior and acupressure can reduce blood glucose levels and body weight in obese prediabetic women

}, keywords = {Acupressure, ADCES7 Self Care Behavior., Obesity, Prediabetes}, doi = {10.5530/pj.2024.16.124}, author = {Acce Basri and Syamsiar Russeng and Nurhaedar Jafar and Ridwan Amiruddin and Yahya Thamrin and Masni Masni and Muhammad Safar and Siti Muslimatun and Anwar Mallongi} } @article {2295, title = {Efficacy and Safety of Traditional Transdermal Patch (Ya-Pok- Dud-Pid) in Primary Knee Osteoarthritis Patients: A Randomized Controlled Trial}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {570-575}, type = {Original Article}, chapter = {570}, abstract = {

Background: Patients with Knee Osteoarthritis (KOA) have a progressive decline in their social and physical abilities, which affects their quality of life. The Thai Traditional Transdermal Patch (Ya-Pok-Dud- Pid; YP) has been widely used for the treatment of KOA. Objective: To determine the clinical efficacy and safety of YP in comparison with diclofenac gel (DG) for the treatment of KOA. Methods: 74 primary KOA Patients were enrolled and randomly assigned to YP groups or DG groups. The outcomes were assessed the Visual Analog Scale (VAS), Time Up and Go (TUG), Active Knee Flexion (AKF) and Passive Knee Flexion, chair sit and reach, and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Results: YP and DG significantly improved VAS, TUG, AKF, PKF, chair sit and reach, and WOMAC (p \< 0.05). Remarkably, YP experienced the same immediate pain relief after day 1 treatment as DG. The VAS scores of the YP group exhibited a significant reduction from 60{\textpm}11.06 to 38.92{\textpm}17.76, while DG decreased VAS score from 61.24{\textpm}17.84 to 39.19{\textpm}20.05 (p \<0.001). However, there was no significant difference between the two treatment groups. For adverse event, skin reaction (rash, itchy, and dry skin) was noted in the YP group because of the participant receiving YP for an extended period. Altogether, YP has a similar effect to diclofenac gel on pain severity and physical function in patients with knee osteoarthritis. Conclusion: YP is recommended as a natural therapeutic agent with efficacy and safety treatment for knee osteoarthritis.

}, keywords = {Diclofenac, Osteoarthritis of knee, Traditional, Transdermal Patch}, doi = {10.5530/pj.2024.16.89}, author = {Chutharat Saereewat and Kusuma Sriyakul and Parunkul Tungsukruthai and Sunyarn Niempoog and Sucharat Tungsukruthai and Chuntida Kamalashiran} } @article {2311, title = {Eosinophil Cell and Mass Appearance in Atypical Mycobacterium Infection of Lymphadenitis}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {664-667}, type = {Research Article}, chapter = {664}, abstract = {

Introduction: Atypical mycobacterium (ATM) is acid fast bacilli not including tuberculosis and may had opportunistic feature in environment either in air or soil. While symptoms of ATM infection may look similar with typical tuberculosis, these specific group of disease were harder to treat and would necessitate longer antibiotics consumption. While PCR may readily available to detect ATM, anatomical pathology method such as biopsy may be a cheaper alternative in low-resource settings to differentiate between atypical and typical mycobacterium infection. Aim: To analyze correlation between eosinophil cells and eosinophil mass with ATM in lymphadenopathy patient. Methods: This study is an analytical observational study with cross-sectional design which aimed to review diagnostic abilities of eosinophil cell and mass to detect ATM. Patient would undergo both PCR as gold standard of diagnosis and cytology biopsy aspiration as comparative diagnostic modalities. Data would be presented from SPSS v. 25. Results: We collected 70 subjects that fulfill inclusion and exclusion criteria. Most samples were dominated by female in relatively young age. There are 37 patients with ATM in which 75,7\% patients cytology result shown expression of eosinophil cells and 71,4\% patients shown eosinophilic mass. Chi-square test revealed that statistical significance existed between eosinophilic cells with ATM. However, such statistical significance was not found between eosinophilic mass and ATM. Conclusion: Eosinophilic cell can be used as alternative diagnostic modalities in diagnosing ATM. Further studies should further examine pathophysiological correlations and diagnostic power.

}, keywords = {Atypical mycobacterium, Cytology, Eosinophil}, doi = {10.5530/pj.2024.16.105}, author = {Neni Wahyu Hastuti and Delfitri Munir and Reno Keumalazia Kamarlis and Bintang Yinke Magdalena Sinag and Adang Bachtiar and Farhat and Amira Permatasari Tarigan and Delyuzar} } @article {2399, title = {Exploration of Adolescent Knowledge Experiences and Efforts to Identify Interventions on the Use of Digital Technology Information Media to Increase Knowledge related to HIV/AIDS Prevention}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1150-1158}, type = {Research Article}, chapter = {1150}, abstract = {

Background: HIV/AIDS has become a pandemic that worries the world community, especially teenagers because of their lack of understanding in tackling the prevention and spread of HIV/AIDS. One of the things that can be done is to identify interventions in the utilization of digital technology information media. Purpose: This study focuses on exploring the experiences of adolescents in efforts and in identifying interventions using digital technology information media to increase knowledge related to HIV/AIDS prevention. Methods: Qualitative research using interpretive descriptive approach and literature review on teenage students of SMA Negeri 4 (SMA A) and SMK Negeri 6 (SMA B) in Pangkep Regency, Class II and Class III. Sampling using t purposive sampling type of criteria sampling. The number of participants is 20 people and 5 participants who fall into the source triangulation category. Semi-structured interview guidelines with in-depth interviews, FGDs and observations using field notes. Results: There are 4 main themes that are obtained, namely: 1) Lack of youth knowledge about HIV/AIDS; 2) Perception of adolescents{\textquoteright} response control towards HIV/AIDS sufferers (ODHA); 3) Work Program in efforts to prevent HIV/AIDS; 4) The needs of adolescents, teachers, health center staff, and the health office regarding plans for developing interventions to increase youth knowledge in efforts to prevent HIV/AIDS. Conclusion: Respondents have inadequate knowledge about HIV/AIDS, show negative attitudes towards PLHIV and are also involved in risky practices that can affect HIV transmission. This shows that the provision of accurate and comprehensive information related to HIV/ AIDS is a component of prevention and control interventions that must be increased so that intervention strategies are needed to alleviate suffering and possibly reduce the negative consequences that may occur.

}, keywords = {HIV/AIDS, Intervention Strategy, knowledge, Model Development, Youth}, doi = {10.5530/pj.2024.16.188}, author = {Rusli Taher and H. Muh. Syafar and A. Indahwaty Sidin and Stang and Oedojo Soedirman and Syamsiar S. Russeng and Ridwan Amiruddin and Andi Armyn Nurdin and Anwar Mallongi} } @article {2261, title = {Factors Affecting the Occurrence of Diarrhea in Infants Aged 7-14 Months in Puskesmas Alak Kupang City}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {388-392}, type = {Research Article}, chapter = {388}, abstract = {

Diarrhea is a disease characterized by changes in the consistency of stools to liquid accompanied by an increase in the frequency of defecation more than usual \> 3 times / day accompanied by changes, with or without blood and or mucus. Factors that cause diarrheal disease are infections, infections can be caused by bacteria, parasites and viruses. Busy parents often pay less attention to health and the impact of an unhealthy environment. The three children have digestive problems, which are still considered a habit and can be cured without having to go to a health facility. The purpose of this study was to identify and analyze the factors that influence the incidence of diarrheal disease in infants aged 7-12 months at the Alak Health Center, Kupang City. The type of research used is an analytical survey with a case control design. The population in this study was divided into case populations, namely all infants aged 7-12 months totaling 137 infants and controls were infants aged 7-12 months who did not experience diarrhea totaling 8,868 infants. Determination of the size of the control sample using a ratio of 1:1 with the case sample so that the number of control samples is the same as the case sample, namely 37 infants and the total sample is 74 infants. The sampling technique is simple random sampling. Analysis of the data used is the chisquare test. The results showed that there was a significant relationship with a history of premature birth (p-value = 0.015 with an odds ratio = 3.434), low birth weight (p-value = 0.015 with an odds ratio = 4.563), exclusive breastfeeding (p-value = 0.015 with an odds value ratio = 3.434), immunization status (p-value = 0.004 with odds ratio = 4.265) and history of allergies (p-value = 0.004 with odds ratio = 4.083) with the incidence of diarrheal disease at the Alak Health Center, Kupang City. Suggestions that health center health workers need to be able to increase prevention efforts from an early age by approaching the community and providing concrete education related to the incidence of diarrhea.

}, keywords = {BBLR, Diarrhea, Exclusive Breastfeeding and Immunization Status, Premature}, doi = {10.5530/pj.2024.16.60}, author = {Deviarbi Sakke Tira and Sonyalin Buifena and Sigit Purnawan and Maria Magdalena Dwi Wahyuni and Marni Marni and Anwar Mallongi} } @article {2342, title = {Garcinia cowa Leaf Ethanolic Extract Induces Vasorelaxation Through eNOS/NO/sGC Pathway, Potassium, and Calcium Channels in Isolated Rat Thoracic Aorta}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {797-804}, type = {Original Article}, chapter = {797}, abstract = {

Background: Garcinia cowa Roxb. ex Choisy (G. cowa) is used in traditional medicine, both for improvement of blood circulation and indigestion, also as an antipyretic and expectorant. Objective: This study investigated the vasorelaxant effects and possible mechanisms of action of G. cowa leaf ethanolic extract (GCE) on the rat isolated thoracic aorta. Methods: The study examined the effects of GCE on isolated rat thoracic aorta, including both endothelium-intact and endothelium-denuded aortic rings, using an organ bath system. Specific inhibitors were used to evaluate the mechanism involved in GCE-induced vasorelaxation. Results: GCE (0.01{\textendash}10 mg/mL) relaxed endothelium-intact aortic rings, that had been precontracted with phenylephrine. Removal of the endothelium or pretreatment of endothelium-intact aortic rings with NꞶ-nitro-L-arginine methyl ester (L-NAME), or 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), significantly decreased vasorelaxation induced by the GCE. Indomethacin or propranolol had no effect on the GCE-induced relaxation of the endothelium-intact aortic rings. In endothelium-denuded aortic rings, the relaxation effect of GCE was significantly blocked by 4-aminopyridine (4-AP) and tetraethylammonium (TEA) at the maximum dose of GCE, but not by glibenclamide. In Ca2+-free Krebs solution, GCE (5 and 10 mg/mL) significantly inhibited extracellular Ca2+ induced contraction in pre-contracted rings with high KCl levels. Conclusions: These findings suggest that GCE exhibits both an endothelium-dependent, which is mediated by an eNOS/NO/sGC pathway, and an endothelium-independent pathway, which involves KCa and KV channels opening and extracellular Ca2+ influx inhibition. Kaempferol, isovitexin, quercetin, apigenin, luteolin, and amentoflavone might play a role in inducing the vasorelaxant effect of GCE.

}, keywords = {Ca2+ channel., Endothelium, Garcinia cowa, K+ channel, Vasorelaxant effect}, doi = {10.5530/pj.2024.16.132}, author = {Siwaporn Praman and Narudol Teerapattarakan and Thaneeya Hawiset} } @article {2381, title = {In Vitro Antiviral Activity of Dried Red Jujube Fruit (Ziziphus jujuba) Ethanol Extract against DENV-2}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1047-1050}, type = {Original Article}, chapter = {1047}, abstract = {

Dengue infection has become one of the most important mosquito-borne diseases worldwide and is caused by the dengue virus (DENV). Recently, neither patent drug, phytopharmaceutical medicine, nor standardized herbal medicine has been officially available against DENV. Dried red jujube fruit (Ziziphus jujuba) ethanol extract has been proven to have an antiviral effect, anti-inflammatory efficacy, and antioxidant properties, which have potential activity against DENV infection. This research was conducted to analyze the antiviral activity of dried red jujube fruit ethanol extract against DENV-2 in vitro. The halfmaximal cytotoxic concentration (CC50) and half-maximal inhibitory concentration (IC50) were examined on Vero cells by a 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, whereas the halfmaximal effective concentration (EC50) was determined using luminescence assay. The selectivity index (SI) value was determined from the ratio of CC50 and EC50. Dried red jujube fruit ethanol extracts inhibited DENV-2 in 24.59\%, 22.39\%, 17.98\%, 14.5\%, 6.42\%, and 1.28\% at 80 μg/mL, 40 μg/mL, 20 μg/mL, 10 μg/ mL, 5 μg/mL, and 2.5 μg/mL, respectively. The extract exhibited antiviral activity against DENV-2, showing a CC50 of 67.73 μg/mL, an IC50 value of 166.18 μg/mL, and an EC50 of 64.87 μg/mL, with an SI of 1.04. The LD50 value was 707.95 mg/kg. Dried red jujube fruit ethanol extract could be a potential candidate for developing an antiviral against DENV-2.

}, keywords = {Antiviral, Dengue virus, DENV-2, dried red jujube fruit, Ziziphus jujuba}, doi = {10.5530/pj.2024.16.169}, author = {Niluh Suwasanti and Cecilia Putri Tedyanto and Silvia Sutandhio and Teguh Hari Sucipto} } @article {2378, title = {Influence of Chamomile Leaves extract in Different Doses on Renal Functions and Diabetic indices in Streptozotocin {\textendash} Induced Diabetic Rat}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1029-1035}, type = {Original Article}, chapter = {1029}, abstract = {

Background: The prevalence of diabetes among Egyptians is rising. Therefore, there is always a demand for innovative natural medicines. Medicinal plants have long been a significant source in search of novel, effective alternatives for human therapy. Chamomile is one of the most widely used medicinal plants, which may help hyperglycemic patients by lowering blood sugar levels. Objectives: To determine how chamomile extract affects the kidneys when albino male rats with chronic diabetes are induced by streptozotocin (STZ). Methods: The study was conducted in the Al-Azhar Faculty of Medicine (Assiut) pharmacology department animal laboratory. For this investigation, a local strain of fifty adult male albino rats was used as the animal model and weighed 120 to 150 g. In this study, rats were divided into five groups, body weight, and systolic blood pressure was measured, and blood samples were collected for measuring blood glucose and insulin level, HbA1c, Na, K, and renal function tests, and histopathological examination was done. Results: After the study, mean glucose levels, HbA1c, urea, creatinine, K, and systolic blood pressure were significantly decreased in group IV \& group V compared to group III. In contrast, body weight serum insulin level and Na increased dramatically in group IV \& group V compared to group III. Conclusion: The serum levels of urea and creatinine in diabetic patients may be positively affected by chamomile. Additionally, short-term chamomile uses benefits diabetic individuals by decreasing loss of body weight, lowering HbA1c, and increasing insulin levels.

}, keywords = {Chamomile leaves, Diabetes mellitus, Streptozotocin}, doi = {10.5530/pj.2024.16.166}, author = {Mohamed Zaeim Hafez Ahmed and Muhammad Abdelbaeth Hassan Elfiky and Elsayed Elagamy Elsayed Mohamed and Ramadan Hassan Ibrahim Thabet and Ahmed Mohamed Gad Allah and Ahmed Abdrabo Elshenawy Elsisi and Ahmed Abdel Nasser Ahmed Mohamed and Tarek Shikhon and Mostafa Abo-akrab and Sayed A.M.Mahmoud and Mohamed AbdelAziz Doma and Wael Ahmed Mahmoud Khattab and Khaled Saleh Ali Elhamaky and Mohamed El- Salamoni and Fatma Mahmoud Abdelraheem and Mahmoud Ahmad Mohamed Azab and Mahmoud Ahmad Mohamed Azab6 and Mohamed E EL-Refaey and Ahmed A. Abd El-Rhman and Ahmed F. Abdel Ghany and Ghada Adel Hegazy} } @article {2373, title = {Juglans regia L.: Source of Bioactive Compounds with Potential Anticancer Activity}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {998-1003}, type = {Original Article}, chapter = {998}, abstract = {

Background: Juglans regia L., commonly known as {\textquotedblleft}walnut{\textquotedblright}, belongs to the Juglandaceae family, with antioxidant, anti-inflammatory, and hypoglycemic medicinal properties. Objective: Describe the anticancer potential of the bioactive compounds present in Juglans regia L. Method: Recent scientific studies were reviewed on the effects of bioactive compounds from Juglans regia L. on inhibiting tumor growth and cancer development in several experimental models. To do this, a scientific literature search was carried out, using databases such as PubMed, Scopus, and Science Direct. Results: Regarding the selected articles, it was found that some bioactive compounds from Juglans regia L. exhibit mechanisms of anticancer action, among which the following stand out: induction of apoptosis, suppression of angiogenesis, and modulation of cell signaling pathways related to cell proliferation and survival. Conclusion: It is concluded that Juglans regia L. contains active metabolites with potential anticancer effects.

}, keywords = {Angiogenesis, Antitumor, Apoptosis, Cancer, Juglans regia L.}, doi = {10.5530/pj.2024.16.161}, author = {Carla Y. Requejo-Rodr{\'\i}guez and Elmer M. Roncal-Alayo and Carmen R. Silva-Correa and V{\'\i}ctor E. Villarreal-La Torre and William A. Sag{\'a}stegui-Guarniz and William A. Sag{\'a}stegui-Guarniz and Walter E. Janampa-Castillo and Jos{\'e} E. Alvarez- Trujillo and Glenda J. Vela-Urbina and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Mar{\'\i}a E. Cotrina-Le{\'o}n and Julio A. Casta{\~n}eda-Carranza and Deivy Y. Dionicio-Rosado} } @article {2234, title = {Measuring Adolescent Mental Health and the Effect on Junevile Deliquency Behavior Tendencies. Case Study in Tana Toraja}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {231-234}, type = {Research Article}, chapter = {231}, abstract = {

Background: Adolescence is a transitional phase of development from childhood to adulthood, involving various changes in the biological, cognitive, and socio-emotional aspects of the adolescent. These changes often lead to confusion in establishing their identity, which can result in behaviors that are not in line with their developmental responsibilities. The tendency towards delinquent behavior in adolescents is one of the forms of behavior that emerges during adolescence due to the dysfunction of various aspects within the adolescent. The presence of dysfunction in these aspects of the adolescent indicates that the adolescent is experiencing mental disorders. The aim of this study is to analyze how the mental health of adolescents influences their tendency to engage in delinquent behaviors. Method: Using a quantitative method with descriptive statistics and testing assumptions using multiple linear regression analysis. Result: Based on the characteristics of adolescents aged 14 to 18 years, it was found that the mental health condition of adolescents has an impact on the tendency of delinquent behavior in adolescents, with a value based on the linear regression model of 0.000 \< 0.05, indicating a significant level. Conclusion: The non-impulsive behavioral aspect is the most significantly influential factor on the tendency of adolescent delinquent behavior with a value of p \< 0.05.

}, keywords = {Adolescent, Juneville delinquency tendency, Mental health, Self-Control}, doi = {10.5530/pj.2024.16.33}, author = {Librawaty Sara Tangibali and Muhammad Syafar and Ridwan M. Thaha and Sudirman Nasir and Hasanuddin Ishak and Sukri Palutturi and Anwar Mallongi} } @article {2410, title = {Obstacles to the Complementary Feeding Assistance Program for Stunted Children Aged 6-24 Months: A Systematic Review}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {October 2024}, pages = {1209-1217}, type = {Review Article}, chapter = {1209}, abstract = {

Stunting is a condition of stunted physical and cognitive growth caused by malnutrition during the development of children under five. UNICEF and WHO recommendations stipulate exclusive breastfeeding for 6 months and breastfeeding for up to two years. Apart from that, it is very important to provide complementary foods for breast milk for 6-23 months. The aim of the research is to determine the obstacles to the Complementary Feeding assistance program for stunted children aged 6-24 months. The method used is a Systematic Literature Review. Health database with search engines Google Scholar, PubMed, Science Direch, ProQuest and Scinapse. The search strategy uses the keywords: Program Constraints, Complementary Feeding, Stunting and Baduta. Identifying research articles for 2017-2023 and using PRISMA flowcharts and literature eligibility criteria based on the PICOS framework. A total of 10,523 articles were identified. Five articles used cross sectional methods, three survey articles, one descriptive analysis article and one cohort article. There were 10 eligible articles that met the inclusion criteria. Based on the results of the identification of Complementary Feeding assistance programs for stunted children aged 6-24 months. There is a correlation between obstacles to the mentoring program related to non-optimal complementary feeding practices (accuracy, diversity and frequency), lack of knowledge and experience, obstacles in communication skills (delivering key messages), selfefficacy/ working mothers, sanitation/environmental conditions, socio-economic, weak regulations and government programs including increasing community-based programs such as posyandu. If children aged 0-23 months receive inappropriate complementary foods, they are at high risk of stunting. Various obstacles to the Complementary Feeding assistance program will influence the program{\textquoteright}s emphasis on promoting children{\textquoteright}s growth and development to prevent stunting. Conclusion: the Complementary Feeding mentoring program is not optimal, due to various obstacles (specific and sensitive) faced in providing Complementary Feeding to stunted children aged 6-23 months.

}, keywords = {Breast milk, Complementary Feeding, Program Barriers}, doi = {10.5530/pj.2024.16.198}, author = {Icha Dian Nurcahyani and Ridwan Amiruddin and Yahya Thamrin and Wahiduddin and Aminuddin Syam and Nurhaedar Jafar and Anwar Mallongi} } @article {2239, title = {Occupational Diseases in Female Workers in the Industrial World, Indonesia: Hazard Types and Exposure Mechanisms {\textendash} Literature Review}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {263-267}, type = {Review Article}, chapter = {263}, abstract = {

Background: Occupational diseases are diseases caused by work and the work environment. Specifically gender, women have a double burden, namely domestic work in the household and the burden of being a breadwinner who works outside the home, women are also faced with reproductive tasks, namely pregnancy, childbirth and breastfeeding, and bioanatomically women have physical strength different from men, so that women are specifically more vulnerable to health risks due to their work, both physically, mental and social. This research will review the types and mechanisms of the spread of Occupational Diseases (OD) in female workers in the industrial world. Methods: The writing of this research was carried out using the Literature Review method which is a literature review method in which scientific articles are selected by researchers related to the research topic. Results: According to the results of the study, the specific risk of occupational diseases in the female worker community is pregnancy and childbirth disorders, Anemia and Sexuall Transmitted Disease (STD), while other accompanying diseases are Pulmonary Obstruction Disease, Tinea pedis, Neurotoksic Symptoms, Noice Induce Hearing Loss (NIHL), Low Back Pain (LBP), MSDs, and Work Stress. Conclusion: Every female worker has a susceptibility to occupational diseases according to the conditions and work environment experienced. The industry must pay attention to programs to improve occupational health by making anticipatory efforts so that occupational diseases do not become a life threat to female workers.

}, keywords = {Female Worker, Hazard, Industry, Occupational Disease}, doi = {10.5530/pj.2024.16.38}, author = {Mirawati Tongko and Yahya Thamrin and Syamsiar S. Russeng and Lalu Muhammad Saleh and Sukri Palutturi and Ridwan Amiruddin and Irwandy and Anwar Mallongi and Maria Kanan and Fahrudin Lahay and Almustari} } @article {2263, title = {Peer Group Empowerment to Improve Teenagers{\textquoteright} Behavior in Consuming Blood Supplement Tablets Through the Youth Integrated Healthcare Center Program}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {400-404}, type = {Research Article}, chapter = {400}, abstract = {

Backgrounds: South Sulawesi Province ranks in the top 7 with a percentage of 58.9\% coverage of TTD provision to adolescent girls. Based on data from the Gowa District Health Service in 2021, it shows that the number of coverage for taking blood-added tablets among young women is 57\% of the accumulated achievements of 26 health centers, where the health center with the lowest number of coverage for taking blood-added tablets is one of the Kanjilo Community Health Centers with an achievement of 18\% of 1239 targets targets. Youth Integrated Healthcare Center with a peer-group approach allows for continuous interaction between peer educators and their peers so that the delivery of information is more intensive. This research aims to determine the effect of peer group empowerment to increase adolescent behavior in consuming blood supplement tablets at the Youth Integrated Healthcare Center, Barombong District, Gowa Regency. Methods: This research uses a quantitative method of quasi-experimental design with a pre-test and post-test group approach. The population in this study were all members of the youth Integrated Healthcare Center in the Kanjilo health center working area, Barombong sub-district, South Sulawesi province, who were divided into two groups, namely the intervention group and the control group, each with 40 people. Results: The results of the study showed that there was a significant effect of peer group empowerment intervention on intention, self-efficacy, knowledge, attitudes, parental support, and teacher support in the intervention group and control group in consuming blood supplement tablets in youth Integrated Healthcare Center with a p-value \< 0.05. Apart from that, the results showed that adolescent Integrated Healthcare Center participants were more disciplined in consuming blood supplement tablets because of peer invitations which made changes in adolescent behavior in a more positive direction. Conclusion: There is a significant influence between the intervention group and the control group before and after being given counseling and peer group empowerment training on adolescent behavior in consuming blood supplement tablets.

}, keywords = {blood supplement tablets, peer groups, Teenagers, youth Integrated Healthcare Center}, doi = {10.5530/pj.2024.16.62}, author = {Nurjanna and Muhammad Syafar and Syria and Ridwan M. Thaha and Abdul Salam and Ridwan Amiruddin and Anwar Mallongi} } @article {2360, title = {Phytochemical Screening, Antioxidant and Anti-Arthritis Potential of Decoction Extract from Caulerpa lentillifera}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {927-932}, type = {Research Article}, chapter = {927}, abstract = {

Caulerpa lentillifera also known as sea grape, is a green seaweed in the Caulerpaceae family known for its nutritional benefits and medicinal properties. This study aimed to examine the phytochemical compounds, total phenolic content, total flavonoid content, and antioxidant and anti-arthritis properties of sea grape decoction extract. The total phenolic content was measured using the Folin-Ciocalteu method, and the total flavonoid content was determined with the aluminum chloride colorimetric method. Antioxidant activities were evaluated using two methods: 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2{\textquoteright}-azinobis-(3- ethylbenzothia-zoline-6-sulfonate) (ABTS). The anti-arthritis activities were assessed using bovine-serum protein. The study identified that the extract contained flavonoids, saponin, terpenoids and coumarins, with the total phenolic content of 343.19 {\textpm} 9.86 μg gallic acid equivalents/ mg dry extract and the total flavonoid content of 268.48 {\textpm} 16.57 μg quercetin equivalents/ mg dry extract. The extract showed antioxidant activity with an IC50 value of 309.05{\textpm}5.91 μg/ml using the DPPH method and 572.33{\textpm}3.47 μg/ml using the ABTS method, respectively. Additionally, it exhibited anti-arthritis properties with an IC50 value of 54.60{\textpm}12.71 μg/ml, which was less than 1.69 times the IC50 value of diclofenac sodium. A strong positive correlation was found between the antioxidant and anti-arthritis activities measured by the ABTS method, with an R{\texttwosuperior} value of 0.9476. Therefore, this study provides initial evidence supporting the antioxidant and anti-arthritis activities of sea grape decoction extract. The extract shows potential for further development as a product for treating arthritis.

}, keywords = {Anti-arthritis activity., antioxidant activity, Caulerpa lentillifera, Phytochemical components}, doi = {10.5530/pj.2024.16.150}, author = {Khemjira Jarmkom and Wanna Eiamart and Prakairat Tunit} } @article {2241, title = {Poikilodermatous Mycosis Fungoides: A Rare Case Treated with Low-Dose Methotrexate}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {276-279}, type = {Case Report}, chapter = {276}, abstract = {

Mycosis fungoides (MF) is a subtype of cutaneous T-cell lymphoma (CTCL) and a primary cutaneous lymphoma. Poikilodermatous MF (PMF) is a rare clinical variant of MF. Systemic chemotherapy, such as methotrexate (MTX), may be administered as monotherapy or in combination at low doses in MF. A 64-year-old man with PMF has been reported. History and physical examination revealed hyperpigmented and hypopigmented macules on the chest, abdomen, both arms, back, and upper legs, along with erythematous macules on the right medial thigh. The diagnosis of PMF is based on clinical manifestations and histopathological features of atypical lymphocyte cell infiltration in the epidermis. In addition, immunohistochemical examination also supports the MF diagnosis. The patient received chemotherapy consisting of monotherapy with MTX at low doses. During the third month of observation following MTX therapy, a few of the hyperpigmented and hypopigmented macules appeared to have diminished; some of the erythematous macules had transformed into hyperpigmented macules, and there were no new lesions. The purpose of therapy is to control the disease. Administration of low-dose MTX as a monotherapy may result in clinical improvement, but further observation is necessary. PMF may have a better prognosis than other clinical variants of MF.

}, keywords = {Cutaneous T-cell lymphoma, Methotrexate, Mycosis fungoides, Poikilodermatous mycosis fungoides}, doi = {10.5530/pj.2024.16.40}, author = {Eva Krishna Sutedja and Frizam Dwindamuldan Sutisna and Endang Sutedja and Kartika Ruchiatan and Yogi Faldian and Laila Tsaqilah and Hermin Aminah Usman and Yovan Rivanzah} } @article {2359, title = {Positive NS1 Antigen in Non-Dengue Virus Infection Serum: Possible Reasons for the Discrepancy with DENV PCR Results}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {923-926}, type = {Original Article}, chapter = {923}, abstract = {

Background and Objective: A specific examination is required to distinguish between DVI and viral, bacterial, and parasitic illnesses because their clinical manifestations are nearly identical. Leukopenia and lymphocytosis are examples of non-specific tests that might be used to get a diagnosis. Non-structural protein 1 (NS1) antigen, anti-DENV antibody, or DENV-specific nucleic acid detection are more specific assays. Methods: Virus isolation or molecular analysis of the detection of DENV nucleic acid ribonucleic acid (RNA) using RT-PCR was used to make the conclusive diagnosis of DVI. The sensitivity of the DENV RT-PCR method ranges from 28.8 to 99\%. NS1 antigen is used as an initial diagnostic option in primary health care because it has a high specificity value (100\%). Researchers want to analyze the positivity in non-DVI samples that have been confirmed by real-time RT-PCR examination with semi-quantitative NS1 antigen examination. Patient population aged 1-65 years with acute fever \<5 days. A total of 130 samples of non-DVI confirmed patients by RT-PCR were examined for NS1Antigen ELISA. Results: With a proportion of 3.08\% of the total sample, the results showed that 4 NS1Antigen ELISA samples were positive. A negative DENV RT-PCR result could indicate either a true negative or a false negative. Conclusion: The type of PCR technology, the primer used, the existence or absence of a DENV mutation, the DENV serotype, and the presence of mismatched nucleotides can all affect variations in DENV PCR sensitivity.

}, keywords = {Dengue Virus Infection., NS1Ag, RT-PCR DENV}, doi = {10.5530/pj.2024.16.149}, author = {I Gusti Agung Ayu Eka Putri Sunari and Aryati Aryati and Faradila Khoirun Nisa Hakim and May Fanny Tanzilia and Ida Parwati and Rismawati Yaswir and Budi Mulyono} } @article {2257, title = {Protective Effects of Rutinoside on Oxidative Induced Articular Cartilage Damage and Catabolic Activity in Rat Chondrocyte}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {360-365}, type = {Research Article}, chapter = {360}, abstract = {

Objective: This study aimed to look into the therapeutic potential of rutinoside in reducing articular cartilage degeneration in a rat model of osteoarthritis generated by monosodium iodoacetate (MIA). Methods: We formed three groups of male Wistar rats: the OA, rutinoside, and control groups. Monosodium iodoacetate (3.0 mg) was injected intra-articularly into the knee joint to cause osteoarthritis. For four weeks, oral administration of rutinoside at 100 mg/kg/day was given to the groups that were given the treatment. Histological examination, immunohistochemistry, and biochemical tests were used to assess the level of articular cartilage injury, oxidative damage, catabolic activity, and biomarker expression. Results: The results showed that treatments with rutinoside significantly reduced the damage to articular cartilage in rats with MIA-induced osteoarthritis. Compared to the osteoarthritis group, the rutinoside-treated groups showed enhanced cartilage structure, proteoglycan content, and chondrocyte organization. Immunohistochemistry revealed reduced NFκB, IL-1β, and MMP-13 expressions in the rutinosidetreated groups, indicating suppressed inflammatory and catabolic activity in chondrocytes. Additionally, rutinoside treatment increased SOD activity and decreased MDA levels, which showed less oxidative damage to the joint. A substantial drop in CTX-II levels was found by biochemical research, indicating less type II collagen breakdown. Conclusion: According to a study, rutinoside effectively reduces oxidative damage and catabolic activity in chondrocytes, which can lead to decreased articular cartilage loss in a rat model of MIA-induced osteoarthritis. The study also found that rutinoside can control critical biomarkers such as NFκB, IL-1β, SOD, MDA, MMP-13, and CTX-II, highlighting its potential as a treatment for osteoarthritis. These findings provide valuable insights into using natural chemicals as a promising treatment for OA and suggest that rutinoside could potentially modulate the critical interplay between oxidative stress, inflammation, and chondrocyte catabolism in osteoarthritis. However, further research is required to understand the underlying molecular mechanisms and evaluate rutinoside{\textquoteright}s translational potential for OA therapy.

}, keywords = {Inflammation, Osteoarthritis, Oxidative stress, Rutinoside}, doi = {10.5530/pj.2024.16.55}, author = {Rena Normasari and Bambang Purwanto and Damayanti Tinduh} } @article {2306, title = {A Quasi-Experimental One Group Pre-Post Test Design in Air Traffic Controller in Indonesia: Progressive Muscle Relaxation}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {638-643}, type = {Research Article}, chapter = {638}, abstract = {

Objectives: The effectiveness of progressive muscle relaxation (PMR) in assessing the general health of air traffic controllers (ATC) is still insufficient, specifically when examining the psychological conditions of workers who use questionnaire instruments. Therefore, this research aimed to evaluate the use of PMR program in ATC by developing a model using biomarkers (saliva) tested on the cocorometer stress diagnostic tool and validity, including observing related determinants in the work environment. Methods: A quasi-experimental method was used, focusing on one group pre-post-test design for 92 respondents across six research areas in Indonesia. All respondents had received training in PMR methods conducted by psychologists. Subsequently, ongoing assistance was provided in implementing relaxation by a trained reminder team for eight weeks to maintain the precision and effectiveness of the intervention. Further analysis was conducted using the Wilcoxon signed rank test to evaluate the success of the intervention. Results: The implementation of PMR program in ATC reduced the incidence of stress levels after the observation. Statistically, the feeling of fatigue was a significant variable that decreased in mean value after the implementation of the relaxation program on the data review. The main benefit of PMR program in improving psychological health conditions (stress) was found in Surabaya branch ATC. Conclusions: The relaxation program was proven to reduce stress levels in ATC, showing an improvement in conditions before and after the implementation of PMR.

}, doi = {10.5530/pj.2024.16.100}, author = {Lalu Muhammad Saleh and Syamsiar S. Russeng and Istiana Tadjuddin and Iva Hardi Yanti and Nurul Mawaddah Syafitri and Yulianah Rahmadani and Mahfuddin Yusbud and Anwar Mallongi} } @article {2291, title = {Renal Resistive Index and Estimated Glomerular Filtration Rate in Nondiabetic Chronic Kidney Disease Stage 3: A Cross-Sectional Analytical Study}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {538-544}, type = {Original Article}, chapter = {538}, abstract = {

Background: Renal resistive index (RRI) and estimated glomerular filtration rate (eGFR) are predictive markers for chronic kidney disease (CKD) progression. Aim: To evaluate RRI value, eGFRcr-cys and renal biomarker in nondiabetic patients with CKD stage 3 in Bangkok, Thailand. Methods: A cross-sectional analytical analysis was conducted involving nondiabetic patients with CKD stage 3, aged 35-85 years. Ultrasound was used to assess the RRI of arteries in both kidneys. Patients underwent assessments of serum and urine 24-hour. Results: Among the 61 participants (67.2\% male; mean age 69.03 {\textpm} 12.59 years), the mean eGFRcr-cys was 41.63 {\textpm} 8.64 mL/min/1.73 m{\texttwosuperior}, and the mean RRI was 0.65 {\textpm} 0.06. Patients were categorized into three RRI groups: low (\<0.65, n=35), intermediate (0.65-0.70, n=14), and high (\>0.70, n=12). The high RRI group showed a mean RRI of 0.73 {\textpm} 0.05 (p \< 0.01). Among those with high RRI group were significant decreased right kidney size (p\<0.05) and they had a lower BMI, averaging 22.49 {\textpm} 3.48. An increase in PP (59.66 {\textpm} 13.84, p=0.04) was also significant in this group. The correlations coefficient of RRI value showed a significant positive correlation with age (p\<0.05) and significant negative with BMI (p\<0.05). In addition, eGFRcr-cys displayed a significant negative correlation with UAGT and 24hUP (p\<0.05) and a significant while eGFRcr-cys positive correlation with both kidney size and urine iNOS(p\<0.01). Conclusion: An increase in RRI is inversely linked to age, BMI, and PP. Lower eGFR is correlated with factors that cause CKD progression.

}, doi = {10.5530/pj.2024.16.85}, author = {Patnaree Wongmanit and Kusuma Sriyakul and Parunkul Tungsukruthai and Ouppatham Supasyndh and Pratya Phetkate} } @article {2235, title = {Safety Assessment of Oral Lysiphyllum strychnifolium Aqueous Extract in Healthy Volunteers}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {February 2024}, pages = {235-240}, type = {Research Article}, chapter = {235}, abstract = {

Background: Lysiphyllum strychnifolium (LS), widely known as Ya nang daeng in Thailand, is a traditional herbal remedy that has long been used to promote health and treat diverse health conditions, especially detoxification, by alleviating the severity of symptoms and lowering the risks associated with toxic exposures. Although it is extensively used in Thailand, human safety studies have been lacking. Thus, this study aimed to examine the safety of using LS capsules in healthy participants through a Phase I clinical trial. Objective: This study aimed to investigate the safety of aqueous extract of LS in twenty-four healthy Thai participants. Method: The participants were received 1,000 mg of LS aqueous extract each morning before their meals for seven days. All participants were examined safety assessment including history taking, physical examination, and laboratory tests at day 0, 8 and 14 (follow-up). Results: The findings showed that there were no significant side effects or abnormalities found during the history taking, physical examination, or laboratory evaluation. Particularly, when compared to baseline, participants who received LS experienced statistically significant reductions in blood sugar, triglyceride, LDL cholesterol, and creatinine (P \< 0.05), but still within normal ranges. Conclusions: Dietary supplementation with 1,000 mg of LS aqueous extract per day may have a beneficial effect on blood sugar and cholesterol management while remaining safe for healthy people.

}, keywords = {Clinical study, Healthy volunteers, Lysiphyllum strychnifolium, Safety, Yanang Daeng}, doi = {10.5530/pj.2024.16.34}, author = {Piracha Jumpa-ngern and Parunkul Tungsukruthai and Chuntida Kamalashiran and Somboon Kietinun and Kesara Na- Bangchang and Kusuma Sriyakul} } @article {2310, title = {Serum Trace Element Levels in Type 2 DM Patients and its Correlation with Glycemic Control}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {June 2024}, pages = {660-663}, type = {Research Article}, chapter = {660}, abstract = {

Background: Type 2 diabetes mellitus, a chronic metabolic disorder, is known to impact serum trace element levels. Objectives: to investigates the association between serum trace elements (Co, Cr, and Cu) and glycemic control in individuals with type 2 diabetes. Material and Methods: A 209 type 2 diabetes patients from Dr. H. Abdul Moeloek Hospital in Bandar Lampung and Hasan Sadikin Hospital in Bandung participated in the study. Patients underwent assessments for serum trace element levels (Co, Cr, and Cu) and glycemic control indicators (FBG and HbA1c). Results: Results indicated significantly lower Co levels in uncontrolled diabetes versus controlled cases (P\<0.05). Co, Cr, and Cu levels displayed a significant negative correlation with HbA1c (P\<0.05), while Cr and Cu showed a significant negative correlation with FBG (P\<0.05). Age did not show significant correlations with serum trace element levels. Conclusion: serum trace element levels (Co, Cr, Cu) are inversely linked to glycemic control in type 2 diabetes individuals.

}, keywords = {Fasting blood glucose, glycemic control, HbA1c, trace element serum, Type 2 diabetes mellitus}, doi = {10.5530/pj.2024.16.104}, author = {Intanri Kurniati and Agustyas Tjiptaningrum and Raja Iqbal Mulya Harahap and Bayu Putra Danan Jaya} } @article {2249, title = {Study on Factors that Influence the High Organizational Citizenship Behavior (OCB) of Makassar Ethnic Nurses in LANTO Hospital DG Pasewang Jeneponto in 2024.}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {April 2024}, pages = {312-318}, type = {Original Article}, chapter = {312}, abstract = {

Background: Organizational Citizenship Behavior (OCB) is behavior carried out by an employee that exceeds formal work obligations, but has a good impact because it supports organizational effectiveness. Culture value is one of the factors for the high level of organizational citizenship behavior in Makassar ethnic nurses. According to the theory that researchers read, it is not only culture values that are a factor in high OCB. There are several factors that influence OCB, including Workplace Variables, HRM Policies \& Practices, Culture, Contextual Factors, Work Centrality, Org Service Orientation, Org Reputation Threat, Dispositional Variables, Org Commitment, Demographic Variables, Personality Variables, Leader Supportive. Researchers became interested because this research only explored cultural values. Researchers want to look for other factors that influence the high OCB of the Makassar tribe at Lanto Dg Pasewang Jeneponto Regional Hospital so that they can be explored in more depth and become input for hospitals and other organizations. Methods: The type of research carried out is qualitative research with a phenomenological approach. The informants in the research were 3 key informants consisting of the hospital director, head of nursing and head of the inpatient room and 7 regular informants consisting of several nurses at Lanto Dg Pasewang Jeneponto Regional Hospital. Results: Based on the results of interviews conducted by writers and ethnic Makassar nurses at Lanto Dg Pasewang Jeneponto Regional Hospital, there are several factors that influence the high level of OCB attitudes. Divided into 2 factors, namely internal and external. Internal factors include aspects originating from individual members of the organization, while external factors relate to the organizational environment and culture within it. Internal and external factors are interrelated in increasing OCB. Internal factors include aspects originating from individual members of the organization which include Dispositional Variables, Organizational Service, Organizational Commitment, Personality Variables, and Work Centrality. External factors relate to the organizational environment and culture within it, which include Workplace Variables, HRM Policies \& Practices, Culture Values, Contextual Factors, Organizational Reputation Treats, Demographic Variables, and Leader Supportiveness. Conclusion: These twelve factors influence the high level of Organizational Citizenship Behavior (OCB) in Makassar ethnic nurses at Lanto Dg Pasewang Jeneponto Regional Hospital.

}, keywords = {Hospitals, Makassar Ethnicity, Nurses, Organizational Citizenship Behavior}, doi = {10.5530/pj.2024.16.47}, author = {Sri Yuyun Afrianti and Andi Indahwaty Sidin and Noer Bahry Noor and Syahrir A. Pasinringi and Stang and Ridwan M. Thaha and Anwar Mallongi} } @article {2331, title = {Vaccinium corymbosum: Phenolic Compound Content and Effect of Fruit Extract on Blood Glucose in Healthy Mice}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {August 2024}, pages = {716-725}, type = {Original Article}, chapter = {716}, abstract = {

Introduction: In the context of the increasing prevalence of metabolic diseases such as diabetes, the search for natural compounds with potential impact on glycemic regulation has become a crucial area of research. Among the numerous options available, Vaccinium corymbosum extract, commonly known as "blueberry", has emerged as a promising candidate due to its rich composition of phytochemicals with antioxidant, anti-inflammatory and hypoglycemic properties. The aim of this study was to determine the total phenolic content (TPC) and the activity of Vaccinium corymbosum ("blueberry") fruit extract on glycemia in healthy mice. Methods: The Folin-Ciocalteau method was applied in order to quantify the phenolic compounds and the BE was administered to 25 mice distributed in six groups: control, negative control, experimental-D1- D2-D3, which were administered the BE in doses of 40, 80 and 120 mg/kg b.w. respectively; and insulin group; which were subjected to the glucose tolerance test (GTT) taking blood samples after 30, 60, 120 and 180 minutes. Results: The total phenolic content (TPC) amount found in the berries was 3.79{\textpm}0.06 GAE/dry weight (mg/g) and 18.96{\textpm}0.28 GAE/solution (mg/L). Statistically significant differences were observed between the three doses of BE and the negative control during GTT as well as induced a significant reduction in area under the curve (AUC) compared to the negative control. Conclusions: the three doses of the BE decreased glucose levels being the dose of 40 mg/kg b.w. the one that produced a statistically significant decrease with respect to the doses of 80 and 120 mg/kg b.w. during GTT.

}, keywords = {Animal studies, Blueberry, Hypoglycemic Effect, Insulin, Phenols, Type 2 Diabetes.}, doi = {10.5530/pj.2024.16.121}, author = {Susana Rubio-Guevara and Olga Castillo-Medina and Marleni Villacorta-Zavaleta and Marleni Villacorta-Zavaleta and Dan Altamirano-Sarmiento and Elena Caceres-Andonaire and Matilde Farias and Nayly Chinchay and Claudia Guerrero and Josue Flores and Edgar Vilela and Sidny Nunez and Janina Sernaque and Felipe Pacherres and Gabriela Mena and Maria Trillo and Julio Amayo and Karyn Olascuaga-Castillo} } @article {2438, title = {Visual Mapping and Future Direction of Marine Products Supplementary and Chemotherapy in The Treatment of Breast Cancer. A Bibliometric}, journal = {Pharmacognosy Journal}, volume = {16}, year = {2024}, month = {December 2024}, pages = {1379-1388}, type = {Research Article}, chapter = {1379}, abstract = {

Marine products have gained attention for their potential benefits in the treatment of breast cancer, offering an alternative or supplementary approach to traditional therapies. While they are not intended to replace established medical treatments like chemotherapy or surgery, marine natural products have shown promise in providing symptom relief, enhancing the quality of life, and potentially improving treatment success for breast cancer patients. Studies have explored the use of marine products in conjunction with chemotherapy for their palliative care benefits and as adjuvants to conventional therapies. Marinederived compounds have been investigated for their anticancer properties, including apoptosis induction, anti-proliferative effects, and modulation of signaling pathways involved in breast cancer progression. These natural products offer a complementary avenue for managing breast cancer, potentially enhancing treatment outcomes, and addressing therapeutic challenges. The utilization of marine products in breast cancer therapy dates back to ancient times when various cultures recognized the therapeutic benefits of plants, herbs, and marine resources. The purpose of this study is to visually map and guide future research on supplementary marine products and chemotherapy in breast cancer based on bibliometric analysis

}, keywords = {Anticancer, Bibliometric, Breast cancer, Chemotherapy, Marine products, Visual mapping}, doi = {10.5530/pj.2024.16.222}, author = {Herin Setianingsih and Nasywa Zahra Sajida Tsuroyya and Prawesty Diah Utami and Riami and Nanang Wiyono} } @article {2131, title = {Accessibility of Mother and Child Health Services to Stunting Incidence in Leti Island, Southwest Maluku District}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {856-860}, type = {Research Article}, chapter = {856}, abstract = {

One of the nutritional problems that can worsen the quality of life of children in achieving growth and development is stunting. Stunting receives greater attention than other nutritional statuses because in addition to a higher prevalence it can also indicate something more serious than just short body size. This type of research is a quantitative study that uses analytic observational with a case control study design to see the effect of the independent variables on the dependent variable. The sampling technique in this study was simple random sampling with a total sample of 164 people, 82 people in the case group and 82 people in the control group. The results of this study indicate that there is an effect between exclusive breastfeeding and health services on the incidence of stunting, while for the basic immunization variable there is no effect on the incidence of stunting. Meanwhile, based on the multivariate test, it was found that the variable that had the most influence on the incidence of stunting was health services. As for suggestions for this research, it is hoped that the Health Service will further improve health services to monitor the growth of toddlers and for mothers of toddlers to visit health services regularly.

}, keywords = {Growth., Health Services, Mother, Stunting, Toddlers}, doi = {10.5530/pj.2023.15.164}, author = {Apia Unmehopa and Sukri Palutturi and Indar and Muhammad Alwy Arifin and Yahya Thamrin and Stang and Anwar Mallongi} } @article {2004, title = {Analysis of Deferred Blood Donor Candidates at Dr. Sardjito Hospital, Yogyakarta, Indonesia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {333-337}, type = {Research Article}, chapter = {333}, abstract = {

Background: The selection of blood donor candidates contributes to the safety of donors and donor recipients. An understanding of the characteristics, demographic characteristics, and types of potential blood donors are essential to obtain an accurate picture of the donor donors, thereby guiding recruitment strategies and providing benchmarks to assess the success of blood donation. Objective: This scientific work aims to analyze the deferred blood donor candidates annually based on the required blood donor characteristics at the Blood Transfusion Unit (BTU) of Dr. Sardjito Hospital, Yogyakarta, Indonesia, from 2017 to 2019. Method: This observational analytic study applied a retrospective design and was conducted at Dr. Sardjito Hospital, Yogyakarta. The data were collected from the donor registration information system and database in the blood request system for the 2017-2019 period. The statistical analysis was conducted using the Chi-Square test in the SPSS version 22. Results: The deferred blood donor candidates in 2017-2019 amounted to 618 (0.82\%) out of 75,067 total blood donors, most of whom were female, reaching an annual percentage of 50.7\% in 2017, 50.9\% in 2018, and 59.1\% in 2019. The age range of both male and female deferred blood donor candidates was 17-30 years. The Hb levels of \< 12.5 g/dL were mostly found in female blood donors, reaching a peak of 82.4\% in 2017, 83.9\% in 2018, and 85.4.6\% in 2019. Voluntary blood donors accounted for 94.7\% (in 2017), 98.6\% (in 2018), and 100\% (in 2019) of the female deferred blood donor candidates. All analytical tests resulted in a p-value of \< 0.0001. Most of the deferred blood donor candidates had blood type O with a p = 0.026. The most common cause of deferral was high or low Hb levels in female blood donors with an age range of 17-30 years. Conclusions: The deferred blood donor candidates in 2017-2019 amounted to 618 (0.82\%) out of 75,067 total blood donors, most of whom were female with the most common deferral reason of Hb levels \< 12.5 g/dL in the age range of 17-30 years.

}, keywords = {Donors rejected, Hemoglobin., Transfusion}, doi = {10.5530/pj.2023.15.50}, author = {Teguh Triyono and Tsaniatul Afifah and Usi Sukorini} } @article {1990, title = {An Analysis of Local Knowledge of Phit-Samdaeng in Yang Sisurat District, Maha Sarakham Province and The Medicinal Plants Used to Relieve Its Symptoms}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {259-265}, type = {Original Article }, chapter = {259}, abstract = {

Introduction: {\textquotedblleft}Phit-Samdaeng{\textquotedblright} is a Thai term often used to refer to an illness of eating unsuitable foods. However, its use in a diagnosis is limited due to the unclear definition and description. This study aimed to compare knowledge of Phit-Samdaeng symptoms and treatments in Northeastern folk medicine, Thai Traditional Medicine, and medicinal plants in the Yang Sisurat District of Thailand. Methods: Semistructured interviews and participatory observations were used to collect data from 12 folk healers. Questions were designed to obtain local knowledge of Phit-Samdaeng and medicinal plants. The data was analyzed using descriptive statistics, comparison and interpretation. Results: Some symptoms of Phit-Samdaeng in the nine scriptures of Thai Traditional Medicine, Tumraya Silajaruek Watprachethupon, and of Kin-Phit and Phit-Kaboon, in Tamraya Boran Isan, were similar in Yang Sisurat. However, the names were different. There were also differences in species and the recipes of herbal remedies among folk healers and in the textbooks. The most used plants to treat Phit-Samdaeng by folk healers were Clerodendrum paniculatum L. and Clausena wallichii Oliv. var. guillauminii (Tanaka) Molino. Only nine species had pharmacological effects relating to Phit-Samdaeng treatment. Conclusions: The knowledge of Phit-Samdaeng symptoms in Yang Sisurat District were consistent with the Northeast folk medicine and Thai Traditional Medicine. The most commonly used species were native plants of Thailand. However, information on the medicinal taste and property from scriptures and pharmacological evidence is lacking. Therefore, the pharmacological activity and toxicity of herbal remedies should be further investigated for efficacy and safety.

}, keywords = {Alternative medicine, Folk knowledge, Herbal medicine, Phit-Samdaeng.}, doi = {10.5530/pj.2023.15.37}, author = {Hatthapan Wipanso and Bhanubong Bongcheewin and Suppachai Tiyaworanant and Suksalin Booranasubkajorn and Natchagorn Lumlerdkij and Pravit Akarasereenont} } @article {2072, title = {Analysis of Lung TB Treatment Strategy in Pangkep District Year 2022}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {524-527}, type = {Original Article }, chapter = {524}, abstract = {

Tuberculosis (TB) is still a world concern with morbidity rates that have not been fully recorded but mortality data continues to increase, so strengthening coordination strategies with various related networks is very important in the target of achieving TB eradication nationally and globally in 2035. This research is a qualitative research carried out to identify phenomena and problems related to pulmonary TB management strategies in Pangkep Regency in October 2022. Data were collected through Focus Group Discussions (FGD), which were then analyzed qualitatively through 3 stages, namely data reduction, data presentation, and data verification as well as drawing conclusions. The results of the study show several important points in the strategy for handling pulmonary TB in Pangkep Regency, namely the applicable policies still follow the policies from the center, access for island areas must have a special strategy, the TB control strategy used is TOSS and there is collaboration between cross-sectors, electronic recording is carried out through SITB and manuals, as well as monitoring and evaluation activities carried out by looking through the system, conducting routine monitoring and evaluation, as well as field visits.

}, keywords = {Policy, Pulmonary Tuberculosis., Treatment strategy}, doi = {10.5530/pj.2023.15.113}, author = {Muhammad Syafar and Ridwan Mochtar Thaha and St. Rosmanely and Rizky Chaeraty Syam and A. Tenri Nurafni Aprilyani} } @article {2196, title = {Analysis of Policy Recommendations in Efforts to Control Positive COVID-19 Cases in South Sulawesi Province, Indonesia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1230-1235}, type = {Research Article}, chapter = {1230}, abstract = {

Introduction: Inconsistent COVID-19 policies have caused the government to experience a degradation in public trust. So, it is necessary to propose policy recommendations for controlling positive COVID-19 cases that receive support from various multi-sectoral areas. Method: This research was conducted in January{\textendash}May 2023. This type of research is qualitative-exploratory, using case study methods through indepth interviews and literature studies of all informants. Sampling was purposive sampling. This research variable uses Patton and Sawicki{\textquoteright}s alternative policy criteria theory (1986). Results: The proposed policy recommendations are increasing COVID-19 vaccine coverage and surveillance for monitoring coronavirus mutations. The two policy recommendations have met technical feasibility because they have clear outcomes, where the outcome of vaccination is to establish herd immunity. In contrast, surveillance of coronavirus mutations has the outcome of analyzing the efficacy of the COVID-19 vaccine. From the economic and financial possibility side, a budget is available with the advantage of carrying out normal activities without any restrictions and efficiency in the health budget. Regarding political viability, the government supports the policy, does not violate the rules, and serves the community{\textquoteright}s needs. Regarding administrative operability, the government as the authorized party is considered to have adequate capability, organizational support, and institutional commitment. Conclusion: The policy recommendations proposed by policymakers and epidemiology experts are increasing COVID-19 vaccination coverage and monitoring surveillance of coronavirus mutations, and it is hoped that the South Sulawesi Provincial Government can consider the proposed policy recommendations.

}, keywords = {COVID-19, Health Policy, Policy Analysis, Surveillance, Vaccination}, doi = {10.5530/pj.2023.15.223}, author = {Sri Nuriana and Balqis and Sukri Palutturi and Indar and Yahya Thamrin and Stang and Anwar Mallongi} } @article {1960, title = {Analysis of The Effect of Leptin, AMPK, Adiponectin, and NPY Markers on Changes in Body Weight of Childhood Epileptic Using Valproic Acid Monotherapy}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {150-153}, type = {Research Article}, chapter = {150}, abstract = {

Introduction: Epilepsy is a neurological disorder that occurs due to abnormal neurons in the brain and an imbalance between excitation and inhibition in the central nervous system. The first line of OAE in children is VPA (Valproate Acid). However, long-term use can cause weight gain with a frequency of 10-70\%. The underlying mechanism of weight gain in patients remains unclear. Purpose: This study aimed to analyze the relationship between levels of biomarkers AMPK, NPY, Leptin, and Adiponectin on changes in body weight in patients with epileptic seizures using VPA monotherapy. Method: This study is an observational cohort design. Data collection in April-June 2019. Inclusion criteria were children aged 2-10 years who used VPA requirement less than two years, not taking any drugs that affect body weight, not diagnose systemic lupus, nephrotic syndrome, and diabetes mellitus. Bodyweight and all biomarkers measurement on subjects who came to the clinic at the time of study and at least after one month of taking VPA. A total of 17 subjects participated in this study. Result: The results of the statistical multivariate analysis test of VPA dosage on changes in body weight and biomarker levels found that Leptin, AMPK, Adiponectin did not significantly increase in body weight (p\>0.05), but NPY significant increase in body weight (p\<0.05). Conclusion: NPY is the most potent for appetite enhancing, preferential effect on carbohydrate intake, weight regulation, energy storage, and expenditure. Increase production of NPY, there is an increase in energy intake and then increases fat storage and body weight.

}, keywords = {Adiponectin, AMPK, Childhood., Epilepsy, Leptin, NPY, Valproic acid, Weight gain}, doi = {10.5530/pj.2023.15.21}, author = {Wardah Rahmatul Islamiyah and Nasronudin and Abdulloh Machin and Iin Ernawati and Yunita Dwi Tanti and Nur Jaya and Farah Medina and Fathia Faza Rahmadanita and Paulus Sugianto} } @article {2124, title = {Analysis of the Phytochemical and Antibacterial Properties of the Indigenous Mizo Medicinal Plant, Helicia Excelsa}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {823-828}, type = {Research Article}, chapter = {823}, abstract = {

Background: Helicia excelsa (Roxb.) Bl. is a scarcely known medicinal plant and is native to Southeast Asia. It is most notably used for the treatment of gastric problems in the Mizo traditional medicine in India. Method: The leaves of H. excelsa were collected from Aizawl, Mizoram, India. An extract was prepared using chloroform. Qualitative phytochemical tests were performed to detect the important phytocompounds. The antioxidant activity was determined by total phenolic content, total flavonoid content, total antioxidant content, DPPH- and ferric-reducing antioxidant power. Antibacterial activity was evaluated by agar well-diffusion method. Results: H. excelsa leaf contains amino acids, alkaloids, carbohydrates, glycosides, phenols, phytosterols, proteins, and tannins. It showed inhibition in selected Gram-negative and Gram-positive bacteria. The phenol, flavonoid and total antioxidant contents were 4.52{\textpm}0.09 gallic acid equivalent (GAE mg/g), 64.27{\textpm}1.04 quercetin equivalent (QE mg/g), 11.39{\textpm}0.45 ascorbic acid equivalent (AAE mg/g) respectively. IC50 value of DPPH-scavenging activity was 5.67{\textpm}0.36. The ferric ion-reducing power showed concentration-dependent activity. The plant extract showed growth-inhibitory actions against Gram-negative bacterium, Escherichia coli, and Gram-positive species, Bacillus cereus and Staphylococcus aureus. :Conclusion H. excelsa leaf contains important bioactive compounds that need to be identified. The antioxidant and antibacterial activities support the basis of its medicinal application.

}, keywords = {Antibacterial activity, Antioxidant, Helicia excelsa, Mizo traditional medicine., Plant extract}, doi = {10.5530/pj.2023.15.157}, author = {Lalbiakngheti Tlau and Lucy Lalawmpuii and P.B. Lalthanpuii and K. Lalchhandama} } @article {2085, title = {Anti-inflammatory Potential of Glycoside Flavonoids from Pterocarpus erinaceus Poir. (Fabaceae) Leaves}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {593-598}, type = {Research Article}, chapter = {593}, abstract = {

Background: Chronic diseases have become one of the leading causes of death worldwide in recent years. Despite tremendous advances in the treatments of diseases, several concerns remain. Those with inflammatory components are alternatively treated or completed in Burkina Faso with medicinal plants. The present study was designed to identify and evaluate the anti-inflammatory potential of glycoside flavonoids from Pterocarpus Erinaceus leaves. Methods: The flavonoids contained in Pterocarpus Erinaceus aerial parts were extracted, identified, and characterized. Sequential soxhlet extraction was subjected to preliminary phytochemical screening, and characterization of isolated flavonoid was done by U.V., I.R., 1H \& 13C N.M.R. and MS. Subsequently, isolates were tested in vitro for their antiinflammatory potential as well as their antioxidant capacities. Results: Five compounds were determined as corresponding to 3{\textquoteright},4{\textquoteright},5,7-tetrahydroxy flavone (luteolin); quercetin-3-O- sophoroside; quercetin- 3-0-β-glucose (isoquercitrin); Kaempferol-3-O-sophoroside and 3,3{\textquoteright},4{\textquoteright},5,7-pentahydroxyflavone-3- rhamnoglucoside (rutin). Concentrations of quercetin-3-O- sophoroside and quercetin-3-0-β-glucose that inhibit 50\% of pro-inflammatory enzymes{\textquoteright} activities were expressed in μg/mL. They were respectively 18.07 {\textpm} 0.78 and 32.27 {\textpm} 2.02 for xanthine oxidase, 1.12 {\textpm} 0.018 and 11.53 {\textpm} 0.52 for lipoxygenase, 26.91 {\textpm} 0.34 and 19.54 {\textpm} 0.25 for acetylcholinesterase. Prevention of the degradation of deoxyribose test gave respectively 19.32 {\textpm} 1.08 μg/mL and 26.21 {\textpm} 2.25 μg/mL for quercetin-3-O- sophoroside and quercetin-3-O- β-glucose while the anti-DPPH free radical potential was 3.41 {\textpm} 0.82 and 2.90 {\textpm} 0.18 μg/ mL. Conclusion: These results may justify the traditional uses of P. erinaceus in treating diseases with an inflammatory component.

}, keywords = {Antioxidant, Compounds, Enzymes, Medicinal plant.}, doi = {10.5530/pj.2023.15.125}, author = {Noufou Ou{\'e}draogo and W. Leila Marie Esther Belem-Kabr{\'e} and A.M. Emmanuel Thiombiano and Tata Kadiatou Traor{\'e} and Lazare Belemnaba and Moussa Ou{\'e}draogo and Innocent Pierre Guissou} } @article {1966, title = {Characterization, Preclinical Efficacy and Toxicity Evaluations of Flavonoids Glycosides based Standardized Fenugreek Seed Extract (FEFLG)}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {90-105}, type = {Original Article }, chapter = {90}, abstract = {

Introduction: Fenugreek seeds, a natural food chain raw material, is known to have many flavonoid glycosides. Objective: Characterization, preclinical efficacy, and safety evaluation of flavonoid glycosidebased standardized fenugreek seed extract (FEFLG). Methods: FEFLG was characterized for a group of flavonoid glycoside marker compounds by HPLC. The CD38+ enzyme inhibition efficacy was assessed in vitro. In addition, acute oral toxicity (AOT) and subchronic, 90-day repeated-dose oral toxicity (in vivo), mutagenicity (AMES test, in vitro) and chromosome aberration test (in vitro) of FEFLG were evaluated. Results: The FEFLG was found to have 49.85\% of total flavonoid glycosides content in FEFLG (25.15\% of Group 1: vitexin, isovitexin and vitexin 2-o- rhamnoside and 24.70\% of Group 2 (vicenin derivatives, schaftoside, iso-schaftoside, orientin and iso-orientin). FEFLG showed CD38+ enzyme inhibition in vitro (IC50= 0.96 μg/ml) equivalent to the positive control, apigenin. FEFLG did not show any toxicity at an acute oral dose of more than 2000 mg/kg (median lethal dose, LD50) with a limit dose of 5000 mg/kg. The 90-day repeated-dose oral administration of FEFLG did not induce significant toxicological changes till the maximum dose of 1000 mg/kg in male and female rats, indicating no observed adverse effect level, NOAEL >= 1000 mg/kg. FEFLG did not show mutagenicity (up to a concentration of 5000 μg/plate) or structural chromosomal aberrations (up to 5000 μg /ml). Conclusion: The CD38+ enzyme inhibitor efficacy in vitro, oral safety in vivo and absence of mutagenicity or genotoxicity of FEFLG indicated its potential for anti-aging applications.

}, keywords = {Acute toxicity, CD38+ enzyme inhibition, Chromosomal aberration., Fenugreek seeds, Flavonoid glycosides, Mutagenicity, Subchronic Toxicity}, doi = {10.5530/pj.2023.15.13}, author = {Prasad A. Thakurdesai and Pallavi O. Deshpande and Mukul P. Pore} } @article {2110, title = {Comparative Evaluation of Microhardness and Color Change of Root dentin using Punica granatum (pomegranate extract), Sodium hypochlorite, Chlorhexidine and Normal saline as an Endodontic irrigant {\textendash} An in vitro study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {732-737}, type = {Original Article}, chapter = {732}, abstract = {

Aim: To evaluate the microhardness and change in color of root dentin using Punica granatum, sodium hypochlorite, chlorhexidine and normal saline as an endodontic irrigant and to implement their use in field of dentistry. Materials and Methods: 60 single rooted anterior teeth extracted due to periodontal and orthodontic reasons were collected. All the samples were decoronated to achieve constant length of 14mm. Patency of root canal was established using 10k file and working length was determined 1mm short of the file length. Each canal was prepared till F3 protaper. After preparation the samples were randomly divided into 4 groups: Group 1: Saline (Control); Group 2: 5\% Sodium Hypochlorite; Group 3: 2\% Chlorhexidine; Group 4: 5\% Punica granatum (pomegranate peel extract). After grouping the samples were longitudinally sectioned. One half of the tooth sample was used for microhardness testing using Vickers microhardness indentor and the other half of sample was used for color change evaluation using spectrophotometer after irrigation with the test solutions on day 1 and day 7th post irrigation. Results: The mean microhardness in all four groups decreased comparatively at post as compared to pre and the decrease was evident highest in sodium hypochlorite followed by chlorhexidine, pomegranate and saline the least. In regard to color change sodium hypochlorite, chlorhexidine and pomegranate all showed visible color changes after 7 day of irrigation with pomegranate showing the highest color change. Higher lightness was shown in Group 2 i.e., sodium hypochlorite whereas redness was seen more in Group 4 i.e., pomegranate and yellowish tint was more visible in Group 3. Conclusion: 5\% Punica granatum has showed negligible effect on microhardness of dentin but showed maximum color change when compared to chlorhexidine, sodium hypochlorite and saline.

}, keywords = {Chlorhexidine., Color change, Endodontic irrigant, Herbal, Microhardness, Punica granatum (pomegranate peel extract), UVVIS spectrophotometer}, doi = {10.5530/pj.2023.15.144}, author = {Ankita singh and Sunil Tejaswi and Kenganora Mruthunjaya and Suneeth Shetty and Ambikathanaya U.K and Sachin B. Manglekar} } @article {2185, title = {A Comparative Study of CFA and MIA Induction Models in Rat Knee Arthritis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1197-1201}, type = {Research Article}, chapter = {1197}, abstract = {

This study presents another comparative review of knee joint arthritis induction in rats using two distinct methods: Complete Freund{\textquoteright}s Adjuvant (CFA) and monosodium iodoacetate (MIA). Different variables are assessed, including bodyweight changes, knee bend scores, and knee diameter measurements, as well as the quantification of interleukin-1β (IL-1β) and C-telopeptide of type II collagen (CTX-II) levels. CFA or MIA induction was used on rats, and 14 days were observed. Our data show that the impact of arthritis induction varies significantly across the two models. Both the CFA and MIA groups showed different changes in terms of bodyweight changes, knee bend scores, and knee diameter variations. Furthermore, the levels of IL-1β and CTX-II, both known indicators of inflammation and cartilage degeneration, were measured. Notably, IL-1β levels in the CFA group were considerably higher than in the MIA-induced rats, although CTX-II concentrations showed a contrary pattern. These findings highlight the need to carefully consider the induction approach when performing arthritis investigations in rats since the model used has a major impact on the reported physiological alterations. This study{\textquoteright}s comparative analysis provides useful information for researchers looking to use rat knee joint arthritis models, laying the groundwork for a better-informed selection of the best induction strategy depending on desired outcome metrics.

}, keywords = {CFA, CTX-II, IL-1β, MIA, Osteoarthritis}, doi = {10.5530/pj.2023.15.217}, author = {Rena Normasari and Bambang Purwanto and Damayanti Tinduh} } @article {2164, title = {Comparison of the Anti-Inflammatory Activity of Flavonoid Bioactive Compounds Acetone Fraction and Steroid Fraction Ethyl Acetate Sungkai Leaves In Vivo and In Silico Studies}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1068-1076}, type = {Original Article}, chapter = {1068}, abstract = {

One of the medicinal plants that is widely used by traditional communities is sungkai (Peronema canescens Jack), which is known to contain secondary metabolite compounds of flavonoids, saponins, tannins, steroids, terpenoids, alkaloids, and phenols. This research aims to isolate secondary metabolite compounds from acetone and ethyl acetate fractions, which act as anti-inflammatory agents in vivo and in silico. Acetone and ethyl acetate fractions were isolated and characterized using UV-Vis and FT-IR. The In Vivo test was carried out on Mus musculus, while the In Silico test was carried out using the IL-10 and IFN-γ receptors, which play a role in inflammation and immunity. Our research results showed that the ethanolic (F1) and n-hexane (F2) fractions of P. canescens extract had good anti-inflammatory activity with percent inhibition values of 58.12\% and 56.59\%, respectively. The characterization results showed that isolate F1 was a flavonoid group, Naringenin compound, while isolate F2 was a steroid group, β-Sitosterol compound. Moreover, from the scoring docking results, β-Sitesterol has tremendous potential as an anti-inflammatory than the compound naringenin.

}, keywords = {Anti-inflamatory; β-Sitesterol; Naringenin, P. canescens Jack}, doi = {10.5530/pj.2023.15.196}, author = {Madyawati Latief and Rahmani and Arliangga Fahrezi and Sutrisno and Indra Lasmana Tarigan} } @article {2108, title = {Decreased Expression of Endocrine Glands Vascular Endothelial Growth Factor (EG-VEGF) in Rat Endometrial After Stimulation with Recombinants FSH Can be Reduce Implantation Rates}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {707-713}, type = {Original Article}, chapter = {707}, abstract = {

Background: Decreased expression of EG-VEGF in human endometrium after administration of ovarian stimulators has been reported to adversely affect endometrial receptivity and low implantation rates. Objective: To determine the effect of recombinant FSH administration on EG-VEGF protein in the endometrium of rats taken in the secretory phase and how it relates to endometrial receptivity. Design: A total of 36 female wistar rats with normal estrous cycles were randomly assigned to the natural cycle group (NC) and two stimulation groups (SC) which were injected with recombinant FSH at 12.5 IU and 25 IU intraperitoneally. Uterine necropsy and blood collection were performed on day 1, day 2, and day 3 after hCG administration. A total of 3 female rats from each group were mated with male rats (two males and three females in one cage). A successful marriage is indicated by the presence of a vaginal plug the next day. The level of EG-VEGF protein expression was assessed by immunohistochemical technique and steroid hormone levels were measured by the Elisa technique. Results: ANOVA test, that the expression of EG-VEGF in the endometrial glands showed a significant decrease from the normal cycle group to the stimulated cycle group 1 (SC 1) and SC2 (P = 0.00), as well as the expression of EG-VEGF in the endometrial stroma. (P = 000). Steroid hormone levels did not show a significant decrease between the normal cycle group and the stimulated cycle group (P = 0.48 and P = 0.13). Conclusion: Decreased EG-VEGF expression in rat endometrium after administration of recombinant FSH is associated with decreased endometrial receptivity which can reduce pregnancy rates.

}, keywords = {EG-VEGF, Endometrial receptivity, rFSH, Secretory phase.}, doi = {10.5530/pj.2023.15.141}, author = {Raden Muharam and Nurhuda Sahar and Kusmardi Kusmardi and Luluk Yunaini and Risqa Novita and Rosalina Thuffi and Conny Riana Tjampakasari and Ponco Birowo and Diyah Kristanty} } @article {1952, title = {Effect of Combination of Soybean and Phaleria macrocarpa Ethanol Extract on IL6, TNFα, VEGF and Fibroblasts in Mice Exposed to UVB}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {6-13}, type = {Original Article}, chapter = {6}, abstract = {

UV exposure causes inflammation and the generation of reactive oxygen species, both of which contribute to skin aging. The purpose of this research was to determine how a combination of Phaleria macrocarpa extract and soybean extract affected the number of fibroblasts, VEGF, IL-6, and TNF alpha expression, and blood levels of IL-6 and TNF alpha in UV-B-exposed mice. In this study, mice were placed into four groups: one control group, three treatment groups, and a combination of Phaleria macrocarpa:soybeans at a 1:1 ratio (com group). The mice were euthanized on days 5 and 21 for histological preparations and then examined under a light microscope. Using an Olympus C-21 microscope with an Optilab Advances camera at 1000x magnification, the fibroblast was studied by counting the number of fibroblast cells per field of view. The immunohistochemical approach was performed to analyze the expression of VEGF, IL-6, and TNF- in skin tissue. The ELISA technique was used to quantify the levels of IL-6 and TNF-alpha. SPSS ver 21 was used to analyze the data. On days 5 and 21, the number of fibroblasts and expression of VEGF, IL-6, and TNF alpha were significantly higher in the combination group than in the control, Phaleria macrocarpa, and soybean treatment groups. However, there was no significant change in IL-6 and TNF alpha levels across groups on days 5 and 21 (p \> 0.05). Finally, a 1:1 mixture of Phaleria macrocarpa and soybeans reduced the number of fibroblasts and the production of VEGF, IL-6, and TNF alpha on days 5 and 21, but not in serum levels.

}, keywords = {Inflammation, Skin wound, UV B radiation}, doi = {10.5530/pj.2023.15.2}, author = {Sumarawati T and Chodidjah and Dina Fatmawati} } @article {1985, title = {Effect of Platelet Concentrates (PCs) Leucodepletion on the Activation and Efficacy of Platelet Transfusion}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {March 2023}, pages = {223-227}, type = {Research Article}, chapter = {223}, abstract = {

Platelet concentrates (PCs) are blood components transfused in thrombocytopenic patients, including patients with blood malignancies. PCs contain leukocytes, which can pose potential side effects and activate platelets, reducing the efficacy of platelet transfusion. The leucodepletion process can be carried out by filtration to reduce the leukocyte count. This study aims to determine the difference between the CD62P expression of nonleucodepleted and leucodepleted PCs and to determine the difference between the Corrected Count Increment (CCI) of patients transfused with nonleucodepleted and leucodepleted PCs. This analytic observational study with a cross-sectional design was carried out on PCs obtained from platelet-rich plasma (PRP-PC). PCs were transfused into 48 blood malignancy patients, Yogyakarta, consisting of two groups i.e the group transfused with nonleucodepleted PCs (24 patients) and the group transfused with leucodepleted PCs (24 patients). CD62P expression in PCs was measured by flow cytometry method, and the CCI of the patients was calculated based on the CCI formula. The difference between the median CD62P expression and CCI of the two groups was analyzed using the Mann- Whitney Test with a significance of p\<0.05. The median CD62P expression of the nonleucodepleted and leucodepleted groups were 34.4\% (16.8{\textendash}94.4\%) and 21.7\% (6.2{\textendash}34.0\%), respectively. There was a statistically significant difference between the CD62P expression of the two groups (p = 0.00). The group transfused with nonleucodepleted, and leucodepleted PCs showed respective median CCI of 18.8 x 109/L (2.4{\textendash}94.8 x 109/L) and 14.7 x 109/L (2.4{\textendash}124.0 x 109/L). There was no statistically significant difference between the CCI of the two groups (p = 0.42). It can be concluded that the CD62P expression in the PCs of the leucodepleted group was significantly lower than those of the nonleucodepleted group and that there was no significant difference between the CCI of both groups.

}, keywords = {CD62P, Corrected count increment, Platelet concentrates}, doi = {10.5530/pj.2023.15.33}, author = {Teguh Triyono and Zelly Dia Rofinda} } @article {1995, title = {The Effect of Preconcenption Moringa Leaf Extract Supplementation on Cotinine Serum Levels in Pregnant Women Exposed to Tobacco Smoke}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {290-293}, type = {Original Article }, chapter = {290}, abstract = {

Background: Moringa oleifera is known for its nutrition content, antioxidant and medical benefit. Tobacco smoke contains various toxic substance and can affect the pregnancy. To reduce the tobacco smoke effect on pregnancy outcome good nutrition is needed. Objective: This study aims to assess the effect of Moringa leaf extract on serum cotinine levels in pregnant women exposed to second-hand tobacco smoke. Method: This is an observational study with a prospective cohort study design the study population was pregnant women which were divided by 2 groups, first group received IFA supplements only (n = 30) and the second group receive IFA and Moringa leaf extract supplements (n = 26). The tobacco smoke exposure data collected with questionnaire, and cotinine serum by blood sample. The tobacco smoke exposure and cotinine serum levels were compered between the two groups. Results: The tobacco smoke exposures at home were higher in MO+IFA group pregnant women then the IFA group pregnant women (p\<0,05). The cotinine serum levels in both groups were found not significantly different (p=0,535). These results indicate that pregnant woman with high exposure of tobacco smoke who MO receive have similar cotinine serum levels with the pregnant woman with lower exposure of tobacco smoke. Conclusion: Moringa leaf extract supplementation to pregnant women with high tobacco smoke exposure has serum cotinine levels similar to pregnant women with lower exposure to tobacco smoke.

}, keywords = {Cotinine, Moringa oleifera., Preconception, Tobacco smoke}, doi = {10.5530/pj.2023.15.41}, author = {Haerani Harun and Anwar Daud and Ridwan Amiruddin and M Sabir and Veni Hadju and Anwar Mallongi and Rahma and Miranti and Tamrin Talebe and M. Faris} } @article {2198, title = {The Effect of Ramania Leaves Extract Gel (Bouea macrophylla Griff) on the Number of Osteoblast (in vivo Study of Post Extraction in Wistar Rats (Rattus norvegicus))}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1219-1223}, type = {Original Article}, chapter = {1219}, abstract = {

Ramania leaves extract contains secondary metabolite compounds such as flavonoids, steroids, phenols and terpenoids which can be used as an alternative medicine for socket wound healing. Flavonoids have anti-inflammatory and antioxidant properties that can accelerate wound healing and can stimulate the formation of osteoblasts. Analyzing the differences in the number of osteoblasts in the negative control group, positive control given aloe vera gel 15\% and ramania leaf extract gel 15\% on day 5, 7 and 14. This study used true experimental design with posttest-only control design, using 27 rats divide into 3 groups. The experimental animals were sacrificed on days 5, 7 and 14 for histopathological observations. Two-Way ANOVA test results obtained p value = 0.013 \<0.05, which indicates that there is a significant difference between the use of 15\% ramania leaf extract gel 15\% and the number of osteoblasts on days 5, 7 and 14. Bonferroni{\textquoteright}s Post Hoc test showed a difference. The number of osteoblasts was significant among the negative control group with ramania leaf extract gel 15\%. Ramania leaf extract gel 15\% was proven to be able to increase the number of osteoblasts and has the potential as an alternative medicine for socket healing after tooth extraction.

}, keywords = {Bouea macrophylla Griff, Flavonoids, Osteoblast, Ramania leaf extract gel, Secondary metabolite, Tooth extraction}, doi = {10.5530/pj.2023.15.221}, author = {Irham Taufiqurrahman and Siti Hajar Norma Gupita and Beta Widya Oktiani and Isyana Erlita and Andi Zulkifli and Veni Hadju and Anwar Mallongi and Eko Suhartono} } @article {2049, title = {The Effect of Safety Climate on Safety Behavior with Safety Motivation as An Intervening Variable on Contractor Workers in PT X}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {411-416}, type = {Research Article}, chapter = {411}, abstract = {

Safety climate in the workplace and safety behaviour of workers need attention to be able to assess what factors are the causes of safe action for workers. This study aims to determine the effect of safety climate on safety behaviour with safety motivation as an intervening variable on contractor workers at PT X. The type of research is analytical observational with a cross sectional design. Questionnaires were given to 380 respondents. The data were analyzed using path analysis to see the direct and indirect effects of safety climate on safety behaviour. The results showed, 361 respondents (95\%) with good safety climate, 367 respondents (96.9\%) with good safety motivation, and 348 respondents (91\%) with good safety behaviour. The path analysis showed that there was no direct influence of safety climate on safety behaviour in contractor workers at PT X (p value \>0.05). However, the safety climate indirectly affects safety behaviour through safety motivation (p value = 0.001). It is recommended to workers that they need to maintain and increase their motivation so the safe work behaviour will still create.

}, keywords = {Contractor workers, Path analysis., Safety behaviour, Safety climate, Safety motivation}, doi = {10.5530/pj.2023.15.93}, author = {Darius Tandiabang and Syamsiar S. Russeng and Lalu Muhammad Saleh and Atjo Wahyu and Yahya Thamrin and Anwar Mallongi} } @article {2133, title = {The Effectiveness of SI-DINI Mobile App (an Education and Early Detection of Leprosy App) on Changes in Community Behavior}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {868-872}, type = {Research Article}, chapter = {868}, abstract = {

Most leprosy case detection in Indonesia is based on passive surveillance. This condition impacts the high number of new cases of leprosy and the disability rate of leprosy. Data from the Ministry of Health of the Republic of Indonesia stated that for 2021, there were 7,201 new cases of leprosy with a disability proportion of 84.6\%. The community{\textquoteright}s reluctance to make early contact is due to low knowledge and fear of stigma. SI-DINI is an android-based application that contains information about leprosy, videos on identifying the characteristics and symptoms of leprosy, and reporting suspected leprosy so that it is hoped that it can change people{\textquoteright}s behavior in a positive direction. This study aims to see the effectiveness of the SI-DINI App in changing people{\textquoteright}s behavior. This study used a quasi-experimental design with a pre and post-test design with intervention and control groups. The use of the SI-DINI App has been proven effective in changing people{\textquoteright}s behavior in terms of knowledge, attitudes and actions. There is a significant increase in the knowledge aspect with p-value = 0.000 (p\<0,05), the attitude aspect p-value = 0.000 (p\<0,05), and the action aspect p-value = 0.000 (p\<0,05). It is hoped that the application of education and surveillance for early detection of leprosy (SI-DINI) can be applied on a broader scope and can be used sustainably and in the future.

}, keywords = {Attitude, Behavior., knowledge, Leprosy, SI-DINI App}, doi = {10.5530/pj.2023.15.166}, author = {Maspa Lapui and Wahiduddin and Ida Leida Maria and A Arsunan Arsin and Ridwan M Thaha and Syamsuar Manyullei and Anwar Mallongi} } @article {2179, title = {Elucidating the Use of the Plant Paeonia Anomala from the Ancient Medical Books Kept in Mongolia}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1163-1165}, type = {Research Article}, chapter = {1163}, abstract = {

Background: It is important to determine and study in detail the action of the main chemical and secondary components contained in Paeonia anomala against diseases. In particular, it is of great practical significance to clarify the use of the plant from ancient medical books and scriptures and to determine which of the six main diseases were used in traditional medicine. Purpose: To compare the information of the ancient medical books written by Mongolian doctors and scientists, who wrote about Paeonia anomala L. and to clarify the taste, potency, strength, and quality. Research materials and methods: Research materials: Sumbe khamba Ishbaljir. {\textquotedblleft}gso dpyad bdud rtsi {\textquoteright}i chu rgyun gyi cha lag gi nang tshan gyi sman so so{\textquoteright}i mngon brjod dang ngos {\textquoteright}dzin shel dkar me long{\textquotedblright}. Wooden printing block with Tibetan script. Toin Jambaldorj. {\textquotedblleft}gso byed bdud rtsi{\textquoteright}i {\textquoteright}khrul med ngos {\textquoteright}dzin bzo rig me long du rnam par shar ba mdzes mtshar mig rgyan zhes bya ba bzhugs so{\textquotedblright}. Wooden printing block with Tibetan script. Research methods: Methods of textual analysis for ancient medical books and checklists were used in the study. Conclusion: The use of Paeonia anomala has been enriched with indications for use in traditional Mongolian medicine, Mongolian folk medicine, Russian folk medicine, and Chinese, Japanese, and Korean traditional medicine. In his book "ngos {\textquoteright}dzin shel dkar me long", the ancient medical scientist Sumbe khamba Ishbaljir wrote the name of the Paeonia anomala plant in Sanskrit as shogandha and in Tibetan as baspru. On the other hand, Toin Jambaldorj noted in his book "mtshar mig rgyan" wrote Paeonia anomala has a warm and equable quality, thus it can create potency. Therefore, it is appropriate to note that this plant in traditional Mongolian medicine is mainly used to treat back pain caused by cold conditions, chronic kidney disease, arthritis, uterine benign tumors, and bladder stones.

}, doi = {10.5530/pj.2023.15.211}, author = {Ariunjargal Tudev and Sansarkhuyag Enkhtur and Khurelbaatar Luvsan and Odontuya Gendaram and Bold Sharav and Ulambayar Lkhamsuren} } @article {2138, title = {Elucidating the Uses of the Plant Veronica Incana from the Ancient Medical Books}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {901-904}, type = {Research Article}, chapter = {901}, abstract = {

Background: Medicinal plant research has been successfully carried out in the field of pharmacy and pharmacology in Mongolia, and dozens of research projects are still being carried out. However, there are still fewer studied medicinal plants of practical importance growing in Mongolia. Therefore, there is a need to register and study the ancient medicinal books written by ancient Mongolian doctors about the relatively little-studied Veronica Incana plant. In addition, taking into account that scientific research on Veronica Incana, which grows in Mongolia, has not been done in the field of medicine. Therefore, the topic was selected for research in this field. Purpose: Comparing the information of the ancient medical books written by Mongolian doctors and scientists, who wrote about Veronica Incana, to clarify the taste, power, and quality. Research materials and methods: 1. Research materials: Sumbe khamba Ishbaljir. gso dpyad bdud rtsi {\textquoteright}i chu rgyun gyi cha lag gi nang tshan gyi sman so so{\textquoteright}i mngon brjod dang ngos {\textquoteright}dzin shel dkar me long. Wooden printing block with Tibetan script. Toin Jambaldorj. gso byed bdud rtsi{\textquoteright}i {\textquoteright}khrul med ngos {\textquoteright}dzin bzo rig me long du rnam par shar ba mdzes mtshar mig rgyan zhes bya ba bzhugs so. Wooden printing block with Tibetan script. 2. Research methods: Methods of textual analysis for ancient books and checklist methods were used in the study. Conclusion: Gandhabhatra plant is used in traditional Mongolian medicinal practices from ancient times, the plant is called Veronica Incana in Latin. Also called Buural gandbadraa in Mongolian. On the other hand, the traditional medical doctors of China{\textquoteright}s Inner Mongolia and Tibet use Gandbadraa, the Latin name Gnaphalium affine D. Don. The appearance, shape, and color of the flowers of these two plants are different. According to the research of the source, the main instruction and usage of the plants are the same: to destroy benign tumors, to remove poison, to treat colds, and to stop cough.

}, keywords = {Ancient medicinal books., Medicinal plants, Traditional Mongolian medicine, Veronica Incana}, doi = {10.5530/pj.2023.15.171}, author = {Sansarkhuyag Enkhtur and Ariunjargal Tudev and Tungalag Dagdanbazar and Selenge Erdenechimeg and Odontuya Gendaram and Ulambayar Lkhamsuren and Bold Sharav} } @article {2123, title = {Evaluation of In vivo Analgesic and Anti-inflammatory Activity of Oroxyulum indicum, Baicalein, Chrysin with Phytochemical Analysis and Molecular Docking Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {811-822}, type = {Research Article}, chapter = {811}, abstract = {

Background: Oroxyulum indicum (OIE) is a native medicinal plant that has been widely employed in Ayurvedic medicine for thousands of years. Though studies have been published citing the analgesic and anti-inflammatory activity of Oroxyulum indicum and chrysin and Baicalein, there has been no comparative study comparing their activittes and confirming them with molecular docking results. Molecular docking study of two phytochemicals Chrysin (PubChem CID 5281607) and Baicalein (PubChem CID 5281605) into the active sites of cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2). Evaluation and validation of Anti-inflammatory and Analgesic effects of a methanolic extract of the stem bark of Oroxylum indicum and its two constituents Chrysin and Baicalein in Charles foster rats with analysis of the phytoconstituent of Oroxyulum indicum through HRMS analysis. Methodology: UHPLC-HRMS/MS analyses were performed on a Dionex Ultimate 3000 RS Series UHPLC system combined with a Q Exactive Plus High-Resolution Accurate Mass Spectrometry System. Hot plate and Tal flick model are used for screening of analgesic activity. TNF-alpha and IL-6 inflammatory markers were examined. Carrageenan model is used for antiinflammatory analysis. Result: Interesting results has been obtained in the docking studies of Chrysin and Baicalein with COX-1 (PDB ID: 1EQG). The hydrogen bond interaction established between the Chrysin and Baicalein with the important amino acid, includes Arg 120, Tyr 355, Ser 530, Met 522 (Figure 1). The binding free energy of the Chrysin and Baicalein with target COX-1 was found to be -7.88 and -7.26 Kcal/mol. Conclusion: There is marked reduction in the TNF Alpha expression in the OIE group which is followed by Baicalein and Chrysine. The Baicalein group shows the most marked cumulative increase in reaction time for tail flick among all the groups of the intervention group followed by Chrysine and OIE.

}, keywords = {Baicalein, Chrysine, Molecular docking, Oroxylum indicum, TNF alpha.}, doi = {10.5530/pj.2023.15.156}, author = {Bhairav Kumar Pathak and Kamlesh M. Palandurkar and Meenakshi Singh and Anshuman Trigunayat and Amit Singh and Reena Giri and Kiran Rajendra Giri} } @article {2060, title = {Experiences and Expectations of Post-Partum Mothers Toward Psychosocial Nursing Services for Mothers Who Have Experienced Postpartum Blues in City of Balikpapan}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {471-478}, type = {Review Article}, chapter = {471}, abstract = {

After giving birth, the mother feels happy to finally be able to meet her beloved baby. However, some mothers actually do not feel happy but appear feelings of sadness, anxiety, and depression after giving birth. As many as 30-75 present of women can experience baby blues after giving birth and one in seven women can experience postpartum depression. Health Education needs to be improved and Nutrition for pregnant women needs attention Micronutrients prevent postpartum depression so that babies are born healthy. Based on the above problems that are still untouched by promotion and prevention health for women overcome the level of emotional anxiety from pregnancy to post-delivery which can be experienced by mothers from mild, moderate to severe. Nurses play a key role related to providing physical and psychological care to support the improvement of the mother{\textquoteright}s condition towards more positive. Mothers are at risk for natural emotional problems requiring someone to be able to give him an understanding of the process he is going through and help him to remain in a more stable condition. This study involved seven participants with diverse characteristics and provided an overview and the high need of postpartum mothers to feel comfortable so that their coping efforts could be achieved so that they did not experience emotional problems after giving birth.

}, keywords = {Baby Blues, Depression, Postpartum, Psychosocial Services.}, doi = {10.5530/pj.2023.15.104}, author = {Ns. Grace C Sipasulta and Indah Nur Imamah and Genevieva E Tanihatu} } @article {2174, title = {Experimental Study of Development Food Safety Booklet using Local Language}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1132-1135}, type = {Research Article}, chapter = {1132}, abstract = {

To prevent food poisoning in Indonesia, it is necessary to have health promotion efforts in the field of food safety using appropriate media. Therefore, this study aims to develop food safety information media, namely local language booklets. For this reason, this study examines the validity and feasibility of local language food safety booklet. The research was conducted in Gorontalo Province from August to October 2022. The development of booklet is done by validating and trial. Validation was carried out using the DELPHI technique with experts in a qualitative descriptive research type. After that, a trial of the booklet was carried out with 20 Village Food Safety Cadres by distributing trial questionnaires and short interviews. Data analysis in this study used content analysis techniques. The results of the validity and feasibility of the local language food safety booklet show that the booklet is very feasible to use. Furthermore, it is hoped that further research can examine the effectiveness of using booklets to convey food safety messages to the wider community.

}, keywords = {Booklet, Cadre, Food Safety}, doi = {10.5530/pj.2023.15.206}, author = {Ridwan Mochtar Thaha} } @article {2156, title = {Factors Affecting the Occurrence of Diarrhea in Infants Aged 7-12 Months in Puskesmas Alak Kupang City}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1024-1028}, type = {Original Article}, chapter = {1024}, abstract = {

Diarrhea is a disease characterized by changes in the consistency of stools to liquid accompanied by an increase in the frequency of defecation more than usual \> 3 times / day accompanied by changes, with or without blood and or mucus. Factors that cause diarrheal disease are infections, infections can be caused by bacteria, parasites and viruses. Busy parents often pay less attention to health and the impact of an unhealthy environment. The three children have digestive problems, which are still considered a habit and can be cured without having to go to a health facility. The purpose of this study was to identify and analyze the factors that influence the incidence of diarrheal disease in infants aged 7-12 months at the Alak Health Center, Kupang City. The type of research used is an analytical survey with a case control design. The population in this study was divided into case populations, namely all infants aged 7-12 months totaling 137 infants and controls were infants aged 7-12 months who did not experience diarrhea totaling 8,868 infants. Determination of the size of the control sample using a ratio of 1:1 with the case sample so that the number of control samples is the same as the case sample, namely 37 infants and the total sample is 74 infants. The sampling technique is simple random sampling. Analysis of the data used is the chisquare test. The results showed that there was a significant relationship with a history of premature birth (p-value = 0.015 with an odds ratio = 3.434), low birth weight (p-value = 0.015 with an odds ratio = 4.563), exclusive breastfeeding (p-value = 0.015 with an odds value ratio = 3.434), immunization status (p-value = 0.004 with odds ratio = 4.265) and history of allergies (p-value = 0.004 with odds ratio = 4.083) with the incidence of diarrheal disease at the Alak Health Center, Kupang City. Suggestions that health center health workers need to be able to increase prevention efforts from an early age by approaching the community and providing concrete education related to the incidence of diarrhea.

}, keywords = {BBLR, Diarrhea, Exclusive breastfeeding, Immunization Status, Premature}, doi = {10.5530/pj.2023.15.188}, author = {Deviarbi Sakke Tira and Sonyalin Buifena and Sigit Purnawan and Maria Magdalena Dwi Wahyuni and Marni Marni and Anwar Mallongi} } @article {2153, title = {Immunization During the Covid-19 Pandemic}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1005-1009}, type = {Original Article}, chapter = {1005}, abstract = {

Objectives: This Study Aims to Analyze the Determinant Factors Associated with Basic Immunization Services for Infants Aged 1-12 Months in Banjarbaru City During the Covid 19 Pandemic. Methods: The Research Design Is an Analytic Research with A Cross Sectional Approach. The Independent Variables Are Mother{\textquoteright}s Knowledge, Mother{\textquoteright}s Anxiety, And Accessibility to Health Facilities, And the Dependent Variable Is Basic Immunization Services. The Research Sample Consisted Of 100 Respondents Who Had Babies Aged 1-12 Months in The Cempaka Health Center, Sungai Ulin Health Center, Sungai Besar Health Center and South Banjarbaru Health Center. The Sampling Technique Was Non-Probability Sampling, Namely Purposive Sampling. The Instruments Used Were A Knowledge Questionnaire, An Anxiety Questionnaire (Dass) And an Accessibility Questionnaire in The Form of a Google Form. Analysis Using the Chi Square Statistical Test. Results: The Results Showed That 58 People (58.0\%) Had Basic Immunization Services According to Age, 44 People (44.0\%) Had Good Knowledge And 55 People (55.0\%) Had Accessibility to Health Facilities. Variables Related to Basic Immunization Services in Banjarbaru City Were Knowledge (P=0.03) And Anxiety (P=0.01). Another Variable in This Study, That Is Accessibility to Health Services, Was Not Related to Basic Immunization Services in Banjarbaru City (P=0.80). Conclusions: It Is Recommended That Basic Immunization Information and Services Be More Proactive. Health Promotion Uses an Interpersonal Approach in The Community to Increase Knowledge, Attitudes and Change People{\textquoteright}s Behavior.

}, keywords = {Accessibility, Anxiety, Health Center, Immunization, knowledge}, doi = {10.5530/pj.2023.15.185}, author = {Yuniarti and Rusmilawaty and Tri Tunggal and Norlaila Sofia and Nur Rohmah Prihatanti and Ahmad Rizani and Anwar Mallongi} } @article {2199, title = {The Impact of Kaempferia galanga L. Extract on Nerve Growth Factor Expression in A Rat Model of Traumatic Brain Injury}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1236-1243}, type = {Research Article}, chapter = {1236}, abstract = {

Introduction: Head injuries contribute significantly to morbidity and mortality globally, and there is need of effective treatment. This study focuses on evaluating NGF (Nerve Growth Factor) expression in a rat model of traumatic brain injury, exploring the potential therapeutic effects of Kaempferia galanga L. extract. Methods: Male Wistar rats were used in the experiment, and traumatic brain injury was induced using Marmarou{\textquoteright}s weight drop model. Four groups of rats were studied: a negative control group, a group with traumatic brain injury without Kaempferia galanga L. extract, and two groups with traumatic brain injury treated with different doses of Kaempferia galanga L. extract. Rats were divided further based on the time of decapitation, either 24 or 48 hours post-injury. NGF expression was assessed using immunohistochemistry. Results: The study confirmed NGF expression variations among groups, with stronger expression observed 48 hours post-injury in rats receiving 1200 mg/kgbb of Kaempferia galanga L. extract. This suggests a potential impact of the extract on NGF expression, likely attributed to its anti-inflammatory and antioxidant properties. Discussion: Kaempferia galanga L. extract has known anti-inflammatory and antioxidant effects, which may contribute to increased NGF expression observed in this study. Conclusion: This study sheds light on the potential benefits of Kaempferia galanga L. extract in promoting NGF expression and improving outcomes in traumatic brain injury, emphasizing the need for further investigation to translate these findings into clinical practice.

}, keywords = {kaempferia galanga, Nerve Growth Factor, Traumatic Brain Injury}, doi = {10.5530/pj.2023.15.224}, author = {Muhammad Fauzan Jauhari and Lucia Yovita Hendrati and Agus Turchan and Asra Al Fauzi and Budi Utomo and Eko Agus Subagio} } @article {2103, title = {Improving the Quality of Assessment and Diagnosis in Nursing Care: A Literature Review}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {703-706}, type = {Review Article}, chapter = {703}, abstract = {

Nursing care involves a series of interactions between nurses with clients and the environment to meet their needs and ensure independence in caring for themselves. Therefore, this research aimed to examine how to improve the quality of assessments and diagnoses in nursing care. Several articles were obtained from Google Scholar, Pubmed, and ProQuest databases, while the research questions were structured using the PICO method and search keywords. The inclusion criteria included articles focused on the quality of assessments and diagnoses in nursing care, applied to health institutions and services, and published in English from 2018-2022. A total of six articles were included after thorough identification, screening, eligibility, and inclusion. The results obtained can be used to improve the quality of assessments and diagnoses in nursing care.

}, keywords = {Nil}, doi = {10.5530/pj.2023.15.140}, author = {Brajakson Siokal and Ridwan Amiruddin and Tahir Abdullah and Yuliana Syam and Sukri Palutturi and Hasnawati Amqam and Rian Adi Pamungkas and Wahyuningsih and Samsualam and Sudarman and Akbar Asfar and Andi Mappanganro}, editor = {Yahya Thamrin} } @article {2061, title = {The Influence of Effective Nurse Communication Application on Patient Satisfaction: A Literature Review}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {479-483}, type = {Review Article}, chapter = {479}, abstract = {

Communication is an important element for building trust and comfort in nursing, and it is the foundation of the nurse-patient relationship. The purpose of this study is to find out how effective communication influences nurses{\textquoteright} perceptions of patient satisfaction. A recent literature review was conducted using the Pubmed, Wiley Online, and Science Direct electronic databases. The review method uses the terms and expressions of the keywords "effective communication," "nurse," and "patient satisfaction." Based on the screening results for inclusion and exclusion criteria, a literature search turned up 10 studies. Effective communication provided by nurses greatly affects patient satisfaction; the better effective communication is carried out, the greater the patient satisfaction will be. With patient satisfaction, nurse communication can improve service by creating good cooperative relationships and fostering trust so as to improve patient recovery. Not only with patients, but effective communication must also be carried out with colleagues and other professions by applying several methods such as ISBAR, PCC, and MCA communication methods. Therefore, health services, especially nurses, should pay more attention to effective communication with patients and implement this effective communication in nursing care activities.

}, keywords = {Effective communication, Nurses, Patient satisfaction.}, doi = {10.5530/pj.2023.15.105}, author = {Brajakson Siokal and Ridwan Amiruddin and Tahir Abdullah and Yahya Thamrin and Sukri Palutturi and Erniwati Ibrahim and Yuliana Syam and Rian Adi Pamungkas and Samsualam and Andi Mappanganro and Wahyuningsih and Anwar Mallongi} } @article {2135, title = {The Investigation of The Network Pharmacology and Mechanism of Action of Centella Asiatica Extract on The Atopic Dermatitis Model}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {881-890}, type = {Research Article}, chapter = {881}, abstract = {

Background: Atopic dermatitis (AD) is a chronic relapsing inflammatory skin condition which has a negative impact on children health. The well-known medicinal plant Centella asiatica extract (CE) is used in herbal skin care products to produce various pharmacological effects in dermatology. However, the molecular target of CE in suppressing inflammatory is largely unknown. Objective: the aim of this study was to examine anti-inflammatory properties and network pharmacology of CE in lipopolysaccharide (LPS)- induced AD in vitro model. Method: RAW264.7 cells were pre-treated with CE and then were stimulated with LPS and then were investigated cell viability, NO production, and the levels of pro-inflammatory mediators. In addition, the Search Tool for Retrieval of Interacting Genes (STRING), SwissTargetPrediction and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to construct the defined mechanism of action and network pharmacology. Results: CE showed the potent inhibitory effects on LPS-induced NO. In addition, CE significantly suppressed the expression of iNOS and COX-2, as well as the production of IL-2, IL-6, IL-10, and TNF- α. Furthermore, the network pharmacological analysis revealed the potential role of CE in biological processes such as regulating JAK/STATs pathway and inhibiting proinflammatory cytokines both of which were linked to AD pathogenesis. Conclusion: Our findings confirm our hypothesis that CE could be developed as a therapeutic therapy for atopic dermatitis due to its pharmacological action and signaling mechanism in the modulation of allergic skin inflammation.

}, keywords = {Atopic dermatitis, Centella asiatica, Network pharmacology, Skin inflammation.}, doi = {10.5530/pj.2023.15.168}, author = {Sucharat Tungsukruthai and Runtikan Pochairach and Aungkana Krajarng and Piracha Jumpa-ngern and Parunkul Tungsukruthai} } @article {2047, title = {Model Prediction of Potential Disease Effects from PM2.5 Emission Among School Children in Coming 30 years in South Tangerang}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {400-404}, type = {Research Article}, chapter = {400}, abstract = {

Background: The largest global environmental health risk factor is the ambient of air pollution, that largely attributed to transportation emissions. One of the main causes of PM2.5 emissions is thought to be onroad transportation. PM2.5 has an impact on health, especially on children that relate to the respiratory system such as asthma, lung cancer, and decreased intelligence. Objective: The research objective was to predict the risk potential disease due to PM2.5 in children from vehicle emissions in South Tangerang City. Method: This research is an observational analytic study with a cross-sectional study design using a dynamic model approach using STELLA software. The environmental and human samples aare used to calculate the exposure level to PM2.5 taken from 32 points in 7 sub-districts of South Tangerang City (North Serpong, Serpong, Pondok Aren, Ciputat, East Ciputat, Pamulang, and Setu). then, meteorological data was also collected. Results: The number of vehicles in the city of South Tangerang is quite high, especially between 11:00 and 15:00 with the majority of vehicles passing by are cars and motorbikes. PM2.5 pollution levels will fluctuate until 2053. The effects of temperature, weather, and humidity might cause an increase in PM2.5 pollutants at specific times. According to the modeling calculation results, even though there are occasions when PM2.5 pollution levels fall, acute respiratory infection (ARI) incidence in children will continue to rise over time. Although PM2.5 emissions fluctuate, exposure to PM2.5 in low concentrations poses a risk to human health.

}, keywords = {Acute respiratory infection., Children, Particulate matter, Transportation}, doi = {10.5530/pj.2023.15.91}, author = {Ernyasih and Anwar Mallongi and Anwar Daud and Sukri Palutturi and Stang and Razak Thaha and Erniwaty Ibrahim and Wesam Al Moudhun} } @article {2117, title = {Phytochemical Profile, Antioxidant and Antibacterial Activity of the Essential Oil of Luma Chequen (Molina) A. Gray from Peru}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {777-780}, type = {Original Article}, chapter = {777}, abstract = {

Background: Luma chequen belongs to Myrtaceae family and it is known as {\textquotedblleft}arrayan{\textquotedblright}. In the traditional medicine from Peru, L chequen is used as aromatic plant, anti-inflammatory and hypocholesterolemic. Objective: To determine the phytochemical profile, evaluate the antioxidant and the antibacterial activity of L. chequen essential oil. Material and Methods: In the analysis of the volatile components a Gas Chromatography coupled to Mass Spectrometry (GC-MS) was used to identify the content of terpenes and sesquiterpenes. 2,2-diphenyl-1-picrylhydrazyl (DPPH) was the method used to determine the antioxidant activity and obtain the half inhibitory concentration (IC50). For the antibacterial activity, a colorimetric macrodilution method was carried out to evaluate the effect of the essential oil of L. chequen against Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922. Results: The analysis by GC-MS showed two major components alpha-pinene (62.89\%) followed by 1,8-cineole (11.94\%), and propanoic acid, 2-methyl-, 2-methylpropyl ester with 8.67\%. In the antioxidant activity against DPPH radical, the essential oil of L. chequen showed an IC50 equivalent to124.60 {\textpm} 2.0 μg/mL. In the antibacterial activity, L. chequen had an MIC (minimum inhibitory concentration) for Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922 of 4.35 {\textpm} 0 μg/mL and 8.71 {\textpm} 0 μg/mL respectively. Conclusion: L. chequen presented monoterpene compounds as main phytoconstituents as well as antioxidant and antibacterial activity in vitro. The essential oil might be used as antimicrobial agent in the future overall against S. aureus.

}, keywords = {Antibacterial., Antioxidant, Aromatic plant, Essential oil, Luma chequeen, Medicinal plant}, doi = {10.5530/pj.2023.15.151}, author = {Julio Luis D{\'\i}az-Uribe and Mar{\'\i}a Elena Salazar-Salvatierra and Julio Reynaldo Ruiz-Quiroz and Oscar Herrera- Calderon and Eddie Loyola-Gonzales and Freddy Emilio Tataje-Napuri and Jos{\'e} Francisco Kong-Chirinos} } @article {2007, title = {Phytochemical Screening, Antibacterial Activity and Fatty Acids from Heliotropium Indicum}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {April 2023}, pages = {350-352}, type = {Research Article}, chapter = {350}, abstract = {

Heliotropium indicum are used in ethnomedicine for treating skin rashes, inflammation, tumors and various diseases of microbial origin. Previous work focused on phytochemical constituents, antibacterial activities and isolated compounds. The whole plant was air dried and pulverized (600 g). It was extracted with ethanol and concentrated to dryness in vacuo (20 g). Screening for phytochemical groups was performed using qualitative methods. The antibacterial activity was performed using agar diffusion and antifungal activity using ditch plate method. Compounds were characterized using Gas-chromatography Mass Spectrometry. The results of the phytochemical screening revealed the presence of phenols, saponins, terpenoids and cardiac glycosides. The results further showed the crude extract of the plant to be moderate to strong antibacterial activity with zones of inhibition ranging from 12.0 + 1.6 mm and 25 +1.7 mm. the crude extracts of Heliotropium indicum demonstrated antibacterial properties which confirmed the traditional use of this plant in treating skin rashes and boil. In addition, the presence of Palmitate and Linoleic acid I the plant as revealed in this study justified the use of this plant in treating hypertension.

}, keywords = {Antibacterial activity, Gas-Chromatography Mass Spectrometry, Heliotropium indicum, Phytochemical.}, doi = {10.5530/pj.2023.15.53}, author = {Idowu and Olajumoke Tolulope} } @article {2170, title = {Role of 1,25(OH)2D On Cytochromes CYP27A1 and CYP27B1 in Periodontitis: A Clinical Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1112-1115}, type = {Research Article}, chapter = {1112}, abstract = {

Background: Vitamins have a great impact on metabolis. Aims: To determine the role of 1,25(OH)2D On Cytochromes CYP27A1 and CYP27B1 in Periodontitis. Material and Method: The investigation was carried out on 45 participants of ages within the range of (30-45 years) who were attending the private dental clinics. Diagnosis of chronic periodontitis was established depending on dental history, clinical examinations (periodontal indices). All participants were examined by the same dentist. They were classified into three groups: Group 1 (control negative): (15) participants with normal serum vitamin D3 level and with pocket depth <=3 mm, good oral health and normal periodontal tissues and no previous history of periodontal diseases. Group 2 (control positive): (15) participants with normal serum vitamin D3 level and periodontitis with pocket depth >=5 mm, they received placebo medication orally, Group3(treatment): (15) participants with vitamin D3 deficiency (below 30 IU), and periodontitis with pocket depth >=5 mm, they received oral Vitamin D3 fast acting liquid soft gel capsule 2000 IU /day for 3 months. 3 blood samples were taken from each participant at 0,45,90 days, for research examinations. CYP27A1, CYP27B1 serum levels was measured for each sample in three groups by ELISA kit. Result: there was a highly significant reduction in CYP27A1 serum level in the treatment group at the ninety days of the study while there was no significant elevation CYP27B1 serum level in all groups during 45,90 days of the study. Conclusion: The present study suggested that the 1,25(OH)2D has effects on serum levels of both Cytochromes CYP27A1 and CYP27B1 and this was associated with periodontitis.

}, keywords = {CYP27, Cytochrome, Periodontitis, Vitamin D}, doi = {10.5530/pj.2023.15.202}, author = {Asmaa Y Thanoon and Faehaa Azher Al-Mashhadane} } @article {2149, title = {Safety Assessment of Supplementation with Cymbopogon citratus Stapf. (Lemongrass) Extract in Patients with Chronic Kidney Disease Stage 3: A Preliminary 90-Days Prospective Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {976-986}, type = {Original Article}, chapter = {976}, abstract = {

Background: Chronic kidney disease is a major public health issue, and due to resource constraints, many can{\textquoteright}t access dialysis. C. citratus, lemongrass is globally prevalent and known to increase urine output without toxicity. Objective: To examine the safety of C. citratus in patients with CKD stage 3. Materials and Methods: The major compound of C. citratus was analyzed using high-performance liquid chromatography (HPLC). 64 patients were enrolled and randomly assigned to control or C. citratus groups. The control group received a placebo, whereas the C. citratus group received 900 mg of C. citratus daily for 90 days. All participants were examined BUN, Scr, Cys-C, and eGFR, liver functions, RBC, HCT, Na+, K+, Cl-, and HCO3, and other biochemical parameters. Results: HPLC showed C. citratus contains of phenolic compounds. Clinically, C. citratus group had no notable side effects on T-Bil, AST, ALT and ALP. Also, maintained eGFR, SCys-C, K+ and Cl level. The level of blood Na+ was significant increase at day 30 (p \< 0.05). The control group had a significant decrease in eGFR and HCO3 levels (p \< 0.05) and a significant increase of Cl- and SCys-C. In addition, no statistical differences had found between groups in eGFR, BUN, Cr, Na+, K+, HCO3, PO4, RBC and HCT levels. Throughout the 90 days, no drug allergies or side effects were reported. Conclusion: Dietary supplementation with C. citratus may have a favorable effect on delaying the course of CKD and is safe to use for patients with CKD stage 3.

}, keywords = {Chronic Kidney Disease, CKD stage 3, Cymbopogon citratus Stapf., Lemongrass, Safety}, doi = {10.5530/pj.2023.15.181}, author = {Patnaree Wongmanit and Parunkul Tungsukruthai and Pratya Phetkate and Daraporn Rungprai and Sucharat Tungsukruthai and Ouppatham Supasyndh and Kusuma Sriyakul} } @article {2053, title = {Tanacetum Parthenium (L.) Sch Bip From Peru: Antioxidant Profile and The Antinociceptive Effect in An Experimental Model}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {June 2023}, pages = {435-437}, type = {Research Article}, chapter = {435}, abstract = {

Background: Tanacetum parthenium (L.) Sch Bip known as {\textquotedblleft}santa mar{\'\i}a{\textquotedblright} (Asteraceae family) is used in Peru for inflammatory diseases and also in colic, stomachache, headaches, diarrhea, among other. Objective: The aim was to determine the antioxidant profile, and analgesic effect of ethanolic extract of flowers and leaves of T. parthenium Material and Methods: Leaves and flowers of T. parthenium were soaked in 96\% ethanol and the obtained extract was analyzed using chemical reactions for identifying each secondary metabolite, 2,2-Diphenyl-1-picrylhydrazyl (DPPH) was used to determine the antioxidant capacity, and the antinociceptive effect was determined by using tail flick method. Results: Qualitative phytochemical study indicates the presence phenolic compounds, alkaloids, flavonoids, saponins and steroids in both extracts. In DPPH assay IC50 showed in leaves and flowers extract 452.10 {\textpm} 10.2 μg/mL and 270.70 {\textpm} 20.6 μg/mL respectively. The antinociceptive effect was better in leaves at doses 300 mg/ Kg than flower extract. Conclusions: The ethanolic extract of flowers of T. parthenium showed a high antioxidant activity and antinociceptive effect in mice.

}, keywords = {Analgesic, Antioxidant, Medicinal Plants., Polyphenols, Tanacetum parthenium}, doi = {10.5530/pj.2023.15.97}, author = {Oscar Herrera-Calderon and Wilfredo Bulege-Guti{\'e}rrez and Luz Alexandra Javier-Silva and Melva Iparraguirre- Meza and Victor Guillermo Sanchez-Araujo and Elizabeth Julia Melgar-Merino and Johnny Aldo Tinco-Jayo and Jos{\'e} Santiago Almeida-Galindo and Josefa Bertha Pari-Olarte} } @article {1858, title = {Analysis of LH Receptor Expression in the Testes of Infertile Azoospermic Non-Obstructive (NOA) Men at High Serum Prolactin Concentrations}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {462-468}, type = {Original Article}, chapter = {462}, abstract = {

Background: Hyperprolactin is one of the endocrine disorders that causes male infertility (11\%). The mechanism is not widely known; it is thought to occur through disruption of LH receptor activity on germ cells. Objective: The aim of study to compare the level of prolactin secretion with receptor expression in non-azoospermic infertile men (NOA). Methods: During the period from July 2019 to July 2021, 40 samples of testicular tissue and serum were obtained from infertile NOA men, aged 25-50 years who were recruited from Ciptomangunkusumo Hospital (RSCM) Jakarta, Faculty of Medicine, Universitas Indonesia and Bunda Hospital Jakarta. Subjects were divided into 4 groups based on prolactin levels (20 ng/ml, 20-50 ng/ml, 50-100 ng/ml and 100ng/ml). This group was tested for significance between groups and continued with a correlation test with the level of LH receptor expression. Results: ANOVA test showed a significant decrease in LH receptor expression between prolactin levels \< 20 ng/mL with levels of 50-100 ng/ml and prolactin levels \> 100 ng/ml (P \< 0.05). Furthermore, the results of the correlation test showed a significant decrease between prolactin levels and LH receptor expression (P \< 0.05). Conclusion: The higher the level of prolactin secretion in this sample, there is a decrease in LH receptor expression, so that testosterone production decreases and the spermatogenesis process will be disrupted.

}, keywords = {Hyperprolactinemia, LH receptor expression, Male infertility, Non obstructive azoospermia (NOA).}, doi = {10.5530/pj.2022.14.123}, author = {Ponco Birowo and Nurhuda Sahar and R. Muharam and Dwi Ari Pujianto and Rosalina Thuffi and Kusmardi Kusmardi and Conny Riana Tjempakasari} } @article {1763, title = {Anti-Ulcer Activity of Spray-dried Powders Prepared from Aerial Parts Extracts of Ampelopsis cantoniensis}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {276-281}, type = {Original Article}, chapter = {276}, abstract = {

Introduction: Ampelopsis cantoniensis is called {\textquotedblleft}Che day{\textquotedblright} in Vietnam and has been used as a traditional treatment for inflammatory diseases. Methods: Plant material and hydroalcoholic extract were processed and analyzed for their physicochemical characteristics. A method using HPLC was validated to quantify ampelopsin. Hydroalcoholic extract was spray dried and the powder obtained was characterized in terms of its physicochemical parameters and potential for antiulcerogenic activity. Results: The analytical method proved to be selective, linear, accurate, sensitive. A. cantoniensiss pray dried extract (ACP) was obtained using colloidal silicon dioxide as adjuvant and was shown to possess 25.94 \% ampelopsisn. It showed significant antiulcer activity in a model of an indomethacin-induced gastric lesion in rats and also produced a gastroprotective effect.

}, keywords = {Ampelopsis cantoniensis, Antiulcer, Spray drying, Vitaceae}, doi = {10.5530/pj.2022.14.34}, author = {Duc Minh Nguyen and Quang Canh Tran and Minh Trung Do and Duc Thinh Pham and Thi Hong Hanh Le and Duy Bac Nguyen and Van Thu Nguyen} } @article {1783, title = {Anxiolytic and Antidepressant-like Effects of Foeniculum vulgare Essential Oil}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {425-431}, type = {Research Article }, chapter = {425}, abstract = {

Introduction: The aim of this research was to determine the anxiolytic and antidepressant-like effects of the essential oils from Foeniculum vulgare aerial parts and seeds. Methods: The oils were extracted by hydro-distillation using a modified Clevenger-type apparatus and chemical composition was performed by Gas chromatography with flame-ionization detection (GC-FID) and Gas chromatography-mass spectrometry (GC{\textendash}MS). Furthermore, an experimental trial was conducted, where 117 participants were divided into three groups, comprising a waiting list control group and two experimental groups treated with essential oils. The anxiety and depression indexes were evaluated by Zung Self-Rating Anxiety Scale (SAS) and Zung Self-Rating Depression Scale (SDS). Results: chemical analysis showed that trans- Anethole was the main component, both in the essential oil from aerial parts (35.5\%) and seeds (79.2\%). Anxiety and depression scores showed a decrease in posttest study phase in comparison with pretest in all experimental groups (p\<0.05), except for depression scores in the group treated with essential oil from aerial parts (p\>0.05). Small changes were found in the case of anxiety for group treated with essential oils from aerial parts (d = 0.41; Δ= 0.40) while moderate (d = 0.86; Δ = 0.85) and small (d = 0.38; Δ = 0.39) changes were found for anxiety and depression respectively, in the group treated with essential oil from seeds. Conclusion: The essential oil from Foeniculum vulgare seeds is more effective to relief anxiety than depression while the essential oil from Foeniculum vulgare aerial parts only exhibit small changes for anxiety.

}, keywords = {Anxiety, Depression, Essential oils, Foeniculum vulgare}, doi = {10.5530/pj.2022.14.54}, author = {Paul Alan Arkin Alvarado-Garc{\'\i}a and Maril{\'u} Roxana Soto-V{\'a}squez and Luis Enrique Rosales-Cerquin and Elda Maritza Rodrigo-Villanueva and Demetrio Rafael Jara-Aguilar and Lurdes Tuesta-Collantes} } @article {1870, title = {Artificial Sweeteners Perturbed Liver Enzymes in Rat Model}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {553-557}, type = {Research Article}, chapter = {553}, abstract = {

In the recent time there has been an increased demand of low-fat or low calorie diet universally. In the mean while the availability of low calorie products has also increased like sugar free drinks, beverages, biscuits, jams and jellies. On contrary to this, some studies suggest that the prolong use of non-nutritive sweeteners alters the homeostasis of glucose and insulin. It results in fluctuation of glucose level in blood and increase in bodyweight. This study intends to evaluate the effect of non-nutritive sweeteners on the liver function test and record the alteration in the levels of ALP, AST and ALT. Seventy rats were divided into seven equal groups, controlled group received distilled water and the rest six were given NNS Sucrose, Stevia, Sucralose, Saccharine Aspartame and Acesulfame-k, respectively. On the evaluation of Alanine aminotransferase ALT, saccharine and aspartame markedly increased the level of ALT from 40U/L to 80 U/L. Both of these NNS have shown the most raised level of Alanine aminotransferase. This represents the stress on the liver associated with the use of NNS and suggests the use to be controlled in humans.

}, keywords = {Albumin, Artificial Sweeteners, Bilirubin, Liver Enzyme}, doi = {10.5530/pj.2022.14.135}, author = {Muthear N Dawood and Shaymaa AH. Jassim and Maab Azmi Fadel and Imad A. Thanoon} } @article {1841, title = {Bioactive Compounds from Purslane (Portulaca oleracea L.) and Star Anise (Illicium verum Hook) as SARS-CoV-2 Antiviral Agent via Dual Inhibitor Mechanism: In Silico Approach}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {352-357}, type = {Original Article }, chapter = {352}, abstract = {

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the COVID-19 pandemic that infects humans and attacks the body{\textquoteright}s immune system. The purpose of the study was to identify the potential of bioactive compounds in purslane (Portulaca oleracea L.) and star anise (Illicium verum Hook) via a dual inhibitor mechanism against SARS-CoV-2 proteases with an in silico approach. The samples were obtained from PubChem and RSCB PDB. Antivirus probability prediction was performed on PASS Online. Virtual screening was performed with PyRx via molecular docking. Visualization was used by PyMol and Discovery Studio. Compounds with the best antiviral potential are indicated by the low binding affinity value to the target proteins, namely SARS-CoV-2 TMPRSS2 and PLpro. The results showed that purslane luteolin has the best antiviral potential. However, further studies are required to validate this computational prediction.

}, keywords = {Antiviral agent, Illicium verum Hook, in silico, Portulaca oleracea L., SARS-CoV-2}, doi = {10.5530/pj.2022.14.106}, author = {Nur Sofiatul Aini and Viol Dhea Kharisma and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Rasyadan Taufiq Probojati and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Dony Novaliendry and Riso Sari Mandeli and Budhi Oktavia and Muhammad Thoriq Albari and Saddam Al Aziz and Muhammad Raffi Ghifari and Okta Suryani and Putri Azhari and Muhammad Arya Ghifari and Devi Purnamasari and Agariadne Dwinggo Samala and Mirella Fonda Maahury and ANM Ansori and Rahadian Zainul} } @article {1747, title = {Comparative Effects of Amlodipine and Candesartan on Blood Pressure and Metabolic Profile in Non-Diabetic Hypertensive Patients}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {February 2022}, pages = {141-147}, type = {Original Article}, chapter = {141}, abstract = {

Introduction: The present study aimed to compare the effects of the angiotensin II receptor blocker candesartan and the calcium channel blocker amlodipine on blood pressure and metabolic profile in nondiabetic hypertensive patients. Methods: The study involved non-diabetic patients with mild to moderate hypertension. They were randomly assigned to receive candesartan or amlodipine for 24 weeks, parameters were evaluated at baseline and after 12 weeks and 24 weeks for each patient group. Results: Candesartan and amlodipine both reduced blood pressure and the HOMA-IR index significantly (P \< 0.05, 24 weeks vs. baseline). Candesartan was more effective than amlodipine in lowering blood pressure and HOMA-IR, although the difference was not significant statistically. Conclusion: Both candesartan and amlodipine are extremely effective at reducing blood pressure in moderate hypertension patients. Candesartan cilexetil has a major benefit in terms of tolerability, as it reduces the risk of developing metabolic dysregulation.

Key words: Amlodipine, Candesartan, Hypertension, Insulin resistance.

}, doi = {10.5530/pj.2022.14.19}, author = {Zeina A Althanoon and Imad AJ Thanoon} } @article {1913, title = {Correlation of the Presence of Non Structural-1 (NS1) Antigen Dengue Virus with Severity of Dengue Infection}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {813-816}, type = {Research Article }, chapter = {813}, abstract = {

Dengue is a major public health threat worldwide, affecting approximately 3 billion people. More than 100 countries in the world located in tropical and subtropical areas, there are at least 100 to 400 million people infected with the dengue virus which causes dengue hemorrhagic fever (DHF). Soluble Non Structural Protein (sNS1) DENV is a soluble NS1 protein that is secreted and found in the serum of patients during acute infection. Because of its presence early in infection, sNS1 is used as a diagnostic indicator of acute dengue infection. NS1 can directly activate platelets through TLR4 and can further increase platelet aggregation, endothelial cell adhesion, and phagocytosis by macrophages that can cause thrombocytopenia so that high sNS1 levels are associated with disease severity. From the results of the study showed p \<0.05. This indicates that there is a correlation between the presence of NS1 and the severity of dengue infection.

}, keywords = {Dengue virus, NS1 antigen, Thrombocytopenia}, doi = {10.5530/pj.2022.14.172}, author = {Ichwan Baihaki and Beti Ernawati Dewi and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Muhammad Badrut Tamam and Devi Purnamasari and Nunuk Hariani Soekamto and ANM Ansori and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Vikash Jakhmola and Maksim Rebezov and Pavel Burkov and Marina Derkho and Pavel Scherbakov and Rahadian Zainul and Muhammad Raffi Ghifari and Asmi Citra Malina AR Tasakka and Tengku Siti Hajar Haryuna} } @article {1777, title = {Cytotoxic Effects of Kirinyuh Herb (Austroeupatorium inulaefolium (Kunth) R. d. King \& H. Robinson) Extracts and Fractions on BSLT, MCF-7 Cells and T-47D Cells}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {374-378}, type = {Research Article }, chapter = {374}, abstract = {

Breast Cancer is the second-highest prevalence of cancer disease in Indonesia, with the number of new cases and deaths continues to increase. Kirinyuh or Austroeupatorium inulaefolium (Kunth) R. D. King \& H. Robinson is a shrub plant, which are widely grown in Indonesia. Traditionally, it is used for woundhealing and information about anticancer potential of A. inulaefolium is still very limited. This study aims to assess the potential of cytotoxic activity of A. inulaefolium on MCF-7 and T-47D breast cancer cells. Tests that carried out in this study were phytochemicals screening, Brine Shrimp Lethality Test (BSLT) and Cytotoxicity assay. The phytochemicals screening showed that EA (leaves extracts levels 1-3), EB (leaves extracts levels 4-6) and EC (stalk extracts) contained tannin, steroids/triterpenoids, flavonoids and phenols. The BSLT results showed that the EB has the smallest LC50 value of 12.86 μg/mL. MTT assay results showed the smallest IC50 value of the extract and the fraction on MCF-7 cells were EA 204.96 μg/ mL and FEA 205.43 μg/mL and T-47D cells were EB 217.03 μg/mL and FEA 192.36 μg/mL. The conclusion of toxicity and cytotoxicity of the herb (leaves and stalks) ethanol 96\% extracts of A. inulaefolium had a very toxic effect on BSLT however had less potential cytotoxicity on MCF-7 cells and T-47D cells.

}, keywords = {BSLT, Cytotoxicity, Kirinyuh (Austroeupatorium inulaefolium (Kunth) R. D. King \& H. Robinson), MCF-7, T-47D}, doi = {10.5530/pj.2022.14.48}, author = {Riskianto and Andreanus Andaja Soemardji and Marselina Irasonia Tan} } @article {1772, title = {Determination Antioxidant Activity of Coffea Arabica, Coffea Canephora, Coffea Liberica and Sunscreens Cream Formulation for Sun Protection Factor (SPF)}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {335-342}, type = {Research Article }, chapter = {335}, abstract = {

Coffee is a highly consumed and popular beverage consumed in many countries. Its ingredients have a powerful antioxidant capacity and have the potential as sunscreen to protect the skin. This study aimed to examine the antioxidant activity of Arabica, robusta and liberica coffee extracts and the SPF activity of the coffee extract cream formulation. Coffee were macerated with three types of solvents with polarity gradients. The fraction of each coffee was analyzed for antioxidant activity using DPPH and formulated into the cream. Furthermore, the cream was analyzed for its SPF activity. The results of this study indicated that the methanol fraction of Robusta and Arabica coffee has the best antioxidant activity with IC50 values of 8.98 (ppm) and 13.13, respectively. Meanwhile, Liberica coffee has the best antioxidant in the ethyl acetate fraction, IC50 = 10.90 (ppm). In addition, the best SPF values for Robusta, Liberica and Arabica coffees were found in F3 cream with the category of Very Good Protection; 36.087 {\textpm} 0.0005; 35.007 {\textpm} 0.0005; 36,867 {\textpm} 0.0005 respectively.

}, keywords = {Antioxidant, Coffee, Cream, SPF}, doi = {10.5530/pj.2022.14.43}, author = {Madyawati Latief and Muhaimin and Heriyanti and Indra Lasmana Tarigan and Sutrisno} } @article {1831, title = {The Effect of Omega-3 Rich Fish Oil on the Kidney Changes in Mice Induced by Azoxymethane and Dextran Sodium Sulfate}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {259-266}, type = {Original Article }, chapter = {259}, abstract = {

Background: The study aimed to investigate the effect of omega-3 rich fish oil to kidney of mice induced by Azoxymethane (AOM) and DSS using histopathology parameters. Method: The experimental mice were induced using 10 mg/kg AOM and 2\% DSS for 2 weeks randomly allocated randomly into four groups as follows; Control Group: mice that not received fish oil, Low Dose Group: mice that received 1.5 mg/day fish oil, Medium Dose Group: mice that received 3 mg/day fish oil, and High Dose Group: mice that received 6 mg/day fish oil. The omega-3 rich fish oil was given for 12 weeks. Result: The administration of high dose omega-3 rich fish oil was able to reduced necrosis and inflammation foci compared to the control group (p\<0.05). Furthermore, the administration of low, medium, and high dose omega-3 rich fish oil was able to significantly reduced vascular edema and cell degeneration foci (p\<0.05). The administration of medium and high dose of omega-3 rich fish oil were able to reduce the amount of fibrosis foci compared to the control group (p\<0.05) compared to the control group. Conclusion: The result suggested anti-nephrotoxic effect of omega-3 rich fish oil in mice induced by azoxymethane and DSS.

}, keywords = {Azoxymethane, Dextran sodium sulfate, Fish oil, Histopathology, Kidney, Mice, Omega-3}, doi = {10.5530/pj.2022.14.94}, author = {Kusmardi Kusmardi and Paulus Anthony Halim and Wachid Putranto and Aryo Tedjo} } @article {1793, title = {The Effect of Pomegranate Peel Ethanol Extract to TNF-α Expression of Mice Colonic Epithelial Cells Induced Using Dextran Sodium Sulfate (DSS)}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {480-488}, type = {Original Article}, chapter = {480}, abstract = {

Introduction: The conventional drugs for inflammatory bowel disease (IBD) have many side effects that impact patient{\textquoteright}s quality of life, leading to the emergence of alternative therapies such as pomegranate peel ethanol extract (PPE). This study aims to investigate the anti-inflammatory effect of PPE by observing TNF-α expression in mice induced chronic inflammation of the colon using dextran sodium sulfate (DSS). Methods: 28 Swiss Webster mice samples were taken and divided into five groups, the control group (6 mice), the negative control group (5 mice), the group that was given DSS and aspirin (6 mice), the group was given DSS and a high dose of PPE (5 mice), and the group was given DSS and a low dose of PPE (6 mice). In mice, distal colonic tissue was taken and then stained immunohistochemically against TNF-α and observed with light microscopy at 400x magnification, and TNF-α expression was assessed using the H-Score. Results: TNF-α expression was significantly lower in the group given a high dose of PPE than the negative control group (p \<0.05), with mean rank scores of 3.00 and 8.00. There was no significant difference between the group given PPE with a high dose and aspirin (p\> 0.05). Conclusion: TNF-α expression in colonic epithelial cells of mice given DSS decreased upon treatment of a high dose of PPE, indicating a mechanism of decreasing inflammation. PPE also has the same effect as aspirin in reducing inflammation.

}, keywords = {Colonic epithelial cells, Dextran sodium sulfate, Mice., Pomegranate peel ethanol extract, TNF-α}, doi = {10.5530/pj.2022.14.61}, author = {Kusmardi Kusmardi and Raja Yasmin Khalilah and E Zuraidah and Ari Estuningtyas and Aryo Tedjo} } @article {1798, title = {Effects of High Intensity Swimming on Heat Shock Protein 70, Superoxide Dismutase and Malondialdehyde of Rattus norvegicus Male Rats}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {524-530}, type = {Original Article}, chapter = {524}, abstract = {

Introduction: This study aims to analyze relationship between physical activity with high intensity swimming by proving the difference in the mean levels of HSP-70, SOD levels and MDA levels in male white rats (Rattus norvegicus) who perform vigorous-intensity physical activity compared to male white rat (Rattus norvegicus) who do not engage in strenuous physical activity. Method: This research is a laboratory experimental research. This research is a True Experimental Research type that uses a Post Test Only Control Group Design research design. The experimental unit consisted of 28 white rats (Rattus norvegicus). The study was started by dividing the rats into 2 groups. Group 0 who did not receive heavy physical activity treatment and group 1 who received heavy intensity physical activity treatment 3 times a week for 4 weeks. Results: The results of the Shapiro-Wilk test showed that the HSP-70 data were normally distributed (p\<0.05). SOD and MDA data for all groups were normally distributed (p\>0.05). The results of the Kruskal Wallis test showed that there was a significant difference in HSP-70 between groups (p \> 0.05), the results of the Mann Whitney test showed that the HSP-70 of the K0 group was significantly different from the K1 group. The results of the analysis of variance with Brown-Forsythe showed that there was a significant difference in SOD between groups (p \< 0.05). The results of the Games Howell test showed that the SOD of group K0 was significantly different from that of group K1. The results of the analysis of variance showed that there was a significant difference in MDA between groups (p \< 0.05). The results of the LSD test showed that the MDA of the K0 group was significantly different from the K1 group. Conclusion: There is a difference in the mean levels of HSP-70 in white male rat (Rattus norvegicus) whoperform strenuous physical activity, lower than male white rat (Rattus norvegicus) who do not engage in strenuous physical activity. There is a difference in the mean SOD levels in male white rat (Rattus norvegicus) which perform strenuous physical activity, lower than male white rat (Rattus norvegicus) who do not do strenuous physical activity. There is a difference in the mean MDA levels in male white rat (Rattus norvegicus) after doing strenuous physical activity, higher than male white rat (Rattus norvegicus) who do not engage in strenuous physical activity.

}, keywords = {HSP-70, MDA., SOD, Strenuous physical activity}, doi = {10.5530/pj.2022.14.66}, author = {Dody Taruna and Bambang Purwanto and Harianto Notopuro and Widjiati and Budi Utomo and Lilik Herawati and Reny I{\textquoteright}tishom and Aryati} } @article {1819, title = {Evaluation of Antiviral Effects and Toxicity of Herbal Medicine Vipdervir Capsules}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {681-689}, type = {Research Article}, chapter = {681}, abstract = {

Background: Antiviral vaccine is not effective, synthetic antiviral drugs are highly toxic, leading to increased interest in herbal medicines as promising antiviral drugs. Recently, Vipdervir has been developed from medicinal herbs with the aim to support and treat diseases caused by viruses such as H5N1 and SARSCoV- 2. In the present study, we assessed Vipdervir{\textquoteright}s antiviral activity against H5N1 and SARS-CoV-2. In addition, we also evaluated the acute toxicity and repeated dose toxicity of Vipdervir in mice and rabbits, respectively. Methods: H5N1 inhibitory effect of Vipdervir was assessed using hemagglutination inhibition assay. Vipdervir{\textquoteright}s SARS-CoV-2 inhibitory effect was evaluated by Plaque Reduction Neutralization assay. Acute and repeated dose oral toxicities of Vipdervir were determined according to OECD 423 and OECD 407 guidelines, respectively. Results: Data show that Vipdervir is effective against both H5N1 and SARSCoV- 2. At concentrations of 3 mg/mL and 5 mg/mL Vipdervir completely inhibits H5N1. At a concentration of 50 μg/mL Vipdervir showed an inhibitory effect on SARS-CoV-2. Acute toxicity data revealed that the LD50 of Vipdervir is greater than 35200 mg/kg, b.wt. in mice. Repeated toxicity data indicated that Vipdervir did not induce significant differences in body weight gain, hematology and clinical biochemistry in compared to the control group. The No Observed Adverse Effect Level of Vipdervir is greater than 613.8 mg/kg b.wt./day in rabbits. No delayed toxicity effects of Vipdervir were observed. Conclusion: Vipdervir capsules were found to be antiviral effective and relatively safe in the tested doses and experimental conditions.

}, keywords = {Antiviral, COVID-19, H5N1, Herbal, SARS-CoV-2.}, doi = {10.5530/pj.2022.14.87}, author = {Thi-Lien Nguyen and Huong Ha Thi Thanh and Kiet Ngo Tuan and Doan Cao Son and Thao Le Quang and Hang Nguyen Thi and Tien Vuong Duy and Quyen Doan Thi Tam and Huan Le Quang} } @article {1846, title = {Genetic Diversity in Commiphora wightii (Arn.) Bhandari (Guggul): An Assessment of Populations in Conservation Sites of Kachchh Region (Gujarat) of India}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {379-387}, type = {Research Article }, chapter = {379}, abstract = {

Introduction: Commiphora wightii (Arn.) Bhandari (Guggul) is native to semi-arid to arid zones. Its oleoresin gum is used for both medicinal and non-medicinal applications. Reportedly, the species faces high degree conservation threats. A network of Four Medicinal Plants Conservation Areas (MPCA) was carved out in Kachchh region- under financial support from National Medicinal Plants Board. The species also occurs in sanctuary and protected by default. It is considered important to assess genetic diversity of these conserved populations. Methods: A total of 38 accessions of Guggul leaves were collected from five study sites and the whole genomic DNA was extracted for each sample. Genetic study was carried out using ISSR technique. Scorable bands were obtained for 14 out of 40 primers tested. A total of 49 bands were obtained of which 20 were polymorphic in nature. UPGMA dendrograms were constructed for individual sites and also a collective dendrogram for all the study sites. Results: All the 8 accessions of Tharawada MPCA were observed to share a high similarity coefficient. Among rest of three sites, genetic diversity was seen to be narrow. The accessions obtained from NSWS displayed good diversity. These accessions were also noted to be distant to the populations captured in the MPCA sites. Conclusions: Established MPCA sites capture the available gene pool of Commiphora wightii of Kachchh region. Since NSWS populations are distant to rest of the region, it is suggested to create another site for this purpose. It is desirable to assess the genetic diversity in rest of the MPCA sites.

}, keywords = {Gene Pool, Guggulu, In-situ conservation, Medicinal Plants Conservation Area, MPCA, UPGMA}, doi = {10.5530/pj.2022.14.111}, author = {Narasimha Baba Brindavanam and Gurinderjit Singh Goraya and Santosh Pal Singh and Amandeep Kumar and Ankita Tiwari and Badari Narayan Sarvepalli and Pankaj Prasad Raturi} } @article {1808, title = {In Silico Phytochemical Compounds Screening of Allium sativum Targeting the Mpro of SARS-CoV-2}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {604-609}, type = {Research Article}, chapter = {604}, abstract = {

The global pandemic of coronavirus disease is still widely spread across the world causing catastrophic effect in both human life and global economy. By the end of year 2021, it has caused a total of 5.437.636 deaths across the world. Indonesia has rich plant biodiversity including medicinal plants that may be used for combating the virus. One of the commonly used medicinal plants comes from Allium species and it has been proved to have antiviral activity. Conducting an in silico study, we screened bioactive compounds that came from Allium sativum to fight against coronavirus through the inhibition of 3CL-Pro, one of the major protease that have an active role for viral replication. Molecular docking of compounds from Allium sativum to 3CL-Pro resulting in the discovery of 5 compounds that have the best binding affinity to 3CL-Pro, which are squalene, 1,4-dihydro-2,3-benzoxathiin 3-oxide, 1,2,3-propanetriyl ester, trans-13-octadecenoic acid and methyl-11-hexadecenoate with binding affinity of -7, -6.5, -5.9, -5.7 and -5.6 kcal/mol, respectively. It is very likely that these compounds can be candidates for therapeutic agents and these candidates need to be studied further.

}, doi = {10.5530/pj.2022.14.78}, author = {Priscilla Listiyani and Viol Dhea Kharisma and Arif Nur Muhammad Ansori and Muhammad Hermawan Widyananda and Rasyadan Taufiq Probojati and Ahmad Affan Ali Murtadlo and Dora Dayu Rahma Turista and Md. Emdad Ullah and Vikash Jakhmola and Rahadian Zainul} } @article {1873, title = {In Silico Screening of Bioactive Compounds from Garcinia mangostana L. Against SARS-CoV-2 via Tetra Inhibitors}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {575-579}, type = {Research Article}, chapter = {575}, abstract = {

The global COVID-19 pandemic caused by SARS-CoV-2 has been the resulted of massive human deaths since early 2020. The purpose of this study was to determine the potential of mangosteen (Garcinia mangostana L.) as an inhibitor of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an in silico approach. The samples were obtained from PubChem and RCSB PDB. Analysis of the similarity of the drug was carried out with the Swiss ADME on the basis of Lipinski rule of five. Prediction of antivirus probabilities was carried out using PASS Online. Molecular screening was performed using PyRx through molecular docking. Discovery Studio was used for visualization. The bioactive compounds with the highest antiviral potential were indicated with the lowest binding affinity to the targeted proteins RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. The results indicated that mangiferin has the greatest potential as a potential antiviral. However, more research is required to validate the results of these computational predictions.

}, keywords = {Antiviral agent, Garcinia mangostana L., in silico, SARS-CoV-2}, doi = {10.5530/pj.2022.14.138}, author = {Nur Sofiatul Aini and Viol Dhea Kharisma and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Rasyadan Taufiq Probojati and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Elsa Yuniarti and Saddam Al Aziz and Muhammad Raffi Ghifari and Muhammad Thoriq Albari and Riso Sari Mandeli and Muhammad Arya Ghifari and Devi Purnamasari and Budhi Oktavia and Amalia Putri Lubis and Fajriah Azra and Fadhilah Fitri and ANM Ansori and Maksim Rebezov and Rahadian Zainul} } @article {1832, title = {In Silico Screening of Bioactive Compounds from Syzygium cumini L. and Moringa oleifera L. Against SARS-CoV-2 via Tetra Inhibitors}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {267-272}, type = {Original Article }, chapter = {267}, abstract = {

The global pandemic of COVID-19 has caused disastrous consequences for both humans and the economy. The purpose of this study was to determine the potential of juwet (Syzygium cumini L.) and moringa (Moringa oleifera L.) as inhibitors of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an in-silico approach. Samples were obtained from PubChem and RSCB PDB databases. The drug similarity analysis was determined using Swiss ADME and the Lipinski rule of five. Prediction of antivirus probabilities is carried out with PASS Online. Molecular screening is performed by molecular docking using PyRx. Visualization was used using PyMol and Discovery Studio. The bioactive compounds with the best antiviral potential had the lowest affinity bonds to the target proteins against RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. Results show that ellagic acid from java plum and myricetin from moringa have the best potential as potential antivirals. However, more research is required to validate the results of these computational predictions.

}, keywords = {Antiviral agent, in silico, Moringa Oleifera L, SARS-CoV-2, Syzygium cumini L.}, doi = {10.5530/pj.2022.14.95}, author = {Nur Sofiatul Aini and Viol Dhea Kharisma and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Rasyadan Taufiq Probojati and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Devni Prima Sari and Muhammad Thoriq Albari and Devi Pernamasari and Muhammad Arya Ghifari and Muhammad Raffi Ghifari and Riso Sari Mandeli and Muhardi and Budhi Oktavia and Trisna Kumala Sari and Titi Sriwahyuni and Putri Azhari and Mirella Fonda Maahury and ANM Ansori and Rahadian Zainul} } @article {1872, title = {In Silico Study of Entry Inhibitor from Moringa oleifera Bioactive Compounds against SARS-CoV-2 Infection}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {565-574}, type = {Research Article}, chapter = {565}, abstract = {

The aim of this study is to screen the content of bioactive compounds of Moringa oleifera and to identify its potential as an antiviral against COVID 19 through an entry inhibitor mechanism using bioinformatics tools. The sample was obtained from PubChem database. Amino acis sequences were obtained from the NCBI. Protein modeling is made through the SWISSMODEL site. The target proteins for this study were SARS-CoV-2 Mpro and RdRp. The protein-inhibitory interaction of the drug from M. oleifera bioactive compounds to SARS-CoV-2 was predicted by molecular docking with PyRx software. The result shows that M. oleifera was a potential antiviral candidate for SARS-CoV-2 with an entry inhibitor mechanism through a compound, especially quercetin. The RFMS value of both interactions between Mpro and quercetion and RdRp with quercetin were not higher than 1.05. This result still needed further research to prove this prediction.

}, keywords = {Active site, COVID-19, Moringa oleifera, Mpro, RdRp}, doi = {10.5530/pj.2022.14.137}, author = {Nala Mawaddani and Ekris Sutiyanti and Muhammad Hermawan Widyananda and Viol Dhea Kharisma and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Vikash Jakhmola and Syamsurizal and Bayu Ramadhani Fajri and Muhammad Raffi Ghifari and Muhammad Thoriq Albari and Muhammad Arya Ghifari and Amalia Putri Lubis and Dony Novaliendry and Dwi Hilda Putri and Fadhilah Fitri and Devni Prima Sari and Alexander Patera Nugraha and ANM Ansori and Maksim Rebezov and Rahadian Zainul} } @article {1908, title = {Increased Risk of Tumor Necrosis Factor-Alpha Levels in Adult Patients with Malignancy Receiving Non-Leucodepleted Packed Red Cells Transfusion}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {778-781}, type = {Original Article }, chapter = {778}, abstract = {

Background and Objectives: Blood transfusion in patients with malignancy may evoke transfusion reactions. Leukocyte, as a major producer of cytokines, including Tumor Necrosis Factor-alpha (TNF-alpha), is considered to correlate to transfusion reactions. This study aims to determine the risk of increased TNFalpha in adult patients with malignancy who received non-leucodepleted (nLD) erythrocyte transfusion compared to those receiving leucodepleted (LD) Packed Red Cells (PRC) transfusion. Materials and Methods: This quasi-experimental study was conducted on adult patients with malignancy who required PRC transfusion and underwent outpatient treatment. The patients were divided without randomization into nLD and LD groups, and then their pre-transfusion TNF-alpha levels and the post-transfusion changes were examined. Results: This study included thirty-one patients fulfilling the inclusion criteria. The TNFalpha levels in nLD and LD groups after transfusion increased significantly (p \< 0.05), i.e., from 0.81 (0.2 - 4.2) pg/mL and 1.7 (0.15 - 6.3) pg/mL to 10.1 (1.4 - 28.9) and 5.9 (0.95 - 12.9) pg/mL. There was no significant difference in the pre-transfusion median TNF-alpha levels between the nLD and LD groups (p = 0.122). However, the post-transfusion median TNF-alpha levels of the nLD group were significantly higher (p = 0.024). It indicated that the increase in TNF-alpha levels is associated with nLD blood products transfused. The Relative Risk of the increased TNF-alpha levels in nLD-PRC transfusion was 2.01 (95\% Confidence Interval: 1,153-3,502). Conclusion: nLD-PRC transfusion poses a 2.01 times risk for increased TNF-alpha levels compared to LD-PRC transfusion.

}, keywords = {Malignancy, Non-leucodepleted, PRC transfusion, Relative risk, TNF-Alpha}, doi = {10.5530/pj.2022.14.167}, author = {Teguh Triyono and Bambang Hendriawan Prasaja Jati and Usi Sukorini} } @article {1852, title = {Indonesian Medicinal Plants with Anti-inflammatory Properties and Potency as Chronic Obstructive Pulmonary Disease (COPD) Herbal Medicine}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {432-444}, type = {Review Article}, chapter = {432}, abstract = {

Indonesia is a tropical country with mega-biodiversity. Several medicinal plants locally have been recognized for their anti-inflammatory properties and are traditionally used to help treat respiratory diseases. Chronic obstructive pulmonary disease (COPD) is one of the diseases known as the high cause of death globally, and one of the treatment efforts is by using anti-inflammatory drugs. In developing alternative remedies for COPD, this review summarizes the potential of Indonesian medicinal plants and their ingredients known to have an anti-inflammatory activity to develop alternative remedies for COPD. Primarily, we focus on the medicinal plants that have been scientifically proven to pose some biological activities, such as legetan warak (Adenostemma lavenia), celery (Apium graveolens), pegagan (Centella asiatica), kenikir (Cosmos caudatus), and kersen (Muntingia calabura). This review is expected to provide more information about Indonesian medicinal plants and their potencies to be developed as COPD herbal medicine and, further, as a treatment to help patients suffering from coronavirus disease (COVID-19).

}, keywords = {Anti-inflammatory, Bioactive compounds, Biological activity, Chronic obstructive pulmonary disease, Indonesian medicinal plants}, doi = {10.5530/pj.2022.14.119}, author = {Min Rahminiwati and Trivadila and Dyah Iswantini and Hiroshi Takemori and Mamoru Koketsu and Rut Novalia Rahmawati Sianipar and Suminar Setiati Achmadi and Ahmad Sjahriza and Betty Marita Soebrata and Armi Wulanawati} } @article {1905, title = {Isolation of a Flavone Apigenin and a Steroids Squalene from Peronema canescens Jack Leaves with Anti-Inflammatory Activities}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {744-752}, type = {Original Article}, chapter = {744}, abstract = {

The leaves of the P. canescens are ethnobotanically used by the community as a remedy for bruises and fever. This study aims to isolate both of ethanol and n-hexane fractions of P. canescens Jack leaves. Isolate then characterized and determined their anti-inflammatory activity with male white mice. Anti- Inflammatory was determined by the volume of exudate and \% inflammation inhibition. The isolates with good anti-inflammatory activity were characterized using UV-Vis and IR spectrophotometry. Our findings showed that the ethanolic (F1) and n-hexane (F2) fractions of P. canescens extract had a good anti-inflammatory activity with percent inhibition values of 58.12\% and 56.59\%, respectively. The characterization results showed that isolate F1 was a flavonoid group, Apigenin compound, while isolate F2 was a steroid group, Squalene compound.

}, keywords = {Anti-inflammatory., Apigenin, P. canescens, Squalene}, doi = {10.5530/pj.2022.14.162}, author = {Indra Lasmana Tarigan and Sutrisno and Rumaida and Indah Pramana Sari Aini and Madyawati Latief} } @article {1926, title = {Kaempferia galanga L. Extract Administration Attenuate Aquaporin-4 Expression in Traumatic Brain Injury: An Experimental Study in Rats}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {893-897}, type = {Original Article }, chapter = {893}, abstract = {

Introduction: Traumatic brain injury (TBI) is still a major health problem in the world. It might cause long-term disability that affect socio-economic life and become nation health burden. Post-traumatic cerebral edema might develop and commit to an unfavorable prognosis. Aquaporin 4 (AQP4) is water channel protein and a key regulator of water metabolism in the brain. Although the mechanism of AQP4 in the regulation of post-traumatic brain edema remains controversial, AQP4-lacking mice show better survival and decreased brain edema. Thus, novel strategies that suppress AQP4 become a potential field. We hypothesized that Kaempferia galanga L. may suppress brain expression of AQP4 following TBI and possibly limit the development of cerebral edema due to its neuroinflammation properties. Method: We conducted TBI to experimental rats, then given Kaempferia galanga L. extract at a dose of 600 mg/kg BW and 1200 mg/kg BW. Evaluation intensity of AQP4 expression by immunohistochemistry was performed 24 and 48 hours later to see its therapeutic effect. Results: Administration of Kaempferia galanga L. extract at a dose of 1200 mg/kg BW showed weak expression of AQP4 in all samples, both 24 and 48 hours following traumatic brain injury treatment. Conclusions: Intensity of AQP4 expression in rats{\textquoteright} brain was lower at 24 and 48 hours after TBI in rats receiving Kaempferia galanga L. extract with dose 1200 mg/ kg BW compared to the other groups. Our result indicates that Kaempferia galanga L. might affect the expression of brain AQP4 in a dose-dependent manner.

}, keywords = {Ayuverdic medicine, Neuroinflammation, Neurotrauma, Post-traumatic cerebral edema}, doi = {10.5530/pj.2022.14.185}, author = {Fajar Herbowo Niantiarno and Agus Turchan and Myrna Adianti and Budi Utomo and Muhammad Arifin Parenrengi and Abdul Hafid Bajamal} } @article {1779, title = {Mechanism of the Bioactive Sargassum cristaefolium in Inhibiting Inflammatory Mediators in a Nitroglycerin-Induced Migraine Model in Rats}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {388-396}, type = {Research Article }, chapter = {388}, abstract = {

Background: Migraine headaches are a form of sterile neurogenic inflammation. The sterile inflammatory process of the trigeminal nerve releases the vasoactive neuropeptide CGRP which stimulates the release of inflammatory mediators. In the incidence of migraine there is an increase in TNF-α and IL-10. Sargassum cristaefolium ethanol extract contains flavonoids, alkaloids, triterpenoids, steroids, and tannins, which has analgesic and anti-inflammatory function. Method: Sargassum cristaefolium was extracted using maceration method with 70\% ethanol as solvent. Animal models were divided into 5 groups and given NTG induction 5 times with 1 day intervals, treated for 3 weeks. All data were analyzed using IBM SPSS version 26.0. Results: Sargassum cristaefolium ethanol extract - CGRP levels β: -0.26, p: 0.17; Sargassum cristaefolium ethanol extract - CGRP expression β: -0.04, p: 0.85; Sargassum cristaefolium ethanol extract - TNF-α levels β: -0.63, p: 0.01; Sargassum cristaefolium ethanol extract - TNF-α expression β: -0.40, p: 0.04; Sargassum cristaefolium ethanol extract - IL-10 levels β: 0.77, p: 0.00; Sargassum cristaefolium ethanol extract - IL-10 expression β: 0.45, p: 0.01. Conclusions: A significant path between the administration of Sargassum cristaefolium ethanol extract and a decrease in TNF-α and an increase in IL-10. But the effect of giving Sargassum cristaefolium ethanol extract on CGRP levels did not have a significant relationship.

}, keywords = {Inflammatory mediator, Migraine, Nitroglycerin, Sargassum cristaefolium}, doi = {10.5530/pj.2022.14.50}, author = {Olivia Mahardani Adam and Jusak Nugraha and Muhammad Hamdan and Agus Turchan} } @article {1910, title = {Nano Transdermal Delivery Potential of Fucoidan from Sargassum sp. (Brown Algae) as Chemoprevention Agent for Breast Cancer Treatment}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {789-795}, type = {Research Article }, chapter = {789}, abstract = {

Conventional chemotherapy substances are associated with mild to severe side effects that affect both healthy and cancer cells. It is presumed to improve therapeutic efficacy in coexistence reducing chemotherapy{\textquoteright}s side effects. Fucoidan is an anticancer bioactive compound derived from Sargassum sp. that has low cytotoxic activity. The purpose of this study was to explore the effectiveness of anticancer activities of fucoidan from Sargassum sp. against breast cancer then analyze the suitability of nano transdermal patch of fucoidan and blueprint the long-term research design of nano transdermal patch as a chemoprevention agent in the chemotherapeutic management of breast cancer. This research was performed through a literature study and in silico study by imposing carbonic anhydrase IX (CA IX) as a marker of hypoxia and metastatic state of cancer cells. The results showed that the fucoidan from Sargassum sp. effectively induced apoptosis and prevented metastasis of breast cancer cells through the Bcl-2, Bcl-w, and bad pathways. Fucoidan, in addition, was predicted to inhibit CA IX by Glu4 Glu5, Leu7, Pro8, and Asp6 residues. Therefore, the delivery of fucoidan is favored to have a local effect on the site of breast cancer cells by nano transdermal patch preparations using fucoidan nanoparticle polymer. Further nano transdermal patch development as a treatment for breast cancer is suggested through the stages of formulation optimization, optimum formula activity testing, patent filing, and distribution in health services.

}, keywords = {Anticancer, Breast cancer, Fucoidan, Nano transdermal, Sargassum sp. .}, doi = {10.5530/pj.2022.14.169}, author = {Syeftyan Muhammad Ali Hamami and Michelle Fai and Ahmad Fariduddin Aththar and M Nizam Zulfi Zakaria and Viol Dhea Kharisma and Ahmad Affan Ali Murtadlo and Muhammad Badrut Tamam and Vikash Jakhmola and Muhammad Hermawan Widyananda and Dora Dayu Rahma Turista and Maksim Rebezov and Nikolai Maksimiuk and Nataliya Kulmakova and Evgeniya Latynina and ANM Ansori and Rahadian Zainul and Riso Sari Mandeli and Devi Purnamasari and Oski Illiandri and Khoirun Nisyak and Ernarisa Fitri} } @article {1856, title = {Nephrotic Syndrome with Focal Segmental Glomerulosclerosis Histological Feature: A Case Report}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {August 2022}, pages = {459-461}, type = {Case Report}, chapter = {459}, abstract = {

Introduction: Nephrotic syndrome is a clinical syndrome of heavy proteinuria and hypoalbuminemia or hypoproteinemia. Renal biopsy is fundamental to assess not only the type but also the degree of disease activity. The overall prognosis and response to treatment often depend on the severity of histological lesions and their reversibility.1,2 Case Presentation: An eighteen years old man with nephrotic syndrome and planned for a kidney biopsy. This case showed a patient with swollen face (especially on the cheek). On Biopsy results showing the glomerulus proliferation of cells and mesangeal matrix, adhesions in (50\%) glomerulus, focal sclerosis in some glomeruli, erythrocyte cells visible in the urinary space and thickening of the basement membrane in some glomeruli, partially atrophic tubules, visible erythrocytes in the tubular lumen. Conclusion: An eighteen years old man with nephrotic syndrome with cushing syndrome and hypokalemia who had a renal biopsy. The histological feature from the renal biopsy was focal segmental glomerulosclerosis. The underlying cause of FSGS is still unclear. Assessing the diagnosis and etiology become important to direct the subsequent clinical approach and therapy

}, keywords = {Focal segmental glomerulosclerosis, Nephrotic syndrome, Renal biopsy}, doi = {10.5530/pj.2022.14.122}, author = {Dian Samudra and Widodo and Nunuk Mardiana and Artaria Tjempakasari and Pranawa and Aditiawardana and Anny Setijo Rahaju} } @article {1769, title = {Pasuchaca (Geranium ruizii Hieron.): A Medicinal Plant of the Geraniaceae Family with Hypoglycemic Effect on Alloxan-Induced Hyperglycemia in Mice}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {315-321}, type = {Original Article}, chapter = {315}, abstract = {

Objective: The current study aims to evaluate the hypoglycemic effect of the hydroalcoholic extract of Geranium ruizii on alloxan-induced hyperglycemia in albino mice. Material and Methods: Geranium ruizii was collected in Huancayo, Junin, Peru. A phytochemical analysis was carried out to confirm the chemical groups. In the pharmacological study, hyperglycemia was induced with alloxan at doses of 170 mg/kg in male albino mice, animals with blood sugar levels above 250 mg/dL were included in the protocol. Mice were randomized into five groups (I: Alloxan 170 mg/Kg; II, III and IV (Geranium ruizii extract: 50; 150 and 300 mg/Kg body weight); and V: glibenclamide, 5mg/Kg B.W. Results: Phytochemical analysis confirmed the presence of tannins, flavonoids, alkaloids, terpenes, saponins and phenolic compounds. It is observed that at doses of 50, 150 and 300 mg/kg reduced blood glucose at 14 days of treatment. Conclusion: The hypoglycemic effect of the hydroalcoholic extract of Geranium ruizii, administered orally in mice with alloxan-induced hyperglycemia was effective with 150 mg/Kg body weight.

}, keywords = {Antidiabetic drugs, Antioxidants, Geranium ruizii, Herbal therapy, Medicinal plants, Pasuchaca}, doi = {10.5530/pj.2022.14.40}, author = {Oscar Herrera-Calderon and Renan Dilton Ha{\~n}ari-Quispe and Johnny Aldo Tinco-Jayo and Josefa Bertha Pari-Olarte and Luz Josefina Chacaltana-Ramos and Eddie Loyola-Gonzales and Melva Iparraguirre-Meza and Mildred Hilda C{\'o}ndor- Privat and Beatriz Lilian Galdos-Vadillo and Jenny Mendoza-Vilcahuaman and Rossibel Juana Mu{\~n}oz-de-la-Torre} } @article {1810, title = {Pharmacobotany, Phytochemical Analysis and Anti-inflammatory effect of the Ethanolic Extract of Luffa operculata}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {622-628}, type = {Research Article}, chapter = {622}, abstract = {

Background: Luffa operculata is a vegetable species well known in the traditional peruvian medicine for its many medicinal properties and cosmetic applications. Objective: The aim objective was to determine the pharmacognostic characteristics of L. operculata as well as observing the pharmacological effect of the ethanol extract of L. operculata fruit on chronic inflammation in rats. Materials and Method: Phytochemical analysis was carried out by using specific chemical reagents for each constituent chemical, the pharmacobotanical study was done with a histological tinction (fruit, steam and leaves), which were stained with Safranin 1\% and Toluidine blue 1\%; the chronical inflammation was assessed by air bag method in Holztman male rats. Doses of 100, 250 and 500 mg/Kg were tested in order to determine the anti-inflammatory effect, which was demonstrated with histopathological evaluation and lymphocytes reduction. Results: The main findings indicate that the ethanolic extract presented saponins, alkaloids, carbohydrates, terpenes and steroids. The efficiency of lymphocyte reduction per field in the histopathological study of the granuloma was 58.4\% with the middle dose of 250 mg/kg (p \< 0.0001), which gives a dose-independent anti-inflammatory effect in rats. Conclusion: Luffa operculata presented anti-inflammatory effect at 250 mg/Kg by oral administration in a chronical experimental model of inflammation in rats.

}, keywords = {Anti-inflammatory., Luffa operculata, Pharmacobotany, Saponins}, doi = {10.5530/pj.2022.14.80}, author = {Jorge Alejandro Arroyo-Sandoval and Manuel Jes{\'u}s Marin-Bravo and Jorge Luis Arroyo-Acevedo and Hugo Jes{\'u}s Justil-Guerrero and Roberto Jes{\'u}s Ch{\'a}vez-Asmat and Josefa Bertha Pari-Olarte and Javier Hern{\'a}n Ch{\'a}vez-Espinoza and Jaime David Torres-L{\'e}vano and Eddie Loyola-Gonzales and Jos{\'e} Santiago Almeida-Galindo and Oscar Herrera-Calderon} } @article {1878, title = {Pharmacognostic Profile of Simplicia and Ethanolic Leaves Extract from Indonesian Piper betle var. nigra}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {610-618}, type = {Research Article}, chapter = {610}, abstract = {

Piper betle var. nigra has potency as an herbal medication. Thus it can be used as a source of medicinal raw materials. Piper betle var. nigra simplicia and extracts must be controlled to obtain unswerving quality and ensure their pharmacological effects by standardizing them through several specific and non-specific parameters. Specific parameters were analyzed organoleptically in the ethanol extract, namely having a thick consistency, brownish-green or blackish-green color, a mild peculiar odor, a bitter, cherish taste, and a slightly spicy flavor. The microscopic simplicia powder profile is as follows: the lower epidermis with idioblasts in oil cells contour and upper epidermis, sclerenchyma, covering hairs, and transport bundles ladder-type thickening, and idioblasts in oil cells contour. Extract content analysis of simplicia and black betle leaves ethanol extract showed water-soluble extract content of 2.77\% and 12.45\% and ethanolsoluble extract content of 1.38\% and 19.1\%. Secondary metabolites in the ethanol extract are flavonoids, polyphenols, tannins, saponins, alkaloids, and steroids. The non-specific parameters of the simplicia and extract are as follows; total ash content of 12.1\% and 7.43\%; acid insoluble ash content of 4.45\% and 1.57\%; drying shrinkage of 14.5\% and 15.85\%; total lead (Pb) contamination 47.5 ppm and 1.2 ppm; and the total cadmium (Cd) contamination \<0.2 ppm. The total bacterial contamination in the extract was 4.3x105 colonies/g. The total yeast contamination was 8.3x105 colonies/g and volumetric mass density of the water-soluble extract of 0.96 g/mL and the volumetric mass density of the ethanol-soluble extract of 1.01 g/mL.

}, keywords = {Black betle, Non-specific parameters, Piper betle var. nigra, Specific parameters, standardization}, doi = {10.5530/pj.2022.14.143}, author = {Herman and Fajar Prasetya and Supriatno Salam and Hifdzur Rashif Rijai and Hadi Kuncoro and Rolan Rusli and Agung Rahmadani and Hady Anshory Tamhid and Kuswandi and Dewanto Harjunowibowo and Islamudin Ahmad and Laode Rijai} } @article {1874, title = {The phytochemical and pharmacological activity of extract Kirinyuh (Chromolaena odorata L.) leaves: A Review}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {October 2022}, pages = {580-586}, type = {Research Article}, chapter = {580}, abstract = {

C. odorata L. is considered to be a plant weed that is scattered in various climates. As a weed, this plant contains a variety of beneficial secondary metabolites. Several studies have shown the benefits of C. odorata L. leaf extract. This study reviews the metabolite content and the pharmacological activities of C. odorata L. leaf extract. A literature search was carried out to obtain various studies related to the use of this plant extract. Secondary metabolites identified in C. odorata L. are alkaloids, flavonoids, tannins, saponins, and steroids. Several reports have also shown that even though it is considered a weed, C. odorata L. leaf extract also provides many benefits due to its pharmacological activities. Various pharmacological activities include anti-inflammatory, anti-microbial, antioxidant, antidyslipidemia, hematologic agent, antidiabetic and anti-cataract, analgesic and antipyretic, wound healing, anti-malaria, mosquito larvicidal, antihypercholesterolemia, and antifungal.

}, keywords = {Characterization, Chromolaena odorata, Kirinyuh, Pharmacological activity, Phytochemical}, doi = {10.5530/pj.2022.14.139}, author = {Erna Harfiani and Yudhi Nugraha and Citra Ayu Aprilia and Feda Anisah Makkiyah and Ratna Puspita and Viol Dhea Kharisma and Muhammad Hermawan Widyananda and Ahmad Affan Ali Murtadlo and Dora Dayu Rahma Turista and Muhammad Badrut Tamam and Riso Sari Mandeli and Mirella Fonda Maahury and Devi Purnamasari and Muhammad Arya Ghifari and Muhammad Thoriq Albari and Muhammad Raffi Ghifari and Asmi Citra Malina A. R. Tasakka and Alexander Patera Nugraha and Rahadian Zainul} } @article {1911, title = {The Potential of Antivirus Compounds in Gletang (Tridax procumbens Linn.) in Inhibiting 3CLpro Receptor of SARS-CoV-2 Virus by In Silico}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {796-805}, type = {Research Article }, chapter = {796}, abstract = {

SARS-CoV-2 virus has caused pandemic disease since the end of 2019. Virus transmission occurs through droplet and infects the host{\textquoteright}s respiratory tract rapidly. Viral propagation occurs through translation process of genome +ssRNA, then it being replicated forming some new body parts of virus and assemblied into virions that ready to infect. During the replication process, the translated viral genome in the form of polyprotein will be cut into smaller components by proteases, which one is 3CLpro. The presence of the 3CLpro receptor is used in drug development through in-silico molecular docking process to minimize failures before laboratory test. The antivirus compounds that used to inhibit the 3CLpro receptor are from gletang plant (Tridax procumbens Linn.). This study aim is to determine the value of binding affinity, the interaction between compounds and receptor, and the effect of drug components. The research was conducted by in-silico through the molecular docking process of 3CLpro receptor and antivirus compounds of gletang (Tridax procumbens Linn.), including betulinic acid, kaempferol and lignan. The results showed that the binding affinity of betulinic acid was -6.6 kcal/mol, kaempferol was -5.6 kcal/ mol and lignan was -5.4 kcal/mol. The interaction form of compounds and receptor was hydrogen bond, electrostatic, hydrophobic, and van der Waals. Compared to baicalein compound as a positive control with the value of binding affinity was -6.7 kcal/mol and its interaction with 3CLpro receptor, showed betulinic acid, kaempferol and lignan have smaller ability but they have the potential to inhibit the 3CLpro receptor.

}, keywords = {3CLpro receptor, Antivirus, Gletang, In-silico, SARS-CoV-2.}, doi = {10.5530/pj.2022.14.170}, author = {Yuna Islamiati and Yani Suryani and Ayuni Adawiyah and Opik Taufiqurrohman and Viol Dhea Kharisma and Devi Purnamasari and Nunuk Hariani Soekamto and Anny Setijo Rahaju and Kuswati and Riso Sari Mandeli and Kawther Ameen Muhammed Saeed Aledresi and Nur Farhana Mohd Yusof and Maksim Rebezov and Shimanovskaya Yanina and Belyakova Natalia and Dmitriy Kulikov and Gulnara Mullagulova and Rahadian Zainul and Muhammad Thoriq Albari} } @article {1782, title = {Preliminary Data on the Antibacterial Activity of Coffea Arabica, Coffea Canephora and Coffea Liberica}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {413-424}, type = {Research Article}, chapter = {413}, abstract = {

The continuous use of synthetic antibiotics will not only kill bacteria but also can accelerate the emergence of resistant pathogenic races. In addition, it can also cause the death of normal flora. Coffee extract is reported to have the potential as a naturally active and non-toxic antibacterial compound suitable for biomedical applications. Extraction using methanol was carried out on green coffee and which had been roasted for three types of Jambi coffee, namely Arabica, Robusta and Liberica coffee and continued with fractionation using hexane and ethyl acetate. The results of the analysis using FTIR showed that OH, C-H, C = C, C = O, C-O, C-N and N-H groups were detected. These functional groups are probably the functional groups that belong to caffeine, trigonelline, nicotinic acid and dehydrocafestol, which are believed to have bacteriostatic effects on some bacteria. The SEM-EDX analysis results of the three types of coffee showed that the dominant elements were O, K and Mg. Potassium and magnesium minerals bind with chlorogenic acid to form salt complexes of chlorogenic acid and magnesium chlorogenic acid complex. The antibacterial activity of the coffee extract and fraction was still low with the diameter of the inhibition zone was still low (0-10 mm). Furthermore, further characterization and tests are needed to confirm the antibiotic potency of the Arabica, Robusta and Liberica coffee ethanol extracts.

}, keywords = {Antibiotics, Coffee, E. coli}, doi = {10.5530/pj.2022.14.53}, author = {Madyawati Latief and Heriyanti and Indra Lasmana Tarigan and Sutrisno} } @article {1822, title = {Review on Literature of the Plant Elephantorrhiza Elephantine on its Healing Properties and Recent Acquired Knowledge of its Medicinal Activities (2000-2020)}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {715-721}, type = {Review Article}, chapter = {715}, abstract = {

Background: The current review article outlines current findings in literature from undertaken studies and review articles on the plant Elephantorrhiza elephantine from the past 20 years to date. The information presented in this article will include the following aspects of the plant. The plant description and taxomony, ethnomedical uses, phytochemistry and pharmacology of Elephantorrhiza elephantine. The article looks to discuss existing hurdles in research found on this plant and how to integrate any previous research with what is currently done in research on the plant. It aims on guiding the path of future research direction on the plant Elephantorrhiza elephantine. Methods: A total of 40 articles were selected and read through. The articles selected had included literature publications with the keywords such as; Elephantorrhiza elephantine, plant description, taxonomic of the plant, ethno medicinal usages, phytochemicals, pharmacological properties and plant toxicity, which were published between the years 2000 {\textendash} 2021. There were 32 articles relevant for this review article and 2 dissertation that were written between the criteria of years. Results: The ethomedicinal uses of Elephantorrhiza elephantine have been investigated by various authors on the anti-microbial activities, anti-inflammatory, anticancer and in ethnoveterinary medicine on how the plant provides relief to individuals with illnesses/disease through its traditional uses. These studies have been conducted on both animals and humans. The experiments performed used the crude extract derived from parts of the plant such as the roots and leaves. These plant parts have phytochemical compounds that are extracted using varying polar solvents. In the animal studies, acetone extracts of E. elephantine roots demonstrated significant activity against a tick-borne disease in cattle livestock and parasite worms in goats. In humans, the dried leaf extracts of E. elephantine was also subjected to various polar solvents and water, investigated for phytochemical content, antioxidant, anti-inflammatory, anti-diabetic and cytotoxic activities, using standard methods. It was reported that the ethanol extract yielded the highest phytochemical content. Conclusion: The gap in knowledge has narrowed on medicinal plants effects of healing properties. This lead by extensive research carried out trying to understand the benefits of traditional medication and why majority of the population uses it as they primary healthcare choice. Investigating the mechanism of action of E. elephantine on its antimicrobial, anti-diabetic, antimalarial, anti-inflammatory and wound healing could lead to an enhanced understanding on the medicinal properties of the plant extracts and a commercialisation of a product in future.

}, keywords = {Antimicrobial, Medicinal plants, Phytochemical content, Plant extracts.}, doi = {10.5530/pj.2022.14.91}, author = {Radebe Tlotlo and Polo-Ma-Abiele Hildah Mfengwana and Dedr{\'e} Olivier} } @article {1767, title = {Screening of Secondary Metabolites and Antioxidant Activity of Wild Edible Termite Mushroom}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {April 2022}, pages = {301-307}, type = {Original Article}, chapter = {301}, abstract = {

Wild edible mushrooms produce a variety of bioactive compounds that are known to have antioxidant properties. Natural antioxidants can protect against oxidative induced free radicals without any side effects. Thus, they are consumed by people for food and nutraceutical values. The purpose of this study was to evaluate the phytochemicals and antioxidant activity of three wild edible termite mushrooms (Termitomyces albuminosus, T. eurhizus and T. robustus). Different phytochemicals were screened in the 50\% ethanol, methanol and water extracts of three termite mushrooms. Total phenolic and flavonoid contents were determined by Folin-Ciocalteau and aluminium chloride method respectively. The antioxidant activity of three termite mushrooms was evaluated by DPPH assay. Qualitative screening of phytochemicals has revealed that alkaloid, steroid, fatty acid, flavonoid, saponin, tannin, carbohydrate and protein are found in the 50\% ethanol, methanol and water extracts of three species of termite mushroom. A high amount of total phenolic and flavonoid content was found in the 50\% ethanol extract of T. albuminosus, T. eurhizus and T. robustus (TPC: 50.28, 54.56 and 57.63 mg GAE/g extract; TFC: 16.30, 18.43 and 18.80 mg QE/g extract respectively). Due to high phenolic and flavonoid content, 50\% ethanol extract of three termite mushrooms has shown high antioxidant activity (i.e., lowest IC50: 710.00 - 714.05 μg/ml). These termite mushrooms have antioxidant properties due to the presence of bioactive secondary metabolites that can potentially be used as a source of natural antioxidants in the form of food and nutraceutical.

}, keywords = {DPPH assay, Flavonoid, phenolic, Phytochemical, Termite mushroom}, doi = {10.5530/pj.2022.14.38}, author = {Anita Kumari Tharu and Mukti Ram Paudel and Ananda Prakash Joshi and Laxman Bhandari and Hari Prasad Aryal} } @article {1800, title = {Utilization of Secondary Metabolites in Algae Kappaphycus alvarezii as a Breast Cancer Drug with a Computational Method}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {June 2022}, pages = {536-543}, type = {Original Article}, chapter = {536}, abstract = {

Breast cancer is one of the worst diseases that affect female people. Long-term treatment with therapy or surgery has a detrimental impact on the patient. The algae Kappaphycus alvarezii has gotten a lot of interest as a breast cancer medication because it contains chemicals that are expected to be anti-cancer. The objectives of this paper were to see how secondary metabolites in algae interact with the Nuclear Factor- kappaB protein kinase in breast cancer. The ligands and proteins were obtained from the PubChem and PDB websites, respectively. Swiss ADME was then used to assess the Pharmacokinetics and Drug likeness Properties. The last stage involved using molecular docking with PyRx and molecular dynamics to identify the interaction and visualization between the ligand and the target protein. The findings of the test revealed that the maraniol chemical had a superior binding capacity with NF kB protein kinase because it has a chromone group that controls transport efficiently in preventing breast cancer proliferation.

}, keywords = {Breast cancer, K. alvarezii, Molecular Docking., NF kB protein kinase}, doi = {10.5530/pj.2022.14.68}, author = {AF Dibha and S Wahyuningsih and ANM Ansori and VD Kharisma and MH Widyananda and AA Parikesit and MT Sibero and RT Probojati and AAA Murtadlo and JP Trinugroho and TH Sucipto and DDR Turista and I Rosadi and ME Ullah and V Jakhmola and R Zainul} } @article {1637, title = {Antibacterial Activities of Cationic Porphyrins and Porphyrin Encapsulated Gold Nanorods on Bacterial Cell Lines}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1086-1096}, type = {Original Article}, chapter = {1086}, abstract = {

Bacterial infections form part of the major causes of mortality and morbidity around the world more especially in developing and under-developed countries. Cationic porphyrins have been reported to display better efficacy in antimicrobial photodynamic therapy activity. The purpose of this study was to synthesise the cationic porphyrins; (TAP) and (TPyP) and evaluate their pharmacokinetics and metabolic interactions with the DNA gyrase subunit A. The antibacterial activity of the nano-conjugates was evaluated against Staphylococcus aureus (ATCC 25925), Enterococcus faecalis (ATCC 29212) and Klebsiella pneumoniae (ATCC 4352) using the micro-dilution assay without light. AutoDock Vina was used to assess the molecular interactions between ligands and the DNA gyrase subunit A. The SwissADME online tool was used to assess the pharmacokinetic properties of the nano-conjugates, while the ADMETlab online tool was used to assess the ability to inhibit the hERG gene, human hepatotoxicity and mutagenicity. The test nano-conjugates showed broad-spectrum antibacterial activity against all tested bacterial strains with the MIC values in a range of 0.42 {\textpm} 0.1 to2.6 {\textpm} 0.7 mg/ml. The nano-conjugates revealed good molecular interaction with DNA gyrase subunit A with their binding free energy in the range of -8.3 to -8.7 kcal/ mol. They are predicted to be P-glycoprotein (P-gp) substrates, able to penetrate the blood-brain barrier and non-inhibitors of cytochrome P450 (CYP) isomers (CYP 2C19, CYP 2C9 and CYP 2D6). Both nanoconjugates have the potential to cause cardiotoxic and mutagenic effects but not hepatotoxic effects. The results show that the synthesized compounds have the potential as anti-bacterial PDT agents.

}, keywords = {Antimicrobial, Bacteria, Porphyrin}, doi = {10.5530/pj.2021.13.141}, author = {Hlapisi N and Maliehe TS and Oluwafemi OS and Songca SP and Linganiso L and Motaung TE} } @article {1390, title = {Antibacterial and Antioxidant Activities of Ethanol Extracts of Some Plants Selected from South Jordan}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {528-534}, type = {Research Article}, chapter = {528}, abstract = {

Three Jordanian medicinal plants; Peganum harmala (P. harmala), Geropogon hybridus (G. hybridus), and Salvia officinalis (S. officinalis) were selected from Al-karak region in order to investigate their antibacterial and antioxidant activities. The crude extract yield of all used plants were varied from 10.6\% in Salvia officinalis and 15.6\% in P. harmala, to 18 \% in G. hybridus. The antibacterial activity of these plants was carried out on four bacterial strain (S. aureus, E.coli, E. aerogenes and B. subtilis). These plant ethanol extracts have effects on the gram positive strains and gram negative bacteria except S. officinalis did not show activity against E. Coli. The minimal inhibition concentration (MIC) of P. harmala S. officinalis and G. hybridus (MIC) ranged from 125 μg/ml to 500 μg/ml. The ethanol crude extract of G. hybridus gave 10 fractions using TLC method, fraction 1,3 and 10 exhibited antibacterial activity against all bacterial strains. Their total phenolic contents were evaluated; the highest total phenol content was observed in G. hybridus with 410 mgGAE/g plant extract followed by P. harmala and S. officinalis with 305 and 203.7 mg/g plant extract, respectively. The antioxidant activity was estimated by using DPPH method. The highest antioxidant activity was obtained with G. hybridus extract and found to be 0.89 mg Trolox/g plant extract. The lowest antioxidant activity was obtained with S. officinalis which was 0.53 mg Trolox/g plant extract. The lowest IC50 (highest antioxidant activity) was observed in G. hybridus with 0.83 mg/ml. Intermediate effect observed in P. harmala with IC50 1.1 mg/ml. The lowest antioxidant activity was obtained in S. officinalis with IC50 1.38 mg/ml.

}, keywords = {Antibacterial, Antioxidant, Ethanol extracts, Peganum harmala}, doi = {10.5530/pj.2021.13.66}, author = {Waleed Khaled Al ani and Ali Abdallah Alqudah and Khaled. A. Tarawneh} } @article {1421, title = {Antihypertensive Effects of Osteospermum Imbricatum in Two Hypertensive Rat Models}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {744-751}, type = {Research Article}, chapter = {744}, abstract = {

Introduction: Osteospermum imbricatum is used traditionally in Eastern Cape, South Africa for the management of hypertension, chest and stomach complaints. This study was aimed at investigating the antioxidant and antihypertensive effects of this plant. Methods: Antioxidant capacity was determined by radical scavenging assays and ferric reducing antioxidant power. Antihypertensive effects after once off treatment with the leaf/root extracts (500 mg/kg) were evaluated in spontaneously hypertensive rats (SHR). The effect of the extracts on established hypertension was determined in Wistar rats treated with Nω-Nitro-L-arginine methyl ester (L-NAME) (40 mg/kg/day) for 4 weeks followed by co-treatment with L-NAME and extracts (200 mg/kg and 400 mg/kg) or amlodipine (5 mg/kg) or normal saline for 4 more weeks. Results: The concentration at which there was 50 \% inhibition (IC50) of DPPH radical by the extracts was lower for the leaf extract (0.79 mg/mL) compared to the root extract (1.15 mg/mL). The leaf extract significantly (p\<0.01) decreased systolic and diastolic blood pressures in both rat models. Conclusion: The extracts of Omsteospermum imbricatu have moderate antioxidants and antihypertensive properties.

}, keywords = {Antioxidants, High blood pressure, Nω-Nitro-L-arginine methyl ester, Spontaneously hypertensive rats}, doi = {10.5530/pj.2021.13.95}, author = {Charlotte Mungho Tata and Constance Rufaro Sewani-Rusike and Olukayode Aremu and Opeoluwa Oyehan Oyedeji and Benedicta Ngwenchi Nkeh-Chungag} } @article {1630, title = {Chemical Composition and In Vitro Antiplasmodial Activity of the Total Alkaloids of the Bulbs of Two Amaryllidaceae Species from Northern Peru}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {1046-1052}, type = {Research Article}, chapter = {1046}, abstract = {

Introduction: The amaryllidaceae family is characterized by presenting alkaloids with powerful pharmacological activities, including antiprotozoal activity. The aim of the present work was to determine the chemical composition and evaluate the in vitro antiplasmodial activity of the total alkaloids of the bulbs of two amaryllidaceae species from northern Per{\'u}. Methods: The total alkaloids were extracted from the bulbs using an acid-base extraction. The chemical composition of the total alkaloids was determined by GC-MS, using galantamine as a reference standard. It was investigated the in vitro antiplasmodial activity against Plasmodium falciparum FCR-3 strain (chloroquine-resistant). Results: 8 alkaloids were identified in the bulbs of Clinanthus incarnatus: lycorine, galanthamine, galanthine, vittatine/crinine, hippamine, 3-O-acetylpowelline, 11,12-dehydroanhydrolycorine, 1-O-acetyllycorine with values of 19.73; 14.99; 10.36; 10.22; 10.16; 10.14; 10.04; 9.85 μg GAL/100 mg of total alkaloid (TA) respectively and 6 alkaloids in the bulbs of Clinanthus ruber: lycorine, anhydrolycorine, 11,12-dehydroanhydrolycorine, 2,4-didehydro-2-dehydroxylycorine, 8-0-dimethylmaritidine, hippamine, with values of 70.2; 18; 4.15; 3.45; 6.8 and 0.1 μg GAL/100 mg TA respectively. The total alkaloids of the species of C. incarnatus and C. ruber at concentrations of 1.0; 2.5; 5.0; 10.0; 25.0 and 50.0 μg/ml presented inhibition percentages of 23.5 {\textpm} 0.46\% to 94 {\textpm} 0.56\% against P. falciparum with (p \<0.05). They also presented IC50 0.375 μg/ml (C. incarnatus) and IC50 0.241 μg / ml (C. ruber). Conclusion: The main component of total alkaloids of the bulbs of two species was lycorine, in adittion, these species showed in vitro antiplasmoidal activity against Plasmodium falciparum FCR-3 strain at the doses tested.

}, keywords = {Clinanthus incarnatus, Clinanthus ruber, Plasmodium falciparum}, doi = {10.5530/pj.2021.13.135}, author = {Maril{\'u} Roxana Soto-V{\'a}squez and Madeleine Vanessa Horna -Pinedo and Luciana R Tallini and Jaume Bastida} } @article {1622, title = {Comparison of Antibacterial Activity of Calcium Hydroxide, Azadirachta Indica (Neem), Ocimum Tenuiflorum (Tulsi) and Punica Granatum (Pomegranate) Gels as Intracanal Medicaments Against Enterococcus Faecalis: An in-vitro Study}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2017}, pages = {988-994}, type = {Research Article}, chapter = {988}, abstract = {

Aim: This study aimed to evaluate the antibacterial activity of Calcium hydroxide, Azadirachta indica (Neem), Ocimum tenuiflorum (Tulsi) and Punica granatum (Pomegranate) gels as intracanal medicaments against Enterococcus faecalis. Methodology: Crude extracts of Pomegranate peel, Neem leaves and Tulsi leaves were used to determine MIC following which gels of 5\% neem, 10\% tulsi and 10\% pomegranate were prepared. Forty-eight single rooted human premolars were procured and inoculated with E.faecalis for 7 days. Specimens were then randomly distributed into 4 groups.

Group I- Calcium hydroxide

Group II- 5\% A. indica (Neem) gel

Group III- 10\% O. tenuiflorum (Tulsi) gel

Group IV-10\%

P. granatum (Pomegranate) gel The experimental gels were then introduced into the samples and were sealed at both ends. The antimicrobial activity of medicaments was assessed by measuring CFU/ml at the end of 1, 3 and 5 days. Results: Calcium hydroxide showed the maximum antibacterial activity (5.3X104 CFU/ml) followed by Pomegranate gel (5.4 X104 CFU/ml) with no statistically significant difference between them. Similarly, no statistically significant difference was observed between the mean CFU/ml values of the neem (10.2 X104 CFU/ml) and tulsi gel (10.2 X104 CFU/ml). However, pomegranate gel showed statistically significant antibacterial activity when compared to Neem and Tulsi. (Table 1, Table 2, Table 3, table 4) (Figure 1). Conclusion: Calcium hydroxide showed the best antibacterial activity against E.faecalis. Among herbal gels, pomegranate showed the maximum antibacterial activity, however, further in-vivo research is required for it to be used as a sole intracanal medicament clinically.

}, keywords = {Calcium hydroxide, Enterococcus faecalis, Herbal, Intracanal medicaments, Microbial sensitivity tests, Root canal therapy}, doi = {10.5530/pj.2021.13.127}, author = {Akanksha Mittal and Sunil Tejaswi and Mruthunjaya K and Suneeth Shetty and Ambikathanaya UK} } @article {1616, title = {Comparison of Colchicine Content in Gloriosa superba L., Root after Pretreatment by Thai Traditional Medicine Methods}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {942-948}, type = {Research Article}, chapter = {942}, abstract = {

Introduction: In Thai traditional medical practice, the roots of Gloriosa superba L. must be treated prior to use as Thai herbal remedies. Colchicine is a major active chemical constituent in the roots. It was reported that lethal doses of colchicine were 7-26 mg. There have been two pieces of evidence that indicated 5 different pretreatment methods of Gloriosa superba L., roots. Therefore, this research aimed to compare the amount of colchicine before and after pre-treated by 5 different methods and compare colchicine content after pretreatment between methods. Methods: Provide five different locations of fresh Gloriosa superba L., roots. Each sample divided into 6 groups. The first group would be treated as a control, the second to the sixth group was pre-treated by roasting, burning, boiling, stewing, and grilling which follow the methods from two pieces of evidence. Subsequently, quantitative analysis by High Performance Liquid Chromatography. Results: The amount of colchicine in roots before and after pre-treated by roasting, burning, boiling, stewing, and grilling methods were significantly reduced by 45.61{\textpm}10.61\% (p=0.000), 37.35{\textpm}14.15\% (p=0.000), 44.55{\textpm}8.60\% (p=0.000), 76.40{\textpm}10.70\% (p=0.000), and 30.35{\textpm}11.31\% (p=0.000), respectively. The stewing method was the greatest decrease amount of colchicine which significantly different from other methods. (p=0.000). Conclusion: All 5 methods were significantly reduced amounts of colchicine in the roots of Gloriosa superba L. They were effective methods to pre-treat the roots of Gloriosa superba L. prior to use as Thai herbal remedies.

}, keywords = {Colchicine, Gloriosa superba L., HPLC, Pretreatment methods, Thai traditional medicine}, doi = {10.5530/pj.2021.13.121}, author = {Sasithorn Tandhavadhana} } @article {1678, title = {Effect of Aporosa villosa Stem Ethanolic Extract on Adipogenesis in 3T3-L1 Adipocytes}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1422-1427}, type = {Research Article}, chapter = {1422}, abstract = {

Background: An excessive fat accumulation is related to development of obesity. Obesity is associated with the induction of insulin resistance and diabetes mellitus conditions. Aporosa villosa is a plant that found in the Northern and Northeastern region of Thailand. Objective: The present study used 3T3-L1 adipocytes for investigating the effect of Aporosa villosa stem ethanolic extract (AS) on adipogenesis. Materials and Methods: 3T3-L1 adipocytes were used for measuring the cytotoxicity of AS at a concentration range of 3-100 μg/mL. After adipocyte cells treated with AS (3-100 μg/mL) for 8 days, the lipid accumulation was detected by Oil Red O staining and adipogenic gene expression were determined by quantitative real-time PCR. Results: AS extracts (3-100 μg/mL) did not show cytotoxicity on cell proliferation. After 8 days of treating 3T3-L1 adipocytes with AS at doses of 3, 10, 30 and 100 μg/mL, the lipid droplets were reduced as compared to non-treated cells. Furthermore, the adipogenic genes were measured. The regulators of adipogenesis, CCAAT/enhancer-binding protein α (C/EBPα), peroxisome proliferatoractivated receptor γ (PPARγ) and sterol regulatory element binding protein 1c (SREBP1c) were found decreasing in AS extracts. The downstream target genes of these regulators cluster of differentiation (CD) 36, fatty acid synthase (FAS) and lipoprotein lipase (LPL) were also reduced by AS treatments. Conclusion: These findings indicate that AS extract has an inhibitory activity on adipogenesis in 3T3-L1 adipocytes via suppressing C/EBPα, PPARγ and SREBP1c.

}, keywords = {Aporosa villosa; Adipogenesis; Obesity}, doi = {10.5530/pj.2021.13.180}, author = {Urarat Nanna and Linda Chularojmontri and Pholawat Tingpej and Rawiwun Kaewamatawong and Sudarat Homhual and Wanwisa Suwannaloet and Thanes Fuangfoo and Jarinyaporn Naowaboot} } @article {1691, title = {The Effect of Mahkota Dewa (Phaleria macrocarpa) Leaf Extract on the Mucin 1 Expression in Mice Colonic Epithelial Cells Induced by Dextran Sodium Sulfate (DSS)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1509-1515}, type = {Research Article}, chapter = {1509}, abstract = {

Background: Inflammatory bowel disease is a chronic inflammation caused by the malignant inflammation response and if not treated, could lead to colorectal cancer. One of the researched treatment is mahkota dewa (Phaleria macrocarpa) leaf extract that has flavonoid compound known to reduce inflammation. This study was aimed to prove that mahkota dewa leaf extract could reduce inflammation of mice colon induced with dextran sodium sulfate (DSS) and observe MUC1 expression from colon epithelial crypt of Lieberkuhn. Methods: This was a laboratory experiment using biological material (paraffin block) taken from 28 mice and divided into 5 groups: normal, aspirin, low and high dose mahkota dewa, and negative control. They were processed into immunohistochemistry and stained microscopic slides. Afterwards, they were observed with 400x magnification and 5 field-of-view of mice colon crypt of lieberkuhn. Then MUC1 expression was counted using ImageJ to obtain mean immunohistochemistry score and analyzed with SPSS. Results: There were significant reduction of MUC1 expressions from normal, aspirin, and high dose mahkota dewa groups compared to the negative control group. The result shown MUC1 expression from high dose mahkota dewa (M=149.90,SD=3.81) and aspirin (M=158.92,SD=5.28) were closer to normal group (M=148.02,SD=5.28). There were no significant results between negative (M=175.39,SD=14.30) and low dose mahkota dewa group (M=149.90,SD=5.02). Conclusion: There was a reduction of MUC1 expression in DSS-induced mice colonic epithelial cells for high dose mahkota dewa group. This shown that high dosage mahkota dewa leaf extract could reduce inflammation like aspirin.

}, keywords = {Anti-inflammatory agent, Colon epithelial cell, Inflammatory bowel Disease, Mahkota Dewa (Phaleria macrocarpa), MUC 1 expression}, doi = {10.5530/pj.2021.13.192}, author = {Kusmardi Kusmardi and Natasha Yemima Situmorang and Endah Zuraidah and Ari Estuningtyas and Aryo Tedjo} } @article {1350, title = {Evaluate the Effect of Herbal Extract Remedy for Treatment of Liver Cirrhosis in in-vitro}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {189-195}, type = {Research Article}, chapter = {189}, abstract = {

Objectives: To evaluate the in-vitro effect of herbal extract recepies, namely XGTQ, in the treatment of liver cirrhosis that induced by Carbon tetrachloride (CCL4) in combination with alcohol and high-fat diet in rats. Materials and Methods: Liver cirrhosis was induced by subcutaneously injecting CC14 (initial dose of 5,0ml/kg, followed by 1,2ml/kg twice a week in 10 weeks) in winstar rats. Then, fed with synthetic food, added 20\% fat, and 0.05\% cholesterol and iron oxalate. Rats were administered a day with fresh water and water mixed with 30\% ethanol in another day. The rats were randomly divided into 5 groups and given distilled water (group 1 or control group and group 2 or cirrhosis group), silymarin (group 3 or reference group) or the herbal recipes, aka XGTQ, drug extract (group 4, 5) for 4 weeks. Blood was collected for biochemical test and livers were dissected to evaluate weight, morphology and quantified 4-hydroxyproline to evaluate fibrosis and collagen accumulation. Results: In cirrhotic wistar rats, the XGTQ herbal drug at 19.6 g/kg/24h and 58.8 g/kg/24h showed the ability of reducing the level of enzymes AST, ALT in the blood (p\<0.01), increasing plasma albumin and decreasing prothrobin time (p\<0.05); improving physical condition, macroscopic and microscopic images of H\&E-stained liver; decreasing the concentration of hydroxyproline in the liver and reducing the level of cirrhosis on the masson-stained templates. The effect of herbal recipes XGTQ increased dramatically with the dose, and was equivalent to silymarin at the dose of 70 mg/kg/24h. Conclusion: The aqueous extract of XGTQ herbal remedy has have a good effect in treatment of liver cirrhosis in in-vitro and to be equivalent to that of silymarin at the dose of 70 mg/kg.

}, keywords = {CCl4, Liver cirrhosis, Silymarin, Wistar Rats, XGTQ herbal extract}, doi = {10.5530/pj.2021.13.27}, author = {Thanh Ha Tuan Nguyen and Ngan Nguyen Hoang and Xuan Thanh Nguyen and Binh Nhu Do and Son Trinh The} } @article {1424, title = {Evaluation of Acute toxicity, In-vitro, In-vivo Antidiabetic Potential of the Flavonoid Fraction of the plant Chenopodium album L}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {765-779}, type = {Research Article}, chapter = {765}, abstract = {

Background: The Chenopodium album L. commonly recognized as Bathua, is widely distributed globally and contains various phytoconstituents that help treat several diseases. However, until now, aerial parts{\textquoteright} antidiabetic potential and the plant{\textquoteright}s acute toxicity at fraction level have never been established. Objectives: To investigate the acute toxicity, the in-vitro, in-vivo antidiabetic potential of the plant at fraction level. Materials and Methods: The aerial parts of the plant were fractionated into different fractions, i.e., flavonoid fraction (CAFF), tannin fraction (CATF), alkaloid fraction (CAAF), saponin fraction (CASF), and were analyzed for in-vitro alpha-amylase inhibition assay. The CAFF, CATF, and CAAF were selected based on in-vitro alpha-amylase inhibition assay results and were further screened for its acute toxicity and in vivo antidiabetic activity using a high-fat diet and streptozotocin-induced diabetes model. The CAFF was characterized by LC-MS, and a molecular docking study was carried out. Results: The in-vitro alpha-amylase inhibition assay revealed that CAFF was found to be more potent than standard Acarbose having IC50 values 122.18 {\textpm} 1.15 and 812.83{\textpm} 1.07 μg/ml, respectively. The CAFF fraction was found to possess potent antidiabetic activity in a dose-dependent manner in both in vitro and in vivo diabetic models and did not produce any sign of severe toxicity. Furthermore, the bioactive CAFF fraction was characterized by LC-MS, showed the presence of quercetin 3-O-(2{\textquoteright}{\textquoteright},6{\textquoteright}{\textquoteright}-di-O-rhamnosyl) glucoside (QRG) or quercetin 3-O-(2{\textquoteright}{\textquoteright},6{\textquoteright}{\textquoteright}-di-Orhamnosyl) galactoside (QRGa) and quercetin 3-O-rutinoside (rutin) (QR). It is predicted from the molecular docking study that the CAFF fraction primarily acts as an alphaamylase inhibitor. Conclusion: The CAFF fraction was found to poses dose-dependent potent antidiabetic activity and did not produce any sign of severe toxicity and primarily act as an alpha-amylase inhibitor.

}, keywords = {Acute toxicity, Alpha-amylase, Antidiabetic activity, Chenopodium album, Lc-Ms, Molecular docking}, doi = {10.5530/pj.2021.13.98}, author = {Neeraj Choudhary and Pranav Kumar Prabhakar and Gopal L Khatik and Subba Rao Chamakuri and Devesh Tewari and Ashish Suttee} } @article {1646, title = {Evaluation of the Anticonvulsant, Anxiolytic, Sedative, and Neuroprotective Activities of Polysaccharides from Mycelium of Two Ganoderma Species}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1161-1173}, type = {Research Article}, chapter = {1161}, abstract = {

Background: Ganoderma lucidum has been used as a medicinal mushroom since centuries in East Asia. Recent reports have shown that metabolites isolated from Ganoderma species have shown effects on central nervous system. Objective:\ To determine the neuroprotective, anticonvulsant, anxiolytic, and sedative effects of Ganoderma sp. and Ganoderma curtisii polysaccharides. Methods: Polysaccharides (Gsp-PS2 or Gc-PS2) were isolated from two Ganoderma mycelia submerged cultures. Acute toxicity effects of Gc-PS2 or Gsp-PS2 on mice were treated orally with doses of 50 - 2000 mg/kg. Anticonvulsant activity was determined using three chemoconvulsants: kainic acid (KA), strychnine, or pentylenetetrazole (PTZ). Anxiolytic-like effects were determined using the elevated plus maze test on mice. GABA release evoked by GC-PS2 or Gsp-PS2 content was determined by HPLC. Neuroprotective effects of Gsp-PS2 or Gc-PS2 were determined by glial activation, histopathological changes, and immunohistochemistry. Results: Gc-PS2 or Gsp-PS2 showed neuroprotective activity by diminishing neuronal death, reducing glial activation and Neu-N expression levels. Gsp-PS2 or Gc-PS2 inhibited convulsions in the KA model. An anxiolytic-like, but not a sedative effect was reported in mice treated with Gc-PS2 or Gsp-PS2. Polysaccharides Gc-PS2 or Gsp-PS2 evoked endogenous GABA release and increased its concentration within the incubation medium. Pretreatment with Gsp-PS2 or Gc-PS2 showed a reduction of the LPSinduced NO production. Gc-PS2 or Gsp-PS2 did not produce toxic effects. Conclusion:\ Ganoderma sp. or Ganoderma curtisii polysaccharides showed neuroprotective and anticonvulsant activities in animal models. The anticonvulsant activity may involve the GABAergic neurotransmision.

}, keywords = {a- and b-glucan, Anticonvulsant, GABA, Ganoderma curtissi, Ganoderma sp, Neuroprotective}, doi = {10.5530/pj.2021.13.149}, author = {Veronica Nunez-Urquiza and Juana Villeda-Hernandez and Elizur Montiel-Arcos and Isaac Tello and Victoria Campos-Pena and Maribel Herrera-Ruiz and Mar{\'\i}a del Carmen Guti{\'e}rrez and Vera Petricevich and Mar{\'\i}a Ang{\'e}lica Santana and Martha Navarro and Ang{\'e}lica Berenice Aguilar-Guadarrama and Gabriel Navarrete-V{\'a}zquez and Irene Perea-Arango and Ismael Leon-Rivera} } @article {1363, title = {Evolution of Biometric Parameters and Oil Fatty Acid Composition of Argan "Argania spinosa L. Skeels" Fruits from Beni- Snassen (Eastern Region of Morocco) During Ripening}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {296-308}, type = {Original Article}, chapter = {296}, abstract = {

Background: Argania spinosa Skeels is an endemic forest essence of Morocco. The argan of the north-east of Morocco remains a virgin subject of study without enough value given to it. Objective: The aim of this study is to asses the evolution of biometric parameters and fatty acids composition of the argan fruits from Beni-Snassen region during ripening. Materials and Methods: 4 fruit shapes harvested over seven months were characterized through the measurement of their biometric parameters (size and weight), and their composition of majority fatty acids. Results: the studied argan tree could be classified into two major groups, namely: early-riped trees with oval or oval-apiculate fruits and late-riped trees with fusiform or spherical fruits. When considering the fruits size and weight, the highest values were recorded on late-ripened fruits, more particularly fusiform shapes. The obtained results showed, on one hand, a significant difference in the unsaturated fatty acids, according to the fruit ripeness stage and shapes, being the later significantly affecting the stearic acid content; and on another hand, it was noted an increase of oleic acid content while linoleic acid decreased. In the maturation stage, the spherical shaped fruits were found to have the highest ratio of unsaturated/saturated fatty acids. Conclusion: The results demonstrated the possibility to predict the kernel{\textquoteright}s weight from the fruit{\textquoteright}s length. The results also showed the good dietary and nutritional quality of spherical shapes and that the biometric parameters are important criteria for the differentiation of argan tree fruits.

}, keywords = {Argan fruits, Beni-Snassen, Biometeric parameters, Fatty Acid, Ripeness}, doi = {10.5530/pj.2021.13.39}, author = {Abdelhak Chergui and Latifa El Hafid and El Amine Ajal and Imane Zakariya and Rachid Nejjari and Mohammed Reda Tazi} } @article {1650, title = {Impact of Solvent Selection on Phytochemical Content, Recovery of Tannin and Antioxidant Activity of Quercus Infectoria Galls}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1195-1204}, type = {Research Article}, chapter = {1195}, abstract = {

Introduction: Quercus infectoria (QI) is medicinal plant well known to exhibit enormous therapeutic values. The main medicinal part of QI plant exists in its edible nutritious gall. This study aimed to determine the effects of extraction solvents on the overall phytochemical content, recovery of tannin and antioxidant activity of the QI galls. Methods: Two solvents of different polarity namely water and methanol, were used to extract bioactive compounds from the QI galls using soxhlet extraction technique. Phytochemical, TLC and HPLC assays were performed to detect and quantify the extracted compounds. DPPH assay was conducted to evaluate the antioxidant potential of the extracted compounds. Results: After 6 hours of extraction at respective solvent boiling points, methanol solvent successfully generated 1.8-fold higher crude yield (34.0\%) compared to water solvent (18.9\%). Phytochemical analysis revealed that both solvent extracts contained different secondary metabolites. The methanol extract was found richer in flavonoid, while the aqueous extract was found richer in phenol, tannin, gallotannin, triterpene and cardiac glycosides. Interestingly, we found that the major type of tannin presence in QI galls was gallotannin (hydrolysable tannin) instead of phlobatannin (non-hydrolysable tannin). The quantification results demonstrated that QI aqueous extract contained significantly higher gallotannin (75.0 μg/mL) compared to QI methanol extract (46.8 μg/mL). Furthermore, the aqueous extract also exhibited significant higher antioxidant activity compared to the methanol extract at concentration of 2 μg/mL. Conclusions: This study strongly support the utilization of water solvent for optimum gallotannin extraction from QI galls.

}, keywords = {Antioxidant, Gallotannin, Phytochemical analysis, Quercus infectoria (QI) galls, Tannin}, doi = {10.5530/pj.2021.13.153}, author = {Nur Alisa Kamarudin and Norhazilah Muhamad and Nik Nur Hakimah Nik Salleh and Suat Cheng Tan} } @article {1712, title = {In silico Study on the Promising Active Components of Terpenoid and Fucoidon from Sargassum sp. in Inhibiting CGRP and TNF-α}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1715-1719}, type = {Research Article}, chapter = {1715}, abstract = {

Introduction: The new discovery of the active substance in Sargassum sp marks the new era for drug industry as it is very effective as the new migraine medication compared to analgesics which have already been popular previously in treating migraine. By using the in silico methods, this study intended to identify the preventive effect of the active substance in Sargassum sp within the stage of pain and inflammation development in migraine. In migraine pathophysiology, the clinical findings would build and verify the role of CGRP and TNF-α. Methods: This research applied a one-shot experimental study and by employing the potential test through PubChem (https://pubchem.ncbi.nlm.nih.gov/), the result of this study proved that tannins, terpenoids and fucoidone were contained in the active substance of Sargassum sp leading to the possession of potential as the drug to treat migraine. Results: Terpenoids and tannin binding affinity value is higher than other substances. Terpenoids and fucoidon had similar amino acid residues with controls. Seaweed metabolites have great potential as inhibitors of CGRP and TNF-α because the binding affinity score is close to control. Conclusion: The active substance in Sargassum sp has an inhibitory effect on the occurrence of CGRP and TNF-α in migraine based on in silico studies.

}, keywords = {CGRP, Fucoidone, in silico, Sargassum sp., Terpenoid, TNF-α.}, doi = {10.5530/pj.2021.13.221}, author = {Olivia Mahardani Adam and Jusak Nugraha and Mohammad Hasan Machfoed and Agus Turchan} } @article {1695, title = {In vitro Wound Healing Potential and Antimicrobial Activity of Clerodendrum Inerme Leave Extracts}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1542-1548}, type = {Review Article}, chapter = {1542}, abstract = {

Background: Clerodendrum inerme is a medicinal plant which exhibited many pharmacological effects. However, wound healing property of this plant has not been investigated. Objective: The present study was designed to evaluate wound healing and antimicrobial activities of C. inerme leaves using the in vitro model with Human keratinocytes (HaCaT). Methods: Cytotoxicity and wound healing effects were determined by MTT and scratch wound healing assay. Antimicrobial activities against cutaneous flora and clinical isolates of bacteria were investigated by broth microdilution assay. Results: The results showed that the water extract of C. inerme leaves did not exhibit cytotoxic effects on HaCaT cells, while ethanol extracts at higher concentrations significantly decreased cell growth with an IC50 value of 386.8 {\textpm} 87.1 μg/mL. The water extract and the lowest concentration (6.25 μg/mL) of the ethanol extract significantly increased percentage of wound closure compared with the untreated group. The water and ethanol extracts of C. inerme displayed a broad spectrum of antibacterial activity, inhibiting growth of Staphylococcus aureus, Staphylococcus.epidermidis, Escherichia coli, and Pseudomonas aeruginosa. The water extract displayed remarkable activity against methicillin-resistant S. aureus with MIC and MBC values ranging from 0.39 to 1.56 μg/mL. Notably, it provided stronger antibacterial activity than vancomycin and also showed antifungal activity against C. albicans. Conclusion: This study confirms the potential of C. inerme leaves for wound healing and antimicrobial therapy and supports the continued utilization of C. inerme leaves in traditional medicine. Further studies are needed to clarify the molecular mechanisms through which it exerts such biological effects.

}, keywords = {Antimicrobial activity, Clerodendrum inerme, Keratinocytes, Scratch assay, Wound Healing}, doi = {10.5530/pj.2021.13.196}, author = {Sueptrakool Wisessombat and Malatee Tayeh} } @article {1610, title = {Inhibitory activity against α-amylase and α-glucosidase by phenolic compounds of quinoa (Chenopodium quinoa Willd.) and ca{\~n}ihua (Chenopodium pallidicaule Aellen) from the Andean region of Peru}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {896-901}, type = {Original Article}, chapter = {896}, abstract = {

Background: Chenopodium quinoa Willd. and Chenopodium pallidicaule Aellen are grains from the Andean region of Peru, which in addition to having a high nutritional value, have health-promoting properties related to the prevention of chronic diseases such as diabetes. Objetive: The present study aimed to identify phenolic compounds associated with an inhibition of carbohydrate hydrolyzing enzymes associated with type 2 diabetes. Material and Methods: Two varieties of quinoa and two varieties of ca{\~n}ihua from the Puno Region in Peru, were evaluated. Total phenolics, total flavonoids, identification of phenolic compounds and antioxidant activity in vitro were measured by Folin-Ciocalteu assay, aluminum chloride colorimetric method, HPLC-DAD and DPPH radical scavenging assay, respectively. In vitro hypoglycemic activity was evaluated through the inhibition of the α-amylase and α-glucosidase enzymes. Results: Gallic acid, rutin and chlorogenic acid were identified by HPLC-DAD in the varieties of quinoa and ca{\~n}ihua. The latter showed significantly higher levels of chlorogenic acid compared to quinoa varieties (p\<0.05). Both Andean grains exhibited inhibition of key-enzymes linked to type 2 diabetes, presenting IC50 values of 7.99 to 34.05 and of 8.07 to 1158 μg/mL for α-amylase and α-glucosidase, respectively. Total phenolics, total flavonoids, DPPH radical scavenging assay, gallic acid and chlorogenic acid showed the greatest contribution to the inhibitory activity of the α-glucosidase enzyme (p\<0.05). Conclusion: Our findings suggest that the phenolic compounds present in the varieties of quinoa and ca{\~n}ihua could modulate the inhibition of carbohydrate hydrolyzing enzymes associated with type 2 diabetes.

}, keywords = {Andean grains, DPPH radical scavenging assay, HPLC-DAD, in vitro antidiabetic activity, Polyphenols}, doi = {10.5530/pj.2021.13.115}, author = {Jorge Coronado-Olano and Ritva Repo-Carrasco-Valencia and Oscar Reategui and Emily Toscano and Elisa Valdez and Mirko Zimic and Ivan Best} } @article {1431, title = {Inotropes in Chronic Beta-Blocker Therapy}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {828-834}, type = {Review Article}, chapter = {828}, abstract = {

The increasing rate of cardiovascular disorders contributes to rising hospitalized patients receive chronic oral beta-blocker therapy. Beta-blockers remain one of the fundamental therapy for chronic heart failure. Still, their role in decompensated heart failure and severe sepsis during hospitalization is often debated and inconsistent in clinical practice. In recent years, evidence of the efficacy and clinical outcomes of beta-blockers in acute heart failure (AHF) have accumulated. Clinical research indicates that chronic beta-blockade withdrawals should be prevented, or as soon as hemodynamic stabilization and euvolemic condition are reached, it should be reinstituted. As a subset of AHF patients with low cardiac output required inotropes, the choice of proper agent is fundamental. Different inotropic agents such as inhibitors of the phosphodiesterase, levosimendan, and dobutamine also their associations with beta-blockers are discussed.

}, keywords = {Beta-blocker, Decompensated heart failure, Inotropes, Severe sepsis}, doi = {10.5530/pj.2021.13.105}, author = {Mochamad Yusuf Alsagaff and Melly Susanti and Mochammad Thaha and Christian Jonatan} } @article {1624, title = {Isolation and Structural Characterization of Compounds from Blumea lacera}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {999-1004}, type = {Research Article}, chapter = {999}, abstract = {

Background: The medicinal plants consider as a rich resource of ingredients which can be used in drug development and synthesis. Blumea lacera (Burm. f.) DC. is generally used in traditional medicine for the treatment of cough, bronchitis, dysentery, wound healing. The aim of this study is to isolate and identify the compounds from the aerial parts of Blumea lacera. Methods: The aerial parts of B. lacera were dried, powdered and extracted using EtOH, and the concentrated extract was partitioned in succession with n-hexane, CH2Cl2, and EtOAc. From the EtOAc fraction, the compounds were isolated through column chromatography and their chemical structures were elucidated by NMR spectroscopy and confirmed by comparison of their NMR data with literature data. Results: Repeated column chromatography of the EtOAc-soluble fraction from the aerial parts of B. lacera resulted in the isolation of β-sitosterol (1), campesterol (2), artemetin (3) and acid paracatechuic (4).

}, keywords = {Asteraceae, Blumea lacera, Column chromatography, Flavonoid}, doi = {10.5530/pj.2021.13.129}, author = {Xuan Phong Pham and Tran Thi Tuyet Nhung and Hoai Nam Trinh and Do Minh Trung and Dang Truong Giang and Binh Duong Vu and Nguyen Trọng Diep and Nguyen Van Long and Van Thu Nguyen and Chu Van Men} } @article {1359, title = {Medicinal Value of Three Agricultural Weed Species of the Asteraceae Family: A Review}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {264-277}, type = {Review Article}, chapter = {264}, abstract = {

Ageratum conyzoides L., Tridax procumbens L. and Bidens pilosa L. are well known plant species of the Asteraceae family that are considered weeds in intensive agriculture. These weeds are traditionally known to have medicinal properties and have been used for therapeutic treatments. However, it is only the lack of proper knowledge, awareness and screening that have limited their use in pharmaceutical sectors. This review attempts to consolidate the traditional, phytochemical and pharmacological studies that have been carried out on Ageratum conyzoides L., Tridax procumbens L. and Bidens pilosa L., which we note are widely spread throughout the world. This study was conducted through a coherent search on Ageratum conyzoides L., Tridax procumbens L. and Bidens pilosa L. with respect to traditional uses, phytochemical and pharmacological studies that have been performed on these three agricultural weeds all over the world. An exploration of reported descriptions of the potential medical importance of three agricultural weed species (A. conyzoides, T. procumbens and B. pilosa) has been presented. The present review would encourage further clinical investigations into these three plants and their extracts to more closely define the range of uses of these herbs for clinical applications. This, in turn, would give a clear understanding whether these weed species might be targeted to be conserved in a sustainable manner rather than eradicated.

}, keywords = {Ageratum conyzoides, Bidens pilosa, Pharmacological, Phytochemical, Traditional use, Tridax procumbens}, doi = {10.5530/pj.2021.13.36}, author = {Mithila Jayasundera and Singarayer Florentine and Kushan U Tennakoon and Bhagirath Singh Chauhan} } @article {1727, title = {Molecular Study of Acalypha indica to Leptin, Alpha Glucosidase, and its Antihyperglycemic Effect on Alpha Glucosidase}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1639-1647}, type = {Research Article}, chapter = {1639}, abstract = {

Introduction: The purpose of this study is to find potential inhibitors of leptin as a proinflammatory adipokine and alpha glucosidase as an enzyme that mediate hyperglycaemia; to alter the chronic complications of obesity from herbal Acalypha indica (Ai). This study was conducted using in silico molecular docking to evaluate the Ai compounds interaction with leptin and alpha glucosidase. The in vitro assay to alpha glucosidase was done to explore antihyperglycemic effect of Ai, as hyperglycaemia is the key process of chronic complication of obesity. Material and Methods: Protein target were leptin and alpha glucosidase; compounds from Ai plant were repundusinic, mauritanin, hesperetin, acaindinin, and glucogalin in pdb format. Molecular docking using autodock vinna. In vitro assay of Ai antihyperglycemic activity was done to alpha glucosidase and was define as IC50 level. Result: The results from the docking analysis demonstrated that compounds from Ai roots contain antihyperglycemic-antiobesity activity which acted by inhibiting leptin and alpha glucosidase receptors. Repundusininc and mauritanin compounds contain hydrogen bond with the greatest leptin enhancer activity on Ser9, Thr35, Glu8, Ser9, Thr25, Gln111, Lys211, Leu7 for repundisinic and Glu8, Thr25, Gly112 and Leu7 for mauritanin. Hesperetin, acaindinin and glucogallin were the most identical compounds with similar affinity binding value to alpha glucosidase. Ai roots was already proven as anti-hyperglycemic-antiobesity which was further confirmed by in vitro assay to alpha glucosidase (IC50 19,429 μg/ml.). Conclusion: The results demonstrated that Ai have anti hyperglycaemic-antiobesity effects and was found to be potentially as antihyperglycemic by in vitro assay to alpha glucosidase.

}, keywords = {Acalypha indica, Alpha glucosidase., Antiobesity, Leptin}, doi = {10.5530/pj.2021.13.211}, author = {Rani Wardani Hakim and Fadilah Fadilah and Tri Juli Edi Tarigan and Sri Widia A Jusman and Erni H Purwaningsih} } @article {1368, title = {Nutritional and Functional Potential of Selliera radicans Cav., a Chilean Native Halophyte}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {341-346}, type = {Original Article}, chapter = {314}, abstract = {

Background: Selliera radicans was recognized as one of the foods consumed by the oldest human settlement in America (Monte Verde, Chile) that had a diet with a high component of plants. Objective: This study aims at investigating nutritional and functional characteristics of S. radicans, a native halophyte from Chile. Materials and Methods: An analysis of total protein, carbohydrate, ash, and moisture from S. radicans leaves was performed, using standard methods. The content of macro and micronutrients was quantified by atomic absorption spectrometry. The inulin content was carried out based on the Seliwanoff reactions. S. radicans leaves were extracted with methanol and the total content of phenolic and flavonoids and antioxidant activity were evaluated by spectroscopic method. Results: Leaves from cultivated plants proved to be a suitable source of proteins (7.5 \% on DW), ash (6.8 \% on DW), and a wide range of macro and micronutrients, where Ca, K, and Na had the highest values. In addition, inulin (2.3\% on DW), total phenolics (63.4 GAE/g LDW) and flavonoids (21.8 QE/g LDW), and antioxidant capacity (10 TE/g LDW) were noted. Conclusions: According to the results, cultivated S. radicans leaves are promising sources of food with beneficial health properties.

}, keywords = {antioxidant activity, Goodeniaceae, Inulin, Macro and Micronutrients, Total flavonoids, Total Phenolics}, doi = {10.5530/pj.2021.13.44}, author = {Maria del Pilar Caramantin Soriano and Flavia Schiappacasse and Patricio Pe{\~n}ailillo and Jaime Tapia and Sergio Wehinger and Camilo A Valenzuela-Vasquez and Sarvia M Dur{\'a}n-Pe{\~n}a} } @article {1417, title = {Pharmacognostic Study of Collection and Study of its Hepatoprotective Activity}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {713-721}, type = {Original Article}, chapter = {713}, abstract = {

Background: The aim of this work is pharmacognostic study of herbal formulation consisting of elecampane rhizomes and roots (Inula helenium L.), fruits of rose (Rosa sp.) and hawthorn (Crataegus sp.), leaves of pepper mint (Mentha piperita L.) and cowberry leaves (Vaccinium vitis-idaea L.), spiny eleuterococcus rhizomes and roots (Eleutherococcus senticosus (Rupr.et Maxim.) Maxim., low cudweed herb (Gnaphalium uliginosum L.s.l.) as well as determination of its hepatoprotective activity. Materials and methods: An electron microscope, HPLC and methods of the State Pharmacopoeia of Russia were used in pharmacognostic study of herbal formulation. The hepatoprotective, antioxidant and choleretic activities of the herbal formulation were studied in vivo model of liver damage induced by tetracycline hydrochloride and 40\% ethanol. Results: The content of biologically active substances (BAS) collected: essential oils - at least 0.30\%; flavonoids in terms of luteolin - not less than 1.0\%; ascorbic acid - not less than 0.5\%; tannins - not less than 3.0\%; arbutin - at least 0.4\%; eleutheroside B - not less than 0.01\%.It has been found that the course administration of herbal formulation to white Wistar rats with liver damage eliminates the prooxidant effect of tetracycline and ethanol, reduces the manifestation of cholestasis and increases the rate of bile secretion for 1-3 hours. Conclusion: The herbal formulation has hepatoprotective activity, antioxidant, choleretic effect and stimulates regenerative and antitoxic processes in the liver in rats with a model of combined liver damage induced tetracycline and ethanol. The obtained research results argue the possibility of using herbal formulation for prevention and complex treatment of liver diseases.

}, keywords = {Hepatoprotective activity, microscopy, Phenolic compounds, standardization}, doi = {10.5530/pj.2021.13.91}, author = {Lubsandorzhieva PB and Rendyuk TD and Dashinamzhilov Zh.B and Dargaeva TD and Ferubko EV} } @article {1330, title = {Phytochemical Screening and Antioxidant Activities of the Seedling Extracts from Inca Peanut Plukenetia volubilis}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {52-58}, type = {Original Article}, chapter = {52}, abstract = {

Background: Plukenetia volubilis L., Inca peanut is an oleaginous plant, widely cultivated as commercially in South East Asia, especially in Thailand. The oil from the seed plant is a greatest interesting a natural source. Objectives: The aims of this study were investigated phytochemical screening, to evaluated the total flavonoids and phenolic compound contents as well as antioxidant activities of seedling extract from P. volubilis. Methods: The dried P. volubilis seedlings of 21 days growing period were extracted by using different solvent including aqueous (ASS), 50\% ethanolic (HESS), and 95\% ethanolic (ESS) extracts. The phytochemical screenings were determined on total phenolic compound (TPC) and flavonoid (TFC) contents. The antioxidation were tested by using 2,2-diphenyl-1-picrylhydrazy radical scavenging (DPPH), 2,2 -azinobis-(3-ethylbenzothiazoline-6-sulphonate) (ABTS+) assay, and ferric reducing antioxidant power (FRAP). Results: The results found that the ESS were significantly highest amount on total phenolic compound (23.0809{\textpm}0.8632 mgGE/gExt ) and flavonoid (466.3839{\textpm}1.5580 mgQE/gExt) contents. In this study, ascorbic acid (IC50 =0.016{\textpm}0.0003 mg/mL) and Trolox (IC50 =0.044{\textpm}0.0008 mg/mL) as standard substances were showed more potent than all of the extracts from P. volubilis seedlings. Surprisingly, the ESS has more potent on free radical scavenging higher than different solvents; DPPH=0.007{\textpm} 0.001 (IC50=mg/mL), ABTS= 1.4065{\textpm} 0.0505 (IC50=mg/mL),and FRAP= 74.4960{\textpm} 2.6067 (mg=TE/gExt). Conclusion: the plant seedling extracts composed with high amount of flavonoids and phenolic compound contents possess valuable to antioxidant activities. The seedling extracts from the plant could apply to supplementary food, cosmetic, pharmaceutical, and horticultural industries. Next study, chemical compositions, the major active compound(s), and biological activities will be clarified.

}, keywords = {antioxidant activity, Flavonoids, Inca peanut seedling, Phenolic compounds, Phytochemical screening, Plukenetia Volubilis}, doi = {10.5530/pj.2021.13.8}, author = {Darunee Puangpronpitag and Puangpaka Tankitjanon and Adisak Sumalee and Ampa Konsue} } @article {1705, title = {Phytochemistry and Biological Evaluation of Daphne gnidium L. Butanol Extract}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1688-1693}, type = {Research Article}, chapter = {1688}, abstract = {

Background: Daphne gnidium L. (Thymelaeaceae) has been used in the Mediterranean basin to treat skin diseases, rheumatism and toothache.\ Objective: the aim of this study was to evaluate the biological activities of butanol extract from the D. gnidium leaves. Methods: A quantitative analysis by high-performance liquid chromatography with a diode array detector (HPLC-DAD) was performed. The antioxidant activities were evaluated by using three different assays: 2,2-diphenyl-l-picrylhydrazyl assay (DPPH assay), deoxyribose degradation assay and Cellular Antioxidant Activity (CAA) assay. The butanol extract was investigated for anti-inflammatory and analgesic activities in animal models. In addition, its effect on the production of NO and lysosomal activity in vivo was assessed. Results: The HPLC-DAD analysis showed the presence of daphnetin. The butanol extract had a remarkable antioxidant activity in the different systems tested. Furthermore, it has an anti-inflammatory effect by inhibiting the xyleneinduced ear edema and reduced the number of abdominal constrictions in mice indicating analgesic effect. It also was found to inhibit (NO) production and lysosomal activity in vivo. Conclusion: These findings support the daphne use in traditional medicine for its analgesic and anti-inflammatory activities. Further investigations to elucidate its mechanism of action are required.

}, keywords = {Analgesic, Anti-inflammatory, Antioxidant, Daphne gnidium, Lysosmal activity, Nitric oxide production.}, doi = {10.5530/pj.2021.13.217}, author = {Amira Horchani and Fadwa Chaabane and Mahassen Barboura and Imen Mokdad-Bzeouich and Aimen Abbassi and Amine Trabelsi and Leila Chekir-Ghedira} } @article {1380, title = {Potential Inhibition by Phaleria macrocarpa Leaves Ethanol Extract on Ki-67 Expression in Distal Colon Mouse}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {March 2021}, pages = {443-449}, type = {Research Article}, chapter = {443}, abstract = {

Ulcerative colitis (UC) has been an important aspect of an incurable chronic inflammatory disease over the last few decades. To find useful therapies for UC, one of which is herbal therapy, many researches have been conducted. Due to its anti-inflammatory effects, Phaleria macrocarpa (PM), an Indonesian indigenous herb, is considered to be the alternative therapy for UC. Phaleria macrocarpa Leaves Ethanol Extract (PMLEE) is then used in this research to determine its effect on UC by using Ki-67 as a marker of proliferation. PMLEE was created from dry PM content undergoing maceration. The animals were classified into six categories: normal, positive control, negative control and PMLEE group (100, 200, 300 mg/kgBW). PMLEE was then injected for 7 consecutive days into BALB/c mice that were caused by dextran sodium sulphate (DSS). DSS is used for modeling UC in the colon tissue of mice. All mice were terminated and then stained with anti-Ki-67 after their colons were extracted. Subsequently, the stained parts were analyzed with ImageJ based on the color intensity produced by the results of H-score. Based on H-score, PMLEE 300mg and 200mg has significantly decreased the expression of Ki-67 compare to the negative control (p=0.001 and p=0.01). PMLEE also has a tendency to be dose dependent based on the significant difference from PMLEE 300mg and 100mg (p=0.002). It then concludes that PMLEE is related to Ki-67 expression in cells, as it was inversely proportional in this analysis.

}, keywords = {Dextran sodium sulphate, Inflamation, Ki- 67, Mahkota Dewa (Phaleria macrocarpa)}, doi = {10.5530/pj.2021.13.56}, author = {Kusmardi Kusmardi and Elvan Wiyarta and Ari Estuningtyas and Nurhuda Sahar and Yurnadi Hanafi Midoen and Aryo Tedjo and Alfred Pakpahan} } @article {1326, title = {Potential of Phaleria macrocarpa Leaves Ethanol Extract to Upregulate the Expression of Caspase-3 in Mouse Distal Colon after Dextran Sodium Sulphate Induction}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {23-29}, type = {Original Article}, chapter = {23}, abstract = {

Ulcerative colitis (UC) is a part of incurable chronic inflammatory disease that has gained importance over the past few decades. A lot of research has been done to find effective treatments for UC, one of which is herbal medicine. Phaleria macrocarpa (PM), an Indonesian native plant, is thought to be an alternative therapy for UC because of its anti-inflammatory properties. Therefore, in this research, Phaleria macrocarpa Leaves Ethanol Extract (PMLEE) is used to assess its effect on UC by using Caspase-3 as apoptosis marker. PMLEE was made from dried material of PM that undergo maceration. Animals were separated into six groups: normal, negative control, positive control, and PMLEE groups (100, 200, 300 mg/kgBW). PMLEE was then injected to BALB/c mice that have been induced by dextran sodium sulphate (DSS) for 7 consecutive days. DSS is used to model UC in mice colon tissue. All animals were sacrificed and their colons were collected then stained with anti-Caspase-3. The stained sections were subsequently examined with ImageJ based on color intensity which generated H-Score as the results. Based on H-Score of each group, PMLEE 300mg has significantly upregulate the expression of Caspase-3 compare to the negative control (p=0.015). PMLEE also has a tendency to be dose dependent based on the significant difference between PMLEE doses. Therefore, it concludes that PMLEE is able to upregulate the expression of Caspase-3 in colon cells as in this study it was directly proportional. Key words: Mahkota Dewa, Inflammation, Apoptosis, Ulcerative colitis.

}, keywords = {Apoptosis, Inflammation, Mahkota Dewa, Ulcerative colitis}, doi = {10.5530/pj.2021.13.4}, author = {Kusmardi Kusmardi and Elvan Wiyarta and Ari Estuningtyas and Nurhuda Sahar and Yurnadi Hanafi Midoen and Aryo Tedjo} } @article {1725, title = {Preclinical Safety Evaluation of Acute and Subacute Intranasal Administration of Polyphenols-based Cinnamon Bark Extract in Laboratory Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1621-1631}, type = {Original Article}, chapter = {1621}, abstract = {

Background: Polyphenols-based standardized cinnamon (Cinnamomum zeylanicum) bark extract (IND02) demonstrated efficacy against allergic rhinitis in animal models and human clinical study. Objectives: To assess the acute and subacute intranasal toxicity of the IND02 nasal solution (IND02-NS). Methods: Acute and 28-days subacute toxicity using the intranasal route of administration of IND02-NS was evaluated using Wistar rats as per Organisation for Economic Co-operation and Development guidelines. For acute intranasal toxicity study, a single dose of 100 μg/rat/day was administered in five male and female rats and observed for the incidence of mortality and signs of toxicity for 14 days. For a 28-days subacute intranasal toxicity study, doses of 20, 50, and 100 μg/rat/day were administered to a group of five male and female rats. Results: The IND02-NS did not show mortality or treatment-related adverse signs during acute (limit dose of 100 μg/rat/day) and subacute intranasal (28-days repeated dose of 20, 50, and 100 μg/rat/day with 14 days of reversal period) administration. The IND02-NS showed a maximum tolerated dose greater than 100 μg/rat during the acute intranasal toxicity study. The no-observed adverse effect level of IND02-NS was 100 μg/rat/day in rats during the subacute intranasal toxicity study. Conclusion: IND02-NS was found safe at 100 μg/rat/day during acute and subacute (28 days repeated dose) for nasal administration in rats.

}, keywords = {Intranasal toxicity, Maximum tolerated dose, Noobserved- adverse-effect level., Polyphenols, Standardized cinnamon bark}, doi = {10.5530/pj.2021.13.209}, author = {Prasad Thakurdesai and Pallavi Deshpande} } @article {1677, title = {Protective effect of Salvia officinalis against cypermethrininduced reprotoxicity in male Wistar rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {November 2021}, pages = {1413-1421}, type = {Research Article}, chapter = {1413}, abstract = {

Background: Medicinal plants are a reservoir of biologically active compounds with therapeutic properties that, over time, have been used for the treatment of various diseases. This study aims to evaluate the protective effect of the aqueous extract of the leaves of Salvia officinalis against cypermethrin-induced toxicity. Methods: 30 male rats weighing approximately 240 g were divided into equal six groups; the control group received tap water, the positive control received the aqueous extract of sage leaves (SLE) at a dose of (0.5g/kg bw), the groups treated with cypermethrin (Cyp1) at 8.33 mg/kg bw and (Cyp2) at 25 mg/kg bw, and the groups treated by cypermethrin combined with aqueous extract of sage SLE+Cyp1 (0.5g/kg bw+8.33 mg/kg bw) and SLE+Cyp2 (0.5g/kg bw+25 mg/kg bw) for four days/week. After 4 weeks of oral administration, epididymal seminal fluid was analyzed via the CASA system, in addition to the histological study testis and epididymis. Results: The obtained results showed a decrease in the absolute weight of the reproductive organs, with a significant decrease in sperm concentration, motility and speed in the cypermethrin-treated group compared to the control. Histological study of the testes and epididymis indicates an alteration in the stages of spermatogenesis in groups Cyp1 and Cyp2 compared to the control. However, the above-mentioned parameters were maintained almost normal in the groups that received the aqueous extract of sage with both doses of cypermethrin. Conclusion: it can be demonstrated that SLE has been shown to protect rats from cypermethrin-induced reprotoxicity.

}, keywords = {Cypermethrin, Histology, Rats, Salvia officinalis, Spermatozoa, Toxicity}, doi = {10.5530/pj.2021.13.179}, author = {Amel CHOUABIA and Samir DJEMLI and Cherif ABDENNOUR and Leila MALLEM and Labiba KAHALERRAS and Fatma Zohra ARKOUB and Narimene BOUABDALLAH and Abdelkrim TAHRAOUI} } @article {1412, title = {Qualitative and Quantitative Analysis of 70\% Ethanol Extract from Ruta angustifolia for Developing Anti-Hepatitis C Agents}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {682-687}, type = {Original Article}, chapter = {682}, abstract = {

Background: Medicinal plants are potential sources for drug candidates. It possesses with various metabolites which have many pharmacology effects. Ruta angustifolia is one of medicinal plants that has been used traditionally for liver disease. Previous study it has been demonstrated to inhibit hepatitis C virus under in vitro cell culture. It decreased protein NS3 level and gave synergistic effect in combination with simeprevir and telaprevir. This plant provides a prospective candidate to develop as anti-HCV Objective: This study evaluates the phytochemistry screening for qualitative assay and determine the concentration of rutin as marker compound for developing R. angustifolia extract as anti-HCV agent. Materials and Methods: R. angustifolia leaves were extracted with 70\% of ethanol. Extract and rutin were analysis their anti-HCV activity by in vitro culture cells of Huh7it. The concentration of rutin was determine by TLC densitometry. Results: The 70\% ethanol extract of R. angustifolia dan rutin exhibit anti-HCV activities with IC50 value of 2.9 {\textpm} 0.8 μg/ml and 28.1 {\textpm} 5.6 μg/ml, respectively. Screening phytochemistry demonstrated to contain flavonoid, terpenoid, alkaloid and polyphenols. TLC densitometry analysis yield the concentration of rutin in extract 0.06 \%. Conclusion: Extract of 70\% ethanol of R. angustifolia has a potential anti-HCV activity. Extract of R. angustifolia may provide a good candidate for developing anti-HCV agents.

}, keywords = {Hepatitis C Virus, Infectious disease, Medicinal plants, Medicine, Ruta angustifolia, Rutin}, doi = {10.5530/pj.2021.13.87}, author = {Tutik Sri Wahyuni and Adita Ayu Permanasari and Lidya Tumewu and Aty Widyawaruyanti and Achmad Fuad Hafid} } @article {1618, title = {Repairing of Renal Tubules in Diabetic Rats (Rattus norvegicus) Diabetes After Administration of Golden Sea Cucumber (Stichopus hermanii)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {958-964}, type = {Research Article}, chapter = {958}, abstract = {

This study aims to analyze the improvement of the histopathological picture of renal tubules in diabetic rats after being given golden sea cucumber extract (Stichopus hermanii). This research uses experimental design laboratories with a post-test only control group design method. The sampling used simple random sampling with 25 white rats divided into five groups, namely groups that were given standard feed without STZ-induced, STZ-induced group, STZ-induced group and given golden sea cucumber extract at a dose of 4.25 mg/kg BW for 21 days, STZinduced group and given golden sea cucumber extract at a dose of 8.5 mg/kg BW for 21 days, and STZ-induced group and given gold sea cucumber extract at a dose of 12.75 mg/kg BW for 21 days. The data on the observation of each group{\textquoteright}s kidney histopathology was carried out at the end of the session. The results of the analysis using the Kruskal-Wallis Test showed significant results, the Mann-Whitney Test showed significant differences between the STZinduced group and the golden sea cucumber extract (Stichopus hermanii) dose of 12.75 mg/kg BW (x=7.4 mg/dl) decreased significantly (p=0.001) compared to the STZ-only-induced group (x=12.6 mg/dl). Administration of golden sea cucumber extract (Stichopus hermanii) at a dose of 12.75 mg/kg BW of rats for 21 days lowered the degree of tubular damage to the kidney rectus of white rats (Rattus norvegicus) male streptozotocin-induced strains.

}, keywords = {Diabetic rat, Stichopus hermanii, Tubular injury}, doi = {10.5530/pj.2021.13.123}, author = {Herin Setianingsih and Satria Erda Wisnumarta and Sareh Arjono Tjandra} } @article {1428, title = {A Review of the Traditional Uses, Medicinal Properties and Phytochemistry of Centaurea benedicta L.}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {May 2021}, pages = {798-812}, type = {Review Article}, chapter = {798}, abstract = {

Centaurea benedicta L. is an annual herbaceous plant which belongs to the Asteraceae family. It is native to the Mediterranean region and western Asia and is commonly known as blessed thistle, holy thistle, St Benedict{\textquoteright}s thistle or spotted thistle. Traditionally, it has been used to treat bubonic plague and possesses diuretic, galactagogue, liver-strengthening and wound healing properties. Recent research studies have investigated its anticancer, antiinflammatory, antioxidant and other therapeutic properties. Several studies have also reported its antimicrobial activity against a range of bacterial pathogens. However, most of these studies were preliminary and only tested relatively high concentrations of the extracts. Additionally, most studies screened a limited number of pathogens. Cnicin is the main chemical compound present in C. benedicta and it has been widely investigated. However, few other compounds from this plant have been identified and/or investigated, and further phytochemical studies are warranted. Interestingly, pure cnicin has good anticancer activity, whilst the crude extracts lack cytotoxic properties. Phytochemical analyses of C. benedicta extracts reveal the presence of multiple flavonoids, tannins, terpenoids and lactones, although few specific phytochemicals within these phytochemical classes have been identified. A limited number of research studies have determined the toxicity profile of C. benedicta in order to evaluate its safety for human use. Substantially more detailed studies are required to rigorously investigate the therapeutic properties and phytochemistry of C. benedicta, which may ultimately lead to the development of new plant-based therapeutic medicines.

}, keywords = {Asteraceae, Blessed thistle, Flavonoids, St Benedict{\textquoteright}s thistle, Tannins, Terpenoids}, doi = {10.5530/pj.2021.13.102}, author = {Gagan Tiwana and Jiahe Fua and Lanping Lu and Matthew J Cheesman and IE.Cock} } @article {1286, title = {Acute Diuretic Activity of the Aqueous Ethanol Root Extract of Corrigiola telephiifolia Pourr. In Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1552-1558}, type = {Original Article}, chapter = {1552}, abstract = {

Objective: This study was undertaken to justify and validate a very frequent traditional use of a very well-known and widely used plant by a large part of the Moroccan population. It{\textquoteright}s about Corrigiola telephiifolia, and the activity in question is the diuretic activity. Methods: The aqueous ethanol root extract of CMethods:orrigiola telephiifolia (200 mg/kg, 400 mg/kg, and 700 mg/kg) was orally administered to rats. The urinary excretion rate and pH, and electrolyte excretion were measured in the urine of saline-loaded rats. Negative control group received only an equivalent volume of distilled water, while the positive control groups received the diuretic drugs hydrochlorothiazide at dose 10 mg/kg. Results: The results showed that hydrochlorothiazide induced significant diuresis and electrolytes excretion at 1, 6 and 24 h after the treatment. Both the higher doses of the extract produced a significant increase in urine volume than the control from the first hour until the end of observation. However, the lowest dose increased significantly only at 24 h after the treatment. With regard to the electrolyte excretion, the tested doses of CTRE which have shown a significant increase in Na+, K+ and Cl-excretion in comparison to normal control rats, are 400 and 700 mg/kg bw. Conclusion: These findings collectively indicate that the extracts of C. telephiifolia have a potential to induce diuresis markedly, and providing evidence, for its traditional use.

}, keywords = {Corrigiola telephiifolia, Diuretic activity, Diuretic plants, Kaliuresis, Urine electrolytes}, doi = {10.5530/pj.2020.12.213}, author = {Imane Zakariya and Omar Elhamdaoui and Zineb ibn lahmar Andaloussi and Abdelhak Chergui and El Amine Ajal and Khalid Taghzouti and Rachid Nejjari} } @article {1160, title = {The Alkaloid Fraction from Melicope latifolia Leaves Inhibits Hepatitis C Virus}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {535-540 }, type = {Research Article}, chapter = {535}, abstract = {

Introduction: Hepatitis C Virus (HCV) is a major health problem, which infects approximately 170 million people among worldwide population. Moreover, there is no vaccine available to prevent HCV infection and the current anti-HCV drugs have not covered all the various genotypes and subtypes. Meanwhile, medicinal plants have been widely used to treat a variety of infectious disease. Our previous study reported that ethanol extract of Melicope latifolia has been shown to exert anti-HCV activity towards a number of different virus genotypes with mainly inhibition mechanism at the entry step. Further separation was needed to purify and identify the active anti-HCV constituent using bioactivity-guided isolation method. Materials and Methods: In vitro Anti-HCV assay was performed using hepatocyte cell line (Huh7it) and HCV genotype 2a (JFH1). The purification of M. latifolia ethanol extract (B1F) was done by liquid-liquid fractionation, vacuum liquid chromatography (VLC), and high-performance liquid chromatography (HPLC). The active fraction was further identified by thin layer chromatography (TLC) and the major constituent was determined by nuclear magnetic resonance (NMR) spectra data analysis. Results: The fractionation of M. latifolia leaves ethanol extract resulted an alkaloid fraction (B1F D2H.3) containing a major constituent N-methylflindersine. This alkaloid fraction was active to reduce HCV JFH1 with an inhibition concentration (IC50) value of 6.21 {\textmu}g/mL, a cytotoxicity concentration (CC50) value of 82.64 {\textmu}g/mL, and a selectivity index value of 13.31. Conclusion: An alkaloid fraction of M. latifolia (B1F D2H.3) was known to have major compound named N-methylflindersine. This alkaloid fraction exhibited strong anti-HCV against JFH1 in vitro. The results indicated that this alkaloid fraction may a good candidate for anti-HCV agent.

}, keywords = {Anti-HCV, Melicope latifolia, N-methylflindersine}, doi = {10.5530/pj.2020.12.81 }, author = {Dwi Susiloningrum and Adita Ayu Permanasari and Myrna Adianti and Lidya Tumewu and Tutik Sri Wahyuni and Mulyadi Tanjung and Aty Widyawaruyanti and Achmad Fuad Hafid} } @article {1146, title = {Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA)}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {562-568 }, type = {Research Article}, chapter = {562}, abstract = {

Objective: To determine the ameliorative effect of the ethanolic extract of Chuquiraga spinosa (ChS) on 7,12-Dimethylbenz[a]anthracene (DMBA)-induced breast cancer in rats. Methods: 36 female Holztman rats were divided into 6 groups. I) The negative control group received physiological saline (PS). II) ChS-200 group received 200 mg/kg of ChS. III) DMBA group was induced with DMBA (20 mg/Kg) dissolved in PS and administrated orally for 15 weeks. IV) DMBA + ChS-50 group, V) DMBA + ChS-250 group, and VI) DMBA + ChS-500 group, which received the extract orally for 15 weeks after DMBA induction. All data were expressed as mean and standard deviation. One-way analysis of variance (ANOVA) followed by Dunnet test was carried out to compare the mean value of different groups Histopathological analysis was evaluated by using Image J software. Results: Hematology showed that the triglyceride level was significantly lowered (P\< 0.01) and high-density lipoprotein (HDL) level was significantly increased (P \<0.01) in groups III, IV and V. Also, ChS extract significantly lowered the C reactive protein (CRP) level (P \<0.01) and malondialdehyde level (P\<0.05). There was a significant decrease in the frequency of DMBA-induced micronucleated polychromatic erythrocyte (P\<0.01). Conclusions: Chuquiraga spinosa showed an ameliorative effect on DMBA-induced breast cancer in rats as well as antioxidant, antitumor and antigenotoxic properties.

}, keywords = {Anticarcinogenic agent, Antioxidant, Breast tumor, Phytochemical, Preventive medicine, Toxicity}, doi = {10.5530/pj.2020.12.85}, author = {Jorge Luis Arroyo-Acevedo and Oscar Herrera-Calderon and Johnny Aldo Tinco-Jayo and Juan Pedro Rojas-Armas and Abdur Rauf and Ren{\'a}n Ha{\~n}ari-Quispe and Linder Figueroa-Salvador and Victor Fern{\'a}ndez-Guzm{\'a}n and Ricardo {\'A}ngel Yuli-Posadas} } @article {1070, title = {Anticancer Activity of Ruellia britoniana Flower on Cervical HeLa Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {29-34}, type = {Original Article}, chapter = {29}, abstract = {

Introduction: Cervical cancer ranks 4th in terms of the mortality rates and incidence of all cancers in women (GLOBOCAN 2018). In last decade, there is a significance progress in cancer therapy followed by an increase in the cost of cancer treatment. Therefore, it is necessary to have therapeutic innovations that are expected to reduce the cost of cervical cancer therapy. One therapeutic innovation that is currently being intensively carried out is herbal medicine. Some researchers have found that some plant extracts have anti-cancer properties that can be an alternative treatment for cancer, such as some plants with the genus Ruellia, such as Ruellia tuberosa and Ruellia squarrosa. However, research on the anticancer activity of the species of Ruellia brittoniana, especially the flowers, is still limited. Objective: Aim of this study is to examine anti-cervical cancer activity of R. brittoniana flower. Methods: R.brittoniana flowers were obtained from Depok, West Java, Indonesia. The flowers are extracted gradually with n-hexane, ethyl acetate, and ethanol solvents. The extracts were evaluated for anticancer activity by MTT method. Results: IC50 values for ethanol extract, ethyl acetate extract and n-hexane extract of R. brittoniana flowers are 116.55 ppm, 52.62 ppm, and 123.09 ppm, respectively, which indicating that ethanol extract has moderate anticancer activity, while ethyl acetate and n-hexane extract of R. brittoniana\ flowers have weak anticancer activity. Conclusion: Ethanol, ethyl acetate, and n-hexane extract of R.brittoniana flowers have a potential to become natural anti-cervical cancer.

}, keywords = {Anticancer, Cervical HeLa cells, Ruellia brittoniana}, doi = {10.5530/pj.2020.12.6}, author = {Nadzila Anindya Tejaputri and Ade Arsianti and Fona Qorina and Qotrunnada Fithrotunnisa and Norma Nur Azizah and Rista Putrianingsih} } @article {1102, title = {Antidiabetic Constituents from Helminthostachys zeylanica (L) Hook (Ophioglossaceae)}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {223-226}, type = {Original Article}, chapter = {223}, abstract = {

Background: The roots of tunjuk langit (Helminthostacshys zeylanica) have been used traditionally in some villages in Indonesia, particularly in Riau Province. Objective: In this study we reported two flavonoids and their antidiabetic activity. Material and methods: Isolation of the metabolites was based on polarity fractionation method. Purification processes were conducted by vacuum liquid chromatography (VLC). Chemical structures were elucidated based on spectroscopy characteristics, including FTIR and 1D/2D NMR. Results: The isolated compounds were identified as ugonin J and K. The antidiabetic activity was measured by α-glucosidase inhibitor assay. The antidiabetic activity of ugonin J was found at IC50 273,13{\textpm}0,402 ppm and Ugonin K was found at IC50 138,21{\textpm}0,263 ppm (moderately active). Conclusion: Therefore this plant can be used traditionally as antidiabetic medicine.

}, keywords = {Antidiabetic, Helminthostacys zeylanica, Ophioglossaceae, α-glucosidase}, doi = {10.5530/pj.2020.12.33}, author = {Fania El Ridhasya and Novia Rahim and Muhammad Almurdani and Rudi Hendra and Hilwan Yuda Teruna} } @article {1184, title = {Antimalarial Activity of Flavonoid Compound Isolated from Leaves of Artocarpus altilis}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {835-842}, type = {Research Article}, chapter = {835}, abstract = {

Introduction: Artocarpus altilis leaves extract has previously been reported as a potential antimalarial drug. Inhibition concentration (IC50) against P. falciparum and effective dose values (ED50) against P. berghei have been reported at 1.32 μg/ml and 0.82 mg/kg, respectively. The aim of this study is to identify the active compound from the ethanol extract of A. Altilis leaves against P. falciparum. Materials and Methods: The isolation of the active compound from the ethanol extract of A. altilis were conducted using chromatography methods, and the chemical structure of the isolated compounds was determined based on NMR and MS spectra data. Antimalarial assay was determined using microscopic method against P. falciparum 3D7 and molecular docking studies was performed using Molegro Virtual Docker version 5.5 program. Results: A flavonoid compound, class of dihydrochalcone was finally isolated from A. altilis and identified as 1-(2,4-dihydroxy phenyl)-3-[8-hydroxy-2-methyl-2-(4-methyl-3- pentenyl)-2H-1-benzopyran-5-yl]-1-propanone (Compound-1). Antimalarial activity test revealed that the compound strongly inhibited P. falciparum growth, with IC50 value of 1.05 μM. An in silico study to determine the mechanism of action of the compound revealed the existence a 3.BPF receptor that possesses a cysteine protease inhibitor of falcipain-2. Conclusion: Compound-1 were isolated from the leaves of A. Altilis is a good candidate of new source in the development of antimalarial drugs. An animal study using this compound is recommended before a clinical trial.

}, keywords = {Artocarpus altilis, Cysteine protease inhibitor, Dihydrochalcones, P. falciparum 3D7}, doi = {10.5530/pj.2020.12.120}, author = {Agriana Rosmalina Hidayati and Aty Widyawaruyanti and Hilkatul Ilmi and Mulyadi Tanjung and Tri Widiandani and Siswandono and Din Syafruddin and Achmad Fuad Hafid} } @article {1165, title = {Antimalarial Effects of the Aqueous Extract of Entandrophragma angolense Bark on Plasmodium berghei Infection in Mice}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {687-698}, type = {Original Article}, chapter = {687}, abstract = {

Background: Research for new antimalarial drugs remains a permanent quest for the control of malaria. Objective: The present study investigates the effects of the aqueous extract of Entandrophragma angolense bark on P. berghei-induced malaria in mice. Methods: Eight weeks old mice, were intraperitoneally infested with 200 μl of blood, containing 1x106 P. berghei-infected-erythrocytes. Parasitaemia was determined using a 10\% giemsa stained blood smear read under optical microscope (x100). The infected animals were randomized into 5 groups of 10 animals each and daily treated for 5 days with the plant extract at 125, 250 and 500 mg/kg. The normal control and malaria control received water while the chloroquine control was treated with 10 mg/kg of chloroquine. Body weight, parasitaemia and survival time were monitored daily during treatment and follow up periods. Five animals from each group were sacrificed under anaesthesia at the end of treatment (d8) and after the follow up period (d28). Venous blood was used for haematological and biochemical tests. Organs (liver, kidneys and spleen) were also collected for biochemical and histological analyses. Results: Administration of the aqueous extract of E. angolense bark to infected mice significantly inhibited parasite development (p \<0.001) with ED50 estimated at 25.32 mg/kg. The extract prevented animal from death, body weight loss, anaemia, leucocytosis, high transaminases (ALT and AST), high bilirubin, creatinine and MDA levels, oxidative stress and anatomical alteration in organs as compared to the malaria control. Conclusion: The E. angolense bark possesses antimalarial properties, supporting its use in traditional medicine to treat malaria.

}, keywords = {Antiplasmodial activity, E. angolense, Malaria infection, Mice, P. berghei}, doi = {10.5530/pj.2020.12.101}, author = {Raceline Gounoue Kamkumo and Abel Narcisse Messi Betene and Patrick Valere Tsouh Fokou and Jean Hubert Donfack and Marius Jaur{\`e}s Tsakem Nangap and Albertine Ngako and Roberto Fokou and Mariscal Brice Tchatat Tali and Florence Ngueguim Tsofack and Th{\'e}ophile Dimo and Fabrice Fekam Boyom} } @article {1223, title = {Anti-migration and Anti-invasion Abilities of Methanolic Leaves Extract of Clerodendrum Inerme on Lung Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1024-1031}, type = {Original Article}, chapter = {1024}, abstract = {

Background: Clerodendrum inerme is a folk medicinal plant used in the treatment of various illnesses such as a cough, scrofulous infection, venereal infection, skin diseases and tumors. It exhibited many pharmacological effects including hepatoprotective, anti-inflammatory, antibacterial, anti-oxidant and anticancer properties. Objective: The purpose of this study was to investigate the influence of methanolic extract of C. inerme leaves on migration, invasion and adhesion activities on human lung adenocarcinoma. Materials and methods: Cytotoxicity, cell motility, migration, invasion and adhesion abilities were detected by MTT, wound healing, trans-well mobilization, modified Boyden chamber and cell adhesion assay, respectively. Results: The results demonstrated that up to 400 μg/mL methanolic leaves extract has low toxicity on A549 cells showing more than 50\% cell viability. At non-cytotoxic and sub-toxic doses (200 and 400 μg/mL) of methanolic leave extract significantly suppressed cell motility, migration, invasion and cell adhesion compared with the untreated control. Conclusion: These results suggested that methanolic leaves extract of C. inerme inhibited migration, invasion and adhesion of A549 cells. These findings showed new therapeutic potential for C. inerme in anti-metastatic therapy.

}, keywords = {Anti-invasion, Anti-migration, Clerodendrum inerme, Human lung adenocarcinoma}, doi = {10.5530/pj.2020.12.145}, author = {Malatee Tayeh and Poonsit Hiransai and Hathaichanok Kommen and Ramida Watanapokasin} } @article {1109, title = {Antioxidant and Antidiabetic Activities of Mempening (Lithocarpus bancanus) Leaves}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {328-334}, type = {Original Article}, chapter = {328}, abstract = {

Background: Lithocarpus bancanus or commonly called as mempening in Talang Mamak Tribe, Indonesia is a plant that is used as a traditional medicine. Objective: This study aim to evaluated antioxidant and antidiabetic activities of L. bancanus leaves extract. Material and Methods: The methanol extract was obtained by maceration of the leaves. The n-hexane, dichloromethane and ethyl acetate fractions were prepared by successive partition process of the methanol extract. Antioxidant activities were evaluated by various antioxidant assays, including DPPH (1,1-diphenyl-2-picrylhydrazyl), FRAP (ferric reducing antioxidant power), CUPRAC (cupric reducing antioxidant capacity), and ABTS (2,2{\textquoteright}-azonobis 3-ethylbenzothiazoline-6-sulfonic acid) method. Total phenolics were estimated based on the Folin{\textendash}Ciocalteu method, while, aluminum chloride methods were employed to estimate total flavonoids. Antidiabetic activies was determined by inhibiting the activity of α-glucosidase method. Results: antioxidant activity assay against DPPH radical as well as the total phenolic and flavonoid content of L. bancanus leaves showed that the methanol extract possessed IC50 value of 39.469 {\textpm} 0.273 μg/mL with total phenol and flavonoid were 11.426 {\textpm} 0.432 mg GAE/g dry weight sample and 15.423 {\textpm} 0.213 mg QE/g respectively. The FRAP, CUPRAC and ABTS values of methanol extract were 3494.302 {\textpm}0.456, 26665.501 {\textpm} 5.940 and 2857.977 {\textpm} 0.715 μM TE/g dry weight sample respectively. Antidiabetic activity of methanol extract with IC50 value of 30.565 {\textpm} 0.331 μg/mL. Conclusion: It could be concluded that leaves of L. bancanus have antioxidant and antidiabetic properties.

}, keywords = {Antidiabetic, Antioxidant, Lithocarpus bancanus, Talang Mamak Tribe}, doi = {10.5530/pj.2020.12.52}, author = {Muhammad Almurdani and Adel Zamri and Titania T Nugroho and Jasril Karim and Yum Eryanti and Rudi Hendra and Hilwan Yuda Teruna} } @article {1243, title = {Antioxidant and the Efficacy of Sophora secundiflora and Methoxyisoflavones in the Immune Function of Pigeons Vaccinated against Paramyxovirus Serotype-1}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1276-1288}, type = {Original Article}, chapter = {1276}, abstract = {

Objective: The present work investigated the effect of oral administration of hydroalcoholic (70\% aqueous ethanol) extract (TeE) of Sophora secundiflora leaves and its organic fractions n-hexane (HeE), ethyl acetate (EaE) and n-butanol (BuE) and major isolated methoxyisoflavones 1 and 2, on the cellular and humoral immune responses to live attenuated avian paramyxovirus-1 (APMV-1) vaccines in pigeons. Methods: The structures of six isolated compounds were elucidated on the basis of chromatographic, chemical, and spectroscopic methods. The samples antioxidative and radical scavenging capabilities of 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2{\textquoteright}-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) radical cation and ferric reducing power were determined. Total phenolic, tannin and flavonoid contents of EaE extract were evaluated. Results: Six compounds were isolated. Three were the methoxyisoflavones5- 7-dihydroxy-4'-methoxyisoflavone (1), 7-hydroxy-4'methoxyisoflavone (2), 5,4{\textquoteright}-dihydroxy-7- methoxy-isoflavone (3), along with isorhamnetin (4) and two quercetin derivatives quercetin 3-glucoside (5) and quercetin 3-rutinoside (6) were isolated. The hydroalcoholic extract, fractions and 4{\textquoteright}-methoxyisoflavones showed radical scavenging effect in the order of EaE \> TeE \> BuE \>compound 1\>compound 2\> HeE. Stimulation of both sero-responses was observed, especially this of EaE. The results showed an increase of macrophage cells, lymphocyte and antibody titers in blood. Conclusion: The presence of 5-hydroxyl group at A-ring may be important to show the immunostimulant and antioxidant activity of compound 1vs compound 2. The present results showed the potential abilities of EaE as antioxidant and immunomodulator agent and these would impart healthy economic benefits in vaccinated birds.

}, keywords = {Antiradical effect, Immune, Isoflavones, Paramyxovirus, Pigeons, Sophora secundiflora}, doi = {10.5530/pj.2020.12.176}, author = {Howaida Ibrahim Abd-Alla and Magda Tohamy Ibrahim and Hanan Anwar Aly Taie and Marwa Abas Hasan and Nagwa M M Shalaby} } @article {1085, title = {Antioxidant and Tyrosinase Inhibitory Properties of an Aqueous Extract of Garcinia atroviridis Griff. ex. T. Anderson Fruit Pericarps}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {71-78}, type = {Original Article}, chapter = {71}, abstract = {

Background: Ultraviolet radiation (UVR) is the major cause for hyperpigmentation, and to prevent this natural products are increasingly being explored as potential skin whitening agents. The aim of this study was to determine the total phenolic and flavonoid content, free radical scavenging activity, anti-tyrosinase activity and the inhibition of melanin content in α-melanocyte stimulating hormone-induced B16F10 melanoma cells of an aqueous extract of Garcinia atroviridis Griff. ex. T. Anderson fruit pericarps. Methods: The aqueous extract was prepared by extraction with distilled water at 105oC for 60 min. Total phenolic and flavonoid content were determined using the Folin-Ciocalteau and aluminium chloride methods, respectively. Scavenging activity was assessed using 2,2-Diphennyl-1-picrylhydrazyl (DPPH) and 2,2'-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS). Tyrosinase activity and melanin content were determined spectrophotometrically. Results: The results showed that the aqueous extract of Garcinia atroviridis fruit pericarps had a phenolic (26.33 {\textpm} 0.77 mg GAE/g plant extract) and flavonoid content (9.31 {\textpm} 0.40 mg QE/g plant extract). The aqueous extract of Garcinia atroviridis significantly inhibited mushroom tyrosinase activity (IC50 of 40.72 {\textpm} 1.83 μg/mL) and cellular tyrosinase activity (at a concentration of 125 μg/mL) in α-melanocyte stimulating hormone-induced B16F10 melanoma cells. The Garcinia atroviridis extract also suppressed melanin content at concentrations of 31.25-125 μg/mL. Correlations of mushroom tyrosinase inhibition with DPPH and ABTS scavenging activities were 0.8673 and 0.9468, respectively. Conclusion: Our findings show that an aqueous extract of Garcinia atroviridis fruit pericarps is a source of natural compounds and antioxidant capacity which can inhibit tyrosinase activity and melanin content. Thus, aqueous extracts of Garcinia atroviridis may be a potential source of skin whitening agents for hyperpigmentation.

}, keywords = {B16F10 cells, Garcinia atroviridis, Melanin, Tyrosinase activity, α-MSH}, doi = {10.5530/pj.2020.12.12}, author = {Moragot Chatatikun and Pitaksit Supjaroen and Patcharaporn Promlat and Chantanapa Chantarangkul and Sutida Waranuntakul and Jiraphat Nawarat and Jitbanjong Tangpong and Jitbanjong Tangpong} } @article {1213, title = {Chemical Composition and Some Biological Activities of the Methanolic Encephalartos ferox Fruit Extract}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1190-1197}, type = {Review Article}, chapter = {1190}, abstract = {

Background: Although literature reports the therapeutic properties of Encephalartos ferox, there are limited pharmacological studies of its fruit. Objective: This study sought to evaluate the antibacterial, antioxidant, anti-quorum sensing and in vitro cytotoxic activities of the methanolic E. ferox fruit extract. Methods: The chemical constituent of the methanolic fruit extract was analysed using gas chromatography-mass spectrometry. Antibacterial activity of the extract was investigated against Staphylococcus aureus (ATCC 25923), Bacillus cereus (ATCC 10102), Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853) using the broth dilution method. The standard 2.2-diphenyl-1-picrylhydrazyl (DPPH) and 2.2-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) methods were used to evaluate the scavenging activities of the extract. Anti-quorum sensing activity was assessed against biosensor strain- Chromobacterium violaceum (ATCC 12472). Cytotoxicity in HepG2 cells was investigated using the tetrazolium-based colorimetric (MTT) assay. Results: The extract revealed eight volatile compounds with cis-Vaccenic acid (87.06\%) and 9-Octadecenoic acid, 1,2,3-propanetriyl ester (5.21\%) as the major components. Antibacterial activity against all tested strains with minimum inhibitory concentration range of 1.56 - 12.5 mg/mL was observed. The DPPH and ABTS assays demonstrated scavenging activities with the median inhibitory concentration (IC50) values of 0.09 mg/mL and 0.003 mg/mL, respectively. The extract also displayed strong anti-quorum sensing activity with 93\% inhibition of violacein production at 25 mg/mL. A half maximum inhibitory concentration (IC50) of 5370 μg/mL was computed in HepG2 cells. Conclusion: The extract has potential to be used as a source of therapeutic compounds in pharmaceutical applications.

}, keywords = {Anti-quorum sensing, Antibacterial, Antioxidant, Cytotoxicity}, doi = {10.5530/pj.2020.12.167}, author = {Phakamani Hopewell Tsilo and Sidney Tsolanku Maliehe and Jabulani Siyabonga Shandu and Rene Khan} } @article {1075, title = {Comparative Pharmacognostical and Pharmacological Evaluation of Costus speciosus (Koen) J.E. Sm. Germplasm Collected from Eastern Ghats of India}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {150-156}, type = {Research Article}, chapter = {150}, abstract = {

Background: Costus speciosus is an erect perennial herb belonging to family Costaceae, an important medicinal plant widely used in several indigenous medicinal formulations. Objective: A comparative evaluation of Pharmacognostical and Pharmacological potential of Costus speciosus for the validation of traditional claims and quality parameters for industry. Materials and Methods: Pharmacognostical studies were performed as per Ayurvedic Pharmacopeia of India and quantification of diosgenin was done through HPTLC. In vitro antidiabetic activity was evaluated by α-amylase inhibition assay based on starch iodine method and in vitro anti-inflammatory were done by using inhibition of protein denaturation assay. Results: The pharmacognostical standards were also laid down for each sample. Morpho-anatomical characters had no distinct variation in all the collected samples of Eastern Ghats. The quantification of diosgenin (without hydrolysis of samples) in the collected germplasm varies significantly from 0.002 to 0.076 \% on dry weight basis. The maximum content was recorded in NBCS-06 from Patiya, Bhubaneswar and was identified as distinct chemotype with high metabolite content. IC50 value of Costus speciosus extract in starch-iodine assay was found to be maximum in NBCS- 6 (87.54 μg/ml) and inhibition of protein denaturation assay was found to be maximum in NBCS- 11 (73.91 μg/ml), respectively. Conclusion: The study suggests that the Costus speciosus germplasm possess potential anti-inflammatory and anti-diabetic activity and comparative pharmacognostical parameters will be useful in collection of location specific potential samples for industrial usage along with quality control of raw materials.

}, keywords = {Anti-diabetic, Anti-inflammatory, Costus speciosus, Diosgenin, HPTLC}, doi = {10.5530/pj.2020.12.22}, author = {Manish Kumar and Ankita Misra and Akanksha Srivastava and Pushpendra Kumar Shukla and L M Tewari and Sharad Srivastava} } @article {1245, title = {Comparison of Cytotoxicity between Ethyl Acetate and Ethanol Extract of White Turmeric (Kaempferia rotunda) Rhizome Extract Against HeLa Cervical Cancer Cell Activity}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1297-1302}, type = {Research Article}, chapter = {1297}, abstract = {

Aim: The aim of this study is to compare between ethanol and ethyl acetate rhizome extract of K.rotunda against HeLa cervical cancer cell in vitro. Material and Methods: Methods used in this research are test the chemical compound of extracts using Thin Layer Chromatography (TLC) and phytochemical screening test, also cytotoxicity test using MTT assay. Result: Ethyl acetate extract contains flavonoid, alkaloid, tannin, and triterpenoid, while ethanol extract have flavonoid, triterpenoid, and alkaloid. In addition, ethanol extract has strong cytotoxic activity (IC50 = 16,939 μg/ml) while ethyl acetate extract has moderate cytotoxic activity (IC50 = 127,9 μg/ml). Each of extracts showed significant results (p <= 0,05) although when compared between concentrations there are several concentrations that are not significant and also small coefficient of determinant values caused by various confounding factors. Conclusion: The ethanol extract of K.rotunda rhizome extract has the higher cytotoxicity activity compared to ethyl acetate extract of K.rotunda rhizome extract against HeLa cervical cancer cell.

}, keywords = {Anti cervical cancer, HeLa, in vitro, Kaempferia rotunda}, doi = {10.5530/pj.2020.12.178}, author = {Surya Dwira and Ariska TP and Fadilah Fadilah and Norma Nur Azizah and Linda Erlina} } @article {1253, title = {Computational Evaluation of ADMET Properties and Bioactive Score of Compounds from Encephalartos ferox}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1357-1362}, type = {Research Article}, chapter = {1357}, abstract = {

Background: Plant based products are recognised as sources of drugs for treatment of diseases. Objective: The study aimed at predicting the physicochemical, pharmacokinetics, drug-likeness and toxicity of the compounds identified from the methanolic Encephalartos ferox fruit extract. Methods: The physicochemical, pharmacokinetics properties and bioactive scores of the compounds were predicted using SwissADME and Molinspiration computational tools. Drug-likeness of the compounds was evaluated based on the Lipinski rule of five (Ro5). In silico mutagenicity, carcinogenicity and inhibition of human ether-a-go-go-related (hERG) gene were also investigated using PreADMET web tool. Results: The physicochemical properties showed the compounds, except 9-Octadecenoic acid, 1, 2, 3-propanetriyl ester to adhere to Ro5. The evaluation of their inhibitory effects profile in several cytochrome P450 isoforms indicate that all the compounds are not the inhibitors of CYP2C19 and CYP3A4 whereas some inhibited CYP1A2, CYP2C9 and CYP2D6. The drug-likeness evaluation employed Ro5 as a filter and all compounds complied with it except for 9-Octadecenoic acid, 1, 2, 3-propanetriyl ester. About 50\% of the tested compound were found to be safe as they did not exhibit antimutagenic and carcinogenic effects. Moreover, the risk of inhibition of hERG gene revealed to be low to medium risk depending on the compound. Conclusion: The calculated physicochemical and pharmacokinetic properties suggest that most of the compounds are safe and have promising oral bioavailability.

}, keywords = {Bioactive score, Compounds, Pharmacokinetic; Drug-likeness, Toxicity}, doi = {10.5530/pj.2020.12.187}, author = {Tsolanku Sidney Maliehe and Phakamani Hopewell Tsilo and Jabulani Siyabonga Shandu} } @article {1079, title = {Correction of Toxic Liver Damage with a Multicomponent Herbal Extract in an Animal Experiment}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {168-172}, type = {Research Article}, chapter = {168}, abstract = {

Background: Digestive diseases constitute a significant part in the overall structure of human diseases. Herbal cholagogues are indicated for a treatment of chronic liver, gall bladder, and bile ducts diseases. The aim of the work is to determine the choleretic effect of a new multicomponent plant extract. Materials and Methods: Multicomponent plant extract was obtained from the following types of plant materials: 300 g of immortelle flowers (Helichrysum arenarium L.), 100 g of tansy flowers (Tanacetum vulgare L.), 100 g of rose fruits (Rosa sp.), 100 g of leaves of common nettle (Urtica dioica L.), 50 g of mint leaves (Mentha piperita L.), 50 g of licorice roots (Glycyrrhiza glabra L.). The extract was standardized by the total flavonoid content. It was calculated and expressed in terms of luteolin and isosalipurposide standards (total flavonoids content: not less than 4\% and 15\% respectively). The animal experiments being done in 80 nonlinear male rats with initial body weight 180-200 g. In order to study a choleretic effect of multicomponent herbal extract, naive rats recieved the single experimental dose of 250 mg/kg. Pharmacotherapeutic activity was studied in white rats with CCl4-induced hepatitis. Results: Studies indicate a pronounced choleretic effect of the studied plant extract, that is comparable with the effect of {\textquotedblleft}Allochol{\textquotedblright} in intact rats experiments. The course administration of a per os (peroral) multicomponent plant extract in a dose of 250 mg/kg to white non-linear rats with tetrachloromethane liver damage has a choleretic effect: it increases the rate of bile secretion, stimulates the synthesis and secretion of cholates with bile, and also the excretion of cholesterol and bilirubin. Conclusion: The obtained research results argue the feasibility of using a multicomponent plant extract containing biologically active substances of phenolic nature in the prevention and comprehensive treatment of liver diseases.

}, keywords = {Choleretic effect, Experimental hepatitis, Multicomponent extract}, doi = {10.5530/pj.2020.12.25}, author = {Ferubko EV and Nikolaev SM and Dargaeva TD and Rendyuk TD} } @article {1068, title = {Cytotoxicity of Soursop Leaves (Annona muricata) against Cervical HeLa Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {20-24}, type = {Original Article}, chapter = {20}, abstract = {

Background: Cervical cancer is the cancer with highest prevalence and the leading cause of women death in Indonesia. Current treatments available for cervical cancer are chemotherapy, radiation, surgery, and nuclear therapy. Unfortunately, these treatments still have several limitations due to serious side effects, development of resistance, and very expensive price. Therefore, it is necessary to develop effective and low-cost therapy to treat cervical cancer. One of which is by utilizing natural sources available in Indonesia such as soursop (Annona muricata) leaves which has been used in folk medicine as a treatment for various diseases, including cancer. However, studies about its cytotoxicity against cervical cancer in Indonesia are still limited. Objective: The aim of this research is to analyze the potency of A.muricataleaves extracts originated from Indonesia as a novel alternative treatment for cervical cancer. Materials and Methods: A.muricata leaves obtained from Serpong, West Java, Indonesia were grounded and macerated in three different solvents with various polarity, namely ethanol (polar solvent), ethyl acetate (semipolar solvent) and hexane (non-polar solvent). Subsequently, the extracts were diluted into 8 various concentrations. Cytotoxicity of A.muricataleaves extracts against HeLa cervical cancer cells were determined by MTT assay and expressed by IC50 value. Results: The results showed that three extracts of A.muricata have strong cytotoxicity against cervical HeLa cells. The highest cytotoxic activity was shown by etanol extract with an IC50 of 35.51 μg/mL, followed by ethyl acetate (IC50: 5.91 μg/mL), and hexane (IC50: 8.39 μg/mL). Conclusion: A.muricata leaves extracts are potential to be developed as a novel alternative therapy for cervical cancer.

}, keywords = {Annona muricata, Cytotoxicity, HeLa cells, Soursop}, doi = {10.5530/pj.2020.12.4}, author = {Fona Qorina and Ade Arsianti and Qotrunnada Fithrotunnisa and NadzilaAnindya Tejaputri and Norma Nur Azizah and Rista Putrianingsih} } @article {1187, title = {Determination of the Chemical Composition of Lady{\textquoteright}s Bedstraw (Galium verum L.) Herb Extract by GC-MS}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {857-863}, type = {Research Article}, chapter = {857}, abstract = {

Background: The research is devoted to the study of the Lady{\textquoteright}s bedstraw (Galium verum L.) herb ethanol extract composition using the method of gas chromatography with mass spectrometric detection. Materials and Methods: Air-dried G. verum L. herb was used for ethanol extract preparation. Hewlett Packard 6890, 5973A GC/MSD System equipped with an HP-5MS quartz capillary column with geometric dimensions of 30 m{\texttimes}0.25 mm{\texttimes}0.25 μm was used for GC-MS analysis. Results: It was established that the Lady{\textquoteright}s bedstraw ethanol extract is rich in biologically active substances that determine its wide spectrum of pharmacological action. 15 compounds were identified by comparing with library mass spectra. Conclusions: G. verum L. is a promising source of crude herbal drugs. In the future, after additional pharmacognostic studies, G. verum L. herb can be recommended for implementation in the State Pharmacopeia of the Russian Federation.

}, keywords = {Ethanol Extract, Galium verum L., Gas chromatography-mass spectrometry, Lady{\textquoteright}s bedstraw}, doi = {10.5530/pj.2020.12.123}, author = {Zaichikova SG and Bokov DO and Kiselevskii MV and Antsyshkina AM and Bondar AA and Prostodusheva TV and Shchepochkina OYu and Gegechkori VI} } @article {1209, title = {Development and Evaluation of New Choleretic Agent}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {962-966}, type = {Original Article}, chapter = {962}, abstract = {

Background: The aim of the research is the determination of pharmacological activity during the development of the optimal way of a new choleretic agent obtaining. The multicomponent herbal medicinal product under the code name Hexaphyte (herbal multicomponent dry extract) is developed. It contains the following species of medicine plant raw materials: Helichrysum arenarium L., Tanacetum vulgare L., Rosa sp., Urtica dioica L., Mentha piperita L., Glycyrrhiza glabra L. in the ratio of 6:2:2:2:1:1. Materials and Methods: Herbal tea was extracted three times with hot water at the temperature of 75-85{\textordmasculine}С; water extracts were combined, filtered and dried. Hexaphyte was standardized by the content of phenolic compounds {\textendash} sum of flavonoids in terms of luteolin standard and isosalipurposide standard. Phenolic compounds (flavonoids) are dominating substances (35-37\%) in the obtained extract. The obtained multicomponent medicine under the code name Hexaphyte was administered per os in the experimental and therapeutic dose of 250 mg/kg to the laboratory animals having experimental induced damages of gallbladder and liver. Results: In Hexaphyte the content of the flavonoid sum (CFS) referred to luteolin standard at a wavelength of 350 nm was not less than 4\%; CFS referred to isosalipurposide standard at a wavelength of 315 nm was not less than 15\%. It was revealed in the results of the realized experiments that it has a choleretic effect superior in a number of indicators to the activity of the Allochol reference drug. The pharmacotherapeutic effect of Hexaphyte at experimental damages of gallbladder and liver is due to the presence of biologically active substances, mainly of phenolic nature. Conclusion: The obtained results of the research argue the feasibility of using the developed multicomponent medicine Hexaphyte containing biologically active substances of phenolic nature in the prevention and complex treatment of hepatobiliary system diseases.

}, keywords = {Choleretic activity, Choleretic herbal medicine Hexaphyte, Experimental damage of liver and gallbladder, Preclinical studies}, doi = {10.5530/pj.2020.12.136}, author = {Ferubko EV and Rendyuk TD and Dargaeva TD and Nikolaev SM} } @article {1227, title = {Green Algae Halimeda macroloba in Spermonde Archipelago: Phytochemical and in vitro Antibacterial Studies}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1000-1004}, type = {Original Article}, chapter = {1000}, abstract = {

Background: Green algae Halimeda macroloba compounds active against human, fish, and shrimp pathogenic bacteria. It is one of the marine natural organisms (MNO) which is a diverse source of secondary metabolites. Objective: We have set our goal towards determining the antimicrobial potential of crude extracts of green algae H. macroloba. Materials and Methods: Three crude mixtures of Marine Natural Product (MNP) were obtained from macroalgae Halimeda macroloba (Lae-Lae island, Spermonde Archipelago) by extraction (n-hexane, ethyl acetate, and methanol were used as solvents). Results: Theses mixtures (phytochemical tests showed they contained steroids, terpenoids, and alkaloids) were screened for their activity against shrimp pathogenic bacteria (Vibrio harveyi (M-120), Aeromonas hydrophilla\ and Vibrio parahaemolyticus (T-170)). The obtained results confirmed weak antibacterial activity of studied extracts of H. macroloba. The ethyl acetate extract was the most potent antimicrobial agent at a concentration of 4 μg/25 μl. The inhibition zones for the growth of A. hydrophilla (the most susceptible microorganism) and V. harveyi were at 8.27 mm and 8.23 mm, respectively (inhibition zone was 15.2 mm for ciprofloxacin which was used as a positive control). Conclusion: They might be even used in the future as alternatives to conventional drugs in aquaculture.

}, keywords = {Antibacterial activity, Halimeda macroloba, Phytochemical screening, Shrimp Pathogenic Bacteria}, doi = {10.5530/pj.2020.12.141}, author = {Lulu Adilla Latifah and Nunuk Hariani Soekamto and Akbar Tahir} } @article {1282, title = {Importance of Cinnamomum Tamala in the Treatment of Various Diseases}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1792-1796}, type = {Review Article}, chapter = {1792}, abstract = {

Cinnamomum tamala is a multipurpose evergreen plant it is a native of India. The plant is commonly known as Indian cassia, Tejpatta, Indian bay leaf etc. All parts of plant possess many major bioactive constituent due to the presence of major phytoconstituent it is useful for the treatment of various diseases or disorders such as Cancer, cardiac diseases, diabetes, Anxiety, depression, ulcer, GI diseases and possess many pharmacological activity includes anti-oxidant, anti-hypercholesterolemia, anti-diarrhoeal, anti-inflammatory, anti-fungal, antibacterial etc. In Ancient time the plant also used as for its medicinal value and it contains a aromatic property due to the presence of these property it is used in perfumery industry and used as mouth refreshing, useful for removal of bad odour from body, mouth and also used in pharmaceutical industries. The leaves of the plant possess flavouring agent property it is used as a flavouring agent in food, curry, fast food, pickles and used as a spice. The main aim of this review/study was to promote and upgrade the knowledge of the use of this multipurpose evergreen plant.

}, keywords = {Cinnamomum tamala, Diseases, Pharmacological activity, Uses}, doi = {10.5530/pj.2020.12.241}, author = {Shashank Tiwari and Shreya Talreja} } @article {1132, title = {In vitro Anti-Amebic Activity of Cage Xanthones from Cratoxylum sumatranum Stem Bark Against Entamoeba histolytica}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {452-458}, type = {Original Article}, chapter = {452}, abstract = {

Background: Amoebiasis is caused by Entamoeba histolytica, which is a pathogenic species living on human colon tissues. The development of new drugs for anti-amebic are still very needed for clinical treatment. Objective: This aims to identify the compounds in Cratoxylum sumatranum for their anti-amoeba activity. Materials and Methods: In this study we used bioactivity-guided isolation and structural analysis to identified anti-amebic compounds from dichloromethane extract of Cratoxylum sumatranum stem bark. Their anti-amebic activity was determined by an in vitro cell-based assay against Entamoeba histolytica and an enzymatic assay on NAD kinase. Results: Two known compounds from the cage xanthone groups, namely cochinchinoxanthone (1) and cochinchinone D (2), were isolated. The structures of the cage xanthone compounds were established by extensive spectroscopic data analysis. Compound (1) showed the greatest level of anti-amebic activity both in cell-based and enzymatic assay, yielding IC50 values of 4.57 and 12.17 μg/mL, respectively. In contrast, compound (2) yielded IC50 values of 5.19 and 12.60 μg/mL, respectively. Conclusion: When considering the demonstrated anti-amebic activities, it becomes apparent that these compounds, isolated from Cratoxylum sumatranum stem bark, have the potential to be further developed into effective anti-amebic medicine against Entamoeba histolytica.

}, keywords = {Amoebiasis, Bioactivity-guided isolation, Cratoxylum sumatranum, Entamoeba histolytica, NAD kinase}, doi = {10.5530/pj.2020.12.70}, author = {Fendi Yoga Wardana and Defi Kartika Sari and Myrna Adianti and Adita Ayu Permanasari and Lidya Tumewu and Tomoyoshi Nozaki and Aty Widyawaruyanti and Achmad Fuad Hafid} } @article {1067, title = {In vitro Cytotoxicity of Hibiscus sabdariffa Linn Extracts on A549 Lung Cancer Cell Line}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {14-19}, type = {Original Article}, chapter = {14}, abstract = {

Background: Lung cancer is the one of the leading causes of cancer death. However, current treatments for lung cancer are expensive and show negative side effects. Therefore, the study concerning natural anticancer from plants has intensified. Hibiscus sabdariffa Linn are Indonesian herb plants which have been consumed as a drink, are known to have anticancer activity against several cancer cell lines. However, its potential cytotoxic activity on A549 lung cancer cell line is still unclear. Objective: This study aimed to identify cytotoxic activity of Hibiscus sabdariffa Linn extracts on A549 lung cancer cell line. Materials and Methods: Hibiscus sabdariffa Linn flowers from Tangerang, province of Banten, Indonesia, were macerated in three different solvents: ethyl acetate, ethanol, and n-hexane. Afterwards, cytotoxic activity of Hibiscus sabdariffa Linn extracts on A549 lung cancer cell line were evaluated using MTT assay. There were eight variety of concentration of the extracts, the experiment has been done triplicate for each concentration. The anticancer activity is expressed by IC50 value. Results: Hibiscus sabdariffa Linn extracts in ethanol, ethyl acetate, and n-hexane showed IC50 value of 374.01 μg/mL, 719.28 μg/mL, and 906.57 μg/mL respectively, in which indicated weak cytotoxic activity on A549 lung cancer cell line. Conclusion: Ethanol, ethyl acetate, and n-hexane extracts of Hibiscus sabdariffa Linn are potential to be further developed as natural anticancer agents.

}, keywords = {A549 Lung Cancer Cell Line, Cytotoxicity, Hibiscus sabdariffa Linn}, doi = {10.5530/pj.2020.12.3}, author = {Qotrunnada Fithrotunnisa and Ade Arsianti and Gerry Kurniawan and Fona Qorina and Nadzila Anindya Tejaputri and Norma Nur Azizah} } @article {1158, title = {Lathraea squamaria L. (Orobanchaceae): A Review of its Botany, Phytochemistry, Traditional Uses and Pharmacology}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {667-673 }, type = {Review Article}, chapter = {667}, abstract = {

This paper presents the results of the review pharmacognostic study of common toothwort, a perennial plant, parasitizing on the roots of trees. Currently, in Russian traditional medicine, there is considerable experience in the use of сommon toothwort (Lathraea squamaria L.) herb and roots as antitumoral, biligenic, infertility-treatment and diuretic drugs. The chemical composition of L. squamaria has not been quite well determined. Phenylethanoid glycosides (acteoside, isoacteoside), iridoid glycosides (aucubin, and aucuboside ester, 6{\textquoteright}-O-glucopyranosyl-aucubin, melampyroside, 6{\textquoteright}-O-glucopyranosyl melampyroside), simple sugars, fatty acids, organic acids, β-sitosterol were identified. Further study of L. squamaria raw materials is a very promising field including implementation in official medicine.

}, keywords = {Aucubin, Chemical compounds, Common toothwort, Iridoids, Lathraea squamaria, Orobanchaceae, Parasitic plants}, doi = {10.5530/pj.2020.12.98}, author = {Bokov DO and Barkalova VE and Suslikova MA and Sokhin DM and Kakhramanova SD and Rendyuk TD and Strelyaeva AV and Antsyshkina AM and Balobanova NP and Prostodusheva TV and Grikh VV and Krasnyuk II1 (junior) and Marakhova AI and Moiseev DV} } @article {1206, title = {Noni Juice (Morinda citrifolia) to Prevent Cancer Progression in Mice Induced DMBA and Cigarette Smoke Exposure}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {946-951}, type = {Original Article}, chapter = {946}, abstract = {

Introduction: Accumulation of polycyclic aromatic hydrocarbons (PAH) in the body commonly lead to degenerative disease such as cancer. This study aims to investigate the potential of Morinda citrifolia to maintain the immune system against toxic exposure. Materials and Methods: This study used Five weeks old male Balb/C mice as animal model. The 7,12-Dimethylbenz(a)anthracene (DMBA) was administrated for six weeks following with 3 days cigarette smoke (CS) exposure then treated with noni juice (M. citrifolia) for two weeks. Experimental animals were divided into six groups. Normal control (N); DMBA+CS; Cisplatin; D1; D2; and D3. Profil of CD4+TNFα+, CD11b+IL6+, CD11b+IFNγ+, CD4+CD25+ IL10+, NK+IL6+ cells was analyzed by flow cytometry and data was analyzed with one-way ANOVA and Post Hoc Tukey HSD test with a significance of p-values \< 0.05. Results: This study show that DMBA+CS induction increasing level of CD11b+IL6+, CD4+CD25+ IL-10+ and NK+ IL-6+ meanwhile decreasing CD4+TNFα+significantly (P\<0.5) than Normal group. Noni juice in dose 90 mg/Kg BW decrease cytokine pro-inflammation (IL-6 and IFNγ) both in macrophage and NK cell profile significantly (P\<0.05). Noni juice in 30 mg/Kg BW could improve the activation CD4+TNFα+ significantly (P\<0.05). Noni juice also has efficacy to control T regulator activation to prevent tumor escape. Conclusion: These results suggest that noni juice has anti-cancer potencies by maintain homeostasis of immune system and could be immune herbal supplement.

}, keywords = {Homeostatic, Immunotoxin, Inflammation, Noni juice, Tumor progression}, doi = {10.5530/pj.2020.12.134}, author = {Didin Wahyu Agustina and Mulya Dwi Wahyuningsih and Sri Widyarti and Aris Soewondo and Hideo Tsuboi and Muhaimin Rifa{\textquoteright}i} } @article {1174, title = {Nutrient Content, Active Compound and Antibacterial Activity of Padina australis against Aeromonas hydropilla}, journal = {Active compound, Antibacterial activity, Padina australis, Nutrient content,}, volume = {12}, year = {2020}, month = {June 2020}, pages = {771-776}, type = {Original Article}, chapter = {771}, abstract = {

Background: Padina australis is one of the brown macroalgae that possess several compounds that can be used for various medicinal properties. Objective: This study aims to analyze the nutrient content, active compounds, and antibacterial activity of Padina australis against Aeromonas hydropilla. Methods: The nutrient content and phytochemical composition of P. australis were examined in this study. The antibacterial effect was evaluated using the disc method against A. hydropilla. Results: The nutrient content of P. australis include 38.5\% carbohydrate, 2.07\% fat, 13.89\% protein, 16.12\% water, 33.34\% ash, 8.54\% total amino acid, and minerals (11.36\% calcium, 0.22\% iron, and 1.81\% potassium). Phytochemical analysis showed that P. australis contained phenols, tannin, flavonoid, and steroid. These compound may be responsible for inhibiting A. hydropilla, with an inhibition zone of 10.5 mm for water extract of P. australis and 10 mm for methanol extract P. australis. Conclusion: This study revealed that P. australis produced antibacterial effect against A. hydropilla which could be potential for further antimicrobial agent development.

}, keywords = {Active compound, Antibacterial activity, Nutrient content, Padina australis}, doi = {10.5530/pj.2020.12.110}, author = {Yuliana Salosso and Siti Aisiah and Lumban Nauli Lumban Toruan and Wesly Pasaribu} } @article {1299, title = {A Perspective Overview on Hygrophila auriculata}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1748-1752}, type = {Review Article}, chapter = {1748}, abstract = {

Hygrophila auriculata, belonging to the family Acanthaceae, is a promising medicinal plant with great economic potential. The medicinal value of H. auriculata has been appreciated in the ancient medical literature. The plant contains terpenoids, alkaloids, flavonoids, and is traditionally known as an aphrodisiac, renal tonic, and for its health-promoting properties. The plant is cultivated throughout India. However, systematic information on the different aspects of this species is not available. In this review, an attempt has been made to present this information.

}, keywords = {Hygrophila auriculata, Pharmacological activity, Phytochemistry}, doi = {10.5530/pj.2020.12.237}, author = {S Dhanalakshmi and N Harikrishnan and N Srinivasan and P Pandian and BA Tanisha and M Tharun Kumar and V Lokesh and N Yuvashri and S Supriya} } @article {1080, title = {Pharmacognostic, Phytochemical and Ethnopharmacological Potential of Cyclamen coum Mill}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {204-212}, type = {Review Article}, chapter = {204}, abstract = {

Background: This review focuses on characterization of Cyclamen coum Mill. (Myrsinaceae), composition and content of biologically active substances presented in the above-ground and underground parts, reporting use of this plant in traditional medicine, predicting possible pharmacotherapeutic effects. Materials and Methods: Various electronic search engines such as Google, Google scholar, scientific literature, electronic databases such as e-Library, Scopus, Web of Science, Pubmed had been searched and data obtained. Results: Cyclamen L. is classified in the Myrsinaceae family now. It is a typical element of the Mediterranean flora. C. coum. is a species characteristic of the Caucasus and Crimea with rounded leaves and rounded corolla lobes, bright and pink-purple flowers. Chemical composition of biologically active substances of C. coum was described in sufficient detail. C. coum contains saponins (coumoside A, coumoside B, cyclaminorin, deglucocyclamin, cyclacoumin, and mirabilin lactone), sterols (stigmasterol and other related compounds), piperidine alkaloid (2-β-D-glycopyranosyl-2-undecil-3,5-dihydroxy-6-carboxypiperidine), flavonoids, phenols, tannins, cardiac glycosides. Antioxidant, antibacterial, antifungal, and antitumor activities are established for different C. coum extracts. Conclusion: C. coum can be used for the production of potential anticancer, antibacterial and antifungal drugs. It should be noted that more pharmacognostic, pharmacological studies are needed for providing further information to use this medicinal plant in the official medicine. Also, standardization procedures for a crude herbal drug should be developed.

}, keywords = {Coumoside A, Coumoside B, Cyclacumin, Cyclamen coum, Cyclaminorin, Deglucocyclamine}, doi = {10.5530/pj.2020.12.31}, author = {Bokov DO and Krasikova MK and Sergunova EV and Bobkova NV and Kovaleva TYu and Bondar AA and Marakhova AI and Morokhina SL and Krasnyuk II and Moiseev DV} } @article {1125, title = {Pharmacopoeial Analysis of Inulin-Containing Medicinal Plant Raw Materials and Drugs}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {415-421}, type = {Review Article }, chapter = {415}, abstract = {

Background: Today, there are some unresolved issues and discussions concerning inulin quantitative determination in medicinal plant raw materials (MPRM). MPRM containing polyfructans or fructosans (inulin and others) are rather complex multicomponent matrixes with many interacting compounds. The article discusses the prospects for further standardization of inulin-containing pharmacopoeial MPRM that include, in addition to polysaccharides (inulin), other biologically active compounds with pharmacological activity. Materials and Methods: Different types of search tools such as Google scholar, Google, scientific literature, normative documentation of Russian Federation (State Pharmacopoeia of Russian Federation IV edition and others) electronic databases such as e-Library, Scopus, Web of Science, Pubmed had been searched and data obtained. Results: The pharmacopoeial spectrophotometric procedures of inulin determination in the Russian Federation are approved in a version that does not fully satisfy modern standardization criteria. Regulatory changes required in the near future. Conclusion: Undoubtedly, to determine inulin quantitatively, it is necessary to modify the existing spectrophotometric procedures and introduce an additional alternative, more specific HPLC-RID (or similar) ones.

}, keywords = {Fructosans, HPLC-RID, Inulin quantitative determination, Polyfructans}, doi = {10.5530/pj.2020.12.64}, author = {Bokov DO and Karabeshkin DI and Samylina IA and Potanina OG and Krasnyuk II and Malinkin AD and Sergunova EV and Kovaleva TYu and Bobkova NV and Antsyshkina AM and Bondar AA and Evgrafov AA and Galiakhmetova EK and Moiseev DV and Bessonov VV} } @article {1214, title = {Phenolic Compounds and Immunomodulating Activity of Chicory (Cichorium intybus L.) Extract}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1104-1107}, type = {Research Article}, chapter = {1104}, abstract = {

Introduction: This research aims to determine the immunomodulating activity of chicory (Cichorium intybus L.) herb extract and to evaluate the prospects of development of the medicine based on it. Methods: Object of the research was dry chicory extract obtained from herb (aerial part) of a wild plant. The chemical composition of the extract was determined by HPLC-MS method. Its immunomodulating action has been explored in vivo experiments involving intact animals, as well as immunosuppressed animals, treated with azathioprine cytostatic agent. Chicory extract was administered at a dose of 30 mg/kg per os 1 time per day for 14 days. As a reference drug, Immunal (Lec Pharma, Slovenia) was used. Chicory extract action on the state of cell immune component was evaluated in delayed hypersensitivity reaction. The humoral immunity condition was evaluated by the count of antibody-forming cells determined by the local hemolysis method. The state of the macrophage component of the immune response was evaluated in the phagocytosis reaction of peritoneal macrophages in relation to colloid liquid ink particles. Results: Dry chicory extract is capable to reduce the suppressive azathioprine effect on the cell-mediated immune response, antibody response, and phagocytosis with macrophages; it does not change the immunity indicators in intact animals. Conclusion: Dry chicory extract contains phenolic complex of biologically active substances, namely oxycoumarins, hydroxycinnamic acids, and flavonoids. Dry chicory extract is an effective immunocorrecting agent; it should be recommended for further study and application aiming for the prevention and treatment of immunodeficiency states.

}, keywords = {Chicory herb, Dry extract, Immunomodulating activity, Phenolic compounds}, doi = {10.5530/pj.2020.12.156}, author = {Saybel OL and Rendyuk TD and Dargaeva TD and Nikolaev SM and Khobrakova VB} } @article {1262, title = {Phytochemical and Antioxidant Evaluation of the Flavonoids and Tannins from Synadenium grantii Hook f, (Ephorbiaceae)}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1421-1428}, type = {Research Article}, chapter = {1421}, abstract = {

Background: The methanol extract (MeE) of the aerial parts from Synadenium grantii Hook f, (Ephorbiaceae) has more Polyphenols and used to treat several diseases. Objective: The aim of this study is isolation, purification and identification of Polyphenols that showed good antioxidant activity. Materials and Methods: In the present study, purification of the MeOH-H2O extract (70:30) from the air-dried aerial parts of S. grantii resulted by different chromatographic tools. The antioxidant activities were evaluated for the examined compounds by several methods using DPPH, Reducing power, ABTS and FRAP assays. Results: A total of 14 compounds were isolated from this plant species for the first time. The results obtained showed that all the examined compounds possess remarkable antioxidant activity through all assays especially compounds 2 and 4 where they showed the highest antioxidant activity among the other compounds and very close to the results of the standard compound BHA. Conclusion: The compounds examined have exhibited antioxidant activity with promising value as natural source antioxidant drugs.

}, keywords = {Antioxidant, Ephorbiaceae, Flavonoids, Synadenium grantii, Tannins}, doi = {10.5530/pj.2020.12.196}, author = {Asmaa S Abd Elkarim and Sahar Abdelaziz and Hany Gouda Attia and Hanan AA Taie and Rafik Monir} } @article {1091, title = {Phytochemical Composition and Evaluation of Marine Algal Sargassum polycystum for Antioxidant Activity and In Vitro Cytotoxicity on Hela Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {88-94}, type = {Original Article}, chapter = {88}, abstract = {

Introduction: Sargassum polycystum is one of marine algal which has a potent antioxidant anticancer activities. This research aims to investigate phytochemical composition, antioxidant activity and in vitro cytotoxicity of marine algal Sargassum polycystum on cervical HeLa cancer. Methods: Sargassum polycystum collected from Dompu beach, Lombok, Nusa Tenggara Barat Province, Indonesia, were extracted into organic solvent of n-hexane, ethylacetate, chloroform and ethanol, respectively. Subsequently, Sargassum polycystum extracts were applied for Thin Layer Chromatography (TLC) analysis, phytochemistry test, total phenolic and total flavonoid contents, as well as for antioxidant activity test by DPPH (2,2-diphenyl-1-picrylhydrazyl) method, and in vitro cytotoxicity evaluation on HeLa cells by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5- diphenyltetrazolium bromide) assay. Results: Phytochemical analysis of S. polycystum extracts are positive for metabolites of flavonoid, steroid, tannin and glycoside. TLC analysis revealed that S. polycystum extracts containing four phytochemical components. Ethylacetate extract of S. polycystum showed the highest total phenolic content, and exhibited greater antioxidant activity than ethanol extract. Total phenolic and total flavonoid content in ethylacetate extract are 548.61 μg/mL and 40.06 μg /mL, respectively. Ethylacetate extract of S. polycystum with IC50 value of 298.3 μg/mL is assigned to have a weak antioxidant activity against DPPH free radical. The results indicate that antioxidant activity of ethylacetate extracts of S. polycystum is directly correlated with its total phenolic and flavonoid content. Moreover, S. polycystum extracts demonstrated a strong anticancer activity on cervical HeLa cells with IC50 ranging from 38.3 μg/mL to 112.8 μg/mL. Conclusion: This work confirmed that S.polycystum are promising natural antioxidant and anti-cervical cancer agents.

}, keywords = {Antioxidant, Cytotoxicity, HeLa cells, phytochemisty, Sargassum polycystum}, doi = {10.5530/pj.2020.12.14}, author = {Ade Arsianti and Anton Bahtiar and Vincent Kharisma Wangsaputra and Norma Nur Azizah and Wilzar Fachri and Lince Dameria Nadapdap and Ajeng Megawati Fajrin and Hiroki Tanimoto and Kiyomi Kakiuchi} } @article {1116, title = {Phytochemical Profile, Antioxidant Activity and Cell Line Study of Marine Red Macroalgae Eucheuma cottonii on Lung A-549 Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {276-281}, type = {Original Article}, chapter = {276}, abstract = {

Introduction: In this century, cancer has increased in incidence and become one of the deadliest disease in the world. However, to date, lung cancer treatments are still not fully effective, quite expensive and very exhaustive for the patient. Eucheuma cottonii is an abundant marine red macroalgae in Indonesia which have a potential anti-lung cancer properties. Aim of this research is to determine phytochemical profile of Eucheuma cottonii extracts, as well as to evaluate its antioxidant and cytotoxic effects on Lung A-549 cancer cells. Methods: Eucheuma cottonii obtained from Sorong beach, West Papua Province, Indonesia, were extracted with three different solvents, that is ethanol, ethylacetate, and n-hexane. These three Eucheuma cottonii extracts were identified for its phytochemical profiles, antioxidant activity by DPPH (2,2-diphenyl-1-picrylhydrazyl) assay, and cytotoxic activity on lung A-549 cells by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay. Results: Phytochemical analysis revealed that Eucheuma cottonii contains metabolites of triterpenoid and alkaloid. Antioxidant activity evaluation showed ethanol extract of Eucheuma cottonii has IC50 value of 559.76 μg/mL against DPPH free radical. Whereas cytotoxicity evaluation showed that ethanol extract and ethylacetate extract of Eucheuma cottonii have cytotoxic effects on Lung A-549 cancer cells, with IC50 value of 251.73 μg/ mL and 261.41 μg/mL, respectively. Conclusion: These results suggesting that Eucheuma cottonii extract could be further developed as a natural anti-lung cancer agent.

}, keywords = {Antioxidant, Cell line study, Eucheuma cottonii, Lung A-549 cells, Phytochemical}, doi = {10.5530/pj.2020.12.43}, author = {Ade Arsianti and Gerry Kurniawan and Nadzila Anindya Tejaputri and Fona Qorina and Qotrunnada Fithrotunnisa and Norma Nur Azizah and Ajeng Megawati Fajrin} } @article {1218, title = {Potential Test of Nephropathy Sonchus arvensis L. Leaves on Male Rats (Rattus norvegicus) Diabetes Mellitus}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1115-1120}, type = {Research Article}, chapter = {1115}, abstract = {

This study aims to determine the type of secondary metabolites compounds of the ethanol Sonchus arvensis\ L leaves extract, the effect of ethanol Sonchus arvensis L leaves extracts the levels of blood glucose and a histopathology picture male white rat induced by streptozotocin. This study used 30 males white rats which were divided into 6 groups, namely the control of normal, negative control, positive control, doses of 200, 300 and 400 mg/kg BW. Results of the study showed that the ethanol Sonchus arvensis L. leaves extracts contained compounds of alkaloids, flavonoids, phenols, saponins and tannins. Sonchus arvensis L ethanol extract at a dose of 300 mg/kg BW is an effective dose in reducing blood glucose levels with an average value of decreasing blood glucose levels 101.6 mg / dL and has an effect on the regeneration of renal tubular cells with an effective dose is 300 mg / kg body weight with an average damage value of 0.28.

}, keywords = {Diabetes, Leaf Sonchus arvensis L, Renal, Tubular}, doi = {10.5530/pj.2020.12.158}, author = {Joni Tandi and I Nyoman Edi Sutrisna and Mentari Pratiwi and Tien Wahyu Handayani} } @article {1202, title = {A Review on Phaseolus vulgaris Linn}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1160-1164}, type = {Review Article}, chapter = {1160}, abstract = {

Medicinal herbs have been discovered and used in traditional medicine practices since antiquated times. Phaseolus vulgaris Linn. (Family-Fabaceae) commonly known as French bean, is a most consuming carbohydrate and protein rich food crop having medicinal values. This plant having diverse compounds like carbohydrate, proteins, flavonoids, Saponins, tannins and phenolic acid. The seeds of Phaseolus vulgaris Linn. Possess having anti-urolithiatic activity and anti- obesity activity. This review provides a summary of phytochemistry and pharmacological effect of Phaseolus vulgaris Linn., The plant can be further investigated for other pharmacological activities as it contains variety of chemical constituents and it is a commonly using food crop and medical remedies of this plant are sync with nature.

}, keywords = {Food crop, Obesity, Phaseolus vulgaris Linn, Urolithiasis}, doi = {10.5530/pj.2020.12.163}, author = {M Devi and S Dhanalakshmi and GE Thillai Govindarajan and BA Tanisha and Talluri Sonalika and JE Ruth and T Avinash and C Jethendra Sri and K Logeswaran and M Nithish Ramasamy} } @article {1304, title = {Review on Plants for Management of Diabetes in India: An Ethno- Botanical and Pharmacological Perspective}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1801-1810}, type = {Review Article}, chapter = {1801}, abstract = {

Background: Diabetes mellitus is a prevalent chronic disease, which is recognized as a common threat to health in the last decade, especially in Asia. It is a lifestyle disease which may cause a number of complications in the body of humans like cardiac failure and dysfunctioning of urinary tract. Materials and Methods: The data is obtained from various search tools and electronic databases like, scientific literature, Google scholar, Google, Pubmed, Web of science and Scopus. Results: Major therapy for diabetes is insulin, oralantidiabetic drugs, and herbal treatment. However, insulin and oral anti-diabetic drugs come with a number of side effects and cannot be afforded by people with below poverty line. The herbal medicines have performed a satisfactory clinical practice for the management of diabetes mellitus. Moreover, pharmacological \& phytochemical screening of medicinal plants has also witnessed the hypoglycaemic effects of these plants in treating diabetes mellitus. Majority of the modern drugs like metformin, atropine, digitalis, etc. are also originated from plants. Conclusion: The current paper presents a review of medicinal plants used for diabetes management in India. The therapeutic potential, ethnobotanical use, and their pharmacological evaluations are highlighted for harnessing the anti-diabetic potential of these plants by the Indian healthcare system.

}, keywords = {Diabetes management, Ethnopharmacology, Herbal drugs, India}, doi = {10.5530/pj.2020.12.243}, author = {Shikha Dixit and Sugandha Tiwari} } @article {1108, title = {Synthesis, Characterization, and Cytotoxicity Evaluation of Gallic Acid Nanoparticles Towards Breast T47D Cancer Cells}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {321-327}, type = {Original Article}, chapter = {321}, abstract = {

Introduction: Gallic acid is a naturally polyphenolic acid which shows cytotoxicity against several cancer cells, as well as it displays chemo-preventive activity which is attributed to its strong apoptosis- inducing and antioxidant effects. Thus, gallic acid has become an attractive substance to be further developed due to its strong cytotoxic activity. This study aimed to synthesize gallic acid nanoparticle coating with alginate-chitosan, and evaluate its cytotoxicity against breast T47D cancer cells. Methods: Gallic acid nanoparticle was synthesized using ionic gelation method. The yield, size and morphology of the nanoparticles were determined by UV-Vis Spectroscopy, Transmission electron microscopy (TEM) and Fourier Transform Infrared (FTIR) spectroscopy. Cytotoxicity evaluation of gallic acid nanoparticle towards breast T47D cancer cell is carried out by MTT(3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazoliumbromide) assay. Results: Spherical nanoparticles of gallic acid with the size of 100-200 nm has been successfully synthesized in 96\% of yield. Compared to gallic acid (IC50: 20.86 μg/mL) and alginate-chitosan nanoparticle (IC50: 38.46 μg/mL), gallic acid coating with alginate-chitosan nanoparticles demonstrated higher cytotoxicity towards breast T47D cancer cells with IC50 value of 9.03μg/mL. Conclusion: Our results clearly confirmed that gallic acid nanoparticles coating with alginate-chitosan showed a strong cytotoxicity towards breast T47D cancer cells, which is potential to be developed as a candidate for new anti-breast cancer agent.

}, keywords = {Cytotoxicity, Gallic acid, Nanoparticle, Synthesis, T47D cells}, doi = {10.5530/pj.2020.12.51}, author = {Ade Arsianti and Anton Bahtiar and Fadilah Fadilah and Vincent Kharisma Wangsaputra and Rafika Indah Paramita and Norma Nur Azizah and Lince Dameria Nadapdap and Ajeng Megawati Fajrin and Hiroki Tanimoto and Kiyomi Kakiuchi} } @article {1216, title = {Tacrolimus Therapeutic Drug Monitoring in Vietnamese Renal Transplant Recipients}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {984-992}, type = {Original Article}, chapter = {984}, abstract = {

Background: Use of tacrolimus (Tac) is pivotal to renal transplant (RT) immunosuppressive maintenance regiments. The most frequently used means of Tac monitoring is the measurement of the trough concentration (C0) in whole blood to maintain drug efficacy and minimize the consequences of overexposure. Most previous studies focused on therapeutic drug monitoring of Tac in renal transplant recipients and assessed the clinical response of patients. Our study aimed to describe a real Tacrolimus therapeutic drug monitoring transplantation and determine the clinical outcomes in Vietnamese adult renal transplant recipients. Methods: This retrospective study including 114 adult renal transplant patients (89 men and 25 women) with a mean age of 35.4 {\textpm} 8.98 years has been performed from August 2012 to March 2018 at Military Hospital 103 (Vietnam). Tac trough concentrations were adjusted according to the target range proposed by the European consensus conference on tacrolimus optimization. Samples for determination of tacrolimus blood levels were subdivided according to the posttransplantation period into three groups (0- 3 months (G1), 3-12 months (G2) and over 1 year (G3). Median Years of follow-up was 15.4 months [range 0.233 to 68.4 months]. Results: A total of 3037 blood samples for the determination of tacrolimus trough concentration were obtained. Median concentrations were 6.7 (4.5 {\textendash} 10.2) ng/ml, 6.4 (5.1 {\textendash} 8.3) and 5.6 (4.5 to 7.1) ng/ml for G1, G2, G3, respectively. After transplantation, three acute rejection (AR) events were documented (Cellular AR: 2, Humoral AR: 1). Cytomegalovirus, BK polyomavirus, Hepatitis B virus and Hepatitis C virus were detected in 7, 4, 7 and 3 renal post- transplant recipients, respectively. There were 5 patients with post-transplant diabetes (NODAT) and all of them had to convert to cyclosporine. 6 patients developed chronic kidney disease (CKD) after transplantation and 2 case with Tac-associated nephrotoxicity with proven biopsy. This observational study provided a real Tacrolimus therapeutic drug monitoring transplantation in Vietnamese renal transplant recipients. Main outcomes were acute rejection, post-transplant viral infections, neurotoxicity, NODAT, CKD, and Tac-associated nephrotoxicity.

}, keywords = {Renal transplantation, Tacrolimus, Therapeutic drug monitoring, Vietnam}, doi = {10.5530/pj.2020.12.139}, author = {Van Anh T Nguyen and Thang Viet Le and Manh Van Bui and Toan Quoc Pham and Son The Trinh and Binh Nhu Do and Lien Huong T Nguyen} } @article {1219, title = {Toxicity Assessment, Evaluation of Antioxidant and Hepatoprotective Activity on Cordia obliqua Fruit Extracts}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1005-1011}, type = {Original Article}, chapter = {1005}, abstract = {

Background: Cordia obliqua Willd plant is a genus of flowering plants in the borage family, Boraginaceae. It is also known as clammy cherry. Very little research was carried out for identification of its medicinal importance when compared to other Cordia species Objective: To determine the safe dose and to explore the in vivo antioxidant and hepatoprotective activity of Cordia obliqua fruits Methods: As per our previous study the ethanolic and aqueous extracts were rich in phytoconstituents and exhibited good in vitro antioxidant effect. So the ethanolic and aqueous extracts were used for evaluation of activity. Acute toxicity study (LD50) was conducted according to OECD guidelines. For hepatoprotective activity paracetamol induced hepatotoxicity was studied using standard drug like Silymarin. The antioxidant potential] of the plant extracts were tested using three tests viz, Reduced GSH, Catalase and SOD activity Results: Acute toxicity studies showed the non-toxic nature of Cordia obliqua fruit extract upto dose of 3000mg/kg body weight. Administration of Paracetamol to rats increased the levels of marker enzymes like ALT, AST and ALP. Increase in the levels of these enzymes in serum indicates damage to the liver cells. Pretreatment with aqueous and ethanolic extracts of Cordia obliqua decreased the levels of ALT, AST, ALP and increased levels of total protein, total bilirubin, direct bilirubin and comparisons histology of cells of extract which are an indication for the hepatoprotective activity. Conclusion: The fruits of Cordia obliqua are safe and effective in treatment of hepatic disorders and prevent oxidation of cells.

}, keywords = {Cordia obliqua, Hepatotoxicity, Paracetamol, Silymarin}, doi = {10.5530/pj.2020.12.142}, author = {G Tharun and S Sivakrishnan and JVC Sharma} } @article {867, title = {Antidiabetic, Antibacterial and Antioxidant Activities of Different Extracts from Brucea javanica (L.) Merr Seeds}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {479-485}, type = {Original Article}, chapter = {479}, abstract = {

Introduction: The seeds of B. javanica are known as herbal material for anticancer, antimalaria and antiamoeba. Limited report is available on their antidiabetic and antibacterial properties. Methods: Methanol (ME) and Ethyl acetate extracts (EAE) were studied for their inhibition activities on α-glucosidase in vitro, including combination of ME with acarbose and inhibition mechanism. Antibacterial activity was tested by well diffusion and microdilution methods. The extracts were evaluated for their in vitro antioxidant property by DPPH assay, as well as their phenolic and flavonoid contents. Results: ME exhibited a strong α-glucosidase inhibition activity (IC50 271.97 μg/ml) compared to EAE and acarbose (IC50 of 1745.05 and 823.99 μg/ml, respectively). A low dose of ME gave an additive inhibition on α-glucosidase when combined with acarbose. By a kinetic analysis, ME was found to inhibit α-glucosidase in a mixed-type inhibition. Both ME and EAE showed strong antibacterial activities against gram negative and positive bacteria. The strongest inhibition was observed against C. violaceum and S. mutans for ME (MIC of both 0.387 mg/ml) and P. aeruginosa for EAE (MIC 2.938 mg/ml). Both extracts showed weaker antioxidant activities than standards; IC50 664.73 and 4225.40 μg/ml, respectively. ME was rich in phenolics (277.54 mg GAE/100 g DW), unlike EAE (1.86 mg GAE/100 g DW). Conclusion: This study can recommend B. javanica seeds as a source for antidiabetic and antibacterial agents. Combination with acarbose may have important role for the treatment of diabetes mellitus.

}, keywords = {Additive inhibition, Antibacterial, Brucea javanica, Mixed type inhibition, α-glucosidase inhibitor}, doi = {10.5530/pj.2019.11.76}, author = {Adelina Simamora and Kris Herawan Timotius and Adit Widodo Santoso} } @article {799, title = {Antitumor and Antioxidant Effects of Flavonoid Fraction of Citrus sinensis peel Extract}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {57-63}, type = {Original Article}, chapter = {57}, abstract = {

Background: Cancer is one of the leading causes of death and globally the numbers of cases of cancer are increasing gradually. However, surgeries, chemotherapies have become safer, but these treatments have debilitating side effects. Flavonoids present in the human diet comprise many polyphenolic secondary metabolites with broad-spectrum pharmacological activities including their potential role as anti-cancer agents. Objective: The objective of the present study was to extract, orange peel flavonoids (Orange Peel Extract) and to screen anticancer potential of OPF. Methods: In the present study tryphan blue dye exclusion, clonogenic assay and nuclear damage studies by ethidium bromide staining were performed to estimate in vitro antitumor properties of Orange Peel Extract and subsequently in vivo studies also performed using the Dalton lymphoma ascites (DLA) tumor model in Swiss albino mice. Results: In vitro studies revealed the moderate toxicity, high regenerative capacity of Orange Peel Extract and also showed changes in nuclear morphology similar to that of apoptotic cells which is one of the important aspect of an anticancer drug. In vivo studies confirmed the anticancer activity of Orange Peel Extract and has increased the average life span of treated animals and restored the antioxidant enzyme levels and hematological parameters to normal which was comparable to that of standard methotrexate. Conclusion: Overall, these findings have proved that out of the two doses (50mg/kg bw and 200mg/kg bw) employed for the study lower dose (50mg/kg) was found to be more effective than higher dose (200mg/ kg). Hence flavonoid fraction of orange peels can be the better alternative to treat cancer.

}, keywords = {Dalton lymphoma ascites, Ethidium bromide, Methotrexate, Orange peel flavonoids, Tryphan blue}, doi = {10.5530/pj.2019.1.11}, author = {Godishala Shirisha and Kiranmai Mandava and Uma Rajeswari Batchu and Kesava Rao Thammana and Vijaya Laxmi Turpu} } @article {1046, title = {Azadirachta indica: Antibacterial Activity of Neem Against Different Strains of Bacteria and their Active Constituents as Preventive in Various Diseases}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1597-1604}, type = {Review Article }, chapter = {1597}, abstract = {

Neem has become valuable plant in the world which shows the solutions for hundreds to thousands problems. Azadirachta indica (Neem) is a rapidly growing evergreen well known tree found Pada generally in various regions of world like America, Africa and India. It has been widely used in Chinese, Ayurveda and Unani medicines across the world especially in Asians countries for the prevention and treatment of diseases. The different parts of neem plant contain biological compounds responsible for antibacterial, antiviral and antifungal activities. It is considered as safe medicinal plants and modulates the numerous biological processes without any adverse effect. Neem tree produces some active compounds which contain biological activities, parts of neem tree such as Root, bark, leaf, flower, seed and fruit together possesses biological activities. Various compounds have been obtained from various parts of neem. Biological activities of few of them have been studied. Hence, the article is aims to utilize the medicinal properties of whole neem plant in various disorders of mankind.

}, keywords = {Antibacterial, Antifungal, Azadirachta indica, Natural antibiotics, Natural products}, doi = {10.5530/pj.2019.11.244}, author = {Oscar Herrera-Calderon and Kainat Ejaz and Mahnoor Wajid and Muzzamil Shehzad and Johnny Aldo Tinco-Jayo and Edwin Enciso-Roca and C{\'e}sar Franco-Quino and Ricardo {\'A}ngel Yuli-Posadas and Victor Chumpitaz-Cerrate} } @article {824, title = {Cakile maritima Scop. Extracts Inhibit Caco2 and HeLa Human Carcinoma Cell Growth: GC-MS Analysis of an Anti-Proliferative Extract}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {258-266}, type = {Original Article}, chapter = {258}, abstract = {

Introduction: Exposure to high levels of antioxidants has been linked to the treatment and prevention of some cancers. Although Cakile maritima has a high antioxidant capacity, it is yet to be tested for the ability to inhibit the proliferation of cancer cells. Methods: Solvent extracts prepared from C. maritima plant material were analysed for antioxidant capacity by the DPPH free radical scavenging assay. Anti-proliferative activities against Caco2 and HeLa cancer cells were determined by an MTS based cell proliferation assay. Toxicity was determined by the Artemia franciscana bioassay. The most potent anti-proliferative extract (hexane) was further investigated using non-targeted GC-MS headspace analysis. Results: Good DPPH radical scavenging activity was calculated for all C. maritima extracts. The methanolic and ethyl acetate extracts had particularly strong antioxidant activity (IC50 of 4.7 and 3.4 μg/mL respectively). Interestingly, the hexane extract which had the lowest DPPH radical scavenging activity (IC50 13.6 μg/mL), was the most potent inhibitor or Caco2 and HeLa carcinoma cell growth, with IC50{\textquoteright}s of 12 and 126 μg/mL respectively. The ethyl acetate extract was also a potent inhibitor of proliferation (IC50 values of 185 and 468 μg/mL against Caco2 and HeLa, respectively). The methanolic extract (IC50 values of 2261 and 2046 μg/mL against CaCo2 and HeLa respectively) displayed only moderate anti-proliferative activity, demonstrating that antioxidant activity did not correspond with anti-proliferative activity. All of the extracts were determined to be nontoxic in the Artemia franciscana bioassay, with LC50 values substantially \>1000 μg/mL. Non-biased GC-MS headspace analysis of the C. maritima hexane extract highlighted several interesting compounds that may contribute to the therapeutic bioactivities of the extract. Conclusion: The lack of toxicity and the anti-proliferative activity of the hexane and ethyl acetate C. maritima extracts against HeLa and Caco2 cancer cell lines indicates their potential in the treatment and prevention of some cancers.

}, keywords = {Anticancer activity, Antioxidant, Brassicaceae, CaCo2, European searocket, HeLa, Oxidative stress}, doi = {10.5530/pj.2019.11.40}, author = {Elsayed Omer and Abdelsamed Elshamy and Rihab Taher and Walaa El-Kashak and Joseph Shalom and Alan White and Ian Cock} } @article {1003, title = {Chemical Constituents and Anti-Ulcer Activity of Ethylacetate Extract of the Leaves of Sanchezia nobilis Hook.F.}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1172-1180}, type = {Original Article}, chapter = {1172}, abstract = {

Study have two objectives. First objective is about the identification of the five components. The second objective is about the antiulcer activity of the ethylacetate extract. Five compounds (1{\textendash}5) were isolated from the leaves of Sanchezia nobilis Hook.F. collected in Nam Dinh province by chromatographic methods. These compounds were identified as: Quercetin (1), Scopoletin (2), Kaempferol-3-O-α-L-rhamnopyranosyl-(1{\textrightarrow}6)-β-D-glucopyranoside (3), Quercetin-3-O-α-L-rhamnosyl-(1{\textrightarrow}6)-β-D-glucopyranosyl-(1{\textrightarrow}3)-β-D-glucopyranoside (4),3{\textquoteright}-Omethyl- 3,4-methylenedioxy ellagic acid (5).Their structures were elucidated by spectroscopic methods, including mass spectrometry (MS) and nuclear magnetic resonance (NMR). Compounds 3, 4, 5 were isolated from the leaves of Sanchezia nobilis Hook.F. for the first time. Evaluation the effect of gastric and duodenal anti-ulcer on cyteamine induced gastric ulcer models indicates at this ethylacetate extract has the effect to improve the extent of ulcer lesions treatment (54,17 \%); obviously reduced the average of number pocket of ulcers (1,85 {\textpm} 0,80) and ulcer index (5,61 {\textpm} 2,69), however, it does not change the area of the ulcer.

}, keywords = {Anti-ulcer activity, Quercetin, Sanchezia nobilis, Scopoletin}, doi = {10.5530/pj.2019.11.182}, author = {Loi Vu Duc and Xuan Bui Thi and Ngoc Tran Minh} } @article {834, title = {Comparison between the Effect of Precipitate and Supernatant Aloe vera Gel on Experimental Cutaneous Wound Healing Using Optical Coherence Tomography}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {405-412}, type = {Original Article}, chapter = {405}, abstract = {

Background: Wound healing is a fundamental response to injured tissue that results in the restoration of tissue integrity. One of the famous herbs that promote wound healing is Aloe vera. Despite well known for its therapeutic effect, several studies reported inconclusive evidence regarding this. Besides, lack of evidence to postulate the superior effect of two components of Aloe vera which are the precipitate and supernatant. Objective: Study compares the effects of precipitate and supernatant in promoting tissue repair. Evaluation takes place by using optical Coherence Tomography (OCT) and is comparable with histopathology study. Methods: Twelve male mice were randomly divided into four groups (precipitate, supernatant, control 50\% ethanol, and normal). 200 mg of Aloe vera was extracted. A standardized 2 cm longitudinal incision wound was created. All mice were given topical Aloe vera, 0.5 g each, once daily and assessment of wound surface was performed using OCT. The animals were sacrificed on day 10 to evaluate histopathologically. Results: R parameter from the OCT was utilized to analyze the data. There is no significant difference in the treatment effect between Aloe vera treated group and control on day 10 post-injury. Treated animals with precipitate did not differ significantly from supernatant treated group. Nevertheless, from histopathology analysis, precipitate showed better wound reepithelialisation, collagen formation and angionesis despite having numerous inflammatory cells. Conclusion: OCT using R parameter is not the best choice to detect wound healing. Nevertheless, from histopathological perspective, Aloe vera accelerates wound healing and precipitate Aloe vera gel does have a superior effect from supernatant in promoting wound healing.

}, keywords = {Aloe vera, OCT, Precipitate, Supernatant, Wound Healing}, doi = {10.5530/pj.2019.11.63}, author = {Kusmardi Kusmardi and Nurrashida Binti Mok Hallim and Aryo Tedjo and Anwar Ibrahim and Salinah} } @article {796, title = {Effects of Withania somnifera Nicotine Induced Conditioned Place Preference in Mice}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {43-47}, type = {Original Article}, chapter = {43}, abstract = {

Background: Herbal medicines can be novel treatment strategies for management of nicotine addiction. Withania somnifera (Ashwagandha) is an Indian medicinal plant of great medicinal value; used in many clinically proven conditions. Objective: In present study we aimed at investigating the effect of withania somnifera extract (WSE) on preventing nicotine mediated effects attributed for the development of addiction. Material and Methods: Mice were treated with nicotine and/or WSE and subjected to nicotine induced conditioned place preference (CPP) in male albino mice was checked. Results: Application of two-way ANOVA showed that with preconditioning and post-conditioning values as a within-subjects (column) factor and treatment as an independent between subject (row) factor. Two-way ANOVA revealed significant effect of treatment [F(3,40)=4.119, p\<0.05], time [F(1,40)=23.76, p\<0.001] and interactiontreatment x time [F(3,40)=5.244, p\<0.01] on Intra-peritoneal (ip) administration of nicotine (1 mg/kg). WSE did not produce any changes in the preference to drug-paired compartment. Factors like treatment [F(3,40) = 0.656, p\>0.05], time [F(1,40) = 7.383, p\<0.01] and interactiontreatment x time [F(3,40) = 0.5748, p\>0.05] showed insignificant effects. Withania somnifera (50,100,200 mg/kg ip) coadministered with nicotine during the 6 days conditioning sessions completely abolished the acquisition of nicotine-induced CPP in mice. Conclusion: Above data indicate that withania somnifera attenuate nicotine induced CPP. Hence it has potential as an anti-addictive therapy.

}, keywords = {Condition place preference, Nicotine, Withania somnifera}, doi = {10.5530/pj.2019.1.8}, author = {Nitin Govindrao Dumore and Milind Janrao Umekar and Brijesh Gulabrao Taksande and Manish Manohar Aglawe and Nandkishor Ramdasji Kotagale} } @article {990, title = {Flavonoids in Passiflora incarnata L. Dry Extract of Russian Origin}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1143-1147}, type = {Research Article}, chapter = {1143}, abstract = {

Background: Flavonoids are one of the main classes of biologically active substances providing the pharmacotherapeutic effect of passionflower (Passiflora incarnata L.) preparations. In this article studies on the standardization of Passiflora incarnata L. dry extract (PDE) by flavonoids are presented. The aim of this work was to study the composition and content of flavonoids in PDE with the help of precise modern physicochemical methods. Materials and Methods: PDE was prepared from crude herbal drug {\textendash} P. incarnata herb of Russian origin. Reverse phase HPLC-UV analysis was performed with Agilent 1100 liquid chromatograph. Chromatographic column was Atlantis C18 (250 mm {\texttimes} 4.6 mm {\texttimes} 5 μm); analytical wavelength {\textendash} 350 nm; mobile phase {\textendash} 0.01\% formic acid solution and methanol: acetonitrile (25:75); column temperature {\textendash} 35{\textdegree}C; analysis time {\textendash} 90 min; flow rate of the mobile phase {\textendash} 0.8 ml/min in gradient elution mode. Commercially available samples of flavonoids were used for identification and quantitative determination. Results: 20 compounds of flavonoid structure are presented in the PDE. 9 flavonoid compounds have been identified, they are: isovitexin, vitexin, rutoside, hyperoside, luteolin, kaempferol, kaempferitrin, orientin, and isoorientin. The content of vitexin is 0,867 {\textpm} 0,011\%, the total flavonoids content in terms of vitexin is 3,762 {\textpm} 0,049\%. Conclusion: The obtained data will be used to create regulatory documentation for drugs based on PDE.

}, keywords = {Dry extract, Flavonoids, Passiflora incarnata, standardization}, doi = {10.5530/pj.2019.11.178}, author = {Guseinov MD and Bobkova NV and Svistunov AA and Tarasov VV and Bokov DO and Sergunova EV and Kovaleva TYu} } @article {945, title = {Glucosinolates, Degradation Products and Myrosinase Activity in Raphanus sativus Linn.}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {866-872}, type = {Original Article}, chapter = {866}, abstract = {

This research was conducted to assess the gluocosinolate (GSL), isothiocyanate (ITC) and myrosinase content in two cultivars of Raphanus sativus Linn. (white and red) roots. LC-ESIMS investigation was done on desulfated GSLs since this methodology has been previously established for efficient GSL analyses. The major GSLs: sinigrin (1) 1,2-dihydroxy-2-phenylethyl glucosinolate (2), 4-hydroxyglucobrassicin (3), glucoraphasatin (4) and 4-methoxyglucobrassicin (5) were found in red radishes; whereas, only 1 and 4 were obtained in white radishes. Myrosinase was analyzed in the tubers due to its ability to catalyze and hydrolyze GSLs into ITCs. This β-thioglucosidase enzyme was found to be over 10 times more active in red tubers (2.05E-02 units) than in white radishes (1.55E-03 units) and the results were linked to the presence/absence of the outer covering of the tubers. Due to the promising medicinal properties of the aglucone derivative of compound 4, 4-methylthio-3-butenyl isothiocyanate (6), the ITC analog was monitored using gas chromatographic mass spectral analyses after myrosinase-mediated hydrolysis. From the results, it can be construed that the occurrence of GSLs 1-5 and the bioactive agent 6 were inherent in the R. sativus cultivars evaluated.

}, keywords = {GC-FID, GC-MS, Glucosinolates, Isothiocyanates, LC-ESI-MS, Myrosinase}, doi = {10.5530/pj.2019.11.139}, author = {Maria Carmen S. Tan and Marissa G. Noel} } @article {940, title = {In vitro Antibacterial, Antioxidant and Anti-Inflammatory Effects of Senecio asperulus and Gunnera perpensa from Mohale{\textquoteright}s Hoek, Lesotho}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {730-739}, type = {Original Article}, chapter = {730}, abstract = {

Background: Traditional medicinal plants have been widely used to treat or manage various ailments for centuries in Lesotho. With an increase in multi drug resistance and undesired adverse events to current drugs challenges, there is a need for alternative drugs. Aim: In this study we aimed at the investigation of antibacterial, antioxidant and anti-inflammatory effects of Senecio asperulus and Gunnera perpensa roots extracted in three solvents of different polarities. Materials and Methods: Antibacterial activity was determined using the disc diffusion method, while antioxidant activity was determined using free radical scavenging of 2,2-diphenyl-1-picrylhydrazyl and the ferric reducing antioxidant power assay. The Lipopolysaccharide (LPS) stimulated RAW 264.7 mouse macrophage in vitro model was used to evaluate the anti-inflammatory activity of both plants. Resveratrol was used as a positive control. Results: Methanol extracts of Senecio asperulus inhibited microbial growth even at the lowest concentration of 50 μg/ml. Senecio asperulus dichloromethane extract was active on most bacteria with MIC{\textquoteright}s between 50 μg/ml and 500 μg/ml. However, the water and methanol extracts of Gunnera perpensa had no activity against all organisms tested. Aqueous extracts of Senecio asperulus and Gunnera perpensa showed free radical scavenging activity yielding EC50 values of 100 μg/ml and 25 μg/ml, respectively. The aqueous extracts of Senecio asperulus showed moderate anti-inflammatory activity from 50 to 200 μg/ml. while the methanol extract was at 200 μg/ml and with no cytotoxicity. No anti-inflammatory activity was observed from all Gunnera perpensa extracts using LPS-induced macrophages, this suggests that this species may be using other mechanisms for anti-inflammatory activity. Conclusion: The antibacterial, antioxidant and anti-inflammatory activities observed from water extracts of Senecio asperulus support its ethnomedicinal use for the management of inflammation related diseases.

}, keywords = {Anti-inflammatory activity, Antibacterial activity, antioxidant activity, Gunnera perpensa, Medicinal plants, Senecio asperulus}, doi = {10.5530/pj.2019.11.116}, author = {Mfengwana Polo-Ma-Abiele H and Mashele Samson S and Manduna Idah T} } @article {1006, title = {In vitro Antioxidant Properties and α-Glucosidase Inhibition of Combined Leaf Infusions from Psidium guajava L., Syzygium polyanthum L., and Annona muricata L.}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1269-1277}, type = {Original Article}, chapter = {1269}, abstract = {

Introduction: Guava (P. guajava), bay (S. polyanthum), and soursop (A. muricata) known as natural medicine. Limited report is available on their antioxidant and α-glucosidase inhibitory activities of leaf infusion. The aims of this research were to compare the antioxidant and α-glucosidase inhibitory activities of leaf infusion from guava, bay, and either as individual or combined infusions, and to analyze the chemical composition of the leaf infusion. Methods: Air dried leaf powder of guava, bay and soursop were infused separately with boiled aquadest. The infusions were analyzed for their antioxidant activity against DPPH. The α-glucosidase inhibitory assay was conducted against α-glucosidase from Saccharomyces cerevisiae. Then the infusions scanned with UV-Vis spectroscopy and analyzed with LC-MS. The synergism activities of the combined infusion were measured. Results: Antioxidant activities of leaf infusions of guava and bay showed a comparable result IC50 12.53 {\textpm} 0.55 and 10.76 {\textpm} 0.20 μg GAE/mL, but the infusion of soursop showed lower (IC50 19.77 {\textpm} 0.35 μg GAE/mL) than BHT as positive control (11.6 {\textpm} 0.31 μg GAE/mL). If soursop infusion was not added, then the mixture of the guava and bay infusion showed an antioxidative synergistic effect. The α-glucosidase inhibitory activities of the guava, bay and soursop infusion (0.083 {\textpm} 0.01; 0.025 {\textpm} 0.007; 0.533 {\textpm} 0.039 μg GAE/mL, respectively) were stronger than acarbose (1285 {\textpm} 148 μg/mL). The α-glucosidase inhibitory activities of the combined infusions showed a synergistic effect. The main constituents of the guava infusion were identified tentatively as chrysin and caffeoylquinic acid, for the bay infusion it was caffeoylquinic, and for the soursop infusion it was luteolin. Conclusions: There is a significant synergism of antioxidant activity of Guava and Bay mixture. The combined infusion of Bay and Soursop or Guava and Soursop showed antagonistic effect.

}, keywords = {Anonna muricata, Leaf infusion, Psidium guajava, Synergism, Syzygium polyanthum, α-glucosidase}, doi = {10.5530/pj.2019.11.197}, author = {Ika Rahayu and Pamela Hendra Heng and Kris H Timotius} } @article {917, title = {A Methanolic Extract of Ocimum basilicum Exhibits Antioxidant Effects and Prevents Selenite-induced Cataract Formation in Cultured Lenses of Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {496-504}, type = {Original Article}, chapter = {496}, abstract = {

Objective: An extract (Methanolic) of the Ocimum basilicum leaf was analysed for potential to abrogate experimental formation of cataract in-vitro. Methods: Phytoconstituents were first detected in O. basilicum extracts (Aqueous or methanolic) by gas chromatographic-mass spectrometric analysis. The putative antioxidant activity of these extracts was then assessed by measuring in-vitro radical-scavenging activity, ion-chelating potential and reducing potency. Potential cytotoxicity of the extract on Human lenticular epithelial B3 (HLE-B3) cells was also sought. Finally, possible prevention of cataract formation by the methanolic extract was gauged in selenite-exposed lenses obtained from Wistar rats. There were 3 groups (8 Lenses in each): Group I (Lenses incubated in Dulbecco{\textquoteright}s modified Eagle{\textquoteright}s medium [DMEM] alone); Group II (Lenses incubated in DMEM with sodium selenite [100 μM/ml]); Group III (Lenses incubated in DMEM with selenite [100 μM/ml] and the O. basilicum methanolic extract (200 μg/ml DMEM). Gross lenticular morphology was assessed. Levels of lenticular malondialdehyde (MDA) and reduced glutathione (GSH) were also measured. Results: A higher intensity of antioxidative activity was noted in the methanolic extract than in the aqueous extract. The methanolic extract exhibited negligible cytotoxicity. On morphological examination, marked opacification was seen in all 8 Group II lenses whereas there was no opacification in 7 of 8 Group III lenses. Near normal mean levels of reduced glutathione and malondialdehyde, were noted within Group III lenses. Conclusion: The methanolic extract of the O. basilicum leaf appears to prevent selenite-induced cataract formation in-vitro.

}, keywords = {Antioxidants, Cataract, Crystallins, Ocimum basilicum, Oxidative stress, Phytoconstituents}, doi = {10.5530/pj.2019.11.79}, author = {Thiraviyam Anand and Mahalingam Sundararajan and Muniyandi Anbukkarasi and Philip Aloysius Thomas and Pitchairaj Geraldine} } @article {1059, title = {Neuroprotective Effect of Sacha Inchi Oil (Plukenetia volubilis L.) in an Experimental Model of Epilepsy}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1591-1596}, type = {Research Article}, chapter = {1591}, abstract = {

Background: Experimental studies have demonstrated that fatty acids such as omega 3 and 6 have anti-inflammatory, anticonvulsant, cardio protective and anti-tumor effects. Objective: The main objective was to determine the protective effect of sacha inchi oil on pentylenetetrazoleinduced seizures in albino mice. Material and Methods: Thirty male Balb/C albino mice of 8 weeks of age were purchased from the National Institute of Health (Lima-Peru). The animals were divided into 5 groups of 6 animals each one. Group I: Control; PTZ (pentylenetetrazole 80 mg / kg, s.c.). II: PTZ + Diazepam (1 mg / kg; s.c.). Group III, IV, V: PTZ + sacha inchi oil at single doses of 250, 500, 1000 mg / kg respectively orally. Sacha inchi oil was administered 30 minutes before induction of seizures by PTZ. Next, various parameters such as latency, seizure frequency, duration and score were scored according to Racine scale. The program Graph Pad Prism v.4 was used for statistical analysis. Results: As result, the experimental group treated with sacha inchi oil at maximum dose of 1000 mg/kg showed better results in response to PTZ induced seizure; low levels of seizures, frequency and duration (P\<0.001; ANOVA, P \<0.001 Post-hoc Dunnett test). Conclusion: It is concluded that Sacha inchi oil presented anticonvulsant effect at the highest doses tested being very similar to Diazepam. The main mechanism could be by reducing free radical and improving GABA levels in the brain.

}, keywords = {Convulsion, Epilepsy, Omega, Pentylenetetrazole, Plukenetia Volubilis, Sacha inchi}, doi = {10.5530/pj.2019.11.243}, author = {Oscar Herrera-Calderon and Ricardo {\'A}ngel Yuli-Posadas and Johnny Aldo Tinco-Jayo and Edwin Enciso-Roca and C{\'e}sar Franco-Quino and Victor Chumpitaz-Cerrate and Linder Figueroa-Salvador} } @article {988, title = {Neuroprotective Effects of Ganoderma curtisii Polysaccharides After Kainic Acid-Seizure Induced}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1046-1054}, type = {Original Article}, chapter = {1046}, abstract = {

Background: Epilepsy is one of the major neurological disorders affecting world population. Although, some Ganoderma species have shown neuroprotective activities, the effects of polysaccharides isolated from Ganoderma curtisii on epileptic seizures have not been reported. Objective: The aims of the present study were to determine whether treatment with a polysaccharide fraction (GCPS-2) from a Mexican Ganoderma curtisii strain can reduce seizures, and the increases in the levels of apoptotic molecules and inflammatory cytokines in kainic acid-induced seizure mouse model. Materials and Methods: Rats were separated in groups: Control group received 2.5\% Tween 20 solution; GCPS-2 groups were administered GCPS-2 (10, 40, or 80 mg/kg); KA group received KA 10 mg/kg; GCPS-2+KA received GCPS- 2 and 30 min later KA. Pathological changes in neuronal morphology, expression of B-cell lymphoma-2, and pro-inflammatory cytokines (interleukin1-β and tumor necrosis factor-α) in the rat hippocampus and cortex were determined by immunohistochemistry. Results: Ganoderma curtisii soluble polysaccharides (GCPS-2) inhibited convulsions in rats. Moreover, treatment with GCPS-2 reduced the increased levels of apoptotic signaling molecules (Bcl-2) and proinflammatory mediators (in the kainic acid-treated hippocampus and cortex). Conclusion: Ganoderma curtisii soluble polysaccharides have a neuroprotective potential against epilepsy, partially through its ability to inhibit neurotoxic events in the in vivo hippocampus and cortex.

}, keywords = {Anti-inflammatory, Anticonvulsant, Ganoderma curtisii, Neuroprotective, β-glucan}, doi = {10.5530/pj.2019.11.164}, author = {Ismael Leon-Rivera and Juana Villeda-Hernandez and Elizur Montiel-Arcos and Isaac Tello and Maria Yolanda Rios and Samuel Estrada-Soto and Angelica Berenice Aguilar and Veronica Nunez-Urquiza and Jazmin Mendez-Miron and Victoria Campos-Pena and Sergio Hidalgo-Figueroa and Eva Hernandez and Gerardo Hurtado} } @article {962, title = {A New LC/MS/MS Method for the Analysis of Phyllanthin in Rat Plasma and its Application on Comparative Bioavailability of Phyllanthin in Different Formulations after Oral Administration in Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {968-975}, type = {Original Article}, chapter = {968}, abstract = {

Introduction: A simple, short UPLC/MS/MS method for quantitation of phyllanthin in rat plasma in less than 2 minutes have been developed and fully validated. The validated method was used to investigate the pharmacokinetic properties of phyllanthin in PA extract and phospholipid complex of PA extract in rat. Methods: The separation was carried out on Acquity C18 (50 x 2.1 mm; 1.7 μm), with a mobile phase of 10 mM aqueous amonium acetate and acetonitrile (10:90; v/v), at a flow rate of 0.2 mL/min. Felodipin was used as internal standard. Phyllanthin is extracted from a small volume of rat plasma (100 μl) by means of liquid-liquid extraction method with tert butyl methyl ether. Electrospray ionization (ESI) mass spectrometry was applied in positive mode at capillary voltage of 4000 V for both phyllanthin and IS, cone voltage of 24 V for phyllanthin and 20 V for IS, desolvation temperature of 360oC, cone gas flow of 25 L/h, collision energy of 12 V for phyllanthin and 10 V for IS. Multiple reaction monitoring (MRM) was used to monitor the transitions at m/z (Q1/Q3) 436.41/355.36 for phyllanthin and 384.20/352.18 for IS. Results: The linear calibration curve of phyllanthin was obtained over the concentration range of 0.5 {\textendash} 100 ng/mL. The intra- and inter-day precisions were less than 7.08 \% and the accuracies were within {\textpm} 7.55\%. The Cmax values of phyllanthin from two different preparations in rat plasma after oral administration of 2.0 mg/kg were 11.44 and 31.44 ng/ml, and the AUC values were 18.07 and 41.43 h.ng/ml, respectively. Conclusion: A simple, short UPLC/MS/MS method for quantitation of phyllanthin in rat plasma in less than 2 minutes have been developed and fully validated. The bioavailability of phyllanthin from the phospholipid complex of PA extract in rat plasma was significantly improved compared with that of raw PA extract after oral administration.

}, keywords = {LC-MS/MS, Pharmacokinetics, Phospholipid, Phyllanthin, Plasma, Quantitation}, doi = {10.5530/pj.2019.11.153}, author = {Nguyen Van Long and Chu Van Men and Anh Vu Tuan and Nguyen Van Manh and Thanh Chu Duc and Ha Bui Thi Thu and Hoang Van Luong and Le Bach Quang and Pham Gia Khanh} } @article {802, title = {Pharmacognostic Specifications, Quercetin and Quercitrin Quantification in Bauhinia malabarica Leaf}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {155-160}, type = {Original Article}, chapter = {155}, abstract = {

Introduction: Bauhinia malabarica Roxb. is a tropical tree that found throughout Thailand. Leaves have a sour taste and have been used in Thai remedies for wound healing, diuretic, dysentery and emmenagogue. Objective: This study aimed to focus on pharmacognostic specification and quantitative analysis of quercetin and quercitrin in B. malabarica leaves. Methods: Various methods such as macroscopic and microscopic evaluations of B. malabarica leaf were studied along with physico-chemical parameters and quantitated quercetin and quercitrin using RP-HPLC. Results and Conclusion: Whole plant, structures of dried powder crude drug, cross section of midrib and leaf measurement were established. Paracytic stomata and multicellular trichome were found on lower epidermis. B. malabarica leaves from 15 sources throughout Thailand were examined the pharmacognostic specification according to WHO guideline. Physico-chemical parameters showed that loss on drying, total ash, acid insoluble ash and water content should not be more than 8.00, 7.08, 1.79 and 8.28 \% of dry weight while ethanol and water soluble extractive values should not be less than 13.78 and 16.47 \% of dry weight respectively. Quercetin and quercitrin were the markers for quantitative analysis using RP-HPLC with diode array detector in B. malabarica ethanolic extract. Quercetin and quercitrin contents were found to be 0.18 g and 0.38 g in 100 g of dried crude drug. Method validation was determined according to ICH guideline. All results were in the acceptable range and could be used for identity, safety, efficacy and quality of B. malabarica leaves in Thailand.

}, keywords = {Bauhinia malabarica Roxb, HPLC, Leaf measurement, Pharmacognostic specification, Quercetin, Quercitrin}, doi = {10.5530/pj.2019.1.26}, author = {Paphitchaya Thetsana and Chayanon Chaowuttikul and Chanida Palanuvej and Nijsiri Ruangrungsi} } @article {891, title = {Phytochemical Screening and Antioxidant Activity Study of Methanol Extract of Stems and Roots of Codonopsis clematidea from Trans-himalayan Region}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {536-546}, type = {Original Article}, chapter = {536}, abstract = {

Aim: The present report aimed to study the therapeutic and phytochemical properties of stems and roots of trans-himalayan plant Codonopsis clematidea. Material and Methods: The crude samples of stems and roots were explored for their chlorophyll, carotenoid and carbohydrate content in order to understand the matrix of these two plant parts. The extraction of phytochemicals was carried out by three different methods viz. sonication, maceration and soxhlet in methanol to identify the best extraction method. Further, analysis of Total Flavonoid Content (TFC) and Total Polyphenolic Content (TPC) were carried out using rutin trihydrate and gallic acid as a reference standard. Antioxidant capacity was estimated using three methods viz. 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2{\textquoteright}-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging assay and Ferric Reducing Antioxidant Power (FRAP) assay. In addition to this, GC-MS analysis was also performed for the identification of volatile constituents of Methanol Extract of Stems (MES) and Methanol Extract of Roots (MER). Results: The MES and Dimethylsulfoxide Extract of Stems (DES) were found to have higher Chlorophyll a (Cha) content in comparison to Chlorophyll b (Chb) and Carotenoids (Cca). Carbohydrate profile showed that stems and roots have the highest content of fructose in comparison to other sugar moieties. The soxhlet method showed the highest percentage extractive yield in the stems as well as roots. Results revealed that the MES showed higher antioxidant potential as compared to the MER. A correlation has also found to exist between the results of TPC, TFC and antioxidant assays, since TPC and TFC are key constituents responsible for the antioxidant potential. Conclusion: These results have been found to suggest the richness of MES in natural phenols, flavonoids and antioxidants. Further, study should be conducted over identification and characterization of compounds present in the extract.

}, keywords = {Antioxidant, Codonopsis clematidea, Fructose, GC-MS, MER, MES}, doi = {10.5530/pj.2019.11.86}, author = {Pushpender Bhardwaj and Mohan Singh Thakur and Sahil Kapoor and Ashwani Kumar Bhardwaj and Ajay Sharma and Shweta Saxena and Om Prakash Chaurasia and Raj kumar} } @article {987, title = {Phytosomal Nanoparticles Preparation of Curcuminoids to Enhance Cellular Uptake of Curcuminoids on Breast Cancer Cell Line MCF-7}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1037-1045}, type = {Original Article}, chapter = {1037}, abstract = {

Objective: Curcuminoids, the bioactive compounds extracted from Curcuma longa consisting of Curcumin (CUR), demethoxycurcumin (DMC) and bisdemethoxycurcumin (BDMC), have shown promising biological effects, including anticancer activity. This study sought to prepare a physically stable phytosomal nanoparticles of curcuminoids (Curs-Phyto) to facilitate uptake of curcuminoids on breast cancer cells line, and further increase the cytotoxicity against cancer cells. Methods: The evaporation combined extrusion technique was employed to prepare phytosomal curcuminoids nanoparticles. The interaction between curcuminoids and phospholipid by a hydrogen bond was confirmed by differential scanning calorimetry (DSC), powder X-ray diffraction (XRD), fourier transform infrared (FT-IR), and 1H nuclear magnetic resonance (1H-NMR). Their physicochemical characterizations and stability in simulated gastric and intestinal media were investigated. The effects of Curs-Phyto on MCF-7 cells were evaluated by flow cytometry, MTS assay and cell cycle analysis. Results: We found that the Curs-Phyto were formed at a spherical shape with good size (~ 180 nm), a narrow size distribution (PDI \< d0.2), high complexation rate (~ 87\%, 95\%, and 90\% for BDMC, DMC, and CUR respectively) and high loading capacity of curcuminoids. More importantly, the Curs-Phyto showed the increased cellular uptake and enhanced cytotoxicity against MCF- 7 cancer cells, compared to free curcuminoids. Conclusion: These results indicated that the phytosome could be a promising oral delivery system for curcuminoids for cancer treatment.

}, keywords = {Cellular uptake, Curcuminoids, FACS analysis, Nanoparticle, Phytosome}, doi = {10.5530/pj.2019.11.163}, author = {Nguyen Van Long and Bui Thi Thu Ha and Anh Vu Tuan and Hoang Van Luong and Nguyen Tung Linh and Thanh Chu Duc and Phung Cao Dai and Chul Soon Yong and Chu Van Men} } @article {914, title = {Protective Role of Eurycoma longifolia Jack Root Extract Against High-Fat Diet Induced Testicular Damage in Sprague-Dawley Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {808-811}, type = {Original Article}, chapter = {808}, abstract = {

Objective: The aims of this study were to investigate the adverse effects of the high-fat-diet (HFD) on the testosterone level and testicular structure of male rats as well as to examine whether Eurycoma longifolia (EL) is able to ameliorate these effects. Methods: Twenty-four male Sprague-Dawley (SD) rats were divided into four groups each containing 6 rats. Group ND was given only normal diet, group NDEL was given normal diet and EL extracts (15 mg/ kg) dissolved in distilled water, group HFD was given only high-fat-diet and group HFDEL was given high-fat-diet and EL extracts (15 mg/kg). EL was administered orally for 12 weeks. The animal{\textquoteright}s testosterone level was measured at week 0, 6 and 12. The rats were sacrificed at the end of 12th weeks and the testes samples were processed for histological examination Results: The testosterone level was significantly increased (p \< 0.05) in the in the treated rats with EL (NDEL and HFDEL) compared with ND and HFD groups. Treatment with HFD revealed a marked degeneration of the seminiferous tubule epithelium and disruption of interstitial cells of the testis thereby interfering with spermatogenesis. Treatment of HFD rats with El reduced the adverse effects of HFD and improved the morphological structure of the seminiferous tubules. Conclusion: These findings revealed that EL has ameliorative effects against the testicular damage caused by high-fat-diet.

}, keywords = {Eurycoma Longifolia, High-Fat-Diet, Seminiferous Tubules Tongkat Ali, Testis, Testosterone}, doi = {10.5530/pj.2019.11.129}, author = {Imad M Al-Ani and Norsidah Ku-Zaifah and Fakhria A. Al-Joufi and Rafidah H.Mokhtar and Norlelawati A. Talib and Ghasak Ghazi Faisal} } @article {964, title = {Quantitative Analysis of Hispidulin Content in Clerodendrum petasites Roots Distributed in Thailand}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1093-1099}, type = {Research Article}, chapter = {1093}, abstract = {

Introduction: Clerodendrum petasites (Lour.) S. Moore (locally known as Mai-Thao-Yaai-Mom), belonging to the Verbenaceae family, is widely formulated into multi-herb remedy, Ben-Cha- Lo-Ka-Wi-Chian remedy, possessing antipyretic activity. C. petasites exhibits many biological activities, such as antioxidant, anti-inflammatory, antipyretic, etc. The flavonoid hispidulin is one of the main active compounds present in C. petasites, containing anti-atheromatous, antitumor and antispasmodic effects. Objective: The present study aimed to determine the hispidulin content in the dried roots of C. petasites using HPLC technique. Methods: C. petasites dried roots, collected from twelve different areas, were extracted with ethanol using Soxhlet apparatus, and then subjected to HPLC-PDA to quantify hispidulin content. The quantitative method using HPLC-PDA technique was validated. Results: The optimized HPLC coupling with PDA detector (HPLC-PDA) was validated for the quantitative analysis of hispidulin content in C. petasites roots in terms of linearity (y = 210,200,536.6667x {\textendash} 448,756.2667; R2 = 0.9997), accuracy (88.82-107.69\% recovery), precision (0.66\% RSD for repeatability precision; 1.17\% RSD for intermediate precision), limit of detection (2.30 μg/mL), limit of quantitation (7.00 μg/mL), specificity (peak purity index = 1.0000) and robustness (\% RSD \< 1). The amount of hispidulin content in the extracts of C. petasites roots conducted from the validated method was found to be 0.0182 {\textpm} 0.0109 g/100 g crude drug. Conclusion: The HPLC-PDA analysis was able to effectively determine hispidulin in C. petasites roots. The hispidulin contents in C. petasites dried roots from various areas in Thailand were revealed which could be used for the specification of this crude drug with reference to its chemical marker.

}, keywords = {Ben-Cha-Lo-Ka-Wi-Chian remedy, Clerodendrum petasites, hispidulin, HPLC-PDA}, doi = {10.5530/pj.2019.11.171}, author = {Thanyathorn Tangsongcharoen and Somchai Issaravanich and Chanida Palanuvej and Nijsiri Ruangrungsi} } @article {1014, title = {Rationale for Manufacturing of Cut-Pressed Granules from Herbal Raw Material Rich in Essential Oil: An Example of Chamomile Flowers and Sweet Flag Rhizome}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1285-1289}, type = {Original Article}, chapter = {1285}, abstract = {

Background: Currently, there are at least 43 different dosage forms present on the Russian Federation pharmaceutical market. A novel, unique dosage form {\textendash} cut-pressed granules (CPG) {\textendash} was developed in order to improve manufacturing characteristics and, therefore, quality of herbal drug products released in tea bags. However, treatment conditions may result in decreased levels of active substances in some of the plants, especially those containing essential oil, which is prone to degradation. The aim of this study was to assess feasibility of CPG manufacturing from herbal raw material rich in essential oil. Materials and Methods: Different morphological groups of raw material from two commonly used medicinal plants, chamomile (Matricaria recutita L.) flowers and sweet flag (Acorus calamus L.) rhizome, were chosen as the objects of the study. Qualitative composition of lipophilic constituents in herbal raw materials and CPG was assessed using thin-layer chromatography. Essential oil content was determined by steam distillation. Results: The results confirmed equivalence of chromatographic profiles for the analyzed raw materials and CPG; thus, granulation didn{\textquoteright}t affect qualitative composition of lipophilic components in chamomile flowers and sweet flag rhizome. The study also showed that the granulation process, in fact, promoted stability of the dosage form: during long-term storage the content of essential oil in all of the assessed cut-pressed granules was equivalent or higher than in corresponding herbal raw material. Conclusions: It can be concluded that Matricaria recutita L. flowers and Acorus calamus L. rhizome can be used as herbal raw material for CPG manufacturing.

}, keywords = {Chamomile, Cut-pressed granules, Dosage form, Essential oil, Herbal drugs, Sweet flag}, doi = {10.5530/pj.2019.11.199}, author = {Olga Trifonova and Olga Evdokimova and Vera Prokofieva and Alexey Matyushin} } @article {848, title = {Reduction of Colchicine Content from Radix Gloriosae Superbae Preparata}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {310-314}, type = {Original Article}, chapter = {310}, abstract = {

Introduction: Gloriosae Superbae Radix is a crude drug employed in Thai herbal remedies for several ailments. Colchicine is known as an active constituent in the roots. It was reported that 7-11 mg. of colchicine may causes lethal effect in human. In Thai traditional medical practice, the roots must be treated prior use to prepare Thai herbal preparations. However, pre-treated method has not yet been well established in any literature. This study aimed to document the pre-treated method and to quantitatively compare the amount of colchicine both before and after pre-treated. Methods: Firstly, interviewing with Thai traditional medicine experts and document the pre-treated methods of Gloriosae Superbae Radix to conclude the 2 commonly used methods. Two pre-treated methods (roasting and burning) were chosen for further study. Colchicine in Gloriosae Superbae Radix from 8 sources were analyzed before and after pre-treat by High Performance Liquid Chromatography (HPLC). Results: After pre-treat by roasting and burning, amount of colchicine in root were significantly decreased by 40.61{\textpm}9.55\% (p=0.000) and 26.79{\textpm}10.89\% (p=0.001), respectively. Comparison of colchicine contents of samples after roasting and burning, the amount of colchicine decreased non statistically insignificantly (p=0.110). Conclusion: Pre-treats of Gloriosae Superbae Radix by roasting and burning had significantly reduce colchicine content. Both methods have been proven to be the effective ways in preparing certain potentially toxic crude drugs before using in compounding into Thai herbal remedies.

}, keywords = {Colchicine, Gloriosae Superbae Radix, HPLC, Pre-treat method, Thai herbal remedy}, doi = {10.5530/pj.2019.11.46}, author = {Sasithorn Tandhavadhana and Chayan Picheansoonthon} } @article {896, title = {Screening and Evaluation of Lectin and Anti-Cancer Activity from the Phloem Exudate/Sap of the Indian Dietary Ethnomedicinal Plants}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {570-578}, type = {Original Article}, chapter = {570}, abstract = {

Objective: Lectins are extremely significant biomolecules to study several biological progressions. In this present investigation, we are screening the crude phloem exudate/ sap sample from different ethnomedicinal plants were evaluated for lectin and anticancer activity. Methods: The lectin activity of crude phloem exudate/sap samples were confirmed by haemgglutination assay and anticancer activity by using trypan blue, MTT and in-ovo CAM angiogenic assay. The tumor cell nuclei resulting in Giemsa stain, AO/EtBr stain, DNA Fragmentation and Caspase- 3 inhibitor assay. Results: Our experimental data show that the phloem exudate/sap sample S2 (Musa Acuminata), sample S4 (Euphorbia Geniculate) exerting the potent lectin activity, sample S5 exerting very low lectin activity against the trypsinized rabbit erythrocytes and decreases the cell viability in EAC cells in-vitro. Sample S2, S4 and S5 exerts significant cytotoxic effect against the various human cancer cell lines and regressed the neovasculature (development of new blood vessels) in the developing CAM embryos when compared to the other crude samples. The apoptotic inducing activity of crude phloem exudate/sap samples was revealed by DNA fragmentation assay, caspase-3 inhibitor assay and cellular morphology were studied by fluorescence staining methods. Conclusion: This study reports that some of the isolated crude phloem exudate/sap samples show potent lectin activity and anti-cancer activity in different human cancer cell lines. The further additional experiment needs to purify and characterize the bioactive lectin components from the potent sample which is responsible for pro-apoptotic, anti-angiogenic activity and mechanism involved.

}, keywords = {Angiogenesis, Apoptosis, EAC, Haemagglutination, Lectin, VEGF}, doi = {10.5530/pj.2019.11.91}, author = {Balaji Kyathegowdanadoddi Srinivas and Madhu Chakkere Shivamadhu and Preethi Saligrama Devegowda and Gurukar Mathew and Theethagounder Tamizhmani and Senthilkumar Gnanavadevel Prabhakaran and Shankar Jayarama} } @article {464, title = {Angiotensin-Converting Enzyme Inhibition of Fractions from Eleusine indica Leaf Extracts}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {25-28}, type = {Original Article}, chapter = {25}, abstract = {

Solvent fractions and decoction of Eleusine indica leaves were tested for their ability to inhibit angiotensin-converting enzyme (ACE), an important component of the Renin-Angiotensin- Aldosterone System which is a critical regulator of arterial blood pressure. The ACE inhibitory activity of each fraction was measured by employing a colorimetric assay based on the hydrolysis of histidyl-hippuryl-leucine (HHL) by ACE. Preliminary assay results revealed that the ethyl acetate fraction exhibited the highest antihypertensive activity with a percent inhibition of 51.51\%. This fraction was considered for further isolation using a bioassay-guided fractionation scheme.

}, keywords = {Bioactive extracts, High-blood pressure, Hypertension, Medicinal, Plant extracts}, doi = {10.5530/pj.2018.1.5}, url = {http://fulltxt.org/article/360}, author = {Jasmin T Tutor and Christine L Chichioco-Hernandez} } @article {474, title = {Anti-inflammatory Activity of Methanolic Extract from Pistacia atlantica Desf. Leaves}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {71-76}, type = {Original Article}, chapter = {71}, abstract = {

Introduction: The extracts of the Pistacia species are known for their anti-inflammatory activity, including fruits and oil of P.\ atlantica. However, the inflammatory effect of the methanolic extract of P.\ atlantica leaves has not been studied. This work aimed at assessing the antiinflammatory and antioxidant activities of P.\ atlantica leaves extract in relation to phytochemical studies of flavonoids. Methods: The extract was obtained using sonication of leaves powder in 80 \% methanol. The analysis of phenolic compounds was carried out using thin-layer chromatography (TLC). The antioxidant activity was evaluated using DPPH, ABTS and FRAP assays. The anti-inflammatory activity was determined by the reduction of carrageenaninduced hind paw edema in mice. Results: The TLC revealed 3 glycosylated flavonoids and gallic acid derivatives. The flavonoids identified corresponded to rutin, quercetrin and other heterosides of quercetin, kaempferol and myricetin. Total phenolics and flavonoids contents were comparable for the male and female trees. The antioxidant activity did not show a significative difference between the two sexes, except for that evaluated by the FRAP assay which was significantly greater for the male tree leaves extract. The leaves extract permitted significative reduction of the edema at h3 and 6 in a dose-dependent manner (100 and 250 mg/kg), while diclofenac used as control reduced the edema at h 1.5. This difference could be explained by the pharmacokinetic and pharmacodynamic properties of diclofenac and P. atlantica leaves compounds. Conclusion: P. atlantica has a strong anti-inflammatory activity and constitutes a potential source for the development of new treatments.

}, keywords = {antioxidant activity, Flavonoids, Methanolic extract, Plantar edema, TLC}, doi = {10.5530/pj.2018.1.14}, url = {http://fulltxt.org/article/369}, author = {Oukacha Amri and Abderrahmane Zekhnini and Abdellah Bouhaimi and Saida Tahrouch and Abdelhakim Hatimi} } @article {743, title = {Antioxidant Activities of Ethanolic and Aqueous Extracts of Asparagus racemosus Roots}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1129-1132}, type = {Original Article}, chapter = {1129}, abstract = {

Background: Asparagus racemosus (AR) is commonly known as shatavari, satawar or satmuli in India and in Thailand it is call sam-sib or rak-sam-sib. The dried root of AR is used in Ayurveda as an antiulcerous and antiinflammatory and has medicinal/pharmacological value. Objective: To investigate the antioxidant activities of Asparagus racemosus root extracts via total phenolic and total flavonoid contents of ethanolic and aqueous extracts. Methods: Antioxidant capacity measurements were carried out by DPPH, ABTS and FRAP methods. Total phenolic and flavonoid contents were determined by the Folin-Ciocalteu method and the aluminum chloride colorimetric method, respectively. Results: The ethanolic extract possessed higher antioxidant capacities than the aqueous extract in the three antioxidant assays (p\<0.05).These results have shown high phenolic and flavonoid contents. The ethanolic extract of AR root possessed higher amounts of phenolic and flavonoid contents than the aqueous extract. Conclusion: The antioxidant capacity of the ethanolic extract was higher than that in the aqueous extract.

}, keywords = {antioxidant activity, Asparagus racemosus, Flavonoid, Phenolic compound}, doi = {10.5530/pj.2018.6.192}, author = {Ladachart Taepongsorat and Surapong Rattana} } @article {630, title = {Antioxidant Activity of Fractions from Garcinia hombroniana Pierre Leaves Extracts}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {682-685}, type = {Original Article}, chapter = {682}, abstract = {

Introduction: Radicals were compounds that generated in normal metabolism and create cell damage. A significant increase of free radical and decreased radical elimination can lead to oxidative stress. Oxidative stress plays an important role in the development of many diseases. Enhanced supply of antioxidants will help prevent the morbidity of many diseases. Garcinia hombroniana Pierre has potency as an antioxidant, but study to evaluate the active fractions as an antioxidant has not been done. Objective: The objective of the study was to evaluate antioxidant activity of fractions separated from ethyl acetate (EtOAc) and methanol (MeOH) extract of Garcinia hombroniana leaves and to obtain active fractions to facilitate finding a pure antioxidant compound. Methods: The extract was fractionated using column chromatography, while antioxidant activity assay was conducted in vitro using spectrophotometric methods with DPPH and FRAP method. Results: EtOAc extract of G. hombroniana leaves yielded EA-8 with radical scavenging percentage 32.67\% (10 ppm, with DPPH method) and EA-11 with antioxidant activity percentage 25.73\% (10 ppm, with FRAP method) as the most active fraction from EtOAc extract, while MeOH extract yielded M-3 with radical scavenging percentage 37.42\% (10 ppm, with DPPH method) and 26.70\% (10 ppm, with FRAP method) as the most active fraction from MeOH extract Conclusion: Most active fractions has good antioxidant activity, worthy for further study to isolate antioxidant compound which is responsible for antioxidant activity. However, the percentage of radical scavenging or antioxidant activity of all active fractions were smaller than quercetin as a positive control.

}, keywords = {Column chromatography, Free Radicals, Spectrophotometric thin layer chromatography}, doi = {10.5530/pj.2018.4.112}, url = {http://fulltxt.org/article/650}, author = {Nita Triadisti and Rani Sauriasari and Berna Elya} } @article {542, title = {Antioxidant Potential and Ionomic Analysis of Two Buckwheat Species from Kashmir Region}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {x}, pages = {XX-XX}, type = {x}, chapter = {XX}, abstract = {

Background: Buckwheat in the past had been the staple food for many regions in the Himalaya\’s and its utilization has declined with time. In recent times buckwheat gained a lot of attention as it has been placed in the list of underutilized crops by FAO. There is a strong sentiment and realization for buckwheat revival because of its neutraceutrical properties due to which it provides the consumers with extra choice for his food basket. In this context the present investigation aimed to evaluate the antioxidant potential and mineral element analysis of two buckwheat species grown in Kashmir region. Methods: To achieve this goal, antioxidant potential of two buckwheat species was done by using standard protocols. For ionomic analysis, atomic absorption spectrophotometry (AAS) was done to unravel the macro-and micro-nutrient composition. Result: Aqueous extract of Fagopyrum tataricum exhibits higher TPC (159.51\±10.3 mg gallic acid equivalent g-1 DW) and TFC (79.49\±9.76 mg rutin equivalent g-1 DW). The F. tataricum samples exhibit high radical scavenging activity (RSa50=26.67\μg ml-1) as compared to F. kashmirianum (RSa50=34.15\μg ml-1). Elemental analysis revealed that calcium (Ca) was found high in F. tataricum (5125\±56.76ppm) while as the iron (Fe) and zinc (Zn) were found in high concentration in F. kashmirianum (1122.5\±25.77ppm) and (122.75\±12.34ppm) respectively. Conclusion: These findings suggested that buckwheat extract possess excellent antioxidant property and is rich source of minerals indispensable for human health. Thus, buckwheat could be a promising alternative in functional food sector for improving the social well-being and diminishing malnutrition especially for the impoverished community.

Key words: Aqueous extract, Antioxidants, AAS, Buckwheat, DPPH, FRAP.

}, keywords = {Aas, Antioxidants, Aqueous extract, Buckwheat, DPPH, FRAP.}, doi = {10.5530/jppcm.2018.2s.xx}, author = {Tanveer Bilal Pirzadah and Bisma Malik and Inayatullah Tahir and Reiaz Ul Rehman} } @article {761, title = {Antioxidant Potential and Ionomic Analysis of Two Buckwheat Species from Kashmir Region}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s83-s88}, type = {Original Article}, chapter = {s83}, abstract = {

Background: Buckwheat in the past had been the staple food for many regions in the Himalaya\’s and its utilization has declined with time. In recent times buckwheat gained a lot of attention as it has been placed in the list of underutilized crops by FAO. There is a strong sentiment and realization for buckwheat revival because of its nutraceutrical properties due to which it provides the consumers with extra choice for his food basket. In this context the present investigation aimed to evaluate the antioxidant potential and mineral element analysis of two buckwheat species grown in Kashmir region. Methods: To achieve this goal, antioxidant potential of two buckwheat species was done by using standard protocols. For ionomic analysis, atomic absorption spectrophotometry (AAS) was done to unravel the macro-and micro-nutrient composition. Result: Aqueous extract of Fagopyrum tataricum exhibits higher TPC (159.51\±10.3 mg gallic acid equivalent g-1 DW) and TFC (79.49\±9.76 mg rutin equivalent g-1 DW). The F. tataricum samples exhibit high radical scavenging activity (RSa50=26.67\μg ml-1) as compared to F. kashmirianum (RSa50=34.15\μg ml-1). Elemental analysis revealed that calcium (Ca) was found high in F. tataricum (5125\±56.76ppm) while as the iron (Fe) and zinc (Zn) were found in high concentration in F. kashmirianum (1122.5\±25.77ppm) and (122.75\±12.34ppm) respectively. Conclusion: These findings suggested that buckwheat extract possess excellent antioxidant property and is rich source of minerals indispensable for human health. Thus, buckwheat could be a promising alternative in functional food sector for improving the social well-being and diminishing malnutrition especially for the impoverished community.

}, keywords = {Aas, Antioxidants, Aqueous extract, Buckwheat, DPPH, FRAP}, doi = {10.5530/pj.2018.6s.16}, author = {Tanveer Bilal Pirzadah and Bisma Malik and Inayatullah Tahir and Reiaz Ul Rehman} } @article {613, title = {Antiradical and Lipid Peroxidation Inhibitory Activity of Ripe and Unripe Fruit of Rubus steudneri Schweinf. (Rosaceae)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {May 2018}, pages = {818-822}, type = {Short Communication}, chapter = {818}, abstract = {

Objectives: A free radical is a molecular species characterized by the presence of an unpaired electron in its outer orbital. Free radicals are highly reactive and are known to damage biomolecules including lipids resulting in a myriad of pathophysiological conditions. The present investigation was carried out to screen antiradical and lipid peroxidation inhibitory activity of ripe and unripe fruit of R. steudneri. Methods: The powdered ripe and unripe fruit materials were extracted by maceration process using methanol. Antiradical activity of extracts was evaluated by DPPH and hydroxyl radical scavenging assays. Lipid peroxidation inhibition assay was carried out by estimating the thiobarbituric acid reactive substances. Both ripe and unripe fruit extracts were screened for the presence of phytochemicals viz. alkaloids, flavonoids, tannins, phenolic compounds, saponins, glycosides, sterols and triterpenoids by standard tests. Results: Preliminary phytochemical analysis indicated that both ripe and unripe fruit extracts contain saponins, alkaloids, phenolic compounds, flavonoids, tannins, sterols and triterpenoids. When compared to unripe fruit extract, ripe fruit extract displayed marked scavenging of DPPH and hydroxyl radicals and inhibition of lipid peroxidation as indicated by lower IC50 values. Conclusion: Overall, ripe fruit extract displayed marked free radical scavenging and lipid peroxidation inhibitory activity. The presence of phenolic and flavonoid compounds in the extracts might be responsible for observed bioactivities of ripe and unripe fruit of R. steudneri.

}, keywords = {Free radical, Lipid peroxidation, Maceration, Phytochemical, Rubus steudneri Schweinf}, doi = {10.5530/pj.2018.4.139}, url = {http://fulltxt.org/article/677}, author = {Raghavendra H.L and Prashith Kekuda T.R} } @article {480, title = {Anti-Staphylococcal and Antioxidant Properties of Crude Ethanolic Extracts of Macrofungi Collected from the Philippines}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2017}, pages = {106-109}, type = {Original Article}, chapter = {106}, abstract = {

Introduction: Macrofungi have been used in the Philippines as source of food and traditional medicines. However, these macrofungi in the Philippines have not yet been studied for different biological activities. Thus, this research determined the potential antibacterial and antioxidant activities of crude ethanolic extracts of seven macrofungi collected in Bataan, Philippines. Methods: Kirby-Bauer disk diffusion assay and broth microdilution method were used to screen for the antibacterial activity and DPPH scavenging assay for the determination of antioxidant activity. Results: F. rosea, G. applanatum, G. lucidum and P. pinisitus exhibited zones of inhibition ranging from 6.55 \± 0.23 mm to 7.43 \± 0.29 mm against S. aureus, D. confragosa, F. rosea, G. lucidum, M. xanthopus and P. pinisitus showed antimicrobial activities against S. aureus with an MIC50 ranging from 1250 \μg/mL to 10000 \μg/mL. F. rosea, G. applanatum, G. lucidum, M. xanthopus exhibited excellent antioxidant activity with F. rosea having the highest antioxidant activity among all the extracts tested (3.0 \μg/mL). Conclusion: Based on the results, these Philippine macrofungi showed antistaphylococcal activity independent of the antioxidant activity. These can be further studied as potential sources of antibacterial and antioxidant compounds.

}, keywords = {Antimicrobial, Antioxidant, Mushrooms, Philippines, Staphylococcus aureus}, doi = {10.5530/pj.2018.1.19}, url = {http://fulltxt.org/article/405}, author = {Christine May Gaylan and John Carlo Estebal and Ourlad Alzeus G. Tantengco and Elena M. Ragragio} } @article {701, title = {Antiurolithiatic Activity of Daucus carota: An In vitro Study}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {880-884}, type = {Original Article}, chapter = {880}, abstract = {

Context: Urolithiasis is a polygenic disorder with complex etiology and even complicated treatment outcomes. Daucus carota is a widely cultivated crop with traditional claims for its antiurolithiatic potential. Aim: Present study was an attempt to investigate the antilithic potential of D. carota root extract (DCRE) against calcium oxalate (CaOx) urolithiasis by employing in vitro methods. Methods: Nucleation, growth and aggregation assay of CaOx crystallization were used. FT-IR analysis was used for characterizing CaOx crystals. Results: DCRE exhibited significant inhibition of nucleation, growth and aggregation of CaOx crystals. It produced a favorable morphological transformation of CaOx crystals from calcium oxalate monohydrate to calcium oxalate dihydrate. FT-IR analysis confirmed formation of calcium oxalate monohydrate crystals to be utilized for growth and aggregation assays. Conclusion: DCRE possesses significant antiurolithiatic activity against CaOx urolithiasis in vitro which could be attributed to its saponins, tannins, flavonoids and polyphenolic content.

}, keywords = {Aggregation, Flavonoids, FT-IR, Nucleation, Urolithiasis}, doi = {10.5530/pj.2018.5.148}, author = {Sweta Bawari and Archana Negi Sah and Devesh Tewari} } @article {617, title = {Assessment of Anti-Protease Property of Nutmeg in Causing Delayed Disintegration of Platelet Rich Fibrin {\textendash} an in vitro Study}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {672-676}, type = {Original Article}, chapter = {672}, abstract = {

Background: Platelet-rich fibrin is a second generation platelet concentrate enhances tissue healing and is in predominant use as a barrier membrane in periodontal regeneration. However, a normal PRF membrane has rapid degradability (1-2 weeks). Myristica fragrans (nutmeg) has been found to have antiprotease property. It was hypothesized if this property helps in inhibiting degradation of PRF. Aim: To assess whether nutmeg has any effect in inhibitingdegradability of PRF membrane and to compare the degradability of PRF at different concentrations (200mg, 100mg, 50mg) of ethanolic and crude extracts of nutmeg. Materials and Methodology: PRF was procured from 30 ml blood from 5 different donors were cut to equal sizes into 35 pieces. They were measured at baseline and dropped in 7 sets of ependorphs containing PBS, PBS containing 200 mg, 100mg and 50 mg crude extract of nutmeg, PBS containing 200 mg, 100mg and 50 mg ethanolic extract of nutmeg. After 1 week the PRF were retrieved and measured. The percentage of remaining PRF was calculated and data analysed. Result: It was found that there was a difference in percentages of remaining PRF between all the groups when compared to the control group, out of which, crude extract of nutmeg 200 mg group alone had a significantly lesser \% of remaining PRF than the control. All ethanolic extract groups had a significantly greater \% of remaining PRF when compared to that of the control. Conclusion: Nutmeg is effective in inhibiting the degradation of PRF membrane.

}, keywords = {Myristica fragrans, Periodontal guided tissue regeneration, Periodontitis, Platelet-rich fibrin, Proteolysis}, doi = {10.5530/pj.2018.4.110}, url = {http://fulltxt.org/article/648}, author = {Darshanaa Arunachalam and Sheeja Varghese and Lakshmi Thangavelu} } @article {723, title = {Chemical Characteristics and In vitro Antidiabetic and Antioxidant Activities of Premna serratifolia L. Leaf Infusion and Decoction}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1114-1118}, type = {Original Article}, chapter = {1114}, abstract = {

Introduction: Leaves of Premna serratifolia L. (local name: arogo) is well known as food ingredient for fish/meat-based soup in Tentena, Indonesia. Evaluation of its bioactivities is needed. Objective: This study aimed to evaluate the \α-glucosidase inhibitory and antioxidant activities of infusion and decoction of P. serratifolia leaves. Methods: The leaf samples were prepared by infusion and decoction and analysed for their \α-glucosidase inhibitory and antioxidant activities, as well as total phenolic contents and LC-MS profiles. Results: The total phenolic content of the decoction was higher than the infusion. The UV spectra of both infusion and decoction showed peak at 325 nm and shoulder at 285 nm. Their LC-MS yielded one dominant component at 132 (100) m/z fragment, which was tentatively identified as caffeic acid. Both infusion and decoction extracts exhibited strong \α-glucosidase inhibition with IC50 of 4.27 and 0.046 \μg GAE/ml, respectively. The IC50 for DPPH scavenging activity of the infusion and decoction were similar; 6.82 and 7.28 \μg GAE/ml, respectively. But the IC50 of the infusion and decoction for ferrous ion chelating activities were different; 161.66 and 28.34 \μg GAE/ ml, respectively. The \α-glucosidase inhibitory and antioxidant activities were related to the phenolic content. Conclusion: The study concludes that both infusion and decoction of arogo leaves have antidiabetic effect and potential antioxidant activity. The decoction of the leaves may increase its antidiabetic capacity.

}, keywords = {Antioxidant, Aqueous extract, Inhibition mechanism, P. serratifolia, α-glucosidase inhibitor}, doi = {10.5530/pj.2018.6.189}, author = {Kris Herawan Timotius and Adelina Simamora and Adit Widodo Santoso} } @article {740, title = {Chemical Composition and Hepatoprotective Activity of Saponaria officinalis on Paracetamol-induced Liver Toxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1196-1201}, type = {Original Article}, chapter = {1196}, abstract = {

Background: The present day life style causing different illness including liver diseases and different health complications. So, there is a need to identify new chemical entities with more efficiency in the treatment of diseases and less side effects. There were many reports in recent times, about identifying new drugs from different medicinal plants and also precursors for synthesis new bioactive molecules for treating various diseases. Objective: The present study was carried out on root parts (rhizomes) of S. officinalis for phytochemical analysis and hepatoprotective activity on paracetmol-induced liver toxicity. Materials and methods: The phytochemical analysis was carried out to know biological active compounds in different extracts of S. officinalis using standard procedures and quantified the total alkaloid and phenolic contents. Hepatoprotective activity of the S. officinalis extracts were carried out by using Paracetmol-induced hepatotoxicity in rats. Results: The phytochemical analysis of S. officinalis roots\’ extracts showed presence of sterols, terpenoids, glycosides, carbohydrates, proteins, flavanoids, alkaloids, phenols, tannins and absence of saponins and oils. The methanolic extract showed more phenolic and alkaloid contents on their quantification. The S. officinalis roots extracts are found to be safe at 2000 mg/kg b. w. in acute toxicity study and showed dose dependent percentage protection on liver toxicity. Methanol extract showed more activity at 500mg/kg b. w. and is comparable with standard drug Liv 52 on altered liver biomarker enzymes AST (SGOT), ALT (SGPT), ALP, total bilirubin and total protein with percentage protection 66.67\%,60.63\%,65.93\%,64.24\% and 60.98\%. Conclusion: The present study results indicates that phytochemical constituent\’s diversity in S. officinalis and those extracts possess hepatoprotective activity. Further studies are needed and should involve the isolation of pure, biologically active compounds.

}, keywords = {Liver, Paracetamol, roots, Saponaria officinalis, Toxicity}, doi = {10.5530/pj.2018.6.205}, author = {Mallikarjuna Rao Talluri and Veda Priya Gummadi and Ganga Rao Battu} } @article {775, title = {Chemical Composition and Hepatoprotective Activity of Saponaria officinalis on Paracetamol-Induced Liver Toxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s129-s134}, type = {Original Article}, chapter = {s129}, abstract = {

Background: The present day life style causing different illness including liver diseases and different health complications. So, there is a need to identify new chemical entities with more efficiency in the treatment of diseases and less side effects. There were many reports in recent times, about identifying new drugs from different medicinal plants and also precursors for synthesis new bioactive molecules for treating various diseases. Objective: The present study was carried out on root parts (rhizomes) of S. officinalis for phytochemical analysis and hepatoprotective activity on Paracetamol-induced liver toxicity. Materials and Methods: The phytochemical analysis was carried out to know biological active compounds in different extracts of S. officinalis using standard procedures and quantified the total alkaloid and phenolic contents. Hepatoprotective activity of the S. officinalis extracts were carried out by using Paracetamol-induced hepatotoxicity in rats. Results: The phytochemical analysis of S. officinalis roots\’ extracts showed presence of sterols, terpenoids, glycosides, carbohydrates, proteins, flavanoids, alkaloids, phenols, tannins and absence of saponins and oils. The methanolic extract showed more phenolic and alkaloid contents on their quantification. The S. officinalis roots extracts are found to be safe at 2000 mg/kg b. w. in acute toxicity study and showed dose dependent percentage protection on liver toxicity. Methanol extract showed more activity at 500mg/kg b. w. and is comparable with standard drug Liv 52 on altered liver biomarker enzymes AST (SGOT), ALT (SGPT), ALP, total bilirubin and total protein with percentage protection 56.17\%, 54.53\%, 61.55\% 57.29\% and 53.66\%. Conclusion: The present study results indicates that phytochemical constituent\’s diversity in S. officinalis and those extracts possess hepatoprotective activity. Further studies are needed and should involve the isolation of pure, biologically active compounds

}, keywords = {Liver, Paracetamol, roots, Saponaria officinalis, Toxicity}, doi = {10.5530/pj.2018.6s.24}, author = {Mallikarjuna Rao Talluri and Veda Priya Gummadi and Ganga Rao Battu} } @article {727, title = {Cholesterol-lowering Effects of Extract from Garcinia daedalanthera in Hyperlipidemic rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1125-1128}, type = {Original Article}, chapter = {1125}, abstract = {

Background: A native plant from Indonesia, Garcinia daedalanthera has been scientifically proven have antidiabetic effects and antioxidant activity. We hypothesized that Garcinia daedalanthera can modulate the lipid profiles of hyperlipidemic rats. Objective: This study aimed to evaluate the antihyperlipidemic potential of Garcinia daedalanthera extract. Materials and Methods: Garcinia daedalanthera leaves extract (GDE) were orally administrated to high fat diet-induced rats for 15 days. After the end of experimental period (43 days) the lipid profiles were estimated along with histopathological liver examination of animals. Results: The results showed that Garcinia daedalanthera extract significantly reduced the level of serum total cholesterol, total triglycerides and low-density lipoprotein as compared to control group with an increasing level of serum high-density lipoprotein. Furthermore, the extract has a favorable effect on histopathological study. Conclusion: This study proved antilipidemic property by lowering altered levels of lipid profile in male wistar rats and suggest lipid lowering effects of Garcinia daedalanthera extract which serves as a new potential natural product for preventing hyperlipidemia.

}, keywords = {Anti-cholesterol, Garcinia, Herbal, In vivo, Pre-clinical study, Rat}, doi = {10.5530/pj.2018.6.191}, author = {Sarah Zielda Najib and Wilzar Fachri and Rani Sauriasari and Berna Elya and Raymond Tjandrawinata} } @article {645, title = {Comparison between Volatile Oil from Fresh and Dried Fruits of Zanthoxylum rhetsa (Roxb.) DC. and Cytotoxicity Activity Evaluation}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {July/2018}, pages = {73-78}, type = {Original Article}, chapter = {73}, doi = {10.5530/pj.2017.3.14}, author = {Sewan Theeramunkong and Maleeruk Utsintong} } @article {648, title = {Comparison between Volatile Oil from Fresh and Dried Fruits of Zanthoxylum rhetsa (Roxb.) DC. and Cytotoxicity Activity Evaluation}, journal = {Pharmacognosy Journal,}, volume = {10}, year = {2018}, month = {July/2018}, pages = {73-78}, type = {Original Article}, chapter = {73}, abstract = {

Introduction: Zanthoxylum rhetsa is a tree found in northern Thailand. It has been used as a traditional herb with medicinal properties. However, the comparison of composition in volatile oil from fresh and dried fruit is still not fully investigated. In study, we evaluated the constituents in oil from fruits of Z. rhetsa and evaluated the cytotoxicity in non-small lung cancer cells. Methods: The hydro distillation was applied to afford the oil. The obtained oil was analyzed by GC-MS and evaluated the cytotoxicity and apoptosis in non-small lung cells by using MTT method and flow cytometry respectively. Results: Fresh and dried fruits provided a higher yield of volatile oil by approximately 10\% and 20\% respectively, compared to other studies. Twenty-eight compounds were identified and the major components of fresh and dried fruits were not distinctly different. The major component, \α-limonene, was found in dried fruits from Phayao, southern Nan and Chiang Rai province. A high content of \β-phellandrene was found in dried fruits from northern Nan province and the (+)-sabinene was found in high content of fresh fruits from southern Nan, Phayao and Chaing Rai province. Furthermore, the cytotoxicity tests displayed that all of oil products were active against lung cancer cells. Among the components investigated, fresh and dried fruits from southern Nan province showed to be the most potent (EC50 = 1.91 \± 0.53, 1.79 \± 0.43 \μL/mL, respectively). Conclusion: Volatile oil of Z. rhetsa exhibited a strong cytotoxic properties against cytotoxic may be potentially used as natural anticancer agents. Key words: Zanthoxylum rhetsa, Local variation, Volatile oil, Chemical composition, Cytotoxic activity.

}, doi = {10.5530/pj.2017.3.14}, author = {Sewan Theeramunkong and Maleeruk Utsintong} } @article {679, title = {Comparison between Volatile Oil from Fresh and Dried Fruits of Zanthoxylum rhetsa (Roxb.) DC. and Cytotoxicity Activity Evaluation}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {827-832}, type = {Original Article}, chapter = {827}, abstract = {

Introduction: Zanthoxylum rhetsa is a tree found in northern Thailand. It has been used as a traditional herb with medicinal properties. However, the comparison of composition in volatile oil from fresh and dried fruit is still not fully investigated. In study, we evaluated the constituents in oil from fruits of Z. rhetsa and evaluated the cytotoxicity in non-small lung cancer cells. Methods: The hydro distillation was applied to afford the oil. The obtained oil was analyzed by GC-MS and evaluated the cytotoxicity and apoptosis in non-small lung cells by using MTT method and flow cytometry respectively. Results: Fresh and dried fruits provided a higher yield of volatile oil by approximately 10\% and 20\% respectively, compared to other studies. Twenty-eight compounds were identified and the major components of fresh and dried fruits were not distinctly different. The major component, \α-limonene, was found in dried fruits from Phayao, southern Nan and Chiang Rai province. A high content of \β-phellandrene was found in dried fruits from northern Nan province and the (+)-sabinene was found in high content of fresh fruits from southern Nan, Phayao and Chaing Rai province. Furthermore, the cytotoxicity tests displayed that all of oil products were active against lung cancer cells. Among the components investigated, fresh and dried fruits from southern Nan province showed to be the most potent (EC50 = 1.91 \± 0.53, 1.79 \± 0.43 \μL/mL, respectively). Conclusion: Volatile oil of Z. rhetsa exhibited a strong cytotoxic properties against cytotoxic may be potentially used as natural anticancer agents.

}, keywords = {Chemical composition, Cytotoxic activity, Local variation, Volatile oil, Zanthoxylum rhetsa}, doi = {10.5530/pj.2018.5.141}, author = {Sewan Theeramunkong and Maleeruk Utsintong} } @article {733, title = {Comparison of Antibacterial Efficacy of Cinnamon Extract and Calcium Hydroxide as Intracanal Medicament against E. fecalis: An In vitro Study}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1165-1168}, type = {Original Article}, chapter = {xx1165}, abstract = {

Background: There has been an increased use of natural products as medicament in endodontic treatment due to the increased adverse effect observed in chemical products used. The natural products used aims to disinfect the root canal and provide a sterile environment as efficiently as the comparable chemical products. Aim: To compare the antibacterial efficacy of cinnamon extract and calcium hydroxide as intracanal medicament against E. fecalis. Materials and Methods: The study is an in vitro randomized controlled study conducted on 40 single rooted permanent teeth. The study sample was divided into two groups- cinnamon extract as intracanal medicament and calcium hydroxide. The intracanal medicament was placed for 7 days. The outcome was measures using colony forming units per ml. Statistical analysis was done using Mann-Whitney\’s test to compare between the two groups. Results: Cinnamon extract intracanal medicament showed higher antibacterial efficacy as compared to calcium hydroxide. (p=0.002). Conclusion: Cinnamon extract showed better antimicrobial efficacy against E. feacalis as intracanal medicament as compared to calcium hydroxide.

}, keywords = {Antibacterial efficacy, Calcium hydroxide, Cinnamon extract, E. feacalis, Intracanal medicament}, doi = {xx10.5530/pj.2018.6.199}, author = {Veerale Panchal and Deepa Gurunathan and Lakshmi Thangavelu} } @article {553, title = {Effect of Thai Folklore Recipe from Abutilon indicum and Mimosa pudica in Streptozotocin-Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {x}, pages = {x}, type = {x}, chapter = {x}, abstract = {

Context: Abutilon indicum and Mimosa pudica were a folklore recipe in Northeastern of Thailand. The recipe was reported that claim to diabetic treatment. Aims: The studies were evaluated to hypoglycemic effect, serum insulin secretion and blood biochemistry in streptozotocin (STZ)-induced diabetic rats. Materials and Methods: The recipe were composed of whole plants from A. indicum and M. Pudica (1:1 w/w) powder. The pound plants were macerated with aqueous (AMA), hydro-ethanol (AMHE) and 80\% ethanol (AME) to crude extracts. The AMA, AMHE and AME at the doses of 125, 250 and 500 mg/kg body weight (b.w.) were administered orally daily in diabetic rats during eight weeks. Fasting blood glucose levels (FBG) were measured at weekly. The serum insulin levels and blood biochemical data including blood urea nitrogen (BUN), creatinine (CREA), total protein (TP), albumin (Alb), serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), alkaline phosphatase (ALP), triglycerides (TG), total cholesterol (TC), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) were estimated at the end of experiment. Results: All doses of the extracts were showed significantly (p\<0.05) decreasing percent age of FBG in diabetic rats. Especially, AME 125 mg/ kg b.w. was showed more potent significantly (p\<0.05) decreasing percentage of FBG at week of 2, 5, 7 and 8. The serum insulin levels of all doses administered with the extracts were significantly (p\< 0.05) higher than diabetic control group. On the other hand, all doses of the extracts were significantly (p\< 0.05) decreasing ALT and ALP lower than diabetic control group. While, AMA and AMHE at the doses of 250 and 500 mg/kg b.w. were increased HDL, but decreased TC, TG and LDL. Conclusion: The study was proved to diabetic treatment and improvement of diabetic stage and blood biochemical parameters. In addition, the experiment was confirmed to folklore traditional use.

Key words: Thai folklore recipe, A. indicum , M. pudica , Fasting blood glucose.

}, keywords = {A. indicum, Fasting blood glucose., M. pudica, Thai folklore recipe}, doi = {10.5530/jppcm.2018.2s.xx}, author = {Ampa Konsue and Chusri Talubmook} } @article {584, title = {Effect of Thai Folklore Recipe from Abutilon indicum and Mimosa pudica in Streptozotocin-Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {480-485}, type = {Original Article}, chapter = {480}, abstract = {

Context: Abutilon indicum and Mimosa pudica were a folklore recipe in Northeastern of Thailand. The recipe was reported that claim to diabetic treatment. Aims: The studies were evaluated to hypoglycemic effect, serum insulin secretion and blood biochemistry in streptozotocin (STZ)-induced diabetic rats. Materials and Methods: The recipe were composed of whole plants from A. indicum and M. Pudica (1:1 w/w) powder. The pound plants were macerated with aqueous (AMA), hydro-ethanol (AMHE) and 80\% ethanol (AME) to crude extracts. The AMA, AMHE and AME at the doses of 125, 250 and 500 mg/kg body weight (b.w.) were administered orally daily in diabetic rats during eight weeks. Fasting blood glucose levels (FBG) were measured at weekly. The serum insulin levels and blood biochemical data including blood urea nitrogen (BUN), creatinine (CREA), total protein (TP), albumin (Alb), serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), alkaline phosphatase (ALP), triglycerides (TG), total cholesterol (TC), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) were estimated at the end of experiment. Results: All doses of the extracts were showed significantly (p\<0.05) decreasing percent age of FBG in diabetic rats. Especially, AME 125 mg/ kg b.w. was showed more potent significantly (p\<0.05) decreasing percentage of FBG at week of 2, 5, 7 and 8. The serum insulin levels of all doses administered with the extracts were significantly (p\< 0.05) higher than diabetic control group. On the other hand, all doses of the extracts were significantly (p\< 0.05) decreasing ALT and ALP lower than diabetic control group. While, AMA and AMHE at the doses of 250 and 500 mg/kg b.w. were increased HDL, but decreased TC, TG and LDL. Conclusion: The study was proved to diabetic treatment and improvement of diabetic stage and blood biochemical parameters. In addition, the experiment was confirmed to folklore traditional use.

}, keywords = {A. indicum, Fasting blood glucose, M. pudica, Thai folklore recipe}, doi = {10.5530/pj.2018.3.79}, url = {http://fulltxt.org/article/512}, author = {Ampa Konsue and Chusri Talubmook} } @article {710, title = {Effects of Asparagus racemosus Root Extracts on Serum Lipid Profiles, Lipid Peroxidation and Superoxide Dismutase in Ovariectomized Rat}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1036-1041}, type = {Original Article}, chapter = {1036}, abstract = {

Background: Once rats have been ovariectomized they have a high risk of cardiovascular disease due to changes in the blood cholesterol and lipid profile. Objective: To investigate the effects of Asparagus racemosus (AR) root extract on the serum lipid profiles, lipid peroxidation and antioxidant levels in ovariectomized rats. Methods: Twenty-five, two month-old female Wistar rats were randomly divided into five groups: SH, OVX,OEE, OAAR and OEAR. The daily doses of 500 mg/KgBW of the AR root extracts for five weeks.The levels of serum TG, TC, HDL, LDL, the liver, kidney and uterine tissue lipid peroxidation and SOD levels were determined. Results: Serum TC and LDL showed no significant differences in any groups. Serum TG of the OAAR and OEAR groups were not significantly different. The serum HDL of the OAAR and OEAR groups were significantly lower than the OEE group. The liver MDA levels of the OAAR and OEAR groups were significantly decreased compared with the OVX and OEE groups while the SOD level of the OAAR group was significantly increased. The MDA levels in the kidney and uterine of the treated group showed no significant difference. The SOD levels in the kidney of the treated group were not different but the SOD levels in uterine were significantly decreased. Conclusion: It can be believed that the lipid profiles were maybe regulated via estrogen.The AR extract has low effects on the lipid profiles at this dose and duration of treatment. The capacity of the extracts to decrease the MDA level and increase the SOD level in this study clearly reflected the antioxidant efficiency of these substances.

}, keywords = {Asparagus racemosus, Lipid profiles, Malondialdehyde, Ovariectomized rat, Superoxide dismutase}, doi = {10.5530/pj.2018.5.175}, author = {Ladachart Taepongsorat and Methin Phadungkit} } @article {699, title = {Ethnobotanical Survey of Medicinal Plants used by Ayta Communities in Dinalupihan, Bataan, Philippines}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {859-870}, type = {Original Article}, chapter = {859}, abstract = {

Objectives: This study documented the species of medicinal plants used by Ayta communities in Dinalupihan, Bataan. The plant parts used for medicinal purposes, preparations, mode of administration of these medicinal plants were determined. The most important species based on use values and informant consensus factors were also calculated. Methods: A total of 26 informants were interviewed regarding the plants they utilize for medicinal purposes. Free and prior informed consents were obtained from the informants. Taxonomic identification was done in the Botany Division of the National Museum of the Philippines. Informant consensus factor (FIC) and use values (UV) were also calculated. Results: Ayta communities listed a total of 118 plant species classified into 49 families used as herbal medicines. The Family Fabaceae was the most represented plant family with 11 species. Leaves were the most used plant part (43\%). Majority of medicinal preparations were taken orally (57\%). It was found that Psidium guajava L. and Lunasia amara Blanco were the most commonly used medicinal plants in the three communities with the use value of 0.814. Conclusion: This documentation provides a catalog of useful plants of the Ayta and serves as a physical record of their culture for the education of future Ayta generations.

}, keywords = {Ayta, Ethnobotany, Medicinal plants, Philippines, Traditional medicine}, doi = {10.5530/pj.2018.5.145}, author = {Ourlad Alzeus G. Tantengco and MARLON LIAN C. CONDES and Hanna Hasmini T. Estadilla and Elena M. Ragragio} } @article {725, title = {Evaluation of in vitro Antioxidant Potential of Amaranthus caudatus L. Grown in Kashmir Region}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1119-1124}, type = {Original Article}, chapter = {1119}, abstract = {

Background: Plants have a well-developed defensive machinery for minimizing the reactive oxygen species (ROS) associated damages in the form of enzymatic and nonenzymatic antioxidants. The in-vitro mechanism of antioxidant action of plant extracts may involve direct inhibition of the ROS generation or ROS scavenging. The antioxidant activity of the extracts may be due to active constituents alone or the combination of constituents. However, the amount of constituents are known to vary according to the change in environment. Method: In our study, antioxidant activity of Amaranthus caudatus L. from two different sites (elevation sites) was investigated at three stages, (vegetative, pre flowering and post flowering) using ethanolic extract (EtOH). Result: The phenolic and flavonoid content increased at all stages from site 1 to site 2. The total reducing power, Ferrous reducing antioxidative power (FRAP), diphenyl picryl hydrazine (DPPH) radical scavenging assay, superoxide dismutase scavenging (SOD) assay and hydrogen peroxide (H2O2) scavenging activity increased from site 1 to site 2 at all the three stages. Conclusion: The results reveal that the altitude and the growth stage have a significant effect on antioxidative potential of Amaranthus.

}, keywords = {Amaranthus, Ethanolic extract, Hydrogen peroxide, Phenolics, Reactive Oxygen Species, Superoxide dismutase}, doi = {10.5530/pj.2018.6.190}, author = {Asiya Ramzan and Inayatullah Tahir and Reiaz Ul Rehman} } @article {622, title = {Hydroalcoholic and Alkaloidal Extracts of Murraya koenigii(L.) Spreng Augments Glucose Uptake Potential against Insulin Resistance Condition in L6 Myotubes and Inhibits Adipogenesis in 3T3L1 Adipocytes}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {633-639}, type = {Original Article}, chapter = {633}, abstract = {

Background: Murraya koenigii, commonly known as \“curry leaves\” is native to India. The highly valued part of the plant is the leaves which possess various biological activities. Objective: The present study aimed to investigate the antidiabetic effect of Murraya koenigii (MK) leaf extracts, of two different solvent ratios. Materials and methods: 70\% hydroalcoholic and alkaloidal extracts of MK leaves were prepared by cold maceration method. Preliminary phytochemical analysis was carried out for both the extracts. In vitro anti diabetic activity was screened by inhibitory action on \α \– amylase, \α \– glucosidase enzymes. Further, the 70\% hydroalcoholic and alkaloidal extracts were assessed for glucose uptake potential, anti - adipogenic property, as well as inhibitory activity on diabetes associated complications. HPTLC quantification of major phytoconstituent was carried out. Results: The study showed presence of various phytoconstituents such as, polyphenols, alkaloids, tannins, reducing sugars etc. The 70\% hydroalcoholic and alkaloidal extracts of MK leaves exhibited \>90\% inhibition against carbohydrate metabolising enzymes compared to aqueous and absolute alcohol extracts. Both the extracts showed enhanced glucose uptake in L6 myotubes attenuating the effect of Palmitate induced insulin resistance. Significant inhibition on adipogenesis was exerted by both 70\% hydroalcoholic and alkaloidal extracts of MK leaves. Besides, marked inhibition of advanced glycation end products was exhibited by the extracts. HPTLC quantification analysis of the aforementioned extracts showed the presence of major phytoconstituent, Mahanine, in it. Conclusion: The results of the present study showed that MK possesses significant antidiabetic property and also exhibited considerable effect in preventing diabetes associated complications. The potent antidiabetic activity of MK could be attributed to the presence of Mahanine, the major active constituent, which is a carbazole alkaloid.

}, keywords = {complications, Diabetes, glucose uptake, L6 myotubes, Mahanine, α - amylase}, doi = {10.5530/pj.2018.4.104}, url = {http://fulltxt.org/article/642}, author = {Parameswari Royapuram Parthasarathy and Janani Murthy and Dinesh Murugan Girija and Srivani Telapolu and Chamundeeswari Duraipandian and Thyagarajan Sadras Panchatcharam} } @article {700, title = {Identification by Docking Simulation and in vivo Effect of Essential Oil from Cinnamommum burmannii as Anti-obesity with Leptin Receptor in the Olfactory System of Mice Balb C}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {875-879}, type = {Original Article}, chapter = {875}, abstract = {

Aim: This study examines the effect of inhalation of essential oil of cinnamon (Cinnamomum burmannii) on the metabolic activity of hormone receptors olfactory system of mice Balb C. Methodology: Effects of agonist or antagonist compounds in cinnamon essential oil on metabolic hormone receptors in the olfactory system are predicted using molecular docking simulation. Changes in the metabolic processes that occur views of changes in body weight, change in food intake, as well as lipid profile and blood glucose of mice. Result: The results showed Expression of leptin receptors (Lep-R) in the brains of mice given either inhalation of essential oils derived from the leaves and stems, in contrast to the control group who did not get essential oils. Provision of essential oils through inhalation increased lep-R expression in the brain of mice. Both in silico and in vivo evidence that essential oils from cinnamon plants are extracted from Cinnamommum burmannii and given by inhalation in Balb C mice are known to improve glucose and lipid metabolism by reducing the concentration of serum leptin concentrations and increased sensitivity to insulin.

}, keywords = {Cinnamomum burmannii, docking simulation, immunohistochemistry, leptin receptors, olfactory system}, doi = {10.5530/pj.2018.5.147}, author = {Kusmardi Kusmardi and Aryo Tedjo and Fadilah Fadilah and Ade Arsianti and Rafika Indah Paramita} } @article {669, title = {Identification by Docking Simulation And In Vivo Effect of Essential Oil From Cinnamommum Burmannii as Antiobesity With Leptin Receptor In The Olfactory System of Mice Balb C}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {July/2018}, pages = {73-77}, type = {Original Article}, chapter = {73}, abstract = {

Aim: This study examines the effect of inhalation of essential oil of cinnamon (Cinnamomum burmannii) on the metabolic activity of hormone receptors olfactory system of mice balb C. Methodology: Effects of agonist or antagonist compounds in cinnamon essential oil on metabolic hormone receptors in the olfactory system are predicted using molecular docking simulation. Changes in the metabolic processes that occur views of changes in body weight, change in food intake, as well as lipid profile and blood glucose of mice. Result: The results showed Expression of leptin receptors (Lep-R) in the brains of mice given either inhalation of essential oils derived from the leaves and stems, in contrast to the control group who did not get essential oils. Provision of essential oils through inhalation increased lep-R expression in the brain of mice. Both in silico and in vivo evidence that essential oils from cinnamon plants are extracted from Cinnamommum burmannii and given by inhalation in Balb C mice are known to improve glucose and lipid metabolism by reducing the concentration of serum leptin concentrations and increased sensitivity to insulin.

Keywords: olfactory system, leptin receptors, Cinnamomum burmannii, docking simulation, immunohistochemistry

}, doi = {10.5530/pj.2017.3.14}, author = {Kusmardi Kusmardi and Aryo Tedjo and Fadilah Fadilah and Ade Arsianti and Rafika Indah Paramita} } @article {548, title = {Larviciding Activity of Acroptilon repens Extract against Anopheles stephensi, Culex pipiens and Culex quinquefaciatus under Laboratory Conditions}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {453-456}, type = {Original Article}, chapter = {453}, abstract = {

Introduction: Due to the emergence of insecticide resistance among the vectors of human diseases, there is a need to explore the use of plant extracts which are safe alternatives to conventional chemical larvicides used in control of vector-borne diseases. The aim of this study was to evaluate the larvicidal activity of Acroptilon repens against third instar larvae of Anopheles stephensi, Culex pipiens and Culex quinquefaciatus. Materials and Methods: The aerial parts of A. repens plants was dried in the shaded places for 3 days at 26-28\°C. The leaves, flowers and stems were blended to crashed form using an electric blender. The larvicidal activity of total extract of A. repens were evaluated against third instar larvae stage of mosquito vectors, An. stephensi, Cx. pipiens and Cx. quinquefaciatus under laboratory conditions with 24h exposure period. Data were subjected to probit regression analysis in order to estimate the lethal concentrations for 50\% and 90\% mortality values. Result: The extract of A. repens exhibited significant larvicidal activity against third instar larvae of An. stephensi, with 24h LC50 of 0.2970 and LC90 of 2.2097 mg/l. The LC50 and LC90 values were 2.5047 and 24.7374 mg/l for Cx. pipiens and 2.9047 and 16.1459 mg/l for Cx. quinquefaciatus. Conclusion: The extract of A. repens can serve as a natural larvicide against An. stephensi, Cx. pipiens and Cx.quinquefaciatus. According to the larvicidal properties of this plant, formulating an extract of A. repens which is known as an abundant agricultural weed in Iran creates an alternative to chemical larvicides and providing a job opportunities.

}, keywords = {Acroptilon repens, Anopheles stephensi, Culex pipiens, Cx. quinquefaciatus, Larvicidal activity, Total extract}, doi = {10.5530/pj.2018.3.74}, url = {http://fulltxt.org/article/507}, author = {Ramesh Toolabi and Mohammad Reza Abai and Mohammad Mehdi Sedaghat and Hassan Vatandoost and Mansooreh Shayeghi and Saeed Tavakoli and Mohammad Sistanizadeh Aghdam} } @article {568, title = {Nephroprotective Effect of Aqueous Extract of Pimpinella anisum in Gentamicin Induced Nephrotoxicity in Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {403-407}, type = {Original Article}, chapter = {403}, abstract = {

Background: Pimpinella anisum known for its various medicinal properties is also a natural antioxidant and a free radical scavenger with no documented evidence as a nephroprotective agent. Objective: To evaluate the nephroprotective activity of aqueous extract of Pimpinella anisum seeds in a rodent model of gentamicin induced nephrotoxicity. Materials and Methods: Wistar albino rats of either sex, weighing 150\–200 g was divided into 5 groups; normal saline, gentamicin 80mg/kg, intraperitoneally for 8 days, aqueous extract of Pimpinella anisum seeds at 1, 2, and 4g/kg, per oral for 8 days, the test extract administered 3 days prior and concurrently with gentamicin for 5 days. Blood urea, serum creatinine, uric acid and blood urea nitrogen analyses and microscopic examination of kidney were performed. Results: Gentamicin treatment caused nephrotoxicity as evidenced by marked elevation in serum urea, serum uric acid, serum creatinine and blood urea nitrogen (107.5\±16.92mg/dl, 0.8\±0.09 mg/dl, 3.05\±0.29 mg/dl, 47.8\±9.07 mg/dl) respectively when compared to the saline treated groups. Co-administration of Pimpinella anisum extract with gentamicin decreased the rise in these parameters in a dose dependent manner. Histopathological analysis revealed epithelial loss with intense granular degeneration in gentamicin treated rats, whereas aqueous extract of Pimpinella anisum mitigated the severity of gentamicin-induced renal damage. Conclusion: To conclude, our data suggest that aqueous extract of Pimpinella anisum exhibits renoprotective effect in gentamicin induced renal damage and further studies on its mechanism of action are warranted.

}, keywords = {Aniseed, Drug induced nephrotoxicity, Gentamicin, Nephroprotective, Pimpinella anisum}, doi = {10.5530/pj.2018.3.66}, url = {http://fulltxt.org/article/532}, author = {Nair Aiswarya and Rao Rashmi R and Shenoy Preethi J and Vinod Chandran and S Teerthanath and Pai Sunil B and KB Rakesh} } @article {505, title = {Pharmacognostic Evaluation of Curcumin on Diabetic Retinopathy in Alloxan-induced Diabetes through NF-KB and Brn3a Related Mechanism}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {324-332}, type = {Original Article}, chapter = {324}, abstract = {

Background: Diabetic retinopathy is one of the most common micro vascular complication of diabetes and involves an abnormal pathology of major retinal pigment epithelium, inter retinal oedema and intraocular neovascularisation where pro-inflammatory proteins including ICAM-1,iNOS and VEGF release by activation of enzyme CaMKII/NF-kB expression Diabetic induced oxidative stress followed by deactivation of Brn3a expression in the retinal ganglionic cells are also early events in pathogenesis of Diabetic retinopathy. These factors are important contributors to the development of clinically significant diabetic retinopathy. Objective: Objective of this study to examine the effect of curcumin with antioxidant and anti-inflammatory properties obtained from Curcuma longa against diabetes-induced retinal vascular damage and its mechanism of action by in-vivo in retinas of rat rendered diabetic by alloxan and in vitro in western blotting and RGC tissue culture. Method: We administered curcumin or saline vehicle to experimental animals daily for 12 weeks. Vascular permeability, expression of CaMK II/NF-kB, Retinal morphology and neuropathic change of the retinal ganglion cells were investigated. Results: As an anti-oxidant, curcumin raised Retinal Ganglionic cells by increasing Brn3a expression during oxidative stress condition and subsequently decreased the expression of inflammatory mediators such as VEGF, iNOS and ICAM-1 as an anti-inflammatory agent by inhibiting CaMKII and NF-kB expression. Conclusion: Curcumin, a common food additive has beneficial effects in experimental studies of diseases that are characterised by increased oxidative stress and inflammatory reactions. It appears to be a useful adjunct therapy to possibly inhibit the progression of retinopathy, sight threatening complication faced by diabetic patients.

}, keywords = {Brn3a, CaKMII, Curcumin, Inflammation, NF-KB, Oxidative stress}, doi = {10.5530/pj.2018.2.56}, url = {http://fulltxt.org/article/486}, author = {Debasish Pradhan and Toffa Dasmohapatra and Gitanjali Tripathy} } @article {533, title = {Pharmacognostic Studies of Psychotria rubra(Lour.)Poir.}, journal = {Pharmacog Journal}, volume = {10}, year = {2018}, month = {January-2018}, pages = {249-255}, type = {Original Article}, chapter = {249}, abstract = {

Objective: Various traditional systems of medicine enlightened the importance of Psychotria rubra (Lour.) Poir to have a great medicinal value. The present study was carried out to provide a scientific basis of the identification and the authenticity of Psychotria rubra (Lour.) Poir with the help of pharmacognostic parameters, which is not done before. Methods: Roots, stems, and leaves of P. rubra were collected for Pharmacognostic studies involving macros, microscopic evaluation, histochemistry and physicochemical parameters analysis like Ash value, Moisture content, Fluorescence analysis and Thin Layer Chromatography et al. Results: Transverse section of root was found like stone cells, calcium oxalate crystal and vessels in circular shape. Transverse section of stem showed the presence of lenticels and stone cell bands. Transverse section of leaf vein revealed the presence of shaft type of porosity. Powder microscopy revealed the presence of cork cells, stone cells, crystals and resin, fibers, needle crystal beam, thread tracheid and scalariform tracheid. Phytochemical investigation was found like alkaloids, flavones, carbohydrates, saponins, tannins and volatile oils. Results obtained in physicochemical parameters like Total ash value, acid insoluble ash and moisture content were 9.77\%, 0.68\% and 1.28\%, respectively. The leaching degree of P. rubra was higher in ethanol(75\%, v/v) and methanol solutions than that in chloroform, petroleum ether, and tetrachloromethane solutions. Thin Layer Chromatography (TLC) of the extract revealed 4 spots with the Rf values 0.47, 0.46, 0.46, 0.47 with the solvent system of chloroform: methanol: water: formic acid(7:3:1:0.1). Conclusion: The observations confirmed that P. rubra has an obvious Pharmacognostic characteristics, which will be useful towards providing a reliable basis for identification, purity, quality and classification of the plant.

}, keywords = {Histochemistry, Identification, Pharmacognostic, Physicochemical, Poir, Psychotria rubra(Lour.)}, doi = {10.5530/pj.2018.2.44}, url = {http://fulltxt.org/article/474}, author = {Gengqiu Tang and Xiaojing Lin and Xiudi Lai and Xue Gong and Shengguo Ji} } @article {592, title = {Pharmacognostical Evaluation of Rhododendron arboreum Sm. from Uttarakhand}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {527-532}, type = {Original Article}, chapter = {527}, abstract = {

Objective: Rhododendron arboreum Sm. commonly known as Burans is an important plant of the Himalayan region. It is the national flower of Nepal and state tree of Uttarakhand. The present study pertains to the pharmacognostical evaluation of R. arboreum from Uttarakhand. Methods: Macroscopy, microscopy by free hand section cutting and with the help of scanning electron microscopy (SEM) were done along with the physicochemical analysis. Preliminary phytochemical studies and fluorescence analysis was also carried out. Results: Results revealed that the leaves contain paracytic or amphiparacytic stomata in cluster form. The epidermal cells were long and spongy. The cells also contain some grooves and papillae throughout the surface. Preliminary phytochemical analysis showed the presence of different secondary metabolites like alkaloids carbohydrates, phenols, proteins, saponins, and tannins. Conclusion: R. arboreum from Uttarakhand region was investigated for its morphological and cytological characteristics with the help of scanning electron microscopy for the first time. The results provide details on the presence of several specific characters which are important for the identification of the genuine crude drug.

}, keywords = {Burans, Himalaya, microscopy, Phytochemical, SEM}, doi = {10.5530/pj.2018.3.86}, url = {http://fulltxt.org/article/519}, author = {Devesh Tewari and Archana Negi Sah and Sweta Bawari} } @article {620, title = {Pharmacophore Modelling of Brassicaceae Members as Potent HIF (Hypoxia Inducible Factor) Inhibitors Involved in Cancer Angiogenesis}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {May 2018}, pages = {798-802}, type = {Original Article}, chapter = {798}, abstract = {

Angiogenesis is considered as an essential pathological feature of cancer due to its interplay between cancer and other diseases. Natural products found to act as antiangiogenic agents that mediate the angiogenic switch between pro and anti angiogenic factors. Among the different targets, HIF is an important and critical factor that stands as a key mediator between angiogenesis, inflammation and cancer. In our study different phytochemicals of Brassicaceae were analysed for their drug like properties and mapped for pharmacophore development. The developed pharmacophore was virtually screened and further subjected to Lipinski and ADMET filters. The molecular interaction studies of the 10 retrieved compounds were studied by binding with HIF. Among the compounds 1stdrug like molecule HTS 0115 (C15H21BrN2O3) was found to have best docked score and its interaction was further validated using dynamics simulation. The compound found to share the pharmacophoric features with progoitrin a biochemical form of glucosinolate with reported anticancer and anti thyroid activities. Thus the drug like compound HTS 0115 can be further optimised as a putative HIF inhibitor in tumor angiogenesis.

}, keywords = {Angiogenesis, Brassicaceae, HIF, Molecular docking, Pharmacophore, Simulation}, doi = {10.5530/pj.2018.4.135}, url = {http://fulltxt.org/article/673}, author = {Jeyavel Renukadevi and Ganesan Nandhinidevi and Muthiah Bavanilatha and Hemanath Tharani and Rajarajan Sathiyabama and Subramani Vasumathi} } @article {719, title = {Phytochemical Screening and Antimicrobial Studies in Leaf Extracts of Indigofera aspalathoides (Vahl.)}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1208-1215}, type = {Original Article}, chapter = {1208}, abstract = {

Introduction: In traditional Indian herbal medicine, the plant Indigofera aspalathoides (Vahl.) has been used to treat various human ailments. Methods and Results: Various phytochemical compounds (Rf value) such as Tannin (1.14), Flavonoid (1.14), Saponin (0.87), Sterol (0.88) and Phenol (0.86) were found in the leaf extract. The antimicrobial effects of the phytoconstituents were examined for three bacterial and fungal species. The highest anti-bacterial and antifungal activities were found in flavonoid compound, where the maximum zone of inhibition was recorded in Staphylococcus aureus 18mm compared to positive control chloramphenicol (24mm). 13mm observed in A. flavus and A. ochraceous where positive control streptomycin exhibits 18mm. GC-MS analysis revealed the presence of three major compounds in 8\α (2H)-Phenanthrenol, 7-ethenyldodecahydro-1,1,4\α, 7-tetramethyl-, acetate, [4\αs(4\α\α, 4b\α, 7\α, 8\α\α, 10\α\α)], Benzoic acid, 4-methyl- , 2-oxo-2- phenylethyl ester and Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1\α,2\α,5\α)] in the crude extracts. The preparative HPLC analysis proved the presence of single peak from the crude flavonoid compounds, where the absorption maximum was between 207-290nm exhibited by the UV spectrum analysis. FTIR spectrum confirmed the presence of amide group, phenol group, carboxylic acid, alkynyl, alkene and aromatic ring. NMR studies proved the presence of phenyl group, methyl group and H2C-CH group and their molecular weight recorded as 353 through the mass spectrum analysis. Conclusion: The identified compound considered as the vital compound to design the \“green antimicrobial drugs\”.

}, keywords = {Antimicrobial activities, GC-MS, HPLC, Indigofera aspalathoides, MS, NMR}, doi = {10.5530/pj.2018.6.207}, author = {Tamilarasan Tamil Kumar and Seeni Mohamed Salique and Mohamed Hussain Muhammad Ilyas and Nooruddin Thajuddin and Annamalai Panneerselvam and Mohamed Khan Syed Ali Padusha and Hussain Syed Jahangir} } @article {726, title = {Sterols from Lentinus tigrinus}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1079-1081}, type = {Original Article}, chapter = {1079}, abstract = {

Aim: To investigate the chemical constituents of the dichloromethane extract of the fruiting bodies of the mushroom Lentinus tigrinus. Materials and Methods: The chemical constituents of L. tigrinus were isolated by silica gel chromatography, while the chemical structures of the isolated compounds were identified by NMR spectroscopy. Results: The dichloromethane extract of the fruiting bodies of L. tigrinus afforded cerevisterol (1), and a mixture of stellasterol (2) and ergosterol (3) in about 4:5 ratio. Conclusion: To the best of our knowledge, this is the first report on the isolation of 1-3 from the fruiting bodies of L. tigrinus.

}, keywords = {Cerevisterol, Ergosterol, Lentinus tigrinus, Polyporaceae, Stellasterol}, doi = {10.5530/pj.2018.6.182}, author = {Consolacion Y. Ragasa and Maria Carmen S. Tan and Ma. Ellenita De Castro and Mariquit M. De Los Reyes and Glenn G. Oyong and Chien-Chang Shen} } @article {751, title = {A Triterpene and a Depside from Parmotrema austrocetratum Elix and J. Johnst.}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s27-s29}, type = {Original Article}, chapter = {s27}, abstract = {

Introduction: Parmotrema austrocetratum Elix and J. Johnst. (syn. Rimelia austrocetrata Elix and J. Johnst.) which belongs to a large genus of lichenized fungi, Parmotrema Massalongo under family Parmeliaceae was investigated for its chemical constituents. Methods: The compounds were isolated by silica gel chromatography and their chemical structures were elucidated by NMR spectroscopy. Results: Chemical investigation of the dichloromethane extract of Parmotrema austrocetratum Elix and J. Johnst. has led to the isolation of zeorin (1) and atranorin (2). Conclusion: P. austrocetratum shares similar chemical characteristic with other Parmotrema species which afforded atranorin. This work highlights the first reported isolation of 1 from P. austrocetratum and the genus Parmotrema.

}, keywords = {Atranorin, Parmeliaceae, Parmotrema austrocetratum, Rimelia austrocetrata, Zeorin}, doi = {10.5530/pj.2018.6s.4}, author = {Consolacion Y. Ragasa and Maria Carmen S. Tan and Virgilio C. Linis and Chien-Chang Shen} } @article {739, title = {Withaferin A attenuates Alcohol Abstinence Signs in Rats}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1190-1195}, type = {Original Article}, chapter = {1190}, abstract = {

Background: Withania somnifera (WS) have been reported to inhibit acquisition and expression conditioned place preference, self-administration and withdrawal anxiety of psychostimulants. In the present work, we have assessed the effect of withaferin A on somatic and affective symptoms of ethanol withdrawal syndrome in rats. Methods: Animals had given free access to ethanol uninterrupted for 21 days through liquid diet. Withaferin A (5, 10 and 20 mg/kg) was injected (ip) either during the development of ethanol dependence phase (days 15 \– 21 or 30 min before ethanol withdrawal assessment. Withdrawal signs characterized by changes in somatic signs were measured in the open field followed by evaluation of anxiety parameters, locomotion, and depressive behavior. Results: Withaferin A treatment 30 min before 24 h postethanol withdrawal assessment did not alter the scores of somatic behavioral signs in ethanol abstinence animals. However, withaferin A (10 and 20 mg/kg, ip) from day 15-21 prevented the ethanol withdrawal-induced elevated scores of somatic behaviors, hyperlocomotion, depressive behavior, and anxiety. Withaferin A treatment did not influence the blood ethanol levels in dependent and withdrawn animals. However, withaferin A administration attenuated the elevated plasma corticosterone and ACTH levels in ethanol-withdrawn rats, suggesting withaferin A induced anti-stress effect and stabilization of HPA axis activity could have facilitated the inhibitory effect of withaferin A on ethanol withdrawal syndrome. Conclusion: The finding supports further investigation of withaferin A and other bioactive components of WS in alcohol addiction.

}, keywords = {Anxiety, Corticosterone, Ethanol withdrawal, HPA axis, Withaferin A.}, doi = {xx10.5530/pj.2018.6.204}, author = {Nandkishor Ramdas Kotagale and Ankit Kedia and Rupali Gite and Shubham Nilkanth Rahmatkar and Dinesh Yugraj Gawande and Milind Janraoji Umekar and Brijesh Gulabrao Taksande} } @article {328, title = {Alpha-Glucosidase Inhibitory Activity and Fractionation of Bioactive Compounds from bark Extracts of Sibucao (Caesalpinia sappan L.) In the Philippines}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {356-360}, type = {Original Article}, chapter = {356}, abstract = {

Diabetes is a chronic disease that affects millions of people around the world. Although conventional medicine is available, it is usually accompanied by serious side effects such as gastrointestinal problem. Thus, the search for alternative medicine from natural sources is of primary importance. Context: The study is concerned with Caesalpinia sappan L. found in the vicinity of Baybay City, Leyte Philippines. Furthermore, it deals with ethanolic and aqueous extracts of the bark only. It was conducted to determine the alpha-glucosidase inhibitory activity of C. sappan to provide evidence to support its efficacy as a folkloric medicinal plant. Aims: This work aimed to evaluate the alpha-glucosidase inhibitory activity of aqueous and ethanolic bark extracts of Sibucao (Caesalpinia sappan L.) and to partially fractionate its bioactive compounds. Settings and Design: Extracts were prepared in increasing concentration to get IC50 values. Samples were analysed in triplicate both for extracts and fractions collected from chromatography. Methods and Material: Caesalpinia sappan L. bark samples were collected from the vicinity of Visayas State University. Plant materials were dried, weighed and stored. Aqueous and ethanolic bark extracts were prepared using water and 20\% ethanol. The total phenolic content of the extracts were determined and the \α-glucosidase inhibitory activity of crude bark and aqueous extracts were measured using the method of Kim et al., 2011. Partial fractionation of bioactive compounds was done successively using gradient elution. The \α-glucosidase inhibitory activity of fractions were then determined and Rf values of active compounds were measured using thin layer chromatography (TLC). Results: Results revealed that aqueous extract (2000 ppm) and ethanolic extract (2000 ppm) show high \α-glucosidase inhibitory activity of 100\% and 59\% respectively. IC50 values of aqueous and ethanolic extract were found to be 300.52 \± 1.467 ppm and 1560.81 \± 2.582 ppm, respectively. TLC of fractions show 7 peaks for aqueous extract and 6 peaks for ethanolic extract in which compound with Rf value 0.70 had the highest inhibitory activity of 65\%. Conclusions: Taken together, the high \α-glucosidase inhibitory activity of aqueous extracts support the effectiveness of C. sappan L. bark decoctions. In addition, results from bioassay-guided fractionation can be used as an effective tool for further isolation and characterization of \α-glucosidase inhibitors from Caesalpinia sappan L. in the Philippines.

}, keywords = {Caesalpinia sappan, Flavonoids, Fractionation, Type II diabetes, α-glucosidase}, doi = {10.5530/pj.2017.3.60}, url = {/files/PJ-9-3/10.5530pj.2017.3.60}, author = {Ea Kristine Clarisse B. Tulin and Ma Theresa P. Loreto and Edgardo E. Tulin} } @article {333, title = {Anti-hyperglycemic and Anti-hyperlipidemic Effects of Extract from Houttuynia cordata Thumb. in Streptozotocin-Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {382-387}, type = {Original Article}, chapter = {382}, abstract = {

Aim: Various properties of Houttuynia cordata Thumb. has been reported. However, few studies on its pharmacological effects have been documented. To elucidate whether there are more pharmacological effects of this plant, this study was therefore, carried out to determine the anti-hyperglycemic and anti-hyperlipidemic effects of 80\% ethanol extract of H. cordata (HCE). Their antioxidant activity and acute toxicity were also conducted. Methods: HCE at a dose of 250 mg/kg was oral given to Streptozotocin-induced diabetic rats daily for 8 weeks. DPPH assay and HCE at the doses of 1,000, 2,000 and 3,000 mg/kg were employed in antioxidant and acute toxicity studies. Results: HCE lowered FBG in the diabetic, but not in the normal treated rats. HCE did not affect the body weight of all rats, but recovered TP, Alb, Glob, BUN, CREA, UA, TB, AST, ALT, ALP, and reduced the elevated CHO, TG and LDL in the diabetic rats. HCE possessed relatively low antioxidant activity with IC50 of 115.98\± 0.82 \μg/mL compared to Vitamin C (42.54+1.37 \μg/ml), but did not produce any symptoms of acute toxicity. Conclusions: The extract of H. cordata may have beneficial properties and is a new agent for diabetic treatment and improve renal and hepatic functions.

}, keywords = {Acute toxicity, Anti-Hyperglycemic, Anti-Hyperlipidemic, Antioxidant, Houttuynia cordata Thumb}, doi = {10.5530/pj.2017.3.65}, url = {/files/PJ-9-3/10.5530pj.2017.3.65}, author = {Patcharee Poolsil and Wilawan Promprom and Chusri Talubmook} } @article {334, title = {Antioxidant Activity, Biochemical Components and Sub-Chronic Toxicity of Different Brown Rice Kefir Powders}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {388-394}, type = {Original Article}, chapter = {388}, abstract = {

Aims: This study aimed to investigate and compare antioxidant activity, biochemical components and subchronic toxicity of brown rice kefir powder from three different coloured rice varieties; Khao Dawk Mali 105 (KDMLKP, white), Red Hawm (RHKP, red), and Hawm Nil (HNKP, dark purple), with cow milk kefir powder (CMKP). Medthods: Antioxidant activity performed by using ferric reducing antioxidant power (FRAP) assay and 2, 2\´-diphenyl-1-picrylhydrazyl (DPPH) assay. Biochemical components values including gamma-aminobutyric acid and alpha-tocopherol were determined using high performance liquid chromatography, but total phenolic compounds was detemined using the Folin-Ciocalteu reagent. Sub-chronic toxicity test, KDMLKP, RHKP and HNKP at the doses of 150 mg/kg were given orally to the rats every day for 90 days. Results: Antioxidant activity showed that brown rice kefir powders were significantly (p\≤0.05) higher than cow milk kefir powder. Interestingly, HNKP provided the highest FRAB value and the lowest IC50 of DPPH assay. HNKP had also the highest biochemical component values. Repeat administration of KDMLKP, RHKP and HNKP did not produce any symptoms of sub-chronic toxicity; mortality, hematological values, and blood biochemistry in the rats. Moreover, RHKP produced HDL increasing without CHO, TG and LDL changing in rats. Conclusions: These data indicate that brown rice kefir powders show no sub-chronic toxicity and exhibit more antioxidant activity and biochemical component values than cow milk kefir powder. Surprisingly, RHKP showed HDL increasing while HNKP had the highest potent antioxidant activity and biochemical components. Thus, both rice kefir powders are safe and probably a new biochemical resource for health.

{\textquoteleft}}, keywords = {antioxidant activity, Biochemical Components, Brown Rice Kefir Powder, Rice, Sub-Chronic Toxicity}, doi = {10.5530/pj.2017.3.66}, url = {/files/PJ-9-3/10.5530pj.2017.3.66}, author = {Supaporn Chunchom and Chusri Talubmook and Sirirat Deeseenthum} } @article {361, title = {Chemical Profile and Biological Activities of Essential oil of Aerial parts of Artemisia monosperma Del. Growing in Libya}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {May 2017}, pages = {578-586}, type = {Original Article}, chapter = {578}, abstract = {

Background: From the bioactivity stand point Artemisia monosperma Del. is reputed to have antispasmodic and anthelmintic properties. Various types of secondary metabolites were reported in A. monosperma plants from different localities. Objective: The current study was planned aiming to investigate the influence of stage of development on the composition, antimicrobial, antiinflammatory and antioxidant activities of the essential oil derived from the aerial parts of the Libyan plants. Material and Methods: A. monosperma volatiles were hydro-distilled from aerial parts of Libyan plants, collected at different stages of growth: before flowering (A1), and at beginning (A2) and by the end (A3) of flowering stage. Yields ranged from 0.16-0.26 ml/100g fresh material (A3, highest). GC/FID and GC/MS analyses were performed. Results: Among 16-20 identified components (97.63-99.00\% of total composition), 11 were common in all samples. A1 and A2 showed close amounts of hydrocarbons (63.56 and 66.55\%), but lesser than A3 (88.36\%); monoterpenoids were mainly represented by sabinene (13.15-22.85\%), \β-pinene (9.00-24.03\%) and \β-cis-ocimene (3.73-12.92\%); while sesquiterpenoids appeared absent. Among oxygenated components (11.29, 31.08 and 35.44 \% in A3, A2 and A1), bornyl acetate was the major monoterpenoid (8.00-31.00\%, highest in A1); and the sesquiterpenoid, \β-eudesmol (8.01\%) was detected in A2 only. Moreover, A2 demonstrated significant antifungal effect against Aspergillus fumigatus and Geotricum candidum (MIC 0.98 and 0.24 \μg/ml). Conclusion: A3 exerted the highest anti-inflammatory activity as compared to the other volatiles. A1 restored the reduced blood GHS level in diabetic animals almost as efficiently as Vitamin E. The antioxidant activity of the volatiles is decreased during the flowering stage, being the highest before flowering (A1); this could be associated to the decreasing bornyl acetate content of the samples.

}, keywords = {Anti-oxidant, Antiinflammatory, Antimicrobial, Artemisia monosperma, Essential oil composition, GC-MS, Libya.}, doi = {10.5530/pj.2017.4.92}, url = {/files/PJ-9-4/10.5530pj.2017.4.92}, author = {Soheir Mohamed El Zalabani and Soad Hanna Tadros and Abeer Mohamed El Sayed and Areej Almaktouf Daboub and Amany Amen Sleem} } @article {429, title = {Chemo-profiling, Antioxidant Potential and Ionomic Analysis of Cichorium intybus L.}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {917-928}, type = {Original Article}, chapter = {917}, abstract = {

Background: Cichorium intybus commonly called as chicory or coffee weed was traditionally used for the treatment of various ailments associated with liver, kidney and heart. The aim of the present study was phytochemical screening, in-vitro evaluation of antioxidant potential, element analysis of wild and cultivated chicory and GC-MS analysis of methanolic leaf extract of wild chicory grown in Kashmir Himalaya. Method: To achieve this goal, the qualitative and quantitative analysis was done to determine the antioxidant potential. Element analysis was done using AAS and metabolite fingerprinting was done using GC-MS to ascertain the presence of active phytoconstituents in chicory leaves. Results: The qualitative screening of leaf extracts from wild and cultivated chicory indicates the presence of important bioactive constituents. The leaf extract of wild chicory constituted the higher amount of total phenol and flavonoid contents and also showed strong radical scavenging activities of DPPH, SOD and hydrogen peroxide radical as indicated by lower values of IC50 compared to cultivated chicory. Furthermore, both extracts of wild chicory showed the highest total antioxidant potential for the reduction of Fe3+ to Fe2+ when compared with cultivated chicory. The results from the elemental analysis shows that leaf extract of wild chicory exhibits higher concentration of elements as compared to cultivated one, thus can be used as a potential bio-fortified crop. The GC-MS analysis determines the presence of 78 different compounds in the methanolic leaf extract of wild chicory. The major phytochemical constituents were phytol (7.96\%) and stigmat-5-en-3-ol (6.45\%). Conclusion: The findings of the present study suggested the therapeutic potential of chicory leaves; particularly wild chicory proves to be a potent source of natural antioxidant against free radical associated damages. Metabolite profiling study revealed important metabolites having potent pharmacological actions.

}, keywords = {Aas, Antioxidant Activities, Cichorium Intybus, GC-MS., Phytochemical analysis}, doi = {10.5530/pj.2017.6.144}, url = {http://fulltxt.org/article/197}, author = {Bisma Malik and Tanveer Bilal Pirzadah and Inayatullah Tahir and Reiaz Ul Rehman} } @article {323, title = {Chronic Toxicity of Leaf Extract from Sphagneticola trilobata (L.) Pruski}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {323-328}, type = {Original Article}, chapter = {323}, abstract = {

Context: Sphagneticola trilobata (L.) Pruski. is a member of the family Asteraceae and has used traditionally in the prevention and treatment of various diseases. Aim: The research was aimed to determine chronic toxicity of 80\% ethanolic leaf extract from S.trilobata (STLE). Materials and Methods: STLE at the doses of 200 or 400 mg/kg b. w. was oral given to the healthy Wistar rats daily for 90 days. Statistical analysis used: Statistical analysis was carried out using F-test (One-Way ANOVA) followed by Duncan\’s New Multiple Range Test. Results: STLE did not produce any signs or symptoms of chronic toxicity. And also, the mortal rat was not observed during a period of an observation. Furthermore, STLE did not alter the body weight, relative organ (liver, pancreas, kidney and heart) weight, hemoglobin (Hb), hematocrit (Hct), red blood cell (RBC), white blood cell (WBC), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), neutrophil, lymphocyte, monocyte, platelet, alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea nitrogen (BUN), creatinine, blood cell characteristics, ultrastructure of RBC, and histological features of hepatic, pancreatic and renal tissues in the STLE treated rats comparing to control rats. Conclusions: These findings indicate that the leaf extract from S. trilobata exerts non chronic toxicity in rats and can be used safely as a traditional medicine or diet complement without any effect on hepatic and renal functions.

}, keywords = {Blood biochemistry, Chronic toxicity, Hematological values, Histological feature, S. trilobata}, doi = {10.5530/pj.2017.3.55}, url = {/files/PJ-9-3/10.5530pj.2017.3.55}, author = {Areeya Suchantabud and Teeraporn Katisart and Chusri Talubmook} } @article {382, title = {Cytotoxic and Antioxidant Effects in Various Tissue Extracts of Plumbago zeylanica: Implications for Anticancer Potential}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {July 2017}, pages = {706-712}, type = {Original Article}, chapter = {706}, abstract = {

Introduction: Complex natural products are emerging as a potent alternate and complement in anticancer therapies due to its multiple mechanisms of action and minimal effects on nontarget cells/tissues. Some of the traditional herbal formulations contain Plumbago zeylanica L, (commonly known as Chitraka or Chitramoolam) to treat various disorders for centuries in Africa and Asia. Methods: The quantity of Plumbagin was detected in different tissues of P. zeylanica through HPTLC analysis. We evaluated and compared the alcoholic tissue extracts of leaf, stem and root of P. zeylanica with standard pure Plumbagin for its in vitro cytotoxic effects (metabolic viability; MTT assay) in A549 Lung cancer cells and antioxidant potential (DPPH free radical scavenging and total phenol content). RNA sequencing and transcriptome analysis was performed in the most potent tissues of P. zeylanica demonstrating efficient pharmacological activity. Results: The root extract containing 1.3\% of plumbagin exhibited strongest scavenging potential with 50\% radical scavenging (IC50\ value of 3.99 g) in comparison with 35.85 g in stem (0.2\% Plumbagin) and 18.06 g in leaf with 0.00007\% Plumbagin. The in vitro cytotoxicity in A549 cells also showed that the root extract was most potent with an IC50\ value of 164.5\ g as compared to extracts from stem (IC50= 379.5\μg) and leaf (IC50= 274.9 g). Conclusion: The strong antioxidant potential shown by the P. zeylanica extract demonstrates its ability to protect the non-target (normal) cells against oxidative stress, while the cytotoxic effects suggest that it could inhibit the growth of cancerous cells. Further, transcriptome analysis predicted the expression of potent gene transcripts coding for quinone biosynthesis in the root tissues of P. zeylanica.

}, keywords = {A549 Cell Line, Alcoholic Root Extract, DPPH assay, HPTLC Quantification, Plumbagin, Transcriptome Analysis}, doi = {10.5530/pj.2017.5.111}, url = {/files/pj-9-5/10.5530pj.2017.5.111/index.html}, author = {Balachandran Karpaga Raja Sundari and Srivani Telapolu and Bilikere S and Dwarakanath and Sadras. P. Thyagarajan} } @article {257, title = {The Efficacy Study of Snake Fruit (Salacca edulis Reinw Var. Bongkok) Extract as Skin Lightening Agent}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {235-238}, type = {Original Article}, chapter = {235}, abstract = {

Introduction: The whitening skin product market has been growing significantly in Asia Pacific. Indonesia is one of those countries that mainly think that having a white color skin is simply beautiful. Therefore, it motivates Indonesian women to buy more whitening product for their beauty needs. Objective: The purpose of this research is to find raw material for whitening product from Indonesian plants that can be useful as skin lightening agents. This study investigated the potential of snake fruit (Salacca edulis Reinw var. Bongkok) ethanolic extract as skin lightening agent. Fruits of Salacca edulis Reinw contains flavonoids which have been reported to play a part in skin depigmentation. Methods: A randomized double-blind study on 17 human volunteers showed marked skin lightening effects using cream containing 3\% extract as there was a significant reduction in skin melanin index which compared favorably with the base cream (p \<0,05). Results: The result strongly suggested that snake fruit ethanolic extract can be used as raw material for skin lightening agents and therefore Indonesia dependency on imported raw materials could be reduced.

}, keywords = {Antioxidant, Melanin index, Salacca edulis Reinw, Snake fruit extract, Tyrosinase}, doi = {10.5530/pj.2017.2.39}, url = {http://phcogj.com/fulltext/306}, author = {Astrid Tilaar and Anna Ranti and Abdul Mun{\textquoteright}im} } @article {322, title = {Fasting Blood Glucose Levels and Hematological Values in Normal and Streptozotocin-Induced Diabetic Rats of Mimosa pudica L. Extracts}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017}, pages = {315-322}, type = {Original Article}, chapter = {315}, abstract = {

Context:M. pudica is a common plant found in moist waste ground, lawns, open plantations and weedy thickets. Aims: The fasting blood glucose levels (FBG) and hematological values of M. pudica aqueous(MPA) and hydro-ethanolic (MPHE) extract were evaluated in normal and streptozotocin (STZ)-induced diabetic rats. Materials and Methods: MPA and MPHE 125, 250 and 500 mg/kg body weight (b.w.) were administered orally and daily to the rats for 8 weeks. The FBG were determined weekly. Red blood cells (RBC), hemoglobin (HM. pudicab), hematocrit (Hct), platelet, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), white blood cells (WBC), lymphocytes, monocytes, neutrophils and eosinophil were evaluated. Results: MPA and MPHE had no effect on blood glucose levels in normal rats. All doses of all extracts showed significantly (p\<0.05) decreasing FBG in diabetic rats. Especially MPA at the dose of 250 mg/kg b.w. showed more potent significantly (p\<0.05) decreasing blood glucose levels than anti-diabetic drug glibenclamide at the end of experiment. All extracts had no effect on RBC, Hb, Hct, platelet, MCH, MCHC, lymphocytes, monocytes neutrophils and eosinophils. Surprisingly, the extracts were decreased WBC and MCV in diabetic rats. In addition, all of the extracts did not produce the alteration of blood cells structure in all rats. Conclusion: This study indicated that the extracts were hypoglycemic effect and improve hematological values in diabetes which confirms the traditional use of the plant.

}, keywords = {Blood glucose level, Hematological values, Mimosa pudica, Red blood cell, White blood cell}, doi = {10.5530/pj.2017.3.54}, url = {/files/PJ-9-3/10.5530pj.2017.3.54}, author = {Ampa Konsue and Chayan Picheansoonthon and Chusri Talubmook} } @article {348, title = {Fractionation and α-glucosidase Inhibitory Activity of Fractions from Garcinia hombroniana Pierre Leaves Extracts}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {May 2017}, pages = {488-492}, type = {Original Article}, chapter = {488}, abstract = {

Background: Diabetes mellitus become one of the biggest global health problems of the 21st century. Type 2 diabetes play role for the majority of cases of diabetes worldwide which is characterized by the increase of postprandial blood glucose level. Maintaining postprandial glucose level through inhibition of \α-glucosidase is one of the essential strategies in the treatment of diabetes. Inhibitory effect of \α-glucosidase was commonly used to identify active compounds potentially to treat diabetes. Natural resources have potency as antidiabetic that can be used in diabetes treatment. Objective: The objective of the study is to separate active fraction in the crude extract of Garcinia hombroniana leaves to facilitate obtaining a pure biologically active compound as the \α-glucosidase inhibitor. Methods: Fractionation to separate active fraction was performed using column and thin layer chromatography methods while \α-glucosidase inhibitory activity assay was performed in vitro using spectrophotometric methods at \λ 400 nm. Results: Ethyl acetate and methanol extract of G. hombroniana yielded 14 and 12 fractions, respectively. Two fractions with the higher percent inhibition compared to other factions are fraction 8 from ethyl acetate extract (FEA8) and fraction 3 from methanol extract (FM3). The IC50 values of FEA8, FM3 and acarbose are 16.370 \μg/mL, 59.042 \μg/mL, and 39.534 \μg/mL respectively. Conclusion: Fraction 8 from ethyl acetate extract of G. hombroniana leaves (FEA8) was separated and known in this study as the most bioactive \α-glucosidase inhibitor agent compared with another extract, fractions, and acarbose.

}, keywords = {Column chromatography, Diabetes mellitus, Fractionation, Thin layer Chromatography, α-glucosidase}, doi = {10.5530/pj.2017.4.79}, url = {/files/PJ-9-4/10.5530pj.2017.4.79}, author = {Nita Triadisti and Rani Sauriasari and Berna Elya} } @article {234, title = {In vitro Studies on Basella rubra Different Extracts as Inhibitors of Key Enzymes Linked to Diabetes Mellitus}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {November 2016}, pages = {107-111}, type = {Original Article}, chapter = {107}, abstract = {

Enzyme, inhibiting carbohydrate metabolism and thereby decreasing glucose level is a class of drugs helpful in the management of type 2 Diabetes mellitus. Naturally existing \α-amylase and \α-glucosidase inhibitors from medicinally significant plants are shown to be effective in the management of postprandial hyperglycemia. In this investigation, leaf extract (BRLE), stem extract (BRSE), fruit extract (BRFRE) and flower extract (BRFLE) of Basella rubra were subjected to evaluate their antioxidant potential and their possible inhibitory effects on \α-amylase and \α-glucosidase. BRLE, BRSE, BRFRE, BRFLE (at concentration 100\μg/ml) exhibited 65.78, 56.84, 63.1, 61.03\% of \α-amylase inhibitory activity respectively with IC50 values of 71.66, 89.69, 73.68, 80.37 \μg/ml respectively. In the same way BRLE, BRSE, BRFRE, BRFLE (at concentration 100 \μg/ml) exhibited 97.63, 92.79, 82.17, 92.71 \% of \α-glucosidase inhibition with an IC50 value of 26.97, 28.53, 41.30, 38.80 \μg/ml respectively. Among the samples, the leaf extract of B. rubra registered higher content of total phenolics and flavonoids and also higher antioxidant activity in DPPH, nitric oxide and NBT radical scavenging assays. Though all the parts had shown potent inhibitory effects on \α-amylase and \α-glucosidase, the highest inhibitory potency was observed in the leaf extract of Basella rubra\ (p\<0.001).

}, keywords = {Basella rubra, Diabetes mellitus, Postprandial hyperglycemia, α-Amylase inhibitory activity}, doi = {10.5530/pj.2017.1.18}, author = {B. Samuel Thavamani and Vanitha Subburaj} } @article {405, title = {Influence of Extraction Parameters on the Yield, Phytochemical, TLC-Densitometric Quantification of Quercetin, and LC-MS Profile, and how to Standardize Different Batches for Long Term from Ageratum conyoides L. Leaves}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {767-774}, type = {Original Article}, chapter = {767}, abstract = {

Introduction: Ageratum conyzoides Linn is one of the Indonesian herbs are used as folk medicine. There are many studies to the therapeutic activity. However, the study of the influence in extraction parameters and how to standardize different batches of plant is still limited. Objective: The present study was designed to investigate the influence of extraction parameters on the variables matter, yield, phytochemical profile, and total quercetin from A. conyzoides L. leaves extract. The study also evaluates Liquid Chromatography-Mass Spectroscopy (LC-MS) and TLC fingerprint profiles of the extract to determine the proper quality of plant material of A. conyzoides L. leaves. Methods: Different temperatures (from 0\°C to 60\°C), solvent types (water and 70\% ethanol (\%v/v), and extraction time (192 h VS 2 h) were used to investigate the influence of extraction parameters. The profiles of extract were performed by TLC and LC-MS method. Results: The extract yield was influenced by temperature, solvent types, and time extraction. Our results suggest that the digestion technique at 60\°C with 70\% ethanol for 2h was recommended for the extraction method to obtained high yield and quercetin content as bioactive compound in A. conyzoides L. leaves extract. The range of quercetin content (40\–52 ppm) combined with TLC and LC-MS profile can be used to determine the proper quality of plant material. Conclusion: All parameter of extraction have an affect on the yield extract and total quercetin on the final extract. Thus, there is a need an optimized method to obtain the suitable method.

}, keywords = {Ageratum conyzoides, Lc-Ms, Quercetin, Standardization., Tlc-Densitometric}, doi = {10.5530/pj.2017.6.121}, url = {http://fulltxt.org/article/174}, author = {Anita Paulina Tambunan and Anton Bahtiar and Raymond Rubianto Tjandrawinata} } @article {340, title = {Neuropathic Pain: Literature Review and Recommendations of Potential Phytotherapies}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {May 2017}, pages = {425-434}, type = {Review Article}, chapter = {425}, abstract = {

Introduction: One of the common syndromes that affect humanity is neuropathic pain (NP), yet poorly understood with no efficient treatment till now. Consequently, it is extremely crucial to seek further evidence for accurate diagnosis and optimum treatment. The aim of this work is to summarize the findings related to neuropathic pain in terms of etiology, types, diagnosis, current and future management prospective, and identify the gaps in neuropathic pain therapy. Methods: A literature investigation was carried out by analyzing classical peer reviewed papers and textbooks, taking into consideration worldwide well established scientific databases mainly PUBMED and SCOPUS to retrieve accessible published literature. The selection of phytotherapies was based upon their potentials in relieving NP in pre-clinical or clinical models. Results: One of the most critical points in this research is that recommendations of the future plans should be focused on the engagement of phytotherapy in the treatment regimen aiming at improving patients\’ quality of life and reaching optimum efficacy and minimum toxicity. Phytotherapies offer relatively low-risk options to NP patients and have an increasing evidence to be the future of neuropathic pain management. Patients suffering from neuropathy are depending increasingly on phytotherapies; however, they need more clinical trials in order to fully understand their mechanism of actions. Conclusion: Health-care specialists should be regularly informed about neuropathic pain current therapies and promising future phytotherapies, bearing in mind the risk/benefit profile of the utilization of these therapies in the amelioration of NP.

}, keywords = {Current therapies, Diagnosis, Mechanisms, Neuropathy Pain, Phytotherapies, Recommendations}, doi = {10.5530/pj.2017.4.72}, url = {/files/PJ-9-4/10.5530pj.2017.4.72}, author = {Karim Raafat and Rawan El-Haj and Dania Shoumar and Rana Alaaeddine and Yousra Fakhro and Natalie Tawil and Farah Shaer and Amani Daher and Natalie Awada and Ali Sabra and Khouloud Atwi and Malak Khaled and Raneem Messi and Nour Abouzaher and Mohamed Houri and Samer Al Jallad} } @article {532, title = {Pharmacognostic Specification and Mangiferin Content of Aquilaria crassna Leaves.}, journal = {Pharmacog Journal}, volume = {10}, year = {2017}, month = {January-2018}, pages = {293-298}, type = {Original Article}, chapter = {293}, abstract = {

Background:\ Aquilaria\ crassna\ Pierre ex Lecomte (Thymelaeaceae) has been used as a medicinal plant in many aspects. Previous research has revealed that A. crassna leaves contain mangiferin as an active compound. Although the active component has been investigated, the pharmacognostic specification and quantification of mangiferin from A. crassna leaves have never been established. Objective: The current study aimed to conduct and develop a pharmacognostic standard according to WHO guidance as well as the validated method for quantifying mangiferin content. Materials and Methods: Dried A. crassna leaves from 15 separated locations throughout Thailand were investigated for pharmacognostic specification. Their mangiferin contents were quantitatively analysed by TLC densitometry with win CATS software. Results: Macroscopic-, microscopic- characteristics and TLC fingerprinting combined with physicochemical parameters were reported in this study. The loss on drying, moisture content, and total ash content as well as acid-insoluble ash content were determined to be 8.62 \± 0.13, 8.16 \± 0.14, 6.82 \± 0.09 and 1.49 \± 0.03\%, respectively. Ethanol- and waterextractive values were found to be 9.05 \± 0.39 and 16.94 \± 0.22 \%, respectively. In addition, the validation method for quantifying the mangiferin content was developed. The contents of mangiferin in A. crassna leaf extract determined by TLC-densitometry and TLC-image analysis were found to be 1.2992 \± 0.5980 and 1.3036 \± 0.5874 \% by dried weight, respectively. The results between these two analytical methods were shown to have an insignificant difference. Conclusion: This study provides the necessary information for authentication and standardisation of A. crassna leaves.

}, keywords = {Aquilaria crassna leaves, Mangiferin, Pharmacognostic specification, TLC image analysis, TLC-densitometry}, doi = {10.5530/pj.2018.2.51}, url = {http://fulltxt.org/article/481}, author = {Worathat Thitikornpong and Boonsri Ongpipattanakul and Chanida Palanuvej and Nijsiri Ruangrungsi} } @article {251, title = {Screening of Ethanolic Extracts of Medicinal Herbal Drugs Against Oral Microbes}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {201-203}, type = {Original Article}, chapter = {201}, abstract = {

Aim: The aim of the present study is to screen the ethanolic extracts of medicinal herbal drugs against oral microbes. Objective: In this study, 3 medicinal herbs were evaluated for antimicrobial activity against five common oral bacteria as a screen for potential candidates for the development of natural antibiotics. Methods: Ethanolic extracts of medicinal herbs were tested for activity against Enterococcus faecalis, Lactobacillus acidophilus, Streptococcus mutans, and Streptococcus sanguis grown in brain heart infusion (BHI) broth. A broth microdilutionassay was used to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). A disk diffusion assay was performed by inoculating bacterial cultures on BHI agar plates with paper disks soaked in each of the medicinal herb extracts. Results: The ethanolic extracts of many of the 3 medicinal herbs showed antimicrobial activity against the five types of pathogenic oral bacteria. The extracts of Caralluma fimbriata, Hemidesmus indicus, and Grape seed effectively inhibited the growth of oral bacteria and showed distinct bactericidal activity. Conclusion: These results suggest that alternative medicines with proven antimicrobial effects, such as Caralluma fimbriata, Hemidesmus indicus, and Grape seed may be useful for the treatment of dental diseases.

}, keywords = {Anti cariogenic, Dental caries, Natural products Pathogenic, Oral bacteria}, doi = {10.5530/pj.2017.2.33}, url = {http://phcogj.com/fulltext/300}, author = {Harsha L and Lakshmi Thangavelu} } @article {227, title = {Toxicology and Oral glucose Tolerance Test (OGTT) of Thai Medicinal Plant Used for Diabetes controls, Phyllanthus acidus L. (EUPHORBIACEAE)}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {December 2016}, pages = {58-61}, type = {Original Article}, chapter = {58}, abstract = {

Aim: The present study aimed to investigate toxicity and oral glucose tolerance test (OGTT) of Phyllanthus acidus leaf extract (PAE) on Wistar rat. Methods: PAE was prepared and administered orally to experimental animals used. The extract was tested for toxicity in rats at a dose of 0, 1,000, 1,500 and 2,000 mg/kg body weight p.o once daily for 14 days. The hypoglycemic effects of PAE on normal rats and orally glucose-induced hyperglycemic rats were compared with distilled water and glibenclamide. A single dose (250 mg/kg body weight) of PAE was administered and blood glucose level was obtained by pricking the tail vain using glucometer at time -30, 0, 30, 60, 120 and 240 minutes. Results: All doses of the extract did not exert any sign or symptom of toxicity and the dead rat was not found. The body weight, white blood cell (WBC), mean corpuscular volume (MCV), platelet (PLT), plateletcrit (PCT), mean platelet volume (MPV), platelet distribution width (PDW), blood chemistry, blood urea nitrogen (BUN), creatinine, alkaling phosphatase (ALP) and organ weight of liver were not significantly different between control and treated rats. However, red blood cell (RBC), hematocrit (HCT), lymphocyte (LYM), and hemoglobin (Hb) at a dose 1,500 mg./kg body weight were significantly lower than those in the control group. The blood glucose levels of PAE treated groups were not different with control and Glybenclamide treated. Conclusion: The findings of the present study can be concluded that the PAE are practically non-toxic at a lower dose.

}, keywords = {Blood glucose, Diabetes, Medicinal plant, Phyllanthus acidus, Toxicity}, doi = {10.5530/pj.2017.1.11}, author = {Napapach Chaimum-aom and Sanong Chomko and Chusri Talubmook} } @article {211, title = {Antioxidant and Hypoglycemic Activities of Clausena anisata (Willd.) Hook F. Ex Benth. Root Mediated Synthesized Silver Nanoparticles}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {579-586}, type = {Original Article}, chapter = {579}, abstract = {

The present study was carried out to examine the hypoglycemic effect of Silver Nanoparticles (SNPs) using ethanolic root extract of Clausena anisata (Willd.) Hook. f. ex Benth. A cost effective and eco friendly technique for green synthesis of SNPs from 1mM AgNO3 solution through the root extract was carried out. The biosynthesized SNPs were characterized using UV spectrophotometry, Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction analysis (XRD), Energy Dispersive Spectroscopy (EDS) and Fourier transform infra-red (FTIR) spectrometry. DPPH assay was done to determine the antioxidant activity and for in vitro hypoglycemic activity glucose uptake by yeast cells, alpha amylase inhibition assay, adsorption capacity and glucose diffusion assay was performed. The SNPs of ethanolic root extract were found to be spherical in shape and up to 32.75 nm average in size. They showed alpha amylase inhibitory activity of 83.60\% at 500 g/ml. The glucose uptake by yeast cells was found to increase with an increase in concentration. The maximum glucose uptake was found to be 69.51\% at 10mM concentration. The molar concentration of glucose was directly proportional to the glucose binding capacity of extracts.The rate of glucose diffusion across the membrane was found to increase from 30 to 180 minutes. The DPPH scavenging activity was found to be potent (74.07\%) at 500 g/ml. The hypoglycemic effect exhibited by the SNPs was revealed by simple in vitro model of yeast cells, mediated by glucose adsorption, increasing glucose diffusion and glucose transport across the cell membrane.

}, keywords = {antioxidant activity, C. anisata, Diabetes, Glucose and Silver nitrate, Silvernanoparticles}, doi = {10.5530/pj.2016.6.10}, author = {Arsia Tarnam Yakoob and Nargis Begum Tajuddin and Muhammad Ilyas Mohammed Hussain and Shilu Mathew and Archunan Govindaraju and Ishtiaq Qadri} } @article {97, title = {Chemical Constituents and in vitro anticancer activity of Tiliacora triandra leaves}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {1-3}, type = {Original Article}, chapter = {1}, abstract = {

Introduction: \ Tiliacora triandra (F. Menispermaceae) is edible and is also known for medicinal values. The leaves are a popular flavoring in Southeast Asia, especially in the northeast of Thailand.\  The objectives of this study were to determine the major constituents of the leaves of T. triandra, and assess their anticancer activities against human cancer cell lines. Methods: The leaves were extracted by a soxhlet apparatus with petroleum ether, dichloromethane, ethyl acetate and water. Major constituents were then purified and identified using chromatographic procedures and various spectroscopic techniques.\  In vitro anticancer activity tests of T. triandra extracts were performed by resazurinmicroplate assay (REMA), and tested with 3 cell lines: oral cavity cancer (KB), lung cancer (NCI-H187) and breast cancer (MCF-7) cell lines. Results: The result indicated that the main compound of T. triandra leaves was oxoanolobine. The methanol extract showed the highest cytotoxic activity against lung cancer (NCI-H187) cell line whereas the water extract exhibited the highest activity against oral cavity cancer (KB) cell line. The IC50 of oxoanolobine against the NCI-H187 cell line was 27.60 \± 4.30 \µg/mL. Conclusion:T. triandra leaves contain oxoanolobine as the major constituent and have the potential of anticancer activity but are required to be investigated further.

}, keywords = {In vitro anticancer activity, Oxoanolobine, Phytochemistry, Tiliacora triandra, Yanang.}, doi = {10.5530/pj.2016.1.1}, author = {Surapong Rattana and Benjamart Cushnie and Ladachart Taepongsorat and Methin Phadungkit} } @article {190, title = {Gas Chromatography - Mass Spectrometry Analysis and In vitro Antioxidant Activity of the Ethanolic Extract of the Leaves of Tabernaemontana divaricata}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {451-458}, type = {Original Article}, chapter = {451}, abstract = {

Objective: To identify phytoconstituents present in an ethanolic extract of the leaves of Tabernaemontana divaricata and to evaluate its in-vitro antioxidant potential. Methods: The extract was subjected to gas chromatography- mass spectrometry analysis to identify phytoconstituents, and screened for hydroxyl, superoxide and 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity, reducing power and metal-chelating activity as a measure of potential antioxidant activity. Results: GC-MS analysis of the extract revealed the presence of 96 phytoconstituents, of which 17 are reported to be bioactive and 11 of these to possess antioxidant potential. When tested in-vitro, the extract exhibited the most potent radical-scavenging activity at a maximum concentration of 10 mg/ml, scavenging effects of 64\%, 67\% and 69\% and corresponding half maximal inhibitory concentration (IC50) values of 6.7 mg/ml, 6.8 mg/ml and 6.2 mg/ml on hydroxyl, superoxide and DPPH radicals, respectively. Ascorbic acid used as a standard (10 mg/ml) showed scavenging effects of 73\%, 73\% and 75\% and corresponding IC50 values of 5.3 mg/ml, 5.8 mg/ml and 5.2 mg/ml, respectively, on hydroxyl, superoxide and DPPH radicals. At 10 mg/ml, the extract and an ethylenediaminetetraacetic acid standard exhibited 68\% and 78\%, respectively, chelation of ferrous ions; at the same concentration, the reducing power of the extract and that of a butylated hydroxytoluene standard was found to be 3.855 and 4.308, respectively. Conclusion: These observations strongly suggest that the ethanolic extract of T. divaricata leaves has potent in-vitro antioxidant activity and thereby could act as a possible therapeutic agent for oxidative stressinduced pathological states.

}, keywords = {antioxidant activity, GC-MS analysis, Metal chelating activity., Phytoconstituents, Reducing power, Tabernaemontana divaricata}, doi = {10.5530/pj.2016.5.7}, author = {Muniyandi Anbukkarasi and Philip A Thomas and Mahalingam Sundararajan and Pitchairaj Geraldine} } @article {210, title = {Gc-Ms Analysis of Ethanolic Stem Extract of Clausena anisata (Willd.) Hook F Ex Benth}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {576-578}, type = {Original Article}, chapter = {576}, abstract = {

Objective: In the present study, the bioactive components present in the ethanol stem extract of Clausena anisata was analyzed by using Gas Chromatography Mass Spectrometry analysis technique (GC-MS). Clausena anisata, a medicinal plant belonging to the family Rutaceae, is represented by 20 species available in India and used traditionally for the treatment of several ailments but there is a requirement to identify its phytoconstituents, its target, mode of action and treatment using plant products either alone or in combination with synthetic drugs. Methods: Clausena anisata stem was procured from Manamettupatti, a village of Pudukottai District, Tamil Nadu. The shade dried stem was powdered and extracted using ethanol by maceration method. One microlitre of the extract was subjected to GC-MS analysis to detect the presence of bioactive compounds present in the stem of C. anisata. Results:The results showed that the ethanol stem extract of C. anisata contained nine bioactive compounds, of which the major one is n-hexadecanoic acid (78.54\%), followed by 8-octadecenoic acid, methyl ester, [E]- (6.638\%). The total number of compounds obtained was compared with National Institutes of Standard and Technology (NIST) library that contains more than 62,000 known compounds based on retention time and molecular mass. Conclusion: In this study, nearly nine compounds have been identified from the ethanolic stem extract of C. anisata using GC-MS analysis which was mainly composed of fatty acids and sterols. The GC-MS analysis is used to understand the nature of active principles present in this plant revealed that the plant can be used as a potential source of new useful drugs.

}, keywords = {C. anisata, Ethanol, GC-MS analysis, maceration and phytoconstituents}, doi = {10.5530/pj.2016.6.9}, author = {Arsia Tarnam Yakoob and Nargis Begum Tajuddin and Shilu Mathew and Muhammad Ilyas Mohammed Hussain and Ishtiaq Qadri} } @article {209, title = {Green synthesis, Antioxidant Potential and Hypoglycemic Effect of Silver Nanoparticles using Ethanolic Leaf Extract of Clausena anisata (Willd.) Hook. F. Ex Benth. of Rutaceae}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {565-575}, type = {Original Article}, chapter = {565}, abstract = {

The current study was conducted to examine the hypoglycemic effect of Silver Nano particles (SNPs) using ethanolic leaf extract of Clausena anisata (Willd.) Hook f. ex Benth. A cost effective and eco-friendly technique for the green synthesis of SNPs from 1mM AgNO3 solution through the leaf extract was carried out. The biosynthesized SNPs were characterized using UV spectro photometry, Field Emission Scanning Electron Microscopy (FESEM), X-ray Diffraction analysis (XRD), Energy Dispersive Spectroscopy (EDS) and Fourier transform infra-red (FTIR) spectrometry. DPPH assay was done to determine the antioxidant activity and for in vitro hypoglycemic activity glucose uptake by yeast cells, alpha-amylase inhibition assay, adsorption capacity and glucose diffusion assay was carried out. The SNPs of ethanol leaf extract were found to be spherical in shape and up to 60.67 nm average in size. They showed alpha-amylase inhibitory activity of 80.32\% at 500 g/ml and IC50 100 g/ml. The glucose uptake by yeast cells was found to increase with an increase in concentration. The maximum glucose uptake was found to be 68.29\% at 10mM concentration. The molar concentration of glucose was directly proportional to the glucose binding capacity of extracts. The rate of glucose diffusion across the membrane was found to increase from 30 to 180 minutes. The DPPH scavenging activity was found to be potent (71.60\%) at 500 g/ml. The hypoglycemic effect exhibited by the SNPs was revealed by simple in vitro model of yeast cells, mediated by glucose absorption, increasing glucose diffusion and glucose transport across the cell membrane.

}, keywords = {Nil}, doi = {10.5530/pj.2016.6.8}, author = {Arsia Tarnam Y and Nargis Begum T and Muhammad Ilyas MH and Shilu Mathew and Archunan Govindaraju and Ishtiaq Qadri} } @article {117, title = {Inhibition of MDR1 in mammary cell carcinoma reverses Multidrug Resistance by SOCS1}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {103-112}, type = {Original Article}, chapter = {103}, abstract = {

Introduction: Suppressors of cytokine signalling (SOCS1), a newly indentified antiapoptotic molecule is a downstream effector of the receptor tyrosine kinase-Ras signalling pathway. Current study has uncovered that SOCS1 may have wide and imperative capacities, particularly because of its close correlation with malignant tumors. Methods: To investigate the impact of SOCS1 on MDR, we analyzed the expression of P-gp and SOCS1 by immunohistochemistry and found there was positive correlation between them. At that point we effectively interfered with RNA translation by the contamination of siRNA of SOCS1 into MCF7/ ADM breast cancer cell lines through a lentivirus, and the expression of the target gene was significantly inhibited. Results: After RNAi the drug resistance was reduced altogether and the expression of MDR1 mRNA and P-gp in MCF7/ADM cell lines demonstrated a significant decrease. Likewise the expression of P53 protein increased in a statistically significant manner (p\≤0.01) after RNAi exposure. Moreover, flow cytometry analysis uncovers that cell cycle and anti-apoptotic enhancing capacity of cells changed after RNAi treatment. Conclusion: These outcomes proposed SOCS1 may take part in breast cancer MDR by managing MDR1 and P53 expression, changing cell cycle and enhancing the anti-apoptotic ability of cells.

}, keywords = {Breast cancer, MDR1gene, Multidrug resistance, RNA interference., SOCS1 gene}, doi = {10.5530/pj.2016.2.2}, author = {Debasish Pradhan and Gitanjali Tripathy and Rakesh Kumar Pradhan and Shaktiprasad Pradhan and Soumyashree Rupambika Moharana} } @article {96, title = {Pharmacognostical, Phytochemical and Nutritional Evaluation of Glinus oppositifolius (L.) Aug. DC}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {31-36}, type = {Original Article}, chapter = {31}, abstract = {

Objective: The primary aim of the study was to establish the pharmacognostic standards along with nutritional values on the important medicinal herb Glinus oppositifolius (L.) Aug. DC., commonly known as Parpata in South India. Material and Methods: Pharmacognostical, physicochemical, nutritional evaluation along with the TLC profiling and preliminary phytochemical screening was carried out. Results: Histological study of different parts of the plant revealed the presence of different cellular structures viz. stem showed the presence of multi cellular to unicellular trichomes, collateral vascular bundles, starch grains etc. Mesophyll of the leaves was embedded with starch grains with clustered calcium oxalate and prism shaped crystals. Anomocytic stomata were present on both the epidermis of the leaf. Powder microscopy exhibited multi cellular trichomes, clustered calcium oxalate, fibres etc. Physicochemical and histochemical studies revealed the presence of various secondary metabolites and different minerals within the acceptable limits. Thin layer chromatographic profiling showed different spots suggesting the presence of specific phytoconstituents in different extracts. The plant also revealed good nutritional value with calorific value of about 245 kcal/100g; Vitamin C 112 mg/100 g and higher amount of calcium etc. Conclusion: The results are beneficial to establish the quality control parameters of the plant species and may be served as future reference for the identification and authentication of the genuine crude drug and also provide sufficient data to recognize the use of the plant as dietary suppliment.\ \  \ 

}, keywords = {Antidiabetic, Histochemical studies., Pharmacognosy, Powder microscopy, standardization, Thin layer Chromatography.}, doi = {10.5530/pj.2016.1.7}, author = {Shantha Thirumalai Ramaseshan and Patchaimal Pitchaiah and Vandana Bharti and Kishore Kumar Ramakrishna and Venkateshwarlu Gaddam and Devesh Tewari and Chinmay Rath and Anupam Mangal and Padhi Madan Mohan and Dhiman Kartar Singh} } @article {185, title = {Pharmacognostical Standardization of Goraksha pods: an important Nutritive and antidiabetic Plant}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {424-429}, type = {Original Article}, chapter = {424}, abstract = {

Objective: Goraksha or cluster beans are an annual legume found throughout India. It is also extensively cultivated for its pods used as vegetable for its high nutritive value, antidiabetic properties and for the source of guargum. Methods: Macroscopy, microscopy, powder microscopy, histochemical studies and preliminary phytochemical studies on the pods of Goraksha has been carried out highlighting its importance along with important diagnostic characters, which will help in the identification of pods both in fresh form as well as in dry form. Results: Study revealed presence of distantly arranged elongated uniseriate warty trichomes in the outer most layer of epidermis, presence of stone cells, simple starch grains and very small calcium oxalate crystals in the hypodermal region. Presence of unevenly thickened row of palisade layer of macro sclereids in the outer most layer of cotyledon region. Phytochemical studies revealed the presence of alkaloids carbohydrates, phenols, proteins, saponins, starch, steroids, and tannins. Conclusion: The pharmacognostical standardization revealed the presence of various specific characters which are important for the identification of the genuine pods of Cyamopsis tetragonoloba (L.) Taub.

}, keywords = {Cluster beans, Goraksha, Pharmacognosy, Pods. Histochemical studies.}, doi = {10.5530/pj.2016.5.2}, author = {Shantha Thirumalai Ramasheshan and Patchaimal Pitchaiah and Prathapa Reddy Maramreddy and Vandana Bharti and Kishore Kumar Ramakrishana and Venkateshwarlu Gaddam and Devesh Tewari and Anupam Kumar Mangal and Madan Mohan Padhi and Kartar Singh Dhiman} } @article {147, title = {Study of Quality Assurance For Peumus Boldus M Products By Botanic Profiling, Extraction Optimization, HPLC Quantification And Antioxidant Assay}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Jan/2016}, pages = {264-272}, type = {Original Article}, chapter = {264}, abstract = {

Introduction: The boldo leaf has several traditional folk medicinal uses, such as for gallbladder, hepatic problems, digestive disorders, rheumatism and others. In the work reported herein, botanic profiling, extraction optimization by Soxhlet, quantification of boldine by an easy/simple to run HPLC method and antioxidant assay are proposed for the quality assurance of boldo dried leaves, standardized extracts, dried extracts, tablets and capsules. Materials and Methods; In this present work we are studying a systematic approach in the quality assurance study of quality assurance for Peumus boldus M products by the ascertainment of pharmacobotanic parameters for boldo identification, investigation of the extraction parameters by Soxhlet method, development and validation of an easy/simple to run HPLC method to quantify boldine in the raw drug, extracts, commercial tablets, capsules and coated tablets, and antioxidant assay. Results: The plant material was submitted to a pharmacognostic evaluation through morpho-anatomical diagnosis, showing that starlike trichomes can be used for boldo authentication. The HPLC validated analytical method is reliable, accurate and precise for boldine quantification. Furthermore, the Soxhlet extraction conditions were optimized. Conclusion: The methods proposed in this paper can be used for the quality assurance of boldo dried leaves, standardized extracts, dried extracts, tablets and capsules.

}, keywords = {antioxidant activity, Boldine, Peumus boldus, Pharmacognostic evaluation, Quantitation.}, doi = {10.5530/pj.2016.3.16}, author = {Cristiane Cardoso Correia Teixeira and Tatiana Pereira de Freitas Cabral and Jo{\~a}o Paulo Barreto de Sousa and Simone de P{\'a}dua Teixeira and Jairo Kenupp Bastos and Luis Alexandre Pedro de Freitas} } @article {214, title = {Study on Silybum marianum Seed through Fatty Acids Comparison, Peroxide Tests, Refractive Index and Oil Percentage}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {595-597}, type = {Original Article}, chapter = {595}, abstract = {

In this study, milk thistle seeds were collected from four regions of Iran (Ahvaz, Lorestan, Kazeroon and Zarghan). The oil extracted from seeds of plant using n-hexane solvent extraction soxhlet. The extracted oil was analyzed by gas chromatography and fatty acids were identified in all four samples. In all four samples, the oil refractive index of Milk thistle oil fatty acids vis. Linoleic acid, Oleic acid, Palmitic acid was evaluated. The Peroxide test and determination of oil percentage was performed in Milk thistle seed oil.

}, keywords = {Extraction, Fatty Acids, Milk Thistle, Oil, Peroxide}, doi = {10.5530/pj.2016.6.13}, author = {Iman Nasrollahi and Ebrahim Talebi and Zahra Nemati} } @article {83, title = {Anti-diabetic Properties of Thymoquinone is unassociated with Glycogen Phosphorylase Inhibition}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {406-410}, type = {Original Article}, chapter = {406}, abstract = {

Background: Nigella sativa L. (Black seed), is commonly used by traditional healers as a remedy for more than four thousand years. The antidiabetic property of N. sativa seeds oil is attributable to the presence of Thymoquinone (TQ). On the other hand many studies have been designed to investigate the possible effects of the TQ in Streptozotocin (STZ) and nicotinamide (NA)-induced diabetes in rats. Aim of the study: The aim of this study was to elucidate the mechanisms underlying the glucose lowering effects of thymoquinone. Methods: In vitro and in silico using glycogen phosphorylase (GPa) enzyme assay and docking tools were used. Results: Oral administration of TQ for 60 days, dose dependently improved the glycemic status in STZ-NA induced diabetic rats. GPa activity was measured in the direction of glycogen synthesis by the release of phosphate from glucose-1-phosphate. TQ at a concentration of 0.05 Mm inhibits GPa activity by only 14.9\%. Conclusion: These results show that TQ at 60 mg/kg b.w is associated with potential antihyperglycemic effects. Furthermore, anti-diabetic properties of TQ are unassociated with glycogen phosphorylase inhibition.

}, keywords = {Diabetes, Docking, Enzyme, Glycogen phosphorylase inhibition, Streptozotocin, Thymoquinone.}, doi = {10.5530/pj.2015.6.16}, author = {Nahid Mahmoud Hassan El-Ameen and Manal Mohamed Elhassan Taha and Siddig Ibrahim Abdelwahab and Asaad Khalid and Fatima Elfatih and Mona Awad Kamel and Bassem Yousif Sheikh} } @article {145, title = {Antimicrobial Effects of Thymoquinone on Entamoeba histolytica and Giardia lamblia}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2015}, month = {December 2015}, pages = {168-170}, type = {Original Article}, chapter = {168}, abstract = {

Background: Parasitic infections are a major difficulty in tropical and subtropical countries. Traditionally medicinal plants have been used in folk medicine to treat parasitic infections and are a valuable source of novel anti-parasitics. Objective: In our search for therapeutic alternatives to anti- protozoal chemotherapy, thymoquinone, the active ingredient of Black cumin (Nigella sativa) was examined. Materials and Methods: Thymoquinone was tested against Entamoeba histolytica and Giardia lamblia using in vitro susceptibility assays and the mortality of the parasites were then obtained using the standard calculations. The compound was also tested for 48 and 72 hours on both parasites. Results: The current study indicate that the mortality of TQ showed 85.5\%, 91.5\% and 96.8\% mortality on E. histolytica for 25 ppm at 24 hr, 48 and 72 hr, respectively, with IC50 2\¥10-19,. On the other hand, this natural compound showed a mortality of 82.83\%, 91.76\% and 96.62\% mortality on G. lamblia for 25 ppm at 24 hr, 48 and 72 hr, respectively, with IC50 4.8\¥10-5. Metrondizole powder gave 70.9\% mortality at 156 ppm at the same times. Conclusion: The current results indicate that TQ is more potent on E. histolytica compared to G. lamblia. Further pharmacological studies were needed to help in the clinical presentation of thymoquinone.

}, keywords = {Entamoeba histolytica, Giardia lamblia., Nigella sativa, Prophetic Medicine, Thymoquinone}, doi = {10.5530/pj.2016.2.12}, author = {Bassem Yousef Sheikh and Manal Mohamed Elhassan Taha and Waleed Syaed Koko and Siddig Ibrahim Abdelwahab} } @article {1449, title = {Assessment of Cytotoxicity of Smokeless Tobacco (Shammah) In Hepg2 and WRL68 Cells Line}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {29th Apr, 2015}, pages = {242-248}, type = {Original Article}, chapter = {242}, abstract = {

Shammah is a traditional form of chewing tobacco [Smokeless tobacco, (ST)] that is commonly used in the Middle east specially Saudi Arabia (KSA), Yemen and Sudan. The cytotoxicity of Sudanese and Yemenis ST hexane and methanol extracts was evaluated using MTT assay. Annexin-V assay has been used to detect the induction of apoptosis. Luminescence based assay also been conducted to check the level of caspases enzyme. The involvement of cell cycle check point arrest has been performed using flow cytometry analysis. The current study found that ST has the capacity to induce cell toxicity in human liver cells. The inhibitory capacity of ST in HepG2 and WRL 68 has been found to be 151 \± 2.5 and 305 \± 11.5 \μg/ml for 24 h. An early apoptosis induction in HepG2 cells was observed by annexin V assay, which clearly exhibited significantly increased early and late apoptosis phases both at 24 and 48 h. Both the caspases-8 and-9 level was found to be increased by the introduction of ST to HepG2 cells significantly (p\<0.05). Moreover the ST extract was able to arrest the cell cycle check point at G2/M phase. A significantly increasing pattern of hypodiploid phases of cells also been observed, which confirm the apoptosis induction again. Collectively, results presented in this study demonstrated that the ST, which is used as a euphoritic substance of abuse also, has significant level of toxicity in human cells. Moreover the mode of cell death was found to be though programmed cell death which is closely associated with cell cycle arrest.

Key words: Hepatotoxicity, In vitro models, Saudi Arabia, Smokeless tobacco, Substance Absue Research Centre, Shammah.

}, keywords = {Hepatotoxicity, In vitro models, Saudi Arabia, Shammah., Smokeless tobacco, Substance Absue Research Centre}, author = {Siddig Ibrahim Abdelwahab and Syam Mohan, and Manal Moahmed Elhassan Taha and Rashad Bin Mohammed Alsanosy and Hamed Karimian} } @article {60, title = {Assessment of Cytotoxicity of Smokeless Tobacco (Shammah) In Hepg2 and WRL68 Cells Line}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Jul-Aug 2015}, pages = {242-248}, type = {Original Article}, chapter = {242}, abstract = {

Shammah is a traditional form of chewing tobacco [Smokeless tobacco, (ST)] that is commonly used in the Middle east specially Saudi Arabia (KSA), Yemen and Sudan. The cytotoxicity of Sudanese and Yemenis ST hexane and methanol extracts was evaluated using MTT assay. Annexin-V assay has been used to detect the induction of apoptosis. Luminescence based assay also been conducted to check the level of caspases enzyme. The involvement of cell cycle check point arrest has been performed using flow cytometry analysis. The current study found that ST has the capacity to induce cell toxicity in human liver cells. The inhibitory capacity of ST in HepG2 and WRL 68 has been found to be 151 \± 2.5 and 305 \± 11.5 \μg/ml for 24 h. An early apoptosis induction in HepG2 cells was observed by annexin V assay, which clearly exhibited significantly increased early and late apoptosis phases both at 24 and 48 h. Both the caspases-8 and-9 level was found to be increased by the introduction of ST to HepG2 cells significantly (p\<0.05). Moreover the ST extract was able to arrest the cell cycle check point at G2/M phase. A significantly increasing pattern of hypodiploid phases of cells also been observed, which confirm the apoptosis induction again. Collectively, results presented in this study demonstrated that the ST, which is used as a euphoritic substance of abuse also, has significant level of toxicity in human cells. Moreover the mode of cell death was found to be though programmed cell death which is closely associated with cell cycle arrest

}, keywords = {Hepatotoxicity, In vitro models, Saudi Arabia, Shammah, Smokeless tobacco, Substance Absue Research Centre}, doi = {10.5530/pj.2015.4.6}, author = {Siddig Ibrahim Abdelwahab and Rashad Bin Mohammed Alsanosy}, editor = {Syam Mohan and Manal Moahmed Elhassan Taha} } @article {82, title = {Cytotoxicity Study of Ethanol Extract of the Leaves of Asam Kandis (Garcinia cowa Roxb.) on T47D Breast Cancer Cell line}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Nov-Dec 2015}, pages = {369-371}, type = {Original Article}, chapter = {369}, abstract = {

Objective: To investigate the cytotoxic effect of ethanolic extract of the leaves of asam kandis (Garcinia cowa Roxb.) against T47D breast cancer cells. Methods: The cytotoxicity of ethanol extract was carried out by measuring the activity of mitochondrial dehydrogenase in living cells that have ability to convert dissolved MTT pale yellow to purple formazan product. The extract was added at various concentrations (0.1, 1, 10 and 100 \μg/mL). The level of cytotoxicity was determined by calculating the IC50 value that was based on the percentage of the cell death after 24 hours treatment with the extract. Cell morphological changes were observed by using inverted microscope. Results: The IC50 value showed that ethanol extract of leaves of asam kandis could resist T47D breast cancer cells with IC50 6.13 \± 3.51 \μg/mL. The statistic results proved that ethanol extract of the leaves of asam kandis could inhibit the growth of T47D breast cancer cells significantly at concentrations of 10 \μg/mL and 100 \μg/mL. Conclusion: The results suggest that ethanol extract of the leaves of asam kandis was potential source of herbal medicine for cancer-related ailments.

}, keywords = {Asam kandis, Beast cancer, Cytotoxicity, Garcinia cowa Roxb, MTT Assay, T47D.}, doi = {10.5530/pj.2015.6.9}, author = {Fatma Sri Wahyuni and Dini Hara Triastuti and Helmi Arifin} } @article {46, title = {Effectiveness of Sidr Honey on the prevention of ethanol-induced gatroulcerogenesis: role of antioxidant and antiapoptotic mechanism}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {157-164}, type = {Original Article}, chapter = {157}, abstract = {

Background: Sider (Ziziphus spina-christi (L.) Desf.) Honey has been used for the treatment of gastrointestinal disorders including peptic ulcer. Aim of the study: The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. Materials and methods: Experimental animals were orally treated with sidr honey (100, 250 and 500 mg/kg, respectively) or omeprazole and subsequently exposed to 95\% ethanol (5 mL/Kg, orally) to induce acute gastroulcerogenesis. Effectiveness of sidr honey was evaluated using ulcer index, pH of gastric juice, mucus content, morphological analyses, glutathione assay and malondialdehyde level. The anti-apoptotic role of sidr honey was studied using immunohistochemical staining of gastric tissues using monoclonal antibodies of Bax pathway. Results: Dose-response studies in ethanol-induced ulcer indicate that sidr honey significantly blocks gastric lesions at lower dose (100 mg/kg). Lipid peroxidation and glutathione depletion were significantly inhibited by sidr honey. Sidr honey modulated the immuno-expression of mitochondrial associated protein (Bax). Conclusion: Thus, sider honey plays a considerable role in gastro protection by acting as a potent antioxidant and antiapoptotic agent. Future study is required to explore its potential clinical usage.

}, doi = {10.5530/pj.2015.3.3}, author = {Manal Mohamed Elhassan Taha and Siddig Ibrahim Abdelwahab and Rashad Elsanousi and Bassem Y. Sheikh and Mahmood Ameen Abdulla and Saif Eldeen Babiker and Husham Elraih and Eldaw Mohamed} } @article {1475, title = {Effectiveness of Sidr Honey on the prevention of ethanol-induced gatroulcerogenesis: role of antioxidant and antiapoptotic mechanism}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {13th Feb, 2015}, pages = {157-164}, type = {Original Article}, chapter = {157}, abstract = {

Background: Sider (Ziziphus spina-christi (L.) Desf.) Honey has been used for the treatment of gastrointestinal disorders including peptic ulcer. Aim of the study: The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. The mechanism of the antiulcer effect of sider honey was studied placing emphasis on its role to block oxidative damage and apoptosis during ethanol-induced gastric ulceration in rats. Materials and methods: Experimental animals were orally treated with sidr honey (100, 250 and 500 mg/kg, respectively) or omeprazole and subsequently exposed to 95\%ethanol (5 mL/Kg, orally) to induce acute gastroulcerogenesis. Effectiveness of sidr honey was evaluated using ulcer index, pH of gastric juice, mucus content, morphological analyses, glutathione assay and malondialdehyde level. The anti-apoptotic role of sidr honey was studied using immunohistochemical staining of gastric tissues using monoclonal antibodies of Bax pathway. Results: Dose-response studies in ethanol-induced ulcer indicate that sidr honey significantly blocks gastric lesions at lower dose (100 mg/kg). Lipid peroxidation and glutathione depletion were significantly inhibited by sidr honey. Sidr honey modulated the immuno-expression of mitochondrial associated protein (Bax). Conclusion: Thus, sider honey plays a considerable role in gastro protection by acting as a potent antioxidant and antiapoptotic agent. Future study is required to explore its potential clinical usage.

Key words: Antiapoptotic Mechanism, Antioxidant Agents, Gastro protection, Monofloral Nectar, Sidr Honey.

}, keywords = {Antiapoptotic Mechanism, antioxidant agents, Gastro protection, monofloral nectar, Sidr Honey.}, author = {Manal Mohamed Elhassan Taha and Siddig Ibrahim Abdelwahab and Rashad Elsanousi and Bassem Y. Sheikh and Mahmood Ameen Abdulla and Saif Eldeen Babiker and Husham Elraih and Eldaw Mohamed} } @article {32, title = {Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {32-36}, type = {Original Article}, chapter = {32}, abstract = {

Introduction: Plectranthus amboinicus (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. Methods: The present study focused on the use of essential oil obtained from the leaves of Plectranthusamboinicusto test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H2O2 induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). Results: Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 \± 0.01 and 87 \± 0.01 \μg/mL respectively. At 200 \μg/mL essential oil protected against 75\% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. Conclusion: Overall, the results showed that essential oil of P. amboinicus is a potent bioactive substance and it could be used in herbal medicine preparations.

}, keywords = {Antigenotoxicity, Cytotoxicity, Essential oil, RT- PCR., Zymogram}, doi = {10.5530/pj.2015.7.3}, author = {Ramaraj Thirugnanasampandan and Gunasekar Ramya and Madhusudhanan Gogulramnath and Rajarajeswaran Jayakumar and M.S. Kanthimathi} } @article {1458, title = {Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil.}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {27th Nov, 2014}, pages = {32-36}, type = {Original Article}, chapter = {32}, abstract = {

Introduction:Plectranthus amboinicus (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. Methods: The present study focused on the use of essential oil obtained from the leaves of Plectranthus amboinicus to test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H2O2 induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). Results: Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 \± 0.01 and 87 \± 0.01\μg/mL respectively. At 200 \μg/mL essential oil protected against 75\% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. Conclusion: Overall, the results showed that essential oil of P. amboinicus is a potent bioactive substance and it could be used in herbal medicine preparations.
Key words: Essential oil , Cytotoxicity , Antigenotoxicity, Zymogram, RT- PCR.

}, keywords = {Antigenotoxicity, Cytotoxicity, Essential oil, RT- PCR, Zymogram}, author = {Ramaraj Thirugnanasampandan and Gunasekar Ramya and Madhusudhanan Gogulramnath and Rajarajeswaran Jayakumar and M.S. Kanthimathi} } @article {1477, title = {Evaluation of Phytoconstituents of Bryonopsis laciniosa fruit by UV-Visible Spectroscopy and FTIR analysis}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {09th Mar, 2015}, pages = {165-170}, type = {Original Article}, chapter = {165}, abstract = {

Objectives: To Investigate the phytochemicals present in Bryonopsis laciniosa fruit. Methodology: Qualitative, Quantitative screening, Compound Identification by UV-Visible method and identification of functional group of the active chemical components were followed by standard procedures. Result: The results showed the presence of phytonutrients like reducing sugar, terpenoids, triterpenoids, aminoacids, anthroquinone, polyphenols, glycosides, anthocyanins, tannins, coumarins, emodins, saponins, total alkaloids, total flavonoids, lignin and serpentine. These substances may be responsible for the health related properties of the plant which are based on antioxidant,anticancer, antipyretic, antiaphoretic, antidiabetic, anti-inflammation, antiheamatisum, antimicrobial and antiviral activity. Conclusion: This study supports the popular use of Bryonopsis laciniosa fruit in preparation of various pharmaceutical formulations for human welfare.

Key words: Bryonia laciniosa, FTIR, Phytochemical screening, Phytonutrients, UV-Vis.

}, keywords = {Bryonia laciniosa, FTIR, Phytochemical screening, Phytonutrients, UV-Vis.}, author = {Ramya Bashyam and Malarvili Thekkumalai and Velavan Sivanandham} } @article {48, title = {Evaluation of Phytoconstituents of Bryonopsis laciniosa fruit by UV-Visible Spectroscopy and FTIR analysis}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {165-170}, type = {Original Article}, chapter = {165}, abstract = {

Objectives: To Investigate the phytochemicals present in Bryonopsis laciniosa fruit. Methodology: Qualitative, Quantitative screening, Compound Identification by UV-Visible method and identification of functional group of the active chemical components were followed by standard procedures. Result: The results showed the presence of phytonutrients like reducing sugar, terpenoids, triterpenoids, aminoacids, anthroquinone, polyphenols, glycosides, anthocyanins, tannins, coumarins, emodins, saponins, total alkaloids, total flavonoids, lignin and serpentine. These substances may be responsible for the health related properties of the plant which are based on antioxidant, anticancer, antipyretic, antiaphoretic, antidiabetic, anti-inflammation, antiheamatisum, antimicrobial and antiviral activity. Conclusion: This study supports the popular use of Bryonopsis laciniosa fruit in preparation of various pharmaceutical formulations for human welfare.

}, keywords = {Bryonia laciniosa, FTIR, Phytochemical screening, Phytonutrients, UV-Vis}, doi = {10.5530/pj.2015.3.4}, author = {Ramya Bashyam and Malarvili Thekkumalai and Velavan Sivanandham} } @article {51, title = {Flavonoids from Eupatorium illitum and Their Antiproliferative Activities}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {178-181}, type = {Original Article}, chapter = {178}, abstract = {

Objective: To isolate the chemical constituents of the aerial parts from Eupatorium illitum, elucidate their structures and evaluate their antiproliferative activity on human cancer cell lines. Materials and Methods: The ethanolic extract of Eupatorium illitum afforded five compounds, which were characterized using spectroscopic techniques and by comparison with data from the literature. Antiproliferative activities of selected isolates were evaluated. Results: The flavonoids Kumatakenin (1), Ermanin (2), 7-methoxy-aromadendrin (3) and Naringenin (4), together with 4-hydroxybenzoic acid (5) were isolated. Compounds 1, 2, 4 and 5 were evaluated for their antiproliferative activity on the human cancer cell lines A549 (lung), HBL-100 (breast), HeLa (cervix), SW1573 (lung), and T-47D (breast) presenting a wide range of bioactivities. In general, best results were observed for 5. Conclusion: Compounds 1-5 are reported for first time from Eupatorium illitum. Isolated phytochemicals show moderate to low antiproliferative activities when evaluated on the aforementioned human cancer cell lines.

}, keywords = {4-Hydroxybenzoic acid, 7-Methoxy-aromadendrin, Ermanin, Eupatorium illitum, Kumatakenin, Naringenin.}, doi = {10.5530/pj.2015.3.6}, author = {Qu{\'\i}rico A Castillo and Jorge Triana and Jos{\'e} L Eiroa and Jos{\'e} M Padr{\'o}n and Gabriela B Plata and Ernesto V Abel-Santos and Luis A. B{\'a}ez and Diana C Rodr{\'\i}guez and Marco A Jim{\'e}nez and Mar{\'\i}a F P{\'e}rez-Pujols} } @article {1478, title = {Flavonoids from Eupatorium illitum and Their Antiproliferative Activities}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {09th Mar, 2015}, pages = {178-181}, type = {Original Article}, chapter = {178}, abstract = {

Objective: To isolate the chemical constituents of the aerial parts from Eupatorium illitum, elucidate their structures and evaluate their antiproliferative activity on human cancer cell lines. Materials and Methods: The ethanolic extract of Eupatorium illitum afforded five compounds, which were characterized using spectroscopic techniques and by comparison with data from the literature. Antiproliferative activities of selected isolates were evaluated. Results: The flavonoids Kumatakenin (1), Ermanin (2), 7-methoxy-aromadendrin (3) and Naringenin (4), together with 4-hydroxybenzoic acid (5) were isolated. Compounds 1, 2, 4 and 5 were evaluated for their antiproliferative activity on the human cancer cell lines A549 (lung), HBL-100 (breast), HeLa (cervix), SW1573 (lung), and T-47D (breast) presenting a wide range of bioactivities. In general, best results were observed for 5. Conclusion: Compounds 1-5 are reported for first time from Eupatorium illitum. Isolated phytochemicals show moderate to low antiproliferative activities when evaluated on the aforementioned human cancer cell lines.

Key words: Eupatorium illitum, Ermanin, 4-Hydroxybenzoic acid, Kumatakenin, 7-Methoxy-aromadendrin, Naringenin.

}, keywords = {4-Hydroxybenzoic acid, 7-Methoxy-aromadendrin, Ermanin, Eupatorium illitum, Kumatakenin, Naringenin.}, author = {Qu{\'\i}rico A Castillo and Jorge Triana and Jos{\'e} L Eiroa and Jos{\'e} M Padr{\'o}n and Gabriela B Plata and Ernesto V Abel-Santos and Luis A. B{\'a}ez and Diana C Rodr{\'\i}guez and Marco A Jim{\'e}nez and Mar{\'\i}a F P{\'e}rez-Pujols} } @article {1459, title = {Immunomodulatory Activity of Atalantia monophylla DC. roots}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {27th Nov, 2014}, pages = {37-43}, type = {Original Article}, chapter = {37}, abstract = {

Objective: The objective of the present study was to evaluate the immunomodulatory activity of the roots of Atalantia monophylla. In the present study Pet. Ether, Chloroform and Methanolic fractions of the ethanolic extract of the roots of Atalantia monophylla, were administered orally, in the doses of 10 mg/kg and 30 mg/kg, to evaluate the immunomodulatory activity. Materials and Methods: The Methanolic fraction showed most significant effect when compared with control group, in the dose of 30 mg/kg, in the E.Coli induced abdominal sepsis and Carbon Clearence Test as models for non-specific immune response. In the models of the Specific immune response, cell mediated immune response to SRBC - delayed type of hypersensitivity (DTH) the methanolic fraction in the dose 30 mg/kg, when compared with control group, showed most significant effect on decrease in footpad edema after treatment. Results: Humoral immune response was assessed by Sheep erythrocyte agglutination test, in which the Methanolic fraction of Atalantia monophylla in the dose of 30 mg/kg showed most significant (p\<0.05) increase in antibody titer after treatment when compared with control group. Conclusion: The present investigation reports that the Methanolic fraction of the ethanolic extract of the roots of Atalantia monophylla, in the dose of 30 mg/kg showed most significant immunomodulatory activity.

Key words:Atalantia monophylla, Immunomodulatory, Phagocytosis, Cell-mediated immune response, Humoral immune response.

}, keywords = {Atalantia monophylla, Cell-mediated immune response, Humoral immune response., Immunomodulatory, Phagocytosis}, author = {V. R. Patil and V. M. Thakare and V.S. Joshi} } @article {34, title = {Immunomodulatory Activity of Atalantia monophylla DC. roots}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {37-43}, type = {Original Article}, chapter = {37}, abstract = {

Objective: The objective of the present study was to evaluate the immunomodulatory activity of the roots of Atalantia monophylla. In the present study Pet. Ether, Chloroform and Methanolic fractions of the ethanolic extract of the roots of Atalantia monophylla, were administered orally, in the doses of 10 mg/kg and 30 mg/kg, to evaluate the immunomodulatory activity. Materials and Methods: The Methanolic fraction showed most significant effect when compared with control group, in the dose of 30 mg/kg, in the E.Coli induced abdominal sepsis and Carbon Clearence Test as models for non-specific immune response. In the models of the Specific immune response, cell mediated immune response to SRBC-delayed type of hypersensitivity (DTH) the methanolic fraction in the dose 30 mg/kg, when compared with control group, showed most significant effect on decrease in footpad edema after treatment. Results: Humoral immune response was assessed by Sheep erythrocyte agglutination test, in which the Methanolic fraction of Atalantia monophylla in the dose of 30 mg/kg showed most significant (p\<0.05) increase in antibody titer after treatment when compared with control group. Conclusion: The present investigation reports that the Methanolic fraction of the ethanolic extract of the roots of Atalantia monophylla, in the dose of 30 mg/kg showed most significant immunomodulatory activity.

}, keywords = {Atalantia monophylla, Cell-mediated immune response, Humoral immune response, Immunomodulatory, Phagocytosis}, doi = {10.5530/pj.2015.7.4}, author = {VR Patil and VM Thakare and VS Joshi} } @article {68, title = {In vitro Acetyl Cholinesterase Inhibitory assay of Acacia catechu Willd Ethanolic Seed Extract}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {280-282}, type = {Original Article}, chapter = {280}, abstract = {

Aim \& objective: The aim of this study was to evaluate acetyl cholinesterase inhibitory activity of Acacia catechu ethanolic seed extract to introduce a new source for management of Alzheimer\’s disease. Background: Alzheimer\’s disease is a complex, multifactorial, progressive, neurodegenerative disease primarily affecting the elderly population and is estimated to account for 50\–60\% of dementia cases in persons over 65 years of age. It is likely that the inhibition of acetyl cholinesterase by Acacia catechu ethanolic seed extract that is rich in flavonoids and antioxidants may aid in the protection of neurodegenerative disorders and ultimately Alzheimer\’s disease. Methods: Anti cholinesterase activity is determined by adopting In vitro standard protocol. Results: According to the obtained results, the inhibitory activity (IC50 values, \μg /ml) of extracts was 204.38 \± 2.54 \μg/ ml. Conclusion: The results indicated and confirmed the traditional use of Acacia catechu ethanolic seed extract for management of central nervous system disorders. It showed the moderate activity in inhibition of acetyl cholinesterase at various concentrations. However, further investigations on identification of active components in the extracts are needed.

}, keywords = {Acacia catechu seed, Acetyl cholinesterase inhibitor, Alzheimer{\textquoteright}s disease, Neurodegenerative, Spectrophotometric analysis.}, doi = {10.5530/pj.2015.5.5}, author = {Lakshmi Thangavelu and Rajendran Ramasamy} } @article {36, title = {Pharmacognostic Evaluation of Indigenous Medicinal Plant Kedrostis foetidissima (Jacq.) Cogn}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {52-57}, type = {Original Article}, chapter = {52}, abstract = {

Introduction: Ingeneral, members of Cucurbitaceae are well exploited for their medicinal, economic and culinary values, however few of them are less exploited. The present study deals with pharamcognostical evaluation of one such plant namely Kedrostis foetidissima (Jacq.) Cogn.called as Appakovai in Tamil. Methods: Pharmacognostic evaluations were carried out by organoleptic evaluation, anatomical studies and powder microscopy of leaves, roots and root tubers. Results: Organoleptic evaluation revealed that the characteristic white tubers, as storage organs, leaves exhibited a foetidodour when crushed. Anatomy of leaves showed lithocysts and anomocytic stomata, root showed the presence of fissured periderm and cleaved vascular bundles and that of root tubers showed 3 or 4 exarch xylem. Powder microscopy of root tubers showed narrow and wide fibers; long, narrow and drum shaped vessels and scattered sclereids. Conclusion: The present Pharmacognostic and Powder microscopic studiesreveals that, the characteristic features of this plantparts resembles, the other members of cucurbitaceae.

}, keywords = {Kedrostis foetidissima, Pharmacognosy, Powder microscopy.}, doi = {10.5530/pj.2015.7.6}, author = {Kavitha R and Chittibabu CV and Subha TS} } @article {1460, title = {Pharmacognostic Evaluation of Indigenous Medicinal Plant Kedrostis foetidissima (Jacq.) Cogn.}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {27th Nov, 2014}, pages = {52-57}, type = {Original Article}, chapter = {52}, abstract = {

Introduction: Ingeneral, members of Cucurbitaceae are well exploited for their medicinal, economic and culinary values,however few of them are less exploited.The present study deals with pharamcognostical evaluation ofone such plant namely Kedrostis foetidissima (Jacq.) Cogn.called as Appakovai in Tamil. Methods: Pharmacognostic evaluationswere carried out by organoleptic evaluation, anatomical studies and powder microscopy of leaves, roots and root tubers. Results: Organoleptic evaluation revealed that the characteristic white tubers, as storage organs, leaves exhibited a foetid odour when crushed. Anatomy of leaves showed lithocysts and anomocytic stomata,root showed the presence of fissured periderm and cleaved vascular bundlesand that of root tubers showed 3 or 4 exarch xylem. Powder microscopy of root tubers showed narrow and wide fibers; long, narrow and drum shaped vessels and scattered sclereids. Conclusion: The present Pharmacognostic and Powder microscopic studiesreveals that, the characteristic features of this plantparts resembles, the other members of cucurbitaceae.

Key words:Kedrostis foetidissima, Pharmacognosy, Powder microscopy.

}, keywords = {Kedrostis foetidissima, Pharmacognosy, Powder microscopy.}, author = {Kavitha R and Chittibabu CV and Subha TS} } @article {79, title = {Preliminary Phytochemical analysis and In vitro Antioxidant, FTIR Spectroscopy, Anti-diabetic activity of Acacia catechu ethanolic seed extract}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Nov-Dec 2015}, pages = {356-362}, type = {Original Article}, chapter = {356}, abstract = {

Objective: To evaluate the preliminary phytochemical analysis and in vitro antioxidant activity, anti-diabetic effect of ethanolic seed extract of Acacia catechu against the alpha amylase and alpha glucosidase digestive enzymes in the pancreas and small intestine. Methods: Preliminary phytochemical analysis was done by adopting the method of Evans. Antioxidant assay is performed by DPPH, ABTS and FRAP assay, Anti diabetic activity was determined by modified method of miller, the extract at different concentrations was tested for mammalian alpha amylase and alpha glucosidase enzyme inhibitory assay under the controlled experimental conditions and subjected to determination of absorbance. Results: The present study reveals the presence of few secondary metabolites and the extract exhibits potent Antioxidant activity and a concentration dependent inhibition of Alpha amylase and Alpha glucosidase. Conclusion: From the present study it can be concluded that ethanolic seed extract of Acacia catechu possessed marked in vitro antioxidant and anti-diabetic effect. The effect was plausibly due to the presence of phenolic contents of Acacia catechu

}, keywords = {Acacia catechu seed, Alpha glucosidase, Alpha-amylase, Antidiabetic, Antioxidant, FTIR Spectroscopy, Phytochemical}, doi = {10.5530/pj.2015.6.7}, author = {Thangavelu Lakshmi and Rajendran Ramasamy and Rathinam Thirumalaikumaran} } @article {1499, title = {Antioxidant and Anticancer Activities of Ocimum basilicum L. cv. Dark Opal (Lamiaceae)}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {3rd Sept, 2014}, pages = {S}, type = {Original Article}, chapter = {32}, abstract = {

Background: Plants used in folk and traditional medicines have been accepted as therapeutic drug development in modern medicine.Although manystudies have been focused on Lamiaceae family,few studies on medical effects of purple basil have been performed until now. Objective: Ocimum basilicum cv. dark opal was chosen for this study as it has been used in Persian traditional medicine and many Iranian dishes. It was considered important to determine the cytotoxicity effect andthe reductive capacity of the purple basil oils and extracts, as this may indicate their potential as antioxidants. Materials and Methods: The reducing power activity of both essential oils of the leaves (before flowering) and the seeds and also methanolic extracts of roots and aerial parts (stem-leaf) (collected prior flowering), and flowers were determined by utilizing of FRAP. Also the MTT assay has been used in order to consider in vitro cytotoxicity of essential oils and extracts on cancerous cell line (MCF-7). Moreover, the extracts were analyzed by HPLC to comprise the rate of some phenolic compounds. Results: The purple basil extracts have more powerful antioxidant activity than the essential oils. MCF-7 revealed to have a meaningful cell death when compared with controls, and the oils were found to be more effective than the extracts. Also the phytochemical analysis of the extracts has led to the identification of 3 phenolic compounds (Rosmarinic acid, p-Coumaric acid and Ferulic acid). Conclusion: Our study tends to validate the traditional use of this medicinal herb as complementary and alternative medicine.

Key Words: purple basil, antioxidant, MCF-7, HPLC.

}, keywords = {3-(4, 4 diphenyltetrazolium bromide assay, 5-dimethylthiazol-2yl)-2, A549 Cell Line, Cytotoxic, Digera muricata, HeLa cell line.}, author = {Mohammadi M and Majd A and Nejadsattari T and Hashemi M} } @article {1510, title = {Evaluation of Wound Healing Potential of Some Indian Herbal Extracts and it{\textquoteright}s Formulation in Acne Vulgaris}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {2nd July 2014}, pages = {37-46}, type = {Original Article}, abstract = {

Objective:Butea monosperma, Barleria prionitis, Casuarina equisetifolia, Dalbergia sissoo, and Lagenaria siceraria are reported to possess anti-acne, anti-infl ammatory, anti-ulcer, and wound healing activity. The present work is aimed at evaluating the wound healing potential of these plant materials in acne vulgaris. Methodology: Individual gel formulations containing extracts of the above mentioned drugs and their polyherbal gels were evaluated by excision and incision wound model (in vivo) in Sprague Dawley rats. Results: The individual gel formulations showed signifi cant reduction in wound size when compared with the untreated group. The rates of wound closure after the application of the gels were compared with the untreated wounds. The polyherbal formulation containing all the extracts was found to be more benefi cial when compared to remaining treated groups. Healing under scab and formation of normal epithelial cells were better than other individual formulations. As well as vascular changes, cellular infi ltration, and necrosis were found less. Conclusion: From the results, it may be concluded that the plants are endowed with signifi cant wound healing activity, thereby justifying its traditional medicinal use in acne vulgaris as a separate entity and in combination. Chemical components such as tannins, fl avonoids, saponins, and alkaloids present in the extracts can be responsible for the foresaid activity.

Key words: Acne, excision model, incision model, wound healing.

}, keywords = {Acne, excision model, incision model, Wound Healing}, author = {S. A. Thube and M. J. Patil} } @article {1524, title = {Pharmacognostic evaluation and chrysazin quantitation of Xyris indica flowering heads}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {26th May 2014}, pages = {16-22}, type = {Research Article}, abstract = {

Objectives: The present study aimed to establish quality specification of Xyris indica L. flowering heads. The pharmacognostic parameters were investigated. Chrysazin contents were analyzed by TLC image analysis using ImageJ software compared to TLC-densitometry. Methods: X. indica flowering heads from 15 different sources in Thailand were collected. Morphological and physicochemical parameters were characterized. Chrysazin was successively extracted and determined by TLC image analysis using ImageJ software and TLC-densitometry. Results: Macroscopic study was illustrated as whole plant drawing. The microscopic study showed fragment of corolla, seeds, pollen grain and staminode. The pharmacognostic parameters revealed that the loss on drying, total ash, acid-insoluble ash and water content should be not more than 6.90, 2.50, 0.41, and 11.12 of \% dry weight respectively while water and ethanol-soluble extractive values should be not less than 6.59 and 4.03 of \% dry weight respectively. TLC fingerprint revealed clearly chrysazin yellow fluorescent band at 365 nm. Chrysazin quantitation by TLC image analysis and TLC densitometry were developed and validated. Chrysazin content was 0.022 \± 0.001 \% dry weight by both methods. There was no statistically significantly difference between these methods. Conclusion: This study provided pharmacognostic specification and chrysazin content of X. indica flowering heads that can be used for basic quality control and standardization of plant material. TLC image analysis using ImageJ software showed reliable and convenient for analysis of chrysazin content in this crude drug.

Key words: Xyris indica, Pharmacognostic specification, Chrysazin, Quantitative analysis, Antimicrobial activities

}, keywords = {Antimicrobial activities, Chrysazin, Pharmacognostic specification, Quantitative analysis, Xyris indica}, author = {Chuanchom Khuniad and Worathat Thitikornpong and Chanida Palanuvej and Nijsiri Ruangrungsi} }