@article {2160, title = {Comics in Health as Alternative Therapy: An Information and Therapeutic Resource for Post-COVID-19 Patients in Ayacucho, Peru}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1047-1051}, type = {Original Article}, chapter = {1047}, abstract = {

The aim of this research was to determine the utility of comics, as an informative and therapeutic resource, in post-COVID-19 patients, in the area of influence of the Camisea project, which is delimited to cities such as Huanta, Tambo, and Cangallo, located in Ayacucho, Peru. The methodology included an observational design, with in and out surveys being conducted during the study. The first survey sought to discover the level of approach of post-COVID-19 patients with the use of comics, while the second examined the effectiveness and usefulness after being exposed to a brochure of four comics (Figure 1) that combined humor and information related to the recovery procedures for COVID-19. The research showed that the usefulness of comics as an informative and therapeutic resource in post-COVID-19 patients in the city of Ayacucho is very significant. This was confirmed by 96\% of those surveyed, since they pointed out that the comics contributed to virus infection recovery and prevention.

}, doi = {10.5530/pj.2023.15.192}, author = {Carlos Rodrigo Infante-Yupanqui and Roberta Garc{\'\i}a-de-la-Cruz and Yanibel Hurtado-Vargas and Rosa Mar{\'\i}a Vega-Guevara and Primy Agripina Alca-Chamba and Rod Rosberg Bendez{\'u}-Perez and Pavel Pool Puclla-Pareja} } @article {2066, title = {Computational Evaluation of the Potential of Salicylate Compound from Syzygium aromaticum on Carbonic Anhydrase I as a Gastric Acid Stimulant}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {489-493}, type = {Original Article }, chapter = {489}, abstract = {

This article explores the potential of the salicylate compound (Syzygium Aromaticum) as a stimulant for Carbonic Anhydrase I in gastric acid secretion, using a computational approach. The research methods include molecular modeling with Pymol and Pyrex, determination of compound structure and interactions with Protein Plus, and examination of physicochemical properties using the Lipinski Rule. The results show that the Binding Affinity of salicylate with Carbonic Anhydrase I ranges from -7.3 to -6.5, with RMSD values of 0, 2.102, and 2.212, indicating good modeling quality. The interaction between salicylate and Carbonic Anhydrase I is also supported by the findings from Protein Plus. Furthermore, the salicylate compound complies with the Lipinski Rule, with a molecular weight of 137, 1 hydrogen bond donor, 3 hydrogen bond acceptors, a log P value of 0.34, and a molar reactivity of 34.16. This study highlights the prospect of salicylate as a potential modulator of Carbonic Anhydrase I.

}, keywords = {Carbonic Anhydrase I, Gastric Acid Stimulant, Molecular docking, Salicylate, Syzygium Aromaticum.}, doi = {10.5530/pj.2023.15.107}, author = {Rahadian Zainul and Rismi Verawati and Rauza Sukma Rita and Fadhli Ranuharja and Musa Ghufron and Agariadne Dwinggo Samala and Herland Satriawan and Muhammad Raffi Ghifari and Devi Purnamasari and Riso Sari Mandeli and Amalia Putri Lubis and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2105, title = {Hepatitis E Inhibited by Rosmarinic Acid Extract from Clove Plant (Syzygium Aromaricum) through Computational Analysis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {518-523}, type = {Original Article }, chapter = {518}, abstract = {

This study aims to evaluate the potential of Rosmarinic Acid as an inhibitor against Hepatitis E by interacting with the active site of the Tyrosine FYN protein. Computational approaches were employed to predict the molecular interactions between Rosmarinic Acid and Tyrosine FYN. The research methodology involved the use of software such as Pymol, Pyrex, Protein Plus, and the Lepinski Rule. Docking analysis was conducted using Pymol to obtain information about the binding energy between Rosmarinic Acid and Tyrosine FYN. The results of the analysis showed that Rosmarinic Acid exhibited a Binding Affinity of -8.3, -8, and -7.9, indicating a strong affinity towards the target protein. Additionally, Root Mean Square Deviation (RMSD) values of 0, 15.905, and 17.014 were used to assess the stability of the formed protein-ligand complex. Analysis using Protein Plus revealed interactions between Rosmarinic Acid and Tyrosine FYN. Furthermore, analysis using the Lepinski Rule to examine the physicochemical properties of Rosmarinic Acid indicated that the molecule had a mass of 360, 5 hydrogen bond donors, 8 hydrogen bond acceptors, a log P value of 1.76, and a molar reactivity of 89.8. These findings highlight the potential of Rosmarinic Acid as an inhibitor of Hepatitis E through its interaction with the Tyrosine FYN protein, providing a basis for the development of potential new therapies in the treatment of this disease.

}, keywords = {Hepatitis E, Molecular Docking., Rosmarinic acid, Syzygium aromaricum, Tyrosine FYN}, doi = {10.5530/pj.2023.15.112}, author = {Sunadi and Saddam Al Aziz and Fadhilah Fitri and Devni Prima Sari and Muhammad Raffi Ghifari and Rismi Verawati and Nita Yessirita and Oski Illiandri and Riso Sari Mandeli and Devi Purnamasari and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2175, title = {In silico ADME and Drug-likeness Evaluation of Phytochemicals from the Leaves of Tabernaemontana divaricata Linn.}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {December 2023}, pages = {1136-1142}, type = {Research Article}, chapter = {1136}, abstract = {

Introduction: Tabernaemontana divaricata is a traditional plant from the family of Apocynaceae, which has wider medicinal activities such brain tonic, anti-epileptic, anti-mania and anti-oxidant. The current predictive study was aimed to know pharmacokinetics and drug likeness of selected phytochemicals present in T.divaricata by using online tool Swiss-ADME. Methods: The air-dried leaves were pulverized and subjected to Soxhlet extraction and percolation using the solvents, namely, ethanol, hydroalcoholic solvent (50:50 and 70:30 ethanol: water) and water to obtain four different extracts. Aqueous extract was made through percolation. Subsequently, gas chromatography-mass spectrometry was used to analyze each extract further. All the bioactive compounds were subjected to in silico ADME and drug-likeness studies and the finalized compounds were undergone cell cytotoxicity activity. Results: All the four extracts have distinct physicochemical properties linked to the chemicals naturally present in large amounts in T. divaricata leaves. The compound 4,4,7a-Trimethylhexahydro-1-benzofuran-2(3H)- one and 2-(4-methylphenyl) indolizine having good drug likeness of 4.50 and 3.50 respectively and good lipophilicity which has the log P value of 2.51 and 3.73 appropriately. IC50 values of compounds were found to be 312.1 {\textpm} 0.2μg/ml for 4,4,7a-Trimethylhexahydro-1-benzofuran-2(3H)-one and 393.7 {\textpm} 0.2μg/ ml for 2-(4-methylphenyl) indolizine. Conclusion: Major bioactive chemicals were found in the aqueous extract and based on the calculated ADME parameters they are anticipated to serve as cytotoxic lead compounds. It is advocated that current predictive results should be authenticated by in vitro and in vivo toxicological and pharmacological assay.

}, keywords = {Apocyanceae, Cell cytotoxicity studies, GC-MS analysis, In silico study}, doi = {10.5530/pj.2023.15.207}, author = {Ayda Cherian and Velmurugan Vadivel} } @article {2104, title = {In Silico Study of Rhamnocitrin Extract from Clove Syzygium Aromaricum in Inhibiting Adenosine A1 Adenylate Cyclase Interaction}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {512-517}, type = {Original Article }, chapter = {512}, abstract = {

This study aims to analyze the potential of Rhamnocitrin, a compound found in clove extract (Syzygium aromaticum), as an inhibitor of Adenylate Cyclase through an in-silico approach. The research method involves the use of software such as Pymol, PyRx, Protein Plus, and Lipinski Rule for molecular interaction analysis and physicochemical characterization of Rhamnocitrin. The analysis results show that Rhamnocitrin has significant affinity towards Adenosine A1 with Binding Affinity values of -6.1, -5.8, and -5.7. RMSD analysis indicates good stability of the formed protein-ligand complexes, with RMSD values of 0, 3.129, and 3.696. Analysis using Protein Plus software reveals the interaction between Rhamnocitrin and Adenosine A1, while the lipinski analysis shows physicochemical characteristics of Rhamnocitrin that meet important criteria, such as a mass of 300, 3 hydrogen bond donors, 6 hydrogen bond acceptors, log P of 2.6, and molar reactivity of 77.27. These findings provide new insights into the development of potential therapies involving clove extract and Rhamnocitrin as inhibitors of Adenylate Cyclase, and further research is needed to validate their effectiveness and safety.

}, keywords = {Adenosine A1, Adenylate Cyclase inhibition, Molecular Docking., Rhamnocitrin, Syzygium aromaricum}, doi = {10.5530/pj.2023.15.111}, author = {Nita Yessirita and Rismi Verawati and Devi Purnamasari and Rollando Rollando and Riso Sari Mandeli and Muhammad Thoriq Albari and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2081, title = {In Silico Study on the Inhibition of Sitogluside from Clove Plant (Syzygium aromaticum) on Interleukin 2 in B and T Cell Proliferation}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {575-580}, type = {Research Article}, chapter = {575}, abstract = {

This research discusses an in-silico study of sitogluside found in the clove plant (Syzygium aromaticum) as a potential inhibitor of B and T cell proliferation through interaction with Interleukin-2. This study utilizes methods such as Swiss Target Prediction, Pymol, Pyrex, Protein Plus, and Lipinski{\textquoteright}s Rule to predict the biological activity and pharmacokinetic characteristics of sitogluside. From the docking simulation results, sitogluside exhibited strong interactions with interleukin-2 with RMSD values of 0, 1.637, and 2.299, and Binding Affinities of -5.7, -5.5, and -5.5, indicating its potential effectiveness as an inhibitor. In addition, sitogluside fulfills Lipinski{\textquoteright}s rule with a molecular mass of 520, 4 hydrogen bond donors and acceptors, a log P value of 2.3, and a molar reactivity of 133, indicating a high potential for good bioavailability in biological systems. These results suggest that sitogluside from the clove plant holds potential as a new therapy in inhibiting B and T cell proliferation, however further research is needed to validate these findings and explore its potential in clinical treatments.

}, keywords = {Cell Proliferation, Interleukin-2, Molecular docking, Sitogluside, Syzygium.}, doi = {10.5530/pj.2023.15.122}, author = {Linda Rosalina and Devi Purnamasari and Rismi Verawati and Okta Suryani and Muhammad Arya Ghifari and Amalia Putri Lubis and Rahadian Zainul and Riso Sari Mandeli and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2067, title = {In Silico Study on the Potential of Guaiacol Extract from Green Tea (Camellia sinensis) as a Stimulant for Carbanoic Anhydrase II in Renal Tubular Acidosis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {494-499}, type = {Original Article }, chapter = {494}, abstract = {

This study explores the potential of Guaiacol, a green tea extract from Camellia sinensis, as a stimulant in renal tubular acidosis through in-silico investigation on the Carbanoic Anhydrase II enzyme. Utilizing comprehensive computational tools including PyMOL, PyRx, Protein Plus, and the Lipinski{\textquoteright}s Rule of Five, a detailed examination of the molecular structure and its interactions with the target enzyme was conducted. The results from Protein Plus revealed interactions between Guaiacol and Carbanoic Anhydrase II. Quantitative parameters were determined with Binding Affinity values of -5, -4.7, and -4.5, along with RMSD values of 0, 0.956, and 1.412. The Lipinski{\textquoteright}s Rule of Five was employed to evaluate the compound{\textquoteright}s drug-like properties, with the findings indicating a molecular weight of 124, one hydrogen bond donor, two hydrogen bond acceptors, a log P of 1.4, and a molar reactivity of 34.65. Overall, these findings suggest that Guaiacol holds promising therapeutic potential in the treatment of renal tubular acidosis.

}, keywords = {Camellia sinensis., Carbanoic Anhydrase II, Guaiacol, Molecular docking, Renal Tubular Acidosis}, doi = {10.5530/pj.2023.15.108}, author = {Rahadian Zainul and Rismi Verawati and Agus Suprijono and Riso Sari Mandeli and Asri Peni Wulandari and Dony Novaliendry and Ritmaleni and Linda Rosalina and Muhammad Arya Ghifari and Amalia Putri Lubis and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2083, title = {Interaction of Cynaroside from Orthosiphon Aristatus Plant Extract on TNF Alpha as a Stimulant in Malaria and Asthma}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {581-586}, type = {Research Article}, chapter = {581}, abstract = {

This research aims to investigate the interaction between cynaroside, a natural compound found in Orthosiphon aristatus plant extract, with TNF Alpha as a stimulant in the context of malaria and asthma. The research method involved an in-silico approach using software such as Pymol, PyRx, Protein Plus, and the Lepinski Rule. The results of the study showed that cynaroside has a significant interaction with TNF Alpha, as indicated by high Binding Affinity values of -9.6, -9.3, and -9.2. Analysis using Protein Plus confirmed the interaction between cynaroside and TNF Alpha. Additionally, evaluation using the Lepinski Rule of Five revealed that cynaroside has physicochemical characteristics suitable as a potential drug compound, with a mass of 448, hydrogen bond donors of 7, hydrogen bond acceptors of 11, log p -0.401, and molar reactivity of 105.2. These findings provide a deeper understanding of the potential of cynaroside in regulating the immune response to malaria and asthma through its interaction with TNF Alpha. These results can serve as an important basis for further research in the development of more targeted and effective therapies for both of these diseases

}, keywords = {Asthma., Cynaroside, Malaria, Molecular docking, Orthosiphon aristatus, TNF Alpha}, doi = {10.5530/pj.2023.15.123}, author = {Rahadian Zainul and Rismi Verawati and Gemini Alam and Khoirun Nisyak and Trisna Kumala Sari and Muhammad Arya Ghifari and Ritbey Ruga and Putri Azhari and Romadhon and Himmatul Barroroh and Riso Sari Mandeli and Devi Purnamasari and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2063, title = {Interaction of Masilinic Acid from Clove Plant (Syzygium aromaticum) with CD81 Antigen in Inhibiting HIV Virus Regulation In Silico}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {484-488}, type = {Original Article }, chapter = {484}, abstract = {

This research explores the interaction of Masilinic Acid from the clove plant (Syzygium aromaticum) with the CD81 antigen to inhibit HIV virus regulation in silico. Using computational methods such as Pymol, Pyrex, and Protein Plus, we demonstrate that Masilinic Acid can significantly interact with the CD81 antigen. The obtained data shows binding affinities of -6.4, -6.2, and -5.7, and RMSD values of 0, 1.885, and 1.952. Further detailed interaction analysis with Protein Plus strengthens these findings, providing evidence of a strong interaction between Masilinic Acid and the CD81 antigen. This study also includes the testing of the Lepinski Rule of Five to assess the potential of Masilinic Acid as a drug candidate, with results indicating a mass of 472, three hydrogen bond donors, four hydrogen bond acceptors, a log P value of 6.2, and a molar reactivity of 134. These results indicate that Masilinic Acid has the potential as an inhibitor of the CD81-HIV interaction, which can be utilized as an effective antiviral strategy. Key words: Masilinic Acid, Clove plant, CD81 antigen, HIV virus, In silico.

}, keywords = {CD81 antigen, Clove plant, HIV virus, In Silico., Masilinic Acid}, doi = {10.5530/pj.2023.15.106}, author = {Rahadian Zainul and Elsa Yanuarti and Siti Amiroch and Muhammad Thoriq Albari and Rismi Verawati and Amalia Putri Lubis and AAA Murtadlo} } @article {2068, title = {Molecular Docking of Thaflavine from Camellia sinensis in Inhibiting B-Cell Lymphoma Through BCl2 Apoptosis Regulator: An In Silico Study}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {500-505}, type = {Original Article }, chapter = {500}, abstract = {

This study aims to analyze the potential of Thaflavine, a compound found in green tea (Camellia sinensis), as an inhibitor in inhibiting B-cell lymphoma through its interaction with the BCl2 apoptosis regulator using an in-silico approach. The research methodology involved the use of software tools such as PyMOL, PyRx, Protein Plus, and the Lepinski Rule. Through molecular docking analysis using PyMOL and PyRx, the findings of this study demonstrate significant interactions between Thaflavine and BCl2, with Binding Affinity values of -5.5, -4.6, and -4.6, and RMSD values of 0, 1.436, and 2.292. The analysis using Protein Plus indicates the presence of interactions between Thaflavine and BCl2. Additionally, the analysis using the Lepinski Rule of Five reveals that Thaflavine meets the criteria as a potential drug compound, with a molecular weight of 549, 9 hydrogen bond donors, 12 hydrogen bond acceptors, a log P value of -2.5, and a molar reactivity of 119.17. The findings of this study provide important contributions to the development of therapies for B-cell lymphoma through an in-silico approach. However, further research is needed for in vitro and in vivo validation.

}, keywords = {Apoptosis Regulator BCl2, B-cell Lymphoma, Camellia sinensis., In-Silico Thaflavine, Molecular docking}, doi = {10.5530/pj.2023.15.109}, author = {Rahadian Zainul and Rismi Verawati and Herland Satriawan and Teresa Liliana Wargasetia and Devi Purnamasari and Amalia Putri Lubis and Bahrun and Riso Sari Mandeli and Muhammad Thoriq Albari and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2119, title = {Phytochemical Screening and Antiinflammatory Activity of the Extract from the Leaves of Desmodium molliculum (Kunth) DC (Fabaceae) in Rats with Acute Inflammation}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {October 2023}, pages = {786-790}, type = {Original Article}, chapter = {786}, abstract = {

Inflammation and pain are the initial response mechanisms to environmental aggression on the human body. The traditional use of plants such as Desmodium Molliculum (Kunth) DC, among the Peruvian population for the treatment of inflammatory diseases, has occurred since ancient times. The objective of this research was to determine the presence of secondary metabolites and evaluate the antiinflammatory activity of Desmodium molliculum (EDM) leaves in rats with acute inflammation induced using carrageenan. The phytochemical profile was performed for the main secondary metabolites with biological activity. Subsequently, 25 rats were divided into 5 groups and treated as follows: Group I and II: Physiological Saline Solution (PSS) by oral administration. Group III: Sodium Diclofenac (25 mg/kg body weight) by intraperitoneal administration. Group IV and V: EDM at 250 mg/kg bw and 500 mg/kg bw by oral administration, respectively; 30 minutes after administration, acute inflammation was induced in Groups II, III, IV, and V using the subplantar edema technique with 1\% w/v carrageenan. The volume displaced by the hind paw was evaluated in all 5 groups using a digital plethysmometer every 60 minutes for 5 hours. The results were obtained from the displaced volume (Mean {\textpm} SD), with the most representative values obtained at 240 minutes, where EDM at 250 mg/kg (0.57 {\textpm} 0.07 ml) bw and 500 mg/kg bw (0.578 {\textpm} 0.051 ml) showed significant anti-inflammatory activity (ANOVA p\<0.05). We concluded that Desmodium Molliculum has anti-inflammatory activity at doses of 250 mg/kg bw and 500 mg/kg bw.

}, keywords = {Acute inflammation, Carrageenan, Desmodium, Dog{\textquoteright}s Paw, Edema Subplantar, Fabaceae.}, doi = {10.5530/pj.2023.15.153}, author = {Karyn Olascuaga-Castillo and Olga Castillo-Medina and Marleni Villacorta-Zavaleta and Dan Altamirano- Sarmiento and Elena Caceres-Andonaire and Maria Llontop and Fatima Malca and Sebastian Noe and Cyntia Blanco-Olano} } @article {2084, title = {Stimulation of Emodin from Aloe Vera on Protein Kinase PIM1 in the Central Nervous System Through In Silico Analysis}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {587-592}, type = {Research Article}, chapter = {587}, abstract = {

This study aims to investigate the potential of Emodin, a compound found in Aloe vera, as a stimulator of Protein Kinase PIM1 in the central nervous system using an in-silico approach. The research method involves the use of software such as Pymol, Pyrex, Protein Plus, and Lepinski Rule. Firstly, the protein structure of the target Protein Kinase PIM1 was obtained from a protein database and prepared using Pymol. Next, the molecular structure of Emodin was imported into Pyrex and subjected to geometry optimization. Docking analysis using Pymol was performed to predict the molecular interactions between Emodin and Protein Kinase PIM1. Additionally, RMSD analysis was conducted to evaluate the stability of the protein-ligand complex formed. The docking analysis results showed that Emodin exhibited significant Binding Affinity, with values of -8.4, -8.3, and -8.2, indicating a strong affinity between Emodin and Protein Kinase PIM1. The RMSD analysis indicated the stability of the protein-ligand complex, with RMSD values of 0, 1.101, and 1.122. Furthermore, analysis using Protein Plus revealed the presence of interactions between Emodin and Protein Kinase PIM1 through hydrogen bonding and hydrophobic contacts. The results of the Lepinski Rule analysis demonstrated that Emodin fulfilled several important criteria in drug design, including a molecular weight of 270, 3 hydrogen bond donors, 5 hydrogen bond acceptors, a log p value of 1.887220, and a molar reactivity of 64.480385. These findings indicate the potential of Emodin as a stimulator of Protein Kinase PIM1 in the central nervous system and provide an important foundation for the development of potential therapies for central nervous system-related disorders.

}, keywords = {Central Nervous System, Emodin, Molecular Docking., PIM1 Kinase, Stimulation}, doi = {10.5530/pj.2023.15.124}, author = {Rahadian Zainul and Rismi Verawati and Ritbey Ruga and Muhammad Arya Ghifari and Devi Purnamasari and Putri Azhari and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {2069, title = {Study on the Inhibition of Sinensetin Extract from Cat{\textquoteright}s Whiskers Plant (Orthosiphon aristatus) on ATP Binding Cassette Sub-Family G Member 2 in Uric Acid}, journal = {Pharmacognosy Journal}, volume = {15}, year = {2023}, month = {August 2023}, pages = {506-511}, type = {Original Article }, chapter = {506}, abstract = {

This study aims to investigate the potential of sinensetin, a compound found in the Cat{\textquoteright}s Whiskers plant (Orthosiphon aristatus), as an inhibitor in inhibiting uric acid through its interaction with ATP Binding Cassette Sub-Family G Member 2 (ABCG2). The in-silico approach was employed using software tools such as Pymol, PyRx, Protein Plus, and Lepinski Rule. The results of molecular docking analysis using PyRx demonstrated significant interactions between sinensetin and ABCG2, with Binding Affinity values of -6.8, -6.6, and -6.6, and RMSD values of 0, 0.785, and 1.379. The analysis using Protein Plus confirmed the interaction between sinensetin and ABCG2, supporting the previous docking findings. Furthermore, the evaluation of pharmacokinetic parameters using the Lepinski Rule of Five revealed that sinensetin meets the criteria as a potential drug compound, with a molecular weight of 372, no hydrogen bond donors, seven hydrogen bond acceptors, a log P value of 3.345, and a molar reactivity of 98.5. This research provides new insights into the development of uric acid therapy through an in-silico approach, and these findings can serve as a basis for further research involving in vitro and in vivo validation.

}, keywords = {ATP Binding Cassette, Molecular docking, Orthosiphon aristatus, Sinensetin, Uric Acid.}, doi = {10.5530/pj.2023.15.110}, author = {Anni Faridah and Rismi Verawati and Budhi Oktavia and Musa Ghufron and Devi Purnamasari and Muhammad Raffi Ghifari and Linda Rosalina and Putri Azhari and Rahadian Zainul and Viol Dhea Kharisma and Vikash Jakhmola and Maksim Rebezov and ANM Ansori} } @article {1930, title = {Left Atrial Myxoma Presented with an Obstructive Shock, Right Ventricle Dysfunction and Pulmonary Hypertension}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {917-920}, type = {Original Article }, chapter = {917-920}, abstract = {

Myxoma is a benign primary cardiac tumour, mostly located in the left atrial. A 43 years old woman was referred with a difficulty of breathing for 3 months. The patients also complained about weakness, swollen legs, enlarged abdomen, and blood-tinged cough. The patient appeared weak with blood pressure of 80/50 mmHg and grade III/IV systolic and diastolic murmurs were found. Transthoracic echocardiography and pathology evaluation conclude a cardiac myxoma. The patient was diagnosed with a LA myxoma with an obstructive shock, right ventricular (RV) dysfunction and pulmonary hypertension, thus a surgical approach was done immediately to prevent embolism and sudden death. Cardiac features are most likely a consequence of obstructed LV inflow. Transthoracic echocardiography is a useful modality to determine the size, location, and mobility of the mass. The persistence of RV dysfunction post-surgical may be due to the chronicity of the myxoma.

}, keywords = {Myxoma, Obstructive shock, Pulmonary hypertension., Right ventricle dysfunction, Transthoracic echocardiography}, doi = {10.5530/pj.2022.14.189}, author = {Wisda Medika Valentidenta and Agus Subagjo and Dandy Hertriwibowo} } @article {1936, title = {Research on External Signs and Chemical Composition of Medicinal Plant Raw Material -Leaves of Ficus Elastica}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {January 2023}, pages = {958-972}, type = {Research Article }, chapter = {958}, abstract = {

Ficus elastica is a species of the plant in the genus Ficus, from the family Moraceae. Ficus elastica, which is the object of our study, has been used for many years in phytodesign, however in terms of medicine, it remains a poorly studied plant. While studying the external signs and chemical composition of medicinal plant raw materials of leaves F{\'\i}cus elastica, chromato-mass spectrometry was used. During the process of studying, some diagnostic signs of Ficus elastica were identified. Chromato-mass spectrometry was used to identify 68 compounds. The maximum amount was accounted for б-D-Glucopyranoside, methyl (28,99\%), Phytol (9,90\%), 2-Hydroxy-3-methylsuccinic acid (6,93\%), Lanosterol (6,13\%), Hydroquinone (5,55\%), 9,12,15-Octadecatrienoic acid, ethyl ester, (Z,Z,Z)- (4,86\%), Lup-20(29)-en-3- one (4,17\%), 1,2-Benzenediol (3,33\%), Lupeol (2,95\%), 16-Allopregnene-3б,9а-diol-20-one 3-O-acetate (2,77\%), 9-Octadecenamide, (Z)- (2,67\%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)- (2,05\%), з-Sitosterol (1,84\%), а-d-Lyxofuranoside, methyl (1,57\%), Dasycarpidan-1-methanol, acetate (ester) (1,52\%), n-Hexadecanoic acid (1,45\%), Hexadecanoic acid, ethyl ester (1,33\%), 1,8-Dioxacyclohexadecane-2,10- dione, 5,6:12,13-diepoxy-8,16-dimethyl- (1,15\%), Vitamin E (0,64\%). Identified morphological features of the leaves of Ficus elastica can be used in diagnosis of this species and may help to develop indicators of authenticity for promising medicinal leaves. As mentioned earlier, by means of chromato-mass spectrometry were identified 68 compounds, and the relative percentage of identified compounds was determined using a simple normalization method.

}, keywords = {Chromato-mass spectrometry, Ficus elastic, Methyl, Phytol, Vitamin E., б-D-Glucopyranoside}, doi = {10.5530/pj.2022.14.197}, author = {Angelina V. Strelyaeva and Anna G. Kharitonova and Larisa B. Vaskova and Alexander N. Luferov and Dmitry O. Bokov and Alina A. Bondar and Natalia V. Bobkova and Nevena Jeremic and Yulia B. Lazareva and Alla M. Antsyshkina and Tatiana V. Prostodusheva and Roman M. Kuznetsov} } @article {1922, title = {Review on Bioactive Potential of Indonesian Forest Essential Oils}, journal = {Pharmacognosy Journal}, volume = {14}, year = {2022}, month = {December 2022}, pages = {873-879}, type = {Review Article}, chapter = {873}, abstract = {

Essential oils are composed of some natural, volatile, as well as aromatic compounds extracted from plants. In recent years, several studies have shown that some of their benefits can be attributed to their antimicrobial, antioxidant, anti-inflammatory, and also immunomodulatory properties. So, essential oils have been proposed as a common elective to anti-microbials or for utilize in combination with other antimicrobials against multidrug-resistant microscopic organisms. Most of the potential data about essential oils were obtained with in vitro and in vivo studies. Several types of essential oils are available in Indonesia which are reported to have biological activity such as antioxidants and antiaging are essential oils of pine (Pinus merkusii), kilemo (Litsea cubeba), agarwood (Aquilaria spp), eucalyptus (Eucalyptus citriodora), and cinnamon (Cinnamomum burmanii). The major chemical compound of pine oil is alpha pinene. Kilemo oil contains geranial. chemical marker compound of agarwood is chromone and sesquiterpenes. Eucalyptus contains citronella. The chemical component of cinnamon oil is cinnamaldehyde. Some essential oils have shown remarkable antioxidant activities when used at specific concentrations which can be due to their richness in phenolic compounds. However, toxicological studies are needed before any recommendation for application can be given. Preformulating and formulation studies will be needed to develop suitable dosage forms in order to introduce optimized pharmaceuticals (high active, low toxic) as alternative of current pharmaceutical dosage forms

}, keywords = {Bioactivity, Chemical compound, Essential oil, Indonesian forest, Pharmaceutics}, doi = {10.5530/pj.2022.14.182}, author = {Yelfi Anwar and Gunawan Pasaribu and M. Nazari V} } @article {1334, title = {Antidepressant-Like Behavioral and Spatial Memory Effects in Peruvian Red Maca (Lepidium meyenii)-Treated Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {81-88}, type = {Original Article}, chapter = {81}, abstract = {

Introduction: Lepidium meyenii, known with the vernacular name of {\textquotedblleft}Maca{\textquotedblright}, is a Brassicaceae family that has been widely used by Peruvian traditional medicine in cases of sexual dysfunction, memory loss, and several other diseases and pathologies. Objetive: The aim of the study was to test the potential effects of aqueous extract of Red Maca (AQ-RM) on antidepressant-like behavioral in male rats and spatial memory in ovariectomized (OVX) rats. Methods: Forced swimming test was used to examine the potential antidepressant AQ-RM activity in male rats. Fluoxetine and amitryptiline were included as reference drugs. Morris Water Maze test was employed to examine the effect of AQ-RM on spatial memory in ovariectomized (OVX) rats. Such effects were compared to exogenous estradiol administration. The potential role of oxidative stress on spatial memory loss was assessed by measuring malondialdehyde (MDA) levels in rats brain homogenates. Results: AQ-RM enhances swimming and climbing activities while reducing the time of immobility in male rats. Meanwhile, it prevents the decrease in the time spent in the target quadrant and displays higher values in the number of crossings in OVX-rats as compared to OVX-control rats. MDA levels in brain homogenates were decreased in OVX-rats receiving AQ-RM. Conclusion: Oral administration of AQ-RM has anti-depressive application in male rats; and increases the ability of learning and memory in OVX rats.

}, keywords = {Antidepressant activity, Forced swimming test, Lepidium meyenii, Morris water maze test, Red Maca, Spatial memory}, doi = {10.5530/pj.2021.13.12}, author = {Roberto O Yba{\~n}ez-Julca and Ivan M Quispe-D{\'\i}az and Daniel Asunci{\'o}n-Alvarez and Kelly S{\'a}nchez-Mu{\~n}oz and Albert Vargas-Go{\~n}as and Jazminy Morote-Guzman and Ronald Yaro-Marcelo and Edmundo A Venegas-Casanova and Rafael Jara-Aguilar and Pedro Buc Calderon and Julio Benites} } @article {1607, title = {Antioxidant and Hepatoprotective Activity of Ethanol Extract of Annona cherimola Mill. On Paracetamol-Induced Liver Toxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {July 2021}, pages = {874-882}, type = {Original Article}, chapter = {874}, abstract = {

Background: Annona cherimola Mill. (A. cherimola) is mainly characterized by its antioxidant and cytoprotective properties due to their content of phenolic compounds. Objective: To evaluate antioxidant and hepatoprotective activity of ethanol extract of leaves from A. cherimola against induced toxicity by paracetamol in rats. Methods: Amount of total phenolics compounds of ethanol extract of A. cherimola Mill. was determined by the Folin-Ciocalteu method and antioxidant activity was evaluated by DPPH method. Three doses of the ethanol extract of leaves of A. cherimola (250, 500 and 750 mg/Kg/day) were administered to rats and it was evaluated biochemical blood parameters: aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) were measured, liver tissue was removed for histopathological analysis. Results: Ethanol extract of leaves from A. cherimola had 41.26 mg GAE/g extract and antioxidant DPPH Scavenging Activity had 85.51\%. A. cherimola reduced blood levels of ALT, AST and ALP, compared to control group Paracetamol, ethanol extract, being more effective at doses of 750 mg/Kg/day. Histopathological evaluation suggested that A. cherimola decreased hepatic necrosis and degenerative process induced by paracetamol. Conclusions: Hepatoprotective activity of ethanol extract of leaves of A. cherimola was demonstrated, being hepatoprotective activity dose dependent and the mechanism may involve antioxidant activity and total polyphenols found in extract of this plant.

}, keywords = {Antioxidants, DPPH, Liver, Paracetamol, Rat}, doi = {10.5530/pj.2021.13.112}, author = {Carmen R. Silva-Correa and V{\'\i}ctor E. Villarreal-La Torre and Jos{\'e} L. Cruzado-Razco and William Antonio Sag{\'a}stegui- Guarniz and Mar{\'\i}a V. Gonz{\'a}lez-Blas and Anabel D. Gonz{\'a}lez-Siccha and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo- Villalaz and Luz M. Guerrero-Espino and Jorge Del Rosario-Ch{\'a}varri and Julio Hilario-Vargas} } @article {1660, title = {Antioxidant Capacity of Chuquiraga Spinosa Less. "Huamanpinta" and Prevention of Carrageenan-Induced Inflammation in Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1287-1296}, type = {Research Article}, chapter = {1287}, abstract = {

Objective: To evaluate the antioxidant capacity of Chuquiraga spinosa extracts and prevention of carrageenan-induced inflammation in mice. Methodology: Experimental design: plant species, erythrocytes and male BALB C53 mice, were considered as biological material. Antioxidant capacity was evaluated in 50\%, 70\%, 96\% and aqueous ethanolic extracts by 2,2-Diphenyl-1-Picrylhydrazyl reduction, malondialdehyde inhibition in oxidized erythrocytes with H2O2 and correlating with polyphenol content equivalent to gallic acid/gram dry extract. Inflammation was evaluated by inoculating carrageenan 2\% in "subcutaneous air bag" of mice: 1) White, 2) carrageenan, 3) dexamethasone 2 mg/kg, 4-6) ethanolic extract 70\% doses 100, 250 and 500 mg/kg respectively; determining nitric oxide, malondialdehyde, total proteins, albumin, leukocytes in exudate and histological changes. Results: Alkaloids, flavonoids, terpenes, phenolic compounds, tannins, carbohydrates, triterpenes, steroids and sesquiterpene lactones were identified; aqueous extract presented greater reduction of 2,2-Diphenyl-1-Picrylhydrazyl (CI50 = 58.99 μg/mL), ethanolic extract 70\% presented greater inhibition of malondialdehyde in erythrocytes (CI50 = 16.44 nm/mL); It was observed that the higher the amount of polyphenols, the greater the reduction of 2,2-Diphenyl-1-Picrylhydrazyl (r=-0.909) and the greater the inhibition of malondialdehyde (r=-0.781). With 500 mg/kg of 70\% ethanolic extract there was greater anti-inflammatory effect inhibiting malondialdehyde, nitric oxide, albumin, total proteins and leukocytes in 55.55\%, 81.92\%, 41.20\%, 31.51\% and 32.45\% (p\<0.01) respectively and less infiltration of leukocytes and lymphocytes in air sac membrane. Conclusion: The extracts of aerial parts of Chuquiraga spinosa showed antioxidant capacity correlated to polyphenol content. The 70\% ethanolic extract prevented inflammation in mice in a dosedependent manner.

}, keywords = {Antioxidant, Ethanolic extract, Leukocytes, Lipoperoxidation, Nitric oxide, Oxidative stress}, doi = {10.5530/pj.2021.13.163}, author = {Hugo Jes{\'u}s Justil-Guerrero and Jorge Luis Arroyo-Acevedo and Juan Pedro Rojas-Armas and Miriam Palomino- Pacheco and Magaly Villena-Tejada and Wilmer Atilio Segura V{\'\i}lchez} } @article {1714, title = {Effect of a Gel Based on Ipomoea batatas (Purple Sweet Potato) on Dermal Wound Healing in Mice}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1720-1726}, type = {Research Article}, chapter = {1720}, abstract = {

Background: Ipomoea batatas (L.) Lam. (I. batatas) is a root native from South America that is characterized by its antioxidant, antimicrobial and anti-inflammatory properties. These properties contribute to the wound healing process. Objective: To evaluate the healing activity of a gel based on I. batatas on dermal wound healing in mice. Material and methods: An acid ethanolic extract (1.5 N hydrochloric acid: Ethanol 96 {\textdegree} 15:85, v / v) was prepared with the peels of the roots of I. batatas "purple sweet potato", which was incorporated into the formulations 0.5\% and 1\% gel. Mus musculus Balb / c with induced injury were distributed in four experimental groups: Group I (Control), which did not receive any treatment. Group II (Gel base), Group III (Gel I. batatas 0.5\%) and Group IV (Gel I. batatas 1\%) received the daily administration of topical treatments for 14 days. Wound closure was determined during the experimentation time, then they were euthanized with sodium pentobarbital 60 mg / kg / pc v.ip. to obtain skin samples for histopathological analysis. Results: Group IV shows a higher percentage of wound closure, which is also evidenced in histopathological changes. Conclusions: The 1\% gel based on the ethanolic extract of the peels of the roots of Ipomoea batatas (L.) Lam. they show healing activity in wounds induced in mice, being the most effective treatment.

}, keywords = {Histology, Ipomoea batatas, Skin., Wound Healing}, doi = {10.5530/pj.2021.13.222}, author = {Carmen R. Silva-Correa and Cristel M. Ortiz-Noriega and V{\'\i}ctor E. Villarreal-La Torre and Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Luz M. Guerrero-Espino and William A. Sag{\'a}stegui-Guarniz and Anabel D. Gonz{\'a}lez- Siccha and Mar{\'\i}a V. Gonz{\'a}lez-Blas and Jos{\'e} L. Cruzado-Razco and Jorge Del Rosario-Ch{\'a}varri and Patricia Contreras- Vera and Julio Hilario-Vargas} } @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 {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 {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 {1323, title = {A New Ursane-Type Triterpene from the Fermented Shallot Allium Ascalonicum}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {January 2021}, pages = {01-07}, type = {Original Article}, chapter = {01}, abstract = {

3,24-acetonideclethric acid (1), a new ursane-type triterpene, and four known compounds including ursolic acid (2), randiasaponin IV (3), ilekudinoside W (4) and (25S)-1β,3β,24β- trihydroxyspirost-5-en 1-O-α-L-rhamnopyranosyl-(1{\textrightarrow}2)- α-L-arabinopyranoside (5), and were isolated from the fermented shallot Allium ascalonicum. Their structures were determined by analysis of HR-ESI-MS, NMR spectral data, as well as comparison with those reported in the literature. All of the saponins (3-5) exhibited antimicrobial activity against three strains Staphylococcus aureus, Escherichia coli, and Candida albicans with IC50 values in the range from 89.49 {\textpm} 2.24 to 95.71 {\textpm} 3.86 μM.

}, keywords = {24-Acetonideclethric acid, 3, Allium ascalonicum, Antimicrobial activity, Saponin}, doi = {10.5530/pj.2021.13.1}, author = {Nguyen Van Chuyen and Nguyen Hong Son and Pham Van Hien and Dang Truong Giang and Ho Ba Ngoc Minh and Ngo Thi Tuyet Mai and Chu Van Men and Ho Anh Son and Vu Binh Duong} } @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 {1719, title = {Pharmacognostic Studies of the Leaves and Fructus of Arctium lappa L. (Asteraceae Bercht. \& J. Presl)}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1734-1745}, type = {Research Article}, chapter = {1734}, abstract = {

Introduction: The state quality assurance system ensures the confidence of consumers that the product meets its quality requirements. In this study, pharmacognostic standards of the leaves and fructus of burdock are specified for the first time. Methods: Microscopic analysis was carried out by using the microscope Carl Zeiss. The UV spectrum were measured on an SF-2000 spectrophotometer. Results: Macroscopically, the leaves are heart-shaped, broad-heart-ovate-shaped with a spaced emarginatedserrate or whole edge, with a wide, wedge-shaped, rounded, uneven base, acute apex, green on the outer surface, grayish slightly pubescent on the inner surface. The fructus are obovate or wedge-compressed, slightly curved, the color is brown/black with spots, or variegated with black spots on a gray background. The microscopic examination of the leaves revealed the presence of epidermis, large submerged and non-submerged stomata of the anomocytic type, 2 types of simple unbranched multi-cellular and glandular capitate trichomes; essential oil glands. Microscopic examination of the leaf petiole revealed the presence of 2 types of simple multi-cellular trichomes, epidermis, angular collenchyma, bicollateral bundles, parenchyma. The stomatal index value is 8.28{\textpm}0.81 per 1cm2. The microscopy of the fructus revealed the presence of elongated cells of the pericarp epidermis; mesocarp; endocarp; endosperm with aleurone grains and drops of fatty oil. The qualitative phytochemical analysis of revealed the presence of polysaccharides, tannins, flavonoids, terpenoids, saponins, phenolic acids. Conclusion: Physical and chemical parameters (moisture, extractive value, ash content) were also specified. These specific data are important for establishing diagnostic indicators for standardization, identification, preparation of new quality standards.

}, keywords = {Analitical standarts, Arctium lappa L., Fructus, Leaves, Pharmacognostic standarts, Phytochemical analysis.}, doi = {10.5530/pj.2021.13.224}, author = {Kolomiets Natalia Eduardovna and Korolev Stepan Alexandrovich and Isaykina Nadezhda Valentinovna and Abramets Natalia Yurievna and Kudryavtseva Darya Vladimirovna and Boev Roman Sergeevich and Zhalnina Ludmila Vladimirovna and Ali Abdujalil Kaid Hasan and Bondarchuk Ruslan Anatolevich} } @article {1641, title = {Phytochemical and Biological Characterization of Aqueous and Ethanolic Extracts of Parthenium hysterophorus}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1122-1133}, type = {Original Article}, chapter = {1122}, abstract = {

Introduction: Parthenium hysterophorus is a plant used in traditional medicine to treat health issues and which could be a source of phytochemicals with possible antioxidant activity without causing cytotoxic effects. Hence, this work was designed to evaluate its phytochemical profile, cytotoxicity, and antioxidant activity. Methods: The aqueous (AE) and ethanolic (EE) extracts of P. hysterophorus flowers were obtained by decoction and ultrasound, respectively. Their phytochemical composition was determined by colorimetric tests and RP-HPLC-MS analysis. Their cytotoxic activity was tested by a hemolysis assay. The antioxidant activity was evaluated with the Trolox equivalent antioxidant capacity (TEAC), 2,2-diphenyl-1- picrylhydrazyl (DPPH), and hydroxyl radical (-OH) scavenging assays. In addition, the effect of the extracts on the activity of the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) from human erythrocytes, was evaluated. Results: The phytochemical screening of the AE and EE by colorimetric test showed the presence of flavonoids, steroids, triterpenes, saponins, coumarins, sesquiterpene lactones, tannins, and carbohydrates. In addition, the RP-HPLC-MS analysis identified some phenolic compounds such as flavonols, methoxyflavonols, flavones, methoxyflavones, and hydroxycinnamic acids. The hemolysis assay showed non-cytotoxic activity by AE, but EE exhibited a hemolytic effect. Furthermore, the AE and EE showed significant antioxidant activity to inhibit radicals in the TEAC, DPPH and -OH scavenging assays. Moreover, the SOD activity only showed a significant increase by AE. However, the two crude extracts increased the CAT activity, at the highest concentrations. Conclusion: P. hysterophorus has phytochemicals with antioxidant activity to inhibit radicals and increase the activity of antioxidant enzymes in vitro.

}, keywords = {antioxidant activity, Cytotoxicity, Parthenium hysterophorus, Phytochemicals}, doi = {10.5530/pj.2021.13.145}, author = {MA Alfaro Jim{\'e}nez and A Zugasti Cruz and SY Silva Belmares and JA Ascacio Vald{\'e}s and CA Sierra Rivera} } @article {1696, title = {Protective Potential of Canthium dicoccum Methanolic Extract Against Hepatic Injury in Rats}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {December 2021}, pages = {1648-1655}, type = {Research Article}, chapter = {1648}, abstract = {

The methanolic extract of leaves of C.dicoccum was evaluated for its hepatoprotective activity against paracetamol induced hepatotoxicity since it is reported to cause oxidative stress in the animal thereby altering the enzymatic levels. Fresh leaves were collected, shade dried and extract was prepared by cold maceration followed by drying in a rota-vapour using methanol to obtain MECD as a sticky semi-solid mass. Thirty rats were taken and divided into 5 equal groups where, Group I, II, and III served as Normal Control, Negative control (PCM 3g/kg), and Positive control (Silymarin 200mg/kg) respectively; whereas, Group IV and V served as test groups where the rats were pre-treated orally with MECD 200mg/kg and 400mg/kg respectively for six days before administering PCM. On the 8th day all groups except Group I was administered with PCM (3g/kg). 48 hours post PCM induction, the animals were anesthetized, blood samples were obtained via retro-orbital sinus plexus and then the rats were sacrificed. The serum was assessed for the evaluation parameters like AST, ALT, ALP, and bilirubin levels. Apart from these; SOD, CAT, and MDA levels were also evaluated and it was concluded that treatment with MECD restored the levels to normal thereby exhibiting hepatoprotective activity. Moreover, histopathological evaluation was carried out to assess the liver for inflammation, infiltration, or necrosis where the MECD treated rats showed promising results.

}, keywords = {Antioxidant enzymes, Canthium dicoccum, Hepatoprotective activity, Liver markers, Paracetamol.}, doi = {10.5530/pj.2021.13.212}, author = {Ravi Kumar Vakkalagadda and Parameshwar Ravula and Kondapuram Parameshwar and Kaspa Saraswathi and P Sindhuri and Rajala Srikala and Kosika Sandeep} } @article {1635, title = {Total Phenol Content and Gastric Anti-Ulcer Activity of Hydroalcoholic Extract of Persea caerulea (Ruiz \& Pav.) Mez. Bark}, journal = {Pharmacognosy Journal}, volume = {13}, year = {2021}, month = {September 2021}, pages = {1072-1078}, type = {Original Article}, chapter = {1072}, abstract = {

Objective: Determine the content of total phenols and evaluate the gastroprotective effect of the extract of Persea caerulea (Ruiz \& Pav.) Mez. in mice with induced gastric ulcer. Material and Methods: The bark of Persea caerulea was macerated in 70\% ethanol and the phenol content was determined using the Folin-Ciocalteu method. The female Mus musculus Balb/c specimens were distributed in the following groups: White Control Group, without indomethacin dosing; Negative Control Group, dosing with indomethacin; Positive Control Group treated with ranitidine at a dose of 50 mg/kg; Groups P. caerulea treated with extract at doses of 50 mg/kg, 100 mg/kg and 200 mg/kg. Gastric ulcer was induced with indomethacin orally at a dose of 50 mg/kg, the procedure was repeated 12 hours later; Gastroprotective treatment was administered 60 minutes after each dose of indomethacin, 6 hours after the last dose, sodium pentobarbital was euthanized and the stomach was resected to determine ulceration using the Marhuenda Scale. Results: Higher percentages of gastric ulcer inhibition were obtained in the P. caerulea 100 mg/kg (80\%) and P. caerulea 200 mg/kg (85.71\%) groups. Conclusions: Extract of Persea caerulea (Ruiz \& Pav.) Mez., At doses of 100 and 200 mg/kg of body weight, has a gastric antiulcerative effect which is related to its content of total polyphenols.

}, keywords = {Gastric ulcer, Indomethacin, Mice}, doi = {10.5530/pj.2021.13.139}, author = {Abhel A. Calder{\'o}n-Pe{\~n}a and Cinthya L. Aspajo-Villalaz and Carmen R. Silva-Correa and V{\'\i}ctor E. Villarreal-La Torre and Mar{\'\i}a V Gonz{\'a}lez-Blas and Orlando E Pretel-Sevillano and Marco L Salazar-Castillo and Maricielo Vaella-Alarc{\'o}n and Franco Huaccha-C{\'a}ceres and Jonatam Le{\'o}n-Soto and Whendy Alaya-Davir{\'a}n and Anabel D. Gonz{\'a}lez-Siccha and William Antonio Sag{\'a}stegui-Guarniz and Luz M. Guerrero-Espino and Julio Hilario-Vargas} } @article {1133, title = {Anti-arthritic Property of Sahacharadi Kashayam Against Freund{\textquoteright}s Complete}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May2020}, pages = {459-464}, type = {Original Article}, chapter = {459}, abstract = {

Introduction: The available modern molecular drugs for the therapy of Rheumatoid arthritis are beset with several side effects and alternative drugs are urgently needed. The present investigation was performed to evaluate the anti-arthritic activity of Sahacharadi Kashayam (SK), an Ayurvedic formulation, against Freund{\textquoteright}s complete adjuvant (CFA) - induced arthritis in rats. Methods: In this experimental trial, SK was administered at doses of 0.5, 1.0 and 1.5 ml/kg body weight orally to adjuvant (CFA) induced arthritic rats. The anti-arthritic activity was evaluated by using paw volume, haematological parameters and arthritic biomarkers. The efficacy of the Kashayam was compared with the standard Leflunomide (10 mg/kg) drug. Results: Significant reduction in paw volume and thickness by SK (0.5 ml dose) has been found and there was considerably improvement in haematological parameters and arthritic markers in CFA rats till 14 days. After 14th day SK treatment with doses (1.0 and 1.5ml), however, reoccurrence of inflammation and pathological changes were observed in rats. Conclusion: The study clearly indicated the anti-arthritic role of SK. Future studies, however, are warranted to provide a new approach in relation to the therapeutic dose and treatment period of SK which may eventually lead to the development of a new category of the anti-arthritic agent.

}, keywords = {Anti-arthritic activity, Arthritis, Biomarkers, Sahacharadi Kashayam}, doi = {10.5530/pj.2020.12.71 }, author = {P Praveen Kumar and K Prabhu and Mudiganti Ram Krishna Rao and Mallika Jain and K Kalaivani and Shruthi Dinakar and Sampad Shil and N Vijayalakshmi} } @article {1225, title = {Antioxidant and Hepatoprotective Activities of Strobilanthes kunthianus against Carbon Tetrachloride-Induced Hepatotoxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1143-1151}, type = {Research Article}, chapter = {1143}, abstract = {

Background: Strobilanthes kunthianus Nees T Anders (Neela kurinji) is a shrub in the grasslands of Nilgiris, Western Ghats in India. It is well known for many biological properties including antioxidant. However, there is no in-vivo antioxidant and hepatoprotective activities has been carried out previously on S. kunthianus. Objectives: The present study was aimed to evaluate the antioxidant and hepatoprotective activities of methanolic flower extract of S. kunthianus (MFESK) against carbon tetrachloride (CCl4)-induced hepatotoxicity in experimental rats. Materials and Methods: The Wistar rats were divided into six groups comprising six animals to each. Group I was served as normal control and group II as CCl4 treated. Both these groups were received sodium CMC (0.3\%, 5 ml/kg). Groups III, IV and V animals were treated with MFESK at different dose levels (100, 150 and 200 mg/kg). Group VI was treated with standard silymarin (100 mg/kg). All these treatments were given orally for eight consecutive days. On the 8th day of treatment, except the normal group I, all the other group of animals from III to VI were received CCl4 in liquid paraffin (1:1, 1 ml/kg, i.p., single dose) after 1 h of the vehicle. On the 9th day, the animals were anesthetized and blood was collected from the abdominal artery, then the serum was separated and used for the biochemical estimations. Serum marker enzymes such as ASAT, ALAT, ALP, TGL, CR, TP, TC, TB and albumin were measured using Ecoline kits by using autoanalyzer. Further, blood serum and the supernatant solution of homogenized liver and kidney were used for the estimation of antioxidant parameters such as CAT, SOD and TBARS by spectrophotometrically. Results: The administration of CCl4 caused a significant increase (P\<0.001) in the levels of ASAT, ALAT, ALP, TGL, TC, TB and TBARS and decrease in the levels of CR, TP, Albumin, CAT and SOD in serum. A significant (P\<0.001 and P\<0.01) restoration of these values towards the normal level was observed in all the three tested doses of MFESK. Similar results were observed for CAT, SOD and TBARS in both liver and kidney tissues. These results designated the strong antioxidant and hepatoprotective nature of MFESK. The histopathological investigation of liver and kidney tissues also confirmed the observed activities. Conclusion: These findings afford incitement for the development of a novel hepatoprotective herbal drugs.

}, keywords = {Antioxidant, Carbon tetrachloride, Hepatoprotective, Hepatotoxicity, Liver disease, Strobilanthes kunthianus}, doi = {10.5530/pj.2020.12.161}, author = {Geetha Balasubramaniam and Mahendran Sekar and Maithili Varadarajan and Shrishailappa Badami} } @article {1224, title = {Antioxidant and Hepatoprotective Activities of Strobilanthes kunthianus against Carbon Tetrachloride-Induced Hepatotoxicity in Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1143-1151}, type = {Research Article}, chapter = {1143}, abstract = {

Background: Strobilanthes kunthianus Nees T Anders (Neela kurinji) is a shrub in the grasslands of Nilgiris, Western Ghats in India. It is well known for many biological properties including antioxidant. However, there is no in-vivo antioxidant and hepatoprotective activities has been carried out previously on S. kunthianus. Objectives: The present study was aimed to evaluate the antioxidant and hepatoprotective activities of methanolic flower extract of S. kunthianus (MFESK) against carbon tetrachloride (CCl4)-induced hepatotoxicity in experimental rats. Materials and Methods: The Wistar rats were divided into six groups comprising six animals to each. Group I was served as normal control and group II as CCl4 treated. Both these groups were received sodium CMC (0.3\%, 5 ml/kg). Groups III, IV and V animals were treated with MFESK at different dose levels (100, 150 and 200 mg/kg). Group VI was treated with standard silymarin (100 mg/kg). All these treatments were given orally for eight consecutive days. On the 8th day of treatment, except the normal group I, all the other group of animals from III to VI were received CCl4 in liquid paraffin (1:1, 1 ml/kg, i.p., single dose) after 1 h of the vehicle. On the 9th day, the animals were anesthetized and blood was collected from the abdominal artery, then the serum was separated and used for the biochemical estimations. Serum marker enzymes such as ASAT, ALAT, ALP, TGL, CR, TP, TC, TB and albumin were measured using Ecoline kits by using autoanalyzer. Further, blood serum and the supernatant solution of homogenized liver and kidney were used for the estimation of antioxidant parameters such as CAT, SOD and TBARS by spectrophotometrically. Results: The administration of CCl4 caused a significant increase (P\<0.001) in the levels of ASAT, ALAT, ALP, TGL, TC, TB and TBARS and decrease in the levels of CR, TP, Albumin, CAT and SOD in serum. A significant (P\<0.001 and P\<0.01) restoration of these values towards the normal level was observed in all the three tested doses of MFESK. Similar results were observed for CAT, SOD and TBARS in both liver and kidney tissues. These results designated the strong antioxidant and hepatoprotective nature of MFESK. The histopathological investigation of liver and kidney tissues also confirmed the observed activities. Conclusion: These findings afford incitement for the development of a novel hepatoprotective herbal drugs.

}, keywords = {Antioxidant, Carbon tetrachloride, Hepatoprotective, Hepatotoxicity, Liver disease, Strobilanthes kunthianus}, doi = {10.5530/pj.2020.12.161}, author = {Geetha Balasubramaniam and Mahendran Sekar and Maithili Varadarajan and Shrishailappa Badami} } @article {1256, title = {Black Horehound (Ballota nigra Linn) Induces Apoptosis in Prostate Cancer Cells (PC-3) Through Intrinsic Signalling Cascade}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1377-1382}, type = {Research Article}, chapter = {1377}, abstract = {

Background: Prostate cancer is the most commonly diagnosed cancer among men. The disease varies widely in its clinical aggressiveness. Ballota nigra Linn (Black horehound) is a three-foot, perennial herb of the family Lamiaceae and it has been shown to have various pharmacological properties such as antioxidant, hypoglycemic, neuro-sedative, antibacterial, insecticidal and anticholinesterase activities. However, the elucidation of B.nigra for its anticancer activity in prostate cancer has not been studied so far. Methodology: Prostate cancer PC3 cells were treated with different concentrations of B.nigra (50, 100, 200 \& 400μg/ml) for the analysis of Bcl-2, Phosphorylation of Bcl2 (p-Bcl2) and tumor suppressor protein p53, Case pase-3 and caspase-9 in PC3 cells. Results: The B.nigra ethanolic leaf extract reduced the levels of anti apoptotic proteins (Bcl-2, p-Bcl2) and increased the level of tumor suppressor protein p53, caspase-3 and 9 significantly (p\<0.05). Conclusion: Results of the study show that B.nigra has potential anticancer activity by modulating intrinsic activity of apoptotic signaling in PC-3 cells. Thus, B.nigra may have a potential therapeutic option for the treatment of prostate cancer.

}, keywords = {Apoptosis, Ballota nigra, Intrinsic pathway, PC3, Prostate cancer}, doi = {10.5530/pj.2020.12.190}, author = {Selvaraj Jayaraman and Ponnulakshmi Rajagopal and Vishnupriya Veeraraghavan and Poonguzhali Sivagnanam and Divya Ravikumar and Sumetha Suga Deiva Suga and Kavin Mozhi James and Surapaneni Krishna Mohan} } @article {1221, title = {Chemical Composition and Content of Polysaccharides from the Yellow Iris (Iris pseudacorus L.) Rhizomes}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1012-1018}, type = {Original Article}, chapter = {1012}, abstract = {

Background: The aim of the present study was to examine the composition and content of the polysaccharide complex and polysaccharide fractions from yellow iris (Iris pseudacorus L.) rhizomes growing in Russian Federation (Moscow region). Materials and Methods: Traditional pharmacognostic methods were used in the analysis of polysaccharides as biologically active substances. The total amount of polysaccharides was determined by a gravimetric procedure with alcohol precipitation. Fractions of polysaccharides were isolated by sequential changing of solvents. The content of monosaccharides was determined by the method of high-performance liquid chromatography with refractometric detection (HPLC-RID) after acid hydrolysis. HPLCRID procedure was performed using Chromatograph Agilent 1260 Infinity, Sugar-Pak column (300{\texttimes}6.5 mm), and isocratic elution mode. Results: Polysaccharide complex was isolated, the total content of polysaccharides in the rhizomes of I. pseudacorus was determined, as well as their distribution by fractions (water-soluble polysaccharides, pectic substances, hemicellulose A, hemicellulose B), the composition of individual sugars (glucose, xylose, galactose, mannose, rhamnose, arabinose) was determined for each fraction. Conclusion: In our experiment polysaccharide complex was first identified and described in detail for I. pseudacorus grown in Moscow region.

}, keywords = {Hemicellulose, Iris pseudacorus L., Pectins, Polysaccharides, Water-soluble Polysaccharides, Yellow iris}, doi = {10.5530/pj.2020.12.143}, author = {Tikhomirova EA and Sorokina AA and Bubenchikova VN and Kostikova EN and Zhilkina VYu and Bessonov VV} } @article {1066, title = {Chemical Fingerprint by HPLC-DAD-ESI-MS, GC-MS Analysis and Anti-Oxidant Activity of Manasamitra Vatakam: A Herbomineral Formulation}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {115-123}, type = {Research Article}, chapter = {115}, abstract = {

Background: Manasamitra Vatakam is a classical ayurvedic herbo mineral formulation used for the treatment of neurodegerative properties and epileptic disorders. The wide range mixture of herbal extracts and minerals were used in the formulation. Aim: The aim of the study implies in performing the chemo-profiling, chromatographic fingerprint analysis by HPLC-DAD-ESI-MS for the selected formulations of Manasamitra Vatakam followed by the identification of bioactive compounds by Gas Chromatography {\textendash} Mass Spectrometric (GC-MS) analysis, to evaluate the diffusion and dilution methods for the determination of anti-bacterial activity in the methanolic extracts of Manasamitra Vatakam (MMV). Materials and Methods: The antibacterial activity was performed by both diffusion and dilution methods whereas the antioxidant activity was performed by free radical scavenging of 2,2-diphenyl-1-picrylhydrazy and hydrogen peroxide scavenging assay method. Results: The estimation of bioactive constituents showed positive results by qualitative analysis. Antibacterial activity of MMV was evaluated against two-gram positive Staphylococcus aureus and Bacillus cereus, two gram negative Escherichia coli and Klebsiella pneumonia by disk diffusion (0.078-10μg mL-1), broth dilution (0.078-10μg mL-1) and broth micro dilution method (0.39-50μg mL-1) respectively. The bioactive constituents were analysed by GC-MS analysis for the methanolic extract of the formulation. Conclusion: To conclude, the formulation was found abundant with phenolic and flavonoid compounds by HPLC-ESI-MS analysis, the bioactive compounds identified are responsible for the anti-bacterial activity. The broth microdilution method performed by resazurin method was observed as the fast screening, sensitive and accurate method for the quantitative determination of antibacterial activity.

}, keywords = {Classical formulation, Diffusion and dilution methods, Heavy metals, MIC, Phytochemicals}, doi = {10.5530/pj.2020.12.18}, author = {Srikalyani V and Ilango K} } @article {1257, title = {Chemopreventive Action of Garcinia Mangostana Linn. on Hepatic Carcinoma by Modulating Ornithine Decarboxylase Activity}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1383-1388}, type = {Research Article}, chapter = {1383}, abstract = {

Ornithine decarboxylase and alpha -L- fucosidase over-expression is associated with advanced hepatocellular carcinoma (HCC) development. The objective of this study was to elucidate the action of Garcinia Mangostana fruit extract (GME) on these overexpressed enzymes and apoptotic proteins in diethyl nitrosamine (DEN) induced hepatocellular carcinoma (HCC) rats. The cancer was induced using DEN to the experimental rats and treated with GME (400 mg/ kg) to find its anticancer property. The lysosomal enzymes such as alpha-L-fucosidase, beta- D-glucosidase, ornithine decarboxylase activity (ODC), apoptotic and antiapoptotic proteins such as Bcl-2, Bax and Bcl-xl and H3 thymidine incorporation assay were done to prove GME{\textquoteright}s chemo preventive property. DEN induction caused significant increase in the activities of ornithine decarboxylase; lysosomal enzymes and increased cell proliferation with decreased apoptosis were observed. In contrast, the groups with GME treated rat{\textquoteright}s elicited significant (P \< 0.001) reduction in ornithine decarboxylase, lysosomal enzymes and decreased cell proliferation with increased apoptosis. GME has effective chemo preventive property and can serve as an anticarcinogenic therapeutic drug against hepatocellular carcinoma.

}, keywords = {Diethyl nitrosamine, G. Mangostana extract, Hepatocellularcarcinoma, Ornithine decarboxylase}, doi = {10.5530/pj.2020.12.191}, author = {Vishnu Priya Veeraraghavan and Sardar Hussain and Janardhana Papayya Balakrishna and Gayathri Rengasamy and Surapaneni Krishna Mohan} } @article {1064, title = {Determination of Sugar Profile in Viburnum Fruits and its Dosage Forms by HPLC-RID}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {February 2020}, pages = {103-108}, type = {Research Article}, chapter = {103}, abstract = {

Background: In the Russian Federation, the viburnum fruits are used to obtain infusions and syrups as medications. This medicinal herbal raw material contains a large number of biologically active substances: vitamins, anthocyanins, proanthocyanidins, flavonoids, hydroxycinnamic acids, iridoids, carbohydrates, organic acids, lipids etc. The research aimed to study one of the biologically active substances group responsible for the formation of the organoleptic properties of aqueous extracts{\textendash}monomeric carbohydrate composition and content. Materials and methods: Dried viburnum (guelder-rose) fruits, an aqueous infusion based on it, and viburnum syrup of industrial manufacture (Russia) were purchased from the pharmacy and prepared for research. For HPLC analysis of monomeric sugars Agilent 1260 Series HPLC system equipped with autosampler/injector, four-channel gradient pump, column thermostat, refractive index detector), software (ChemStation Version B.01), column (Waters Sugar-Pack I, 10 μm, 300 {\texttimes} 6.5 mm) were used. Isocratic elution was performed using purified water (with the addition of Ca-EDTA 0.05 mg/ml) as the mobile phase, at a flow rate of 0.5 mL/min. The column was maintained at 80{\textdegree}C, the refractive index detector {\textendash} at 35{\textdegree}C. The injection volume was 10 μL, analysis time {\textendash} 20 min. Results: The main free carbohydrates of viburnum fruits and preparations based on them are glucose, fructose, and sucrose. The total content of simple sugars in the viburnum fruits is 28.393 {\textpm} 0.528\%, in the infusion {\textendash} 0.499 {\textpm} 0.015\%, in the syrup {\textendash} 69.736 {\textpm} 1.551\%. The characteristic ratio of glucose: fructose: sucrose in dried viburnum fruits is 8.1:5.4:1, in infusion {\textendash} 7.0:5.7:1, and in syrup {\textendash} 9.2:8.8:1. The sugars{\textquoteright} degree of passing into infusion is 74.34\%. Conclusion: The composition and content of carbohydrates determined by HPLC-RID are an important characteristic data. It can be used for viburnum fruits Russian pharmacopoeial standardization along with the quantifying total content of organic acids.

}, keywords = {Guelder-rose, HPLC-RID, Monomeric carbohydrates, Viburnum fruits}, doi = {10.5530/pj.2020.12.16}, author = {Bokov DO and Sergunova EV and Marakhova AI and Morokhina SL and Plakhotnaia ON and Krasnyuk II and Bessonov VV} } @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 {1145, title = {Hypoglycemic Effect of Kalanchoe pinnata (Lam) Pers. Leaf Extract}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {557-561}, type = {Research Article}, chapter = {557}, abstract = {

Introduction: Kalanchoe pinnata (Lam) Pers (Crasulaceae) is a succulent ornamental plant. In Costa Rica, the leaves are used as a coadjuvant treatment for Diabetes Mellitus based on traditional knowledge of natural remedies. Moreover, there are some studies mentioning its use for Diabetes Mellitus as medicinal plant in several countries. This research aimed to demonstrate the antidiabetic properties of hydroalcoholic extracts of K. pinnata leaves through phytochemical screening, alpha amylase inhibition and rodent models. Methods: Crude extracts of K. pinnata leaves were prepared by infusion and decoction using water:ethanol (70:30) as a solvent. The extracts prepared by decoction (LAED, lyophilized-water:ethanoldecoction) and by infusion (LAEI, lyophilized-water:ethanol-infusion) were analyzed by FolinCiocalteu, HPLC and capacity of inhibition of α-amylase activity. To determine hypoglycemic activity in rats, extracts were administered orally at doses of 250, 500 and 750 mg/Kg and blood sugar levels were monitored over a four hours period using a glucometer. Results: A significant reduction (p \< 0.05) in blood glucose was observed after one hour in rats treated with 500 mg/Kg of LAED extract. Treatment with 750 mg/Kg LAEI induced a statistically significant reduction in blood sugar at 90, 180 and 240 min, showing that the glucose-lowering effect of this extract was greater at a higher concentration. Conclusions: This study confirmed the hypoglycemic effect of K. pinnata extracts in the acute phase in rats and supports the use of this Crassulaceae as a home remedy.

}, keywords = {Antidiabetic activity, Diabetic, Extract, Kalanchoe pinnata}, doi = {10.5530/pj.2020.12.84}, author = {Ana L Ag{\"u}ero-Hern{\'a}ndez and Catalina Rosales-L{\'o}pez and Cristina Herrera and Andr{\'e}s Vargas-Picado and Rodrigo Mu{\~n}oz and Ana Abdelnour-Esquivel} } @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 {1291, title = {Lutein: A Comprehensive Review on its Chemical, Biological Activities and Therapeutic Potentials}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1769-1778}, type = {Review Article}, chapter = {1769}, abstract = {

Background: Lutein is a naturally occurring carotenoid found in high amounts in flowers, grains, fruits and green vegetables with green leaves include spinach, kale and carrots. The market for lutein encompasses pharmaceutical, dietary supplement, food, animal and fish feed industries. Objective: The present review aimed to provide an updated and comprehensive analysis of lutein, including its chemistry, biological properties and therapeutic potentials. Methods: Relevant literatures were collected from several scientific databases, include Google Scholar, Pubmed and ScienceDirect between 2000 to till date. Following a detailed inclusion and exclusion screening process, the information obtained was summarized. Results: Information on the sources, chemistry and biological properties including antioxidant, anti-arthrisits, antiinflammatory, hepatoprotective, cardioprotective, anti-cataract, antidiabetic, anticancer and bone remodelling activities, as well as food industry processing for lutein were tabled. Lutein can be considered powerful antioxidants along with multifaceted molecular targets, such as NF-ҡB, PI3K/Akt, Nrf-2, HO-1 and SIRT-1 signaling pathways in various pathological conditions. Conclusion: The present review observe the chemical, pharmacological properties, in addition to the therapeutic potentials of lutein. It is hoped that the information can provide a good reference to aid in the development and utilization of lutein in phytopharmaceuticals and food industries.

}, keywords = {Antioxidant, Inflammatory cytokines, Lutein, Molecular targets, Pharmacology, Transcription factors}, doi = {10.5530/pj.2020.12.239}, author = {Nurul Iman Nurul Fuad and Mahendran Sekar and Siew Hua Gan and Pei Teng Lum and Jaishree Vaijanathappa and Subban Ravi} } @article {1248, title = {Microscopic Investigations and Pharmacognosy of Striga orobanchioides Benth}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {September 2020}, pages = {1325-1331}, type = {Research Article}, chapter = {1325}, abstract = {

Objective: To study delineate Pharmacognosy of the stem of plant Striga Orobanchioides Benth (Scrophulariaceae), prime plant in Indian system of medicine. A comprehensive account on standardization of herbal drug Striga Orobanchioides Benth by using microscopic as well as Pharmacognostic parameters. In the field of herbal medicines, the main issues are quality, purity, and effectiveness, as in many cases herbal drugs are knowingly or unknowingly substituted or adulterated with similar species or varieties. Methods: The macroscopy, microscopy, physicochemical analysis, preliminary phytochemical testing of the powder of plant stem and other WHO recommended methods for standardization was done. Results: T S of young as well as old stem was studied. T.S. of the young stem confirmed the presence of thin epidermal layer, fairly wide cortex and thin vascular cylinder having the pith disintegrated or retained as homogeneous parenchymatous tissue. T.S. of the old stem confirmed the presence of cortical cells, parenchyma cells, sclerenchyma cells, vascular tissue. The lower conical part of the stem has epidermis cortical zone and vascular cylinder continued from its wide upper part. The cortical zone consists of parenchymatous ground tissue with sealed masses of sclerenchyma cells. The xylem tissue becomes gradually narrow and thin in the end of the stem. It includes compact radial lines of vessels, filnes and xylem rays. Conclusion: The above parameters, being reported to the first time for the studied plant species, and are significant towards establishing the microscopic and Pharmacognostic standards for future identification and authentication of genuine herbal drug. It can be concluded that the Pharmacognostic outline of Striga Orobanchioides plant is beneficial in developing standards for quality, purity and sample identification.

}, keywords = {Pharmacognosy, Stem, Striga Orobanchioides}, doi = {10.5530/pj.2020.12.182}, author = {Sunayana Vikhe and Rahul Kunkulol} } @article {1196, title = {Modern Approaches to the Analysis of Kelp (Laminaria sp.) as Pharmacopoeial Herbal Drugs and Food Products}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {June 2020}, pages = {929-937}, type = {Review Article}, chapter = {929}, abstract = {

Background: Currently, the chemical composition of Laminaria J.V. Lamour. species is well studied; they have found applications in the food, cosmeceutical and pharmaceutical industries. The main groups of biologically active compounds are polysaccharides (alginic acid, laminarin, mannitol, fucoidan, and others) and minerals (iodine compounds, magnesium, potassium, calcium, iron) that are determined according to pharmacopoeial and All-Union State Standards requirements. Materials and Methods: For data obtaining various types of search tools and engines such as Google, Google scholar, scientific literature (including Russian sources), normative documentation of Russian Federation (State Pharmacopoeia of Russian Federation IV edition, All-Union State Standards, and others) electronic databases such as e-Library, Scopus, Web of Science, Pubmed were used. Results: In the course of this review study, a modern characteristic of the kelp thallus as a pharmaceutical, cosmeceutical, food substance of plant origin is presented. The data on the chemical composition, harvesting, and processing of raw materials are summarized. The standardization and safety issues of kelp thallus are considered taking into account modern pharmacopoeial and food international requirements. The approaches to the qualitative and quantitative analysis of biologically active compounds (polysaccharides, iodine) and the determination of safety indicators are studied. Conclusions: The regulatory documentation that is used in the quality control of kelp needs to be finalized and updated. For pharmacopoeial analysis, all possible physicochemical methods (gravimetric, titrimetric, spectrophotometric) should be presented in the newly approved monograph. In this case, modern procedures should be developed, including HPLC with various types of detection (determination of the carbohydrates profile and polysaccharides, including methods with acid and enzyme hydrolysis). This will ensure the required level of quality, the safety of kelp (Laminaria) raw materials.

}, keywords = {alginic acid, Fucoidan, Iodine, Kelp, Laminaria japonica, Laminaria saccharina, Laminarin, Mannitol}, doi = {10.5530/pj.2020.12.132}, author = {Bokov DO and Potanina OG and Nikulin AV and Shchukin VM and Orlova VA and Bagirova GB and Kakhramanova SD and Al- Khafaji H and Balobanova NP and Evgrafov AA and Samylina IA and Krasnyuk II and Golubeva OA and Kuleshova ES and Moiseev DV and Bessonov VV} } @article {1207, title = {Paronychia argentea: A Critical Comprehensive Review on its Diverse Medicinal Potential and Future as Therapeutics}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {August 2020}, pages = {1172-1179}, type = {Review Article}, chapter = {1172}, abstract = {

Background: Paronychia argentea has been used since long as a traditional medicine for the treatment of diabetes, kidney stones, anti-microbial and many other human diseases. However, the plant has not been explored much. In the present scenario of drug resistance and toxicity associated with available drugs, there is a need for elaborated studies of plants like Paronychia argeneta which had been used as folk medicines. Aim and Objectives: The present article is focused on reviewing the ethnopharmacology, phytochemistry, traditional usage, biological activities, of Paronychia argentea which has been used in traditional medicinal system for ages. The aim of the study was to assess the ethnopharmacological usage of this plant and to explore therapeutic potentials and future opportunities for research. Materials and Methods: Information on the traditional usage and studies of the Paronychia argentea was gathered from from various journals, MSc dissertation, conference abstract, local books. Various search engines including Google Scholar, Baidu Scholar, Elsevier, ACS, Pubmed, Web of Science, CNKI and EMBASE were used to collect the information along with libraries. Results: Paronychia argentea has played an important role in traditional medicines in Algeria, Portugal, Israel and Jordan. The aerial parts of this plant are used as diuretics in Algerian traditional medicines and are used as antiurolithiasis. Leaf decoction of this plant is also used as diuretic. Paronychia argentea has been used as analgesic, treatment of stomach ulcer, anorexia, and flatulence in Portugal. Scientific studies on extracts of Paronychia revealed a wide range of pharmacological activities including anti-microbial activity, anti-oxidant, nephroprotective activity. Moreover, few reports have given contradictory data for usage of Paronychia when compared with its traditional usage. As in the case of alpha-amylase inhibitory efficacy of PA, it was observed that PA inhibits alpha-amylase activity but later on it was proven that PA does not have a hypoglycemic effect. Main bioactive metabolites present in this plant include alkaloids, flavonoids, volatile oils, etc. Conclusions: Based on this review, there are evidences from various studies regarding pharmacological effects of this plant as nephroprotective, anti-oxidant, anti-microbial activity. Some indications from in vitro studies have confirmed the inhibitory activity of this plant extract against alpha amylase enzyme. The available literature showed that most of the activities of the Paronychia can be accredited to the flavonoids present in them. Data regarding mechanisms of action of this plant along with pharmacokinetics, toxicology studies is still limited, which indicate the need of such studies for the clinical usage of this plant.

}, keywords = {Anti-microbial, Anti-oxidant, Bioactivity, Herbal medicine, Nephroprotective, Oxidative stress, Paronychia argentea, Therapeutic value, Ulcerative colitis}, doi = {10.5530/pj.2020.12.165}, author = {Vishnu Priya Veeraraghavan and Sardar Hussain and Janardhana Papayya Balakrishna and Surapaneni Krishna Mohan} } @article {1317, title = {Pharmacological Screening of Anti Lice and Antidandruff Activity of Ethanolic Extract of Leaves of Datura metel}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1653-1657}, type = {Research Article}, chapter = {1653}, abstract = {

It should be noticed that there is no drugs is available to treat lice and dandruff both are very great public health concern. So it is necessary to screen a drug especially of herbal origin to treat the both head lice and dandruff without affecting eyes. In the present study, Datura metel leaf extracts was evaluated for their insecticidal properties using head lice as an insect model. The study was conducted from November 2019 to March 2020. Plant sample (leaf) of Datura metel was collected from anantapur, Andhra Pradesh, India in November 2019. The various concentration of ethanolic extract of leaves of Datura metel was prepared by using distilled water. 20\%, 40\%, 60\% were used. A colony of P.humanus capitis was collected by combing the hair of 20-25 infected children at the age group of 10-15. Head lice were reared in the glass vessels covered with nylon mesh containing tufts of hairs. The hair tufts was impregnated with appropriate doses for the screening. Pure culture of M.furfur (MTCC: 1374) was obtained from institute of Microbial type of culture collection, Chandigarh, India. The culture was maintained in SDA medium. The current study afford scientific basis for the ethnomedical use of this plant as antilice application. It is concluded that it can be optimistic that the present work proved Datura metel of dual therapeutic advantage to be a potential phytochemical target in the design of a drug for the treatment of both lice and dandruff.

}, keywords = {Anti dandruff, Anti lice, Datura metel, Ethnomedical use, Pharmacological screening}, doi = {10.5530/pj.2020.12.225}, author = {Sreedhar V and J Mastanaiah and B Chakrapani and D Venkata Narayana and B Nagendra Babu and M Sushma and C Usha Sree and N Krishna Sree} } @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 {1120, title = {Phenolic Compounds from Caesalpinia sappan}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {410-414}, type = {Research Article}, chapter = {410}, abstract = {

Introduction: Caesalpinia sappan L., a traditional ingredient of food and beverages in South East Asia, was investigated for its chemical constituents. Methods: The compounds were isolated by 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 heartwood of C. sappan resulted in the isolation of sappanchalcone (1), caesalpiniaphenol G (2), and quercetin (3). Conclusion: Three phenolic compounds have been successfully isolated from C. sappan.

}, keywords = {Analgesic, Caesalpinia sappan, Caesalpiniaceae, Homoisoflavonoids}, doi = {10.5530/pj.2020.12.63}, author = {Van Ba Nguyen and Binh Duong Vu and Gia Khanh Pham and Bach Quang Le and Van Chuyen Nguyen and Chu Van Men and Van Thu Nguyen} } @article {1106, title = {Prospects for the Use of Spinach (Spinacia oleracea L.) Containing Phytoecdysteroids and Polyphenols}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {March 2020}, pages = {246-250}, type = {Original Article}, chapter = {246}, abstract = {

Background: Phytoadaptogens, biologically active compounds increasing the nonspecific resistance of the human organism, are well known for the prevention and correction of stressful conditions. Phytoadaptogens group includes phytoecdysteroids and polyphenols, that are characterized by the multiplicity of pharmacological effects in combination with the low toxicity. According to literature data, spinach (Spinacia oleracea L.) is a promising source of these compounds. This work aims to systematize data on the chemical composition of biologically active compounds of spinach, that determine its adaptogenic properties and concentration methods in the spinach processing for use in specialized foods and dietary supplements. Materials and Methods: Manifold electronic search engines, electronic databases, and libraries such as Google, Google scholar, Crossref, Indian Science Abstracts, Emerging Sources Citation Index, e-Library, Scopus, Web of Science, Pubmed, Chemical Abstracts, Index Copernicus, scientific literature had been searched and data obtained. Results: Botanical characteristics of spinach, main cultivation conditions, the latest data on the chemical composition of raw spinach material cultivars and extracts based on it are presented in this study. Schemes for the obtaining of products enriched with polyphenols and ecdysteroids are considered, and ways of proper purification are mentioned. Conclusion: It is recommended to introduce spinach into the diet of healthy people in order to increase the functional reserves of a person during periods of hypovitaminosis, overwork, intense physical exertion, and also to compensate for the adverse effects of external factors. Spinach extracts containing phytoecdysteroids (20-hydroxyecdysone) and polyphenols (flavonoids) can be used as a prophylactic to overcome the negative effects of stress, accelerate recovery after strong physical and mental stress, particularly for people with extreme occupations, athletes, and those who are engaged in hard physical labor.

}, keywords = {20-hydroxyecdysone, Flavonoids, Phytoecdysteroids, Polyphenols, Spinach leaves, Spinacia oleracea}, doi = {10.5530/pj.2020.12.38}, author = {Bokov DO and Sidorova YuS and Mazo VK and Bessonov VV} } @article {1320, title = {Representatives of the Genus Goryanka (Epimedium L) {\textendash} a Promising Source of Raw Materials for the Creation of Medicines for the Treatment of Erectile Dysfunction in Men}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1710-1715}, type = {Research Article}, chapter = {1710}, abstract = {

Erectile dysfunction and multiple mechanisms of its development are one of the most pressing problems of modern medicine. In the twenty-first century, millions of men around the world suffer from sexual disorders, and the number of such patients is only growing from year to year. The flavonoid icariin, contained in plants of the genus Epimedium L., is a promising pharmacologically active substance used for erectile dysfunction, due to its ability to affect type 5 phosphodiesterase, inhibiting its activity. To date, domestic and foreign pharmaceutical companies produce biologically active food additives and herbal preparations, which include Goryanka extract. But the range of standardized herbal medicines is very small.

}, keywords = {Drug, Epimedium Estrellita, Icariin, Impotence}, doi = {10.5530/pj.2020.12.231}, author = {Bukinich Darya Dmitrievna and Salova VG and Odintsova EB and Rastopchina OV and Solovyovа NL and Kozlova AM and Krasniuk II (jun) and Krasniuk II and Kozlova Zh M} } @article {1292, title = {Resveratrol: Latest Scientific Evidences of its Chemical, Biological Activities and Therapeutic Potentials}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1779-1791}, type = {Review Article}, chapter = {1779}, abstract = {

Background: Resveratrol is a non-flavonoid polyphenol possesses many biological properties with great potential to develop into various products. In order to cure a wide variety of diseases, resveratrol has attracted a great deal of attention for medicinal purposes. Objective: The present review aimed to provide a comprehensive literature summary of latest scientific evidences on the chemistry, biological properties and therapeutic potentials of resveratrol. Methods: To complete this review, relevant literatures were collected from several scientific databases, including Google Scholar, Pubmed and ScienceDirect, using keywords {\textquotedblleft}source{\textquotedblright}, {\textquotedblleft}chemistry{\textquotedblright}, {\textquotedblleft}bioavailability{\textquotedblright}, {\textquotedblleft}pharmacokinetics{\textquotedblright}, {\textquotedblleft}isolation{\textquotedblright}, {\textquotedblleft}anticancer{\textquotedblright}, {\textquotedblleft}analgesic{\textquotedblright}, {\textquotedblleft}antiinflammatory{\textquotedblright}, {\textquotedblleft}antidiabetic{\textquotedblright}, {\textquotedblleft}nephroprotective activity{\textquotedblright}, {\textquotedblleft}neuroprotective activity{\textquotedblright}, {\textquotedblleft}antiobesity{\textquotedblright}, {\textquotedblleft}cardioprotective effects{\textquotedblright}, {\textquotedblleft}antioxidant{\textquotedblright}, {\textquotedblleft}anti-aging{\textquotedblright} with resveratrol. After a detailed screening process for inclusion and exclusion, the information obtained was summarised. Results: The information on the source, chemistry, bioavailability, biological and therapeutic potentials of resveratrol were tabled. In various pathological conditions, resveratrol can be considered as powerful antioxidants along with multidimensional molecular targets such as NF-ҡB, MAPK, AMPK, SIRT-1, Nrf-2, m-TOR, PI3K/Akt and PPAR-γ signaling pathways. Conclusion: Based on the existing knowledge, we may believe that resveratrol has a significant therapeutic potential for the treatment of various diseases. To accelerate the development and utilization of resveratrol as promising products, in-depth studies should be focused on exploiting its properties and developing phytopharmaceuticals.

}, keywords = {Bioavailability, Inflammatory cytokines, Molecular targets, Pharmacology, Resveratrol, Toxicity}, doi = {10.5530/pj.2020.12.240}, author = {Nur Mursyida Saad and Mahendran Sekar and Siew Hua Gan and Pei Teng Lum and Jaishree Vaijanathappa and Subban Ravi} } @article {1305, title = {The Role of Recombinant Parathormone derivative in Bone healing. Making the Unfavorable, Favorable - A Systematic Review}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1753-1768}, type = {Review Article}, chapter = {1753}, abstract = {

Background: Teriparatide is a recombinant parathormone derivative encompassing the first 1-34 amino acids off PTH, which is said to contain potent anabolic capability. It is said to induce osteoblastogenesis thereby placing an essential role in bone healing. The aim of this systematic review is to evaluate the best available evidence from randomized controlled trials analyzing the effectiveness of teriparatide on bone regeneration and healing in osteoporotic patients and patients with fractures. Aim: This systematic review aims to assess whether Teriparatide enhances bone regeneration and healing in terms of improving clinical, radiographic, histologic parameters and Biomarkers of Bone formation and resorption. Materials and Methodology: A comprehensive search was done in databases such as {\textquoteleft}PubMed{\textquoteright}, {\textquoteleft}Google Scholar and {\textquoteleft}Cochrane{\textquoteright} databases based on pre-determined eligibility criteria. Randomized control trials assessing the effectiveness of Teriparatide in Bone healing in fractures as well as osteoporosis were selected after thorough screening. Results: The selected 13 studies compared teriparatide to either placebo or another anti-resorptive drug. Out of the 13, 8 studies were done to evaluate the improvement and healing of bone in Osteoporotic patients whereas 5 studies were done on improvement in fracture healing. The studies evaluated outcome parameters such as Clinical and Radiological improvement, Biomarkers of Bone resorption and formation and Safety.6 studies assessed clinical parameters, 12 studies assessed radiological parameters, 7 studies assessed biomarkers, 11 studies assessed safety parameters by means of occurrence of any adverse effects. All the 8 studies done on osteoporotic patients showed a good improvement. Of the 5 studies on fracture healing, only 2 studies showed beneficial effects while the other 3 did not show any benefits. Conclusion: Teriparatide could have beneficial effects in bone healing in osteoporotic patients and is well tolerated. However, the results are inconclusive whether they have beneficial effects in treating fractures. More Homogenous Randomized control trials are required to ascertain whether teriparatide could improve bone healing.

}, keywords = {Bone healing, Fracture, Parathormone, Recombinant derivative, Teriparatide}, doi = {10.5530/pj.2020.12.238}, author = {S Swarna Meenakshi and Sheeja S Varghese} } @article {1321, title = {Seagrass in the Control of Hyperglycemic and Hyperlipidemic States of Streptozotocin Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {November 2020}, pages = {1716-1721}, type = {Research Article}, chapter = {1716}, abstract = {

Background: The present study intended to evaluate the beneficial effects of the seagrass Halophila beccarii, against induced diabetes mellitus in rat models. Halophila beccarii is a type of Seagrass abundant in Pulicat Lake of Andhra Pradesh, India. Objective: Evaluating the anti-hyperglycemic and anti-hyperlipidemic properties of seagrass extract in comparison with standards. Materials and Methods: STZ induced diabetic rat models were adopted to analyze the effect of long-term treatment with seagrass extract on blood glucose, HbA1c and serum lipids. Results: The methanolic extract of seagrass demonstrated a significant drop of blood glucose levels (52\%), in diabetic rats, after 6 h of supplementation. After 40 days of treatment with 500 mg/day of seagrass extract, STZ diabetic rats exhibited tremendous decrease in fasting blood glucose with significant improvement in glycemic control as evidenced by controlled levels of HbA1c. Lower levels of triglycerides, total cholesterol, LDL and VLDL cholesterols and higher levels of HDL cholesterol in STZ-induced diabetic rats provided an evidence for significant anti hyperlipidemic property of seagrass extract. Conclusion: Phytochemicals of seagrass like phenols, flavonoids and bioactive lipids contribute to the anti-hyperglycemic and anti-hyperlipidemic activities and Halophila beccarii extract serves as a natural supplement in the management of diabetes.

}, keywords = {Diabetes mellitus, FBG, Halophila beccarii, HbA1c, HDL, LDL}, doi = {10.5530/pj.2020.12.232}, author = {M Vani and P Uma Maheswari Devi} } @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 {883, title = {Anatomical and Histochemical Characterization of Leaves of Luffa cylindrica (L.) M. Roem}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {511-514}, type = {Original Article}, chapter = {511}, abstract = {

Background: Luffa cylindrica (L.) M. Roem. (Cucurbitaceae) is an herbaceous plant used for food as compose salads and do sweets and also used in traditional medicine as treat parasitic infections and intestinal diseases. Although this information, there are not many relates about anatomic characters for use in your quality control. Objective: The aim was investigating the anatomical characters of petiole and leaf blade and characterizing the metabolites in the leaf blade of L. cylindrica. Materials and Methods: Semipermanent histological slides were prepared for analysis of petiole and leaf blade in optical microscopy. Histochemical tests were also performed in the leaf blade. Results: The anatomical study revealed information about the type of trichomes, cuticle, vascular bundles and arrangement of the tissues that determine the botanical identity of this species. It was also identifying, for the first time, the presence of two types of trichomes in both of leaf blades faces. The histochemistry allowed determining which metabolites are in the leaf blade and also their location. Conclusion: The study described new characters for L. cylindrica and the results provide support to quality control of the species.

}, keywords = {Anatomy, Cucurbitaceae, Histochemistry, Luffa cylindrica, microscopy}, doi = {10.5530/pj.2019.11.81}, author = {La{\'\i}s Emanuelle Bernardo Vieira and Rafaela Damasceno S{\'a} and Karina Perrelli Randau} } @article {862, title = {Antidiabetic Aptitude of Cordia sebestena and its Outcome on Biochemical Parameters, Serum Electrolytes, and Hematological Markers}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {418-423}, type = {Original Article}, chapter = {418}, abstract = {

Objective: The present study investigated the antidiabetic outcome of ethanolic extract of Cordia sebestena fruit (EECSF) in streptozotocin (STZ)-induced diabetogenic rodents and evaluated its consequence to improve the level of biochemical parameters, serum electrolytes level, and hematological indices along with its impact on body weight. Materials and Methods: The albino rodents were selected to observe oral glucose tolerance test by oral intake of aqueous glucose solution (4 g/kg, body weight) in normal rodents and assessment of blood glucose level after administration of EECSF at 100 and 200 mg/kg and standard drug glibenclamide at 0.6 mg/kg, body weight. Antidiabetic activity was estimated in the chronic biological model by STZ (65 mg/kg/i.p.)-induced diabetes in rodents escorted by the determination of blood glucose. Further pharmacological research was carried out to explore the effect of EECSF on body weight, variations in biochemical parameters including aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, total bilirubin, and total protein, transformations in serum electrolytes such as Na+, K+, Cl-, and Ca2+ along with estimation of hematological indices such as red blood cells, white blood cells, hemoglobin, lymphocytes, neutrophils, eosinophils, and monocytes. Results: It was discovered that EECSF significantly lowered the blood glucose level of diabetic rodents along with enhancement in body weight. Correspondingly, EECSF significantly ameliorated the biochemical parameters, serum electrolytes, and hematological indices. Conclusion: The results demonstrated the antidiabetic potential of EECSF in STZ-induced diabetes in rodents, and it could be selected to benefit from diabetes and its affiliated complexities inclusive of anemia, diabetic nephropathy, retinopathy, neuropathy, and hepatitis.

}, keywords = {Anemia, Antidiabetic, Cordia sebestena, Glucose, Streptozotocin}, doi = {10.5530/pj.2019.11.65}, author = {Sachin Chaudhary and Harish Chandra Verma and Mandeep Kumar Gupta and Hitesh Kumar and Sudhansu Ranjan Swain and Ramesh Kumar Gupta and Abdel-Nasser El-Shorbagi} } @article {1054, title = {Antioxidant Activity, HPTLC Fingerprint and Discriminant Analysis of Plantago major Leaves from Diverse Origins in Indonesia}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1483-1489}, type = {Original Article}, chapter = {1483}, abstract = {

Introduction: Plantago major L. (Plantaginaceae) is a perennial herb having contribution to the folk medicine all around the world, including Indonesia with wide geographical distribution. Plant materials origin is one factor that significantly influences the quality of herbal medicines. Materials and Methods: In this paper, High-Performance Thin Layer Chromatography (HPTLC) method using pattern-oriented approach has been employed to evaluate the quality of Plantago major leaves collected from seven origins in Indonesia. To differentiate the antioxidant capacities of those plant materials, the crude extracts were tested using 1,1-diphenyl-2-picrylhydrazyl (DPPH), total phenolics, and total flavonoids assay methods. Results: The results showed that radical scavenging activity, total phenolics, and total flavonoids of plant material from seven origins were significantly different. Moreover, HPTLC fingerprints analyzed with chemometrics showed an ability to discriminate the leaves samples from various origins as well as detect chemicals responsible for discrimination. Two models using principal component analysis (PCA) and partial least squares (PLS-DA) were built in chemometrics test. The PCA model was able to describe the studied samples by using four principal components with a value of explained variance of 95\%, whereas PLS-DA model accurately classified the leaves samples with prediction ability of 100\%. In the PCA, loading plot of the first PC showed that peaks number 10 and 12 are the most important peaks for clustering of the samples. Conclusions: Plantago major collected from different origins revealed different radical scavenging activity and concentration of total phenolics as well as total flavonoids. HPTLC fingerprints coupled with chemometrics analysis can be used as an alternative to marker-oriented method for the quality control of Plantago major.

}, keywords = {Chemometrics, Flavonoids, Herbal medicines, Pattern-oriented, Phenolics, PLSDA}, doi = {10.5530/pj.2019.11.229}, author = {Kartini Kartini and Christina Avanti and Chutima Phechkrajang and Omboon Vallisuta} } @article {1035, title = {Chemical Constituents and Antifungal Activity of Leaf Essential Oil from Oreopanax ecuadorensis Seem. (Pumamaki), Endemic Plant of Ecuador}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1544-1548}, type = {Research Article}, chapter = {1544}, abstract = {

Background: Oreopanax ecuadorensis Seem. is a plant from Ecuador, that is found in the Andean region of the country. The plant is commonly used in protective rituals, and as an antiflu, analgesic and disinfectant medicine. Aim: The research aims to extract and analyze the chemical composition and evaluation of its antifungal potential of the essential oil extracted from its leaves. Methods: steam distillation was used for the extraction of essential oil, the evaluation of its components was performed by GC/MS, and the antifungal evaluation by the disc diffusion method. Results: The essential oil was obtained with a yield of 0.05\%. 33 compounds were detected of which 30 were identified, corresponding to 99.28\%; the most abundant molecules were: thujene \<α-\> (36.63\%), followed by bicyclogermacrene with (8.76\%), pinene \<β-\> with (8.32\%) and limonene with 5.15\%. Three of the four strains evaluated were affected by the oil at concentrations of 1.25\%, inhibiting its growth. The strains were: Trichophyton mentagrophytes, Trichophyton rubrum and Microsporum canis. Conclusion: The essential oil shows good antifungal activity, which could be less than 1.25\%. In this way, this medicinal plant is valued by verifying ancestral knowledge in the use of medicinal plants by the Andean people of Ecuador.

}, keywords = {Antifungal activity, GC/MS, Oreopanax ecuadorensis, Puma Maki}, doi = {10.5530/pj.2019.11.236}, author = {Paco Noriega and Bryan Vergara and Carlos Carillo and Tatiana Mosquera} } @article {974, title = {Comparative Evaluation of Anti-Inflammatory Potential of Ethanolic Extract of Leaf, Bark and Flower of Tecoma stans with Ibuprofen- An In vitro Analysis}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1088-1092}, type = {Research Article}, chapter = {1088}, abstract = {

Background: Endodontics has always been indebted to pharmaceutical sciences to provide it with necessary analgesics and anti-inflammatory agents. More specifically, there has always been a need for anti-inflammatory phytotherapeutic agents as the commercially available synthetic anti inflammatory drugs have their own limitations due to undesirable side effects. Hence, novel potent analgesic and anti-inflammatory drugs without considerable side effects from the natural sources are under evaluation. Tecoma stans (Bignoniaceae) is an ornamental plant found throughout India. It has been shown to have variety of medicinal properties. In the present study, we have shown that potential anti inflammatory activity of different parts of Tecoma stans (T.stants) and compared with standard drug. Aim: To evaluate the in vitro anti inflammatory potential of different parts of T.stans ethanolic extract and to compare the anti inflammatory activity with standard drug ibuprofen. Methodology: The ethanolic extraction of T.stans{\textquoteright}s bark, leaves and floweres was done as per the standard method. Different concentrations (100, 200, 300, 400 and 500 μg/ml) of the extracts were used for anti-inflammatory activity by inhibition of albumin denaturation. All samples were analyzed in triplicate. The results were statistically analyzed. Results: All the three parts of the plant extract have shown to have anti inflammatory activity in a dose-dependent manner. However, the leaf and flower extracts of T.stans were found to have 100 percent anti-inflammatory pontential than standard drug ibuprofen. Conclusion: It is concluded from the present findings that T.stants possess anti-inflammatory properties which could be due to presence of active constitutents presen in the plant extracts. Hence, T.stans may serve as one of the anti inflammatory herbal durgs for Endontic infection-induced inflammation and related to dental diseases. Further studies on the identification of the active principles present in the leaf and flower extract are warranted to assertatin its potentials.

}, keywords = {Anti-inflammatory Effect, Bark, Flower, Leaf, Tecoma stans}, doi = {10.5530/pj.2019.11.170}, author = {Swarna SK and Nivedhitha MS and Vishnu Priya V and Gayathri R and Selvaraj J and Madhan K and Shyamala Devi B} } @article {1027, title = {Detailed Pharmacognostical and Phytochemical Screening of Stem and Stem Bark of Ficus semicordata Buch.-Ham. Ex sm. - An Extra Pharmacopoeial Drug of Ayurveda}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {October 2019}, pages = {1303-1311}, type = {Original Article}, chapter = {1303}, abstract = {

Introduction: Stem bark of Bhumi udumbara (Ficus semicordata Buch.-Ham. ex Sm.) is used traditionally in the treatment of leprosy, ulcer, dysentery, wound, pregnancy, complaints of gastric, liver, bladder and various disorders. In present study, stem and stem bark of F. semicordata are explored for their microscopic including powder microscopy, physiochemical and preliminary phytochemical aspects. Materials and Methods: Stem and stem bark of the plant, after proper authentication by BSI Kolkata, were evaluated following standard procedures. Results: Stem is hard, cylindrical, cut pieces measures about 10 - 25cm in length and 0.4 {\textendash} 0.8 cm in diameter. Diagrammatic transverse section of stem shows outer cork followed by wide parenchymatous cortex with prismatic and rhomboidal crystals, starch grains and tannin content. Powder light brown in colour; odour woody; taste tasteless to astringent; texture fibrous. Stem bark is hard, single quilled after drying, outer dark reddish brown in colour with presence of lenticels, longitudinal cut fibres, rough in surface. Diagrammatic section, of the bark, shows outer several layered cork followed by cortical region along with medullary rays. Powder tortilla(brown) in colour; odour slightly aromatic; taste astringent; texture fibrous. Loss on drying at 110{\textdegree}C was found to be 7.41\% and 8.60\% of stem and stem bark respectively. HPTLC results shows 3 peaks and 0 peak at 254 and 366 nm of stem and 3 peaks at 254 and 366 nm of stem bark respectively. Discussion and Conclusion: Woody stem and presence of brown content, tannin, rhomboidal and prismatic crystals in stem and stem bark are the diagnostic characters.

}, keywords = {Anukta Dravya, Bhu-udumbara, Bhuindumer, Extra-pharmacopoeial, Ficus semicordata}, doi = {10.5530/pj.2019.11.202}, author = {Gupta Shashi and Acharya Rabinarayan and Harisha CR and Shukla Vinay} } @article {870, title = {Effect of Porana paniculata Whole Plant on Blood Glucose Levels and Lipid Profile of STZ Induced Diabetic Rats}, journal = {Pharmacognosy Journal}, year = {2019}, month = {March 2019}, pages = {xx-xx}, type = {Original Article}, chapter = {xx}, abstract = {

Background: To establish the antidiabetic potential of Porana paniculata whole plant belongs to Convolvulaceae family. Methods: Extraction and preliminary phytochemical screening were conducted by standard methods. Antidiabetic activity was evaluated by streptozotocin induced diabetic rats where the hydroalcoholic extract of plant was administered orally at a dose of 250 and 500 mg/kg for 30 days. Blood glucose levels were estimated at 1st, 10th, 20th and 30th day of study. Lipid profile was studied 30th day of study and body weight of the animals was measured at day 1 and 30. Results: Plant extract significantly (p\<0.01) reduced the blood glucose levels at both the tested dose levels of 250 and 500 mg/kg. The lipid profile was estimated in which the plant extract showed significant improved in both tested dose level that is 250 and 500 mg/kg. The body weight of the animals under study was also estimated on day 1 and 30 in which a good control was observed by the plant extract. Conclusion: Antidiabetic activity of Porana paniculata whole plant extract may be due to the presence of various phytoconstituents. Present study gives a scientific evidence for the folklore claim of the plant under study for its use in diabetes.

}, keywords = {Diabetes, Folklore, lipid profile, Porana paniculata, Streptozotocin}, doi = {10.5530/pj.2019.11.xx}, author = {Sanjeeva Kumar A and Raveendra Reddy Juturu and Rama Mohan Gupta Vankadari} } @article {1031, title = {The Effect of Ultraviolet-B Radiation Exposure on Hibiscus cannabinus Linn with its Phytochemical and Pharmacological Responses}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {November 2019}, pages = {1540-1543}, type = {Research Article}, chapter = {1540}, abstract = {

Aim: Exposure of UV-B Radiation on\ Hibiscus cannabinus Linn and to evaluate both Phytochemical and Pharmacological responses. Objective: UV-B can increase the nutrients contents from plants, plants become tastier and increases the yield and UV-will make plants resistant to fungal infections and stimulate the production of phytomarkers. Material and Methods: Hibiscus cannabinus Linn seeds were soaked with 50\% H2O2 for 12 hours and then inoculated with the Azospirillum. UV-B radiation cabinet was provided by UV lamps which are above 15 cm from control maintained. Normal daylight exposed control group Seedlings irradiated for 2 hour per day (12.30 pm to 2.30 pm) for 20 days. Results and Discussion: 20 days treatment increases total phenolic contents and sugars content were decreased in uncovered leaf tissue. Protein content was at first diminished but expanded on the 20 day of UV-B treatment. Also, perform pharmacological studies no toxic elements are observed 20 days treatment and pharmacological activity by using anticancer activity by using human colon HT-29 cancer cell line. UV light exposed plants shows good anticancer activity when compared with non UV exposed Plant.

}, keywords = {Cancer cells line HT-29, Hibiscus cannabinus Linn, Total Phenolic Contents, UV-B radiation}, doi = {10.5530/pj.2019.11.235}, author = {T Sundarrajan and V Velmurugan and MK Kathiravan and K Manikandan and KS Lakshmi and MR Ganesh} } @article {907, title = {Effectiveness of Moringa oleifea Extract in Attenuating the Toxic Effect on Platelet Count: An Experiment on Cadmium Exposed Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {689-693}, type = {Original Article}, chapter = {689}, abstract = {

Aims and Objective: To determine the role of Moringa oleifera on total platelet count alterations (T-PC) in rats treated with cadmium. Materials and Methods: In the present study female adult Wistar Albino rats, (180-200) gm were divided into, Group I-normal control, Group II-pretreated control, group III-cadmium treated , group IV- pre-treated with Moringa oleifera leaf extract (MOE) and then administered oral cadmium for a day, with n=6 each Results: Indicate that the pre-treatment with MOE (100 mg/kg/bw) prior to cadmium infusion augmented the level of total platelet count (p<=0.001) as compared to the cadmium-exposed group, which might have a role in clotting mechanisms also. Conclusion: Moringa oleifera extract has a beneficial effect on platelet count in cadmium-induced animal model.

}, keywords = {Cadmium, Clotting Mechanisms, Moringa oleifera, Platelet Count, Toxicity}, doi = {10.5530/pj.2019.11.109}, author = {Vinodini NA and Pratik Kumar Chatterjee and Kunal and Suman VB and Rashmi KS and Nayanatara AK and Anupama N and Ramesh M. Bhat and Sheela Joice P} } @article {984, title = {Evaluation of Antibacterial Activity of Lemongrass Oil Against Oral Clinical Isolates {\textendash} An In vitro Study}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1023-1028}, type = {Original Article}, chapter = {1023}, abstract = {

Background: There are 1,200 oral species out of which 400 are potentially important and 20 organisms are periopathic. Periodontal flora plays the important role in initiation and progression of periodontal diseases. There are various conservative and surgical procedures to treat and prevent periodontal diseases. Local drug delivery agents reduce microbial burden, blocks collagenase activity and inhibits bone loss; out of which tetracycline is common in use. Unwanted side effects and resistance of microorganisms towards antibiotics due to their widespread use have modified the general prescription about their efficacy. Various researches elucidate that herbal extracts exhibit wide range of antibacterial activity. In recent years, Lemongrass essential oil gains scientific interest as it targets even the periodontal pathogens. The purpose of this study is to comparatively evaluate the antibacterial activity of lemongrass essential oil with that of tetracycline. Aim and objective: To comparatively evaluate the antibacterial activity of lemongrass essential oil with tetracycline against Streptococcus mutans, Staphylococcus epidermidis and Lactobacillus and to determine the minimal inhibitory concentration of lemongrass essential oil. Study design: In vitro. Materials and Methods: It is an in vitro study done to demonstrate the antimicrobial activity of lemongrass against the oral microbes. Based on their involvement in various clinical conditions Streptococcus mutans, Staphylococcus epidermidis and Lactobacillus were selected for the study. These organisms were inoculated to a solid media and incubated overnight aerobically at 37{\textdegree}C to obtain a pure culture. The culture was made as a suspension in sterile saline with the turbidity matching 0.5 Macfarland standard. This is used to make a lawn culture on the Mueller Hinton Agar. Antimicrobial effect of tetracycline was tested using standard disc of doxycycline 30 mcg (Himedia, SD012) and sterile disc was used to prepare lemongrass essential oil which contained 10 μl, 15 μl and 20μl. In each category 5 discs were tested to get a mean zone of inhibition. After 24 hours of incubation the zone of inhibition was measure in mm using a scale. The measured zone size was tabulated and compared among the groups. Results: The minimal inhibitory concentration of lemon grass essential oil was estimated to be 10μl. Statistically significant zone of inhibition and antibacterial zone was greater in lemongrass essential oil than tetracycline for Streptococcus mutans and Staphylococcus epidermis. Conclusion: Lemongrass essential oil showed higher antibacterial activity than tetracycline. Hence, it can be used as a good alternative to tetracycline or adjunctive in the treatment of periodontitis.

}, keywords = {Antibacterial, Lemongrass essential oil, Minimal inhibitory Concentration, Tetracycline}, doi = {10.5530/pj.2019.11.161}, author = {Paavai Ilango and Vasugi Suresh and Ayswarya V Vummidi1 and Vanessa Ravel and Veejai Chandran and Arulpari Mahalingam and Vineela Katam Reddy} } @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 {884, title = {Flavonoids of East Asian Species Serratula manshurica Kitag}, journal = {Pharmacognosy Journal}, year = {2019}, month = {March 2019}, pages = {xx-xx}, type = {Original Article}, chapter = {xx}, abstract = {

Aim/ Background: The flavonoid composition of the East Asian species Serratula manshurica Kitag. (Family Asteraceae) growing in the Primorsky Territory, the Amur region and in the South of the Khabarovsk Territory of Russia was studied. Materials and Methods: Flavonoids quercetin-4{\textquoteright}-O-β-D-glucuronopyranoside (1) and apigenin-7-O-β-D-glucuronopyranoside (2) were isolated from Serratula manshurica by methods of liquid extraction and recrystallization. The structures of the isolated compounds were identified by UV, NMR spectroscopy and mass spectrometry with electrospray ionization. Separation and quantitative content of flavonoids in the extracts of the aerial part (Leaves, stems, inflorescences) of Serratula manshurica was observed by RP HPLC. Results and Conclusion: The change in the amount of some flavonoids in various phenological phases in the overhead part of Serratula manshurica Kitag was studied. It was revealed that the maximum concentration of flavonoid aglycones in the plant was observed during the before budding in the budding period and their glycosides prevaily in the flowering phase. Widespread across the Far East, Serratula manshurica is promising and renewable source of bioactive compounds.

}, keywords = {Flavonoids, Leaves, NMR spectroscopy, Serratula manshurica, Steams}, doi = {10.5530/pj.2019.11.xx}, author = {Myagchilov Aleksey V and Sokolova Larisa I and Gorovoy Peter G and Dmitrenok Pavel S} } @article {989, title = {GC-MS Analysis of Bioactive Phytochemicals in Methanol Extract of Aerial Part and Callus of Dipterygium glaucum Decne}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {1055-1063}, type = {Original Article}, chapter = {1055}, abstract = {

Introduction: This study was designed to evaluate the phytocomponents present in aerial part and in vitro induced callus methanol extracts of Dipterygium glaucum by Gas Chromatography-Mass Spectrometry (GC-MS) technique. Methods: GC-MS analysis of aerial part sample and callus produced from leaf of D. glaucum extracted in methanol solvents was performed using GC-MS QP 2010 Plus (Shimadzu, Japan) system comprising an auto sampler (AOC-20i) and a gas chromatograph interfaced to a mass spectrometer. Results: This study was carried out to identified and comparative analysis of bioactive phytochemicals from aerial part extract and callus extract of D. glaucum. This analysis revealed that both the extracts have 69 different types of phytochemical components in varying quantities. Some of the important phytochemical compounds were Stigmasterol, β-sitosterol, γ-sitosterol, Campesterol, Squalene, n-Hexadecanoic acid, Stearic acid, Myristic acid, Quinazoline, Linalyl acetate etc. These chemical compounds have anticancer, antitumor, anti-inflammatory, antidiabetic and antioxidants properties. Conclusion: This study represents the detection and identification of different phytochemical compounds from aerial part and callus extract of D. glaucum. Thus, due to the presence of various important bioactive phytocomponents this plant is recommended as a pharmaceutically important plant.

}, keywords = {Callus, Campesterol, Capparidaceae, Fatty Acid, Stigmasterol, Terpenoids}, doi = {10.5530/pj.2019.11.165}, author = {Choudhary D and Shekhawat JK and Kataria V} } @article {947, title = {The Identification of Bioactive Compounds from Turbinaria ornata (Turner) J. Agaradh and Computational Studies}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {873-883}, type = {Original Article}, chapter = {873}, abstract = {

Aim/Background: The present work was carried out to identify some of the bioactive components present in the Brown seaweed Turbinaria ornata by GC-MS technique, and to ascertain its medicinal properties. Materials and Methods: GC-MS analysis of some of the potent volatile constituents present in the pet ether of Turbinaria ornata was performed. MD simulations were performed for complex structures of human secretory PLA2 and P38 kinase. GC-MS chromatogram showed peaks indicating the presence of various compounds of interest. The interpretation of the mass spectrum of GC-MS was done using the Database of Indian Institute of Crop Processing Technology (IICPT). Twenty compounds were identified in pet ether extract of Turbinaria ornata. All 20 compounds were screened using PASS online activity prediction server, for the possession of anti-inflammatory potency and the selected target proteins were subjected to molecular docking studies. MD simulations were also performed for the top listed compound 16 which was identified from D3P extract (2,3-Diphenylcyclopropyl)methyl phenyl sulfoxide, trans-). Similarly, the complex structure of PLA2 (phospho-ethanolamine, PE) and P38 kinase (3-(2-pyridine-4-ylethyl)-1H-indole) were simulated for comparative study. Results and Conclusion: Based on the in silico results, the binding affinities for compounds of T. ornata were judged against known standards for its capability to restrain inflammation and to promote possibility for scheming potential antiinflammatory lead from natural compounds were discussed.

}, keywords = {Bioactive components, Brown algae, GC-MS, Molecular docking and simulation studies, T. ornata}, doi = {10.5530/pj.2019.11.140}, author = {S. Deepa and K. Sujatha and D Velmurugan} } @article {878, title = {In vivo Toxicopathological Evaluation of a Purified Bioflocculant Produced by Arthrobacter humicola}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {May 2019}, pages = {486-492}, type = {Original Article}, chapter = {486}, abstract = {

Introduction: In spite of the commendable flocculating activities of microbial flocculants, a good number of them potentiate significant toxicity. This study evaluated the in vivo toxicological implications of treatment with the Purified bioflocculant (PB) from Arthrobacter humicola using OECD guidelines. Materials and Methods: In the acute toxicity assessment, a single oral administration of 2000 mg/kg body weight (b.w.) of PB was given to the Wistar rats and the animals were observed for 2 weeks. The daily dose toxicity testing was performed through daily oral treatment with graded doses (50, 200 and 500 mg/kg b.w.) of PB for 4 weeks. Clinical signs of toxicity, behavioral changes, hematological and biochemical parameters were thereafter evaluated. Results: PB at 2000 mg/kg b.w. produced no treatment-mediated signs of toxicity, behavioral changes or mortality in the animals. Thus, its no-observed-adverse-effect level was estimated to be above 2000 mg/kg b.w. In the repeated dose toxicity testing, treatments with PB also revealed no significant differences in the feeding patterns, lipid profiles, hematological and clinical biochemistry parameters when compared with the control group. Although, at 500 mg/kg b.w. PB, a significant increase was observed in the serum activities of alkaline phosphatase, nonetheless, cage side observations recorded no treatment-induced signs of toxicity and macro-histopathological examinations of all the investigated organs also revealed no obvious morphological changes. Conclusion: The overall results suggested that PB was well tolerated by the animals and is endowed with monosaccharides bearing functional groups of flocculation importance, thus, suggesting its potential application as a safe actinomycetes bioflocculant for water treatment.\ 

}, keywords = {Actinomycetes, Arthrobacter humicola, Bioflocculant, Hematological, Polysaccharides, Wastewater treatment}, doi = {10.5530/pj.2019.11.77}, author = {Mayowa Oladele Agunbiade and Sabiu Saheed and Esta Van Heerden and Carolina Henritta Pohl} } @article {818, title = {Investigation on Pharmacognostic Parameters of Sirunagapoo (Mesua ferrea L): A Traditional Indian Herbal Drug}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {225-230}, type = {Research Article}, chapter = {225}, abstract = {

Introduction: Flower buds of Sirunagapoo (Mesua ferrea) are used in Siddha system of medicine as carminative, astringent and anti-vatha. It is traditionally used to treat various diseases like cough, venerial, white discharge, diarrhea, over-bleeding and peripheral neuritis. It is one of the major ingredients in Amukkara choornam, Inji choornam and Elathi choornam which are used for indigestion, loss of appetite and gastritis. Methods: Pharmacognostic characters of M. ferrea flower bud were studied through powder microscopy. Both ethanol and aqueous extracts were investigated for phytochemical screening, total phenolic content, in vitro antioxidant and anti-inflammatory properties and the ethanolic extract was subjected to GC-MS analysis. Results: Powder microscopy of flower buds of M. ferrea revealed the presence of brachysclereids, macrosclereids, starch grain, crystals and parenchyma cells. The powdered material exhibited 6.07\% of loss on drying, 2.93\% of total ash, 11.34\% of water-soluble extractive and pH value 5.35. Data showed the presence of sterols only in ethanol extract and phenols, flavanoids, saponins and coumarins in both ethanol and aqueous extracts. Ethanolic extract was found to contain higher concentration of total phenols (1030 mg GAE/L) when compared to aqueous extract. Totally forty compounds were detected in GC-MS analysis and the major compound is eugenol (61\%) and cinnamaldehyde (15\%). In vitro studies revealed antioxidant in terms of DPPH free radical scavenging property (IC-50 = 229.7 mg/ml) remarkable anti-inflammatory activity using RBC membrane stabilization assay (70.27\%) were noted. Conclusion: This study provides the pharmacognostic standards, phytochemical profile, major volatile compounds and in vitro properties of Mesua ferrea flower bud.

}, keywords = {GC-MS, In vitro studies, Mesua ferrea, Pharmacognosy, Phytochemicals}, doi = {10.5530/pj.2019.11.35}, author = {Perumal Rajalakshmi and Vellingiri Vadivel and Natesan Ravichandran and Pemaiah Brindha} } @article {846, title = {Morpho-anatomical Observations on Homoeopathic Plant Drug Hygrophila spinosa T. Anderson}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {286-291}, type = {Original Article}, chapter = {286}, abstract = {

Background: Hygrophila auriculata (Schumach.) Heine synonym Hygrophila spinosa T. Anderson is used in the homoeopathic system of medicine belongs to the family Acanthaceae. Plant contains terpenoids, alkaloids, flavonoids and is traditionally known as an aphrodisiac, renal tonic and for its health-promoting properties, this drug is most popularly used by homoeopathic practitioners for the treatment of urticaria, conjunctivitis, gastroenteritis, nausea etc. Complete morphological characterization of whole plant has not been reported so for. This study may provide complete information on the basis of morphological, anatomical and powdered studies. That will assist to differentiate between adulterants and authentic raw drug to maintain the quality of drugs. Objective: The aim of the present study is to examine the morpho-anatomical, powder and fluorescence analysis of whole plant i.e. root, stem, and leaf of the plant used in homoeopathy. Material and methods: The macroscopical, microscopical and powdered analysis of drug was performed. For morphological study simple observational methods applied while for anatomical and bio-statistical parameters microscopy including powder microscopy was performed by using different methods. Results: The drug was in form of dried pieces of leaves, small quadrangular pieces of stem with spines and roots. Microscopy showed few features like aerenchymatous cortex in the middle region of root; semi-quadrangular outline, four vascular bundles at each corner in young stem and developing fascicular vascular bundles between them, in mature stem 6 vascular bundles viz. 4 vascular bundles at corner and 2 vascular bundles present in between opposite to each other; broad cortical aerenchyma in mature stem, leaf amphistomatous, anomocytic stomata, crescent-shaped meristele in leaf. Conclusion: Present study can assist the diagnostic characters of Hygrophila spinosa may be taken as pharmacognostical standards for the identification of plant drug.

}, keywords = {Drug, Homoeopathy, Macroscopy, microscopy, Organoleptic}, doi = {10.5530/pj.2019.11.44}, author = {Digvijay Verma and Shilpi Singh and Renu Arya and Soundararajan Rajan and Bhopal Singh Arya and Anil Khurana and Raj Kumar Manchanda} } @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 {957, title = {Optimization Method for Determination of Swelling Factor Linum usitatissimum Seeds}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {936-943}, type = {Original Article}, chapter = {936}, abstract = {

Aim: Aspire of the investigation is to amend the method for determination of swelling factor of seeds, so it can be determined to optimize the minimum errors which will be reproducible. Swelling factor is play key role if the phytoconsitituent rich in mucilage and polysaccharide which constitute a diverse class of biological macromolecules. Background: Sugar molecules play a broad range of physiochemical properties which are widely used for applications in Pharmacy and the present investigation work is related to determine the effect of parameters such as quantity of seed, volume and nature of solvent, time interval of agitation, time of measurement of result, Effect of quantity of seeds on swelling factor determination. Solvent Optimized technic gives superlative results over IP method. Methods: The swelling factor of Linum usitatissimum was evaluated by using different polar to non-polar solvents by using the standard procedure. During the determination, the role of physical parameter were calculated by comprising the swelling factor with agitation and temperature. Results: According to the observations, the lower concentration levels of swelling index used as an alternative binder to starch. keeping one parameter as variable while all other parameters constant, it was observed that the swelling index of gives better results using the solvents plain distilled water, seeds moistened with alcohol. It was also observed that agitation at every three hours till the process of 24 hours is maintained would give better results, keeping one parameter as variable while all other parameters constant.

}, keywords = {Formulation parameter, Seed, Swelling index}, doi = {10.5530/pj.2019.11.149}, author = {S Dhanalakshmi and C N Hemalatha and Sai Ramya Bharathi and C Dhivya and S Vanishree and V Rekha and V Vijayalakshmi and A Hari priya and Sai Monisha} } @article {922, title = {Phytochemical Screening, HPTLC Fingerprinting and Invitro Antioxidant Activity of Root Extract of Asparagus racemosus}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {July 2019}, pages = {818-823}, type = {Original Article}, chapter = {818}, abstract = {

Background: Asparagus racemosus is a climber shrub used in Indian medicine for centuries. It has been used as galactogogue and nerve tonic in folk medicine. The recent research on A. racemosus has revealed its disease fighting properties such as anti-bacterial, immunomodulatory, cardio protective, anti-stress, etc. Phytochemicals present in the plants are associated with their therapeutic capabilities. Hence, phytochemical screening of a therapeutic plant is essential. Materials and Methods: A preliminary qualitative screening of phytoconstituents present in the ethanol and aqueous extract of the plant was done. high-performance thin layer chromatography (HPTLC) was used to create a phytochemical fingerprint of the plant extract. Further, a series of antioxidant assays, i.e., 2,2-diphenyl-1- picrylhydrazyl (DDPH) radical, Nitric oxide (NO) radical, Superoxide (SO) radical and 2,2{\textquoteright}-azinobis( 3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging assays were done. Results: The phytochemical screening and the HPTLC fingerprint showed the presence of phenolic compounds, flavonoids, glycosides, triterpenoids, saponins etc. They also showed free radical scavenging property and hence can be used as potential primary antioxidant. Conclusion: A preliminary screening created a phytochemical profile of A. racemosus extracts. These phytoconstituents may be linked to the various known therapeutic applications of the plant. This may aid in further extensive studies for identifying and isolating compounds with potential therapeutic value in A. racemosus.

}, keywords = {Antioxidants, Asparagus racemosus, Chromatography, Phytochemistry, Phytoconstituents, Therapeutics}, doi = {10.5530/pj.2019.11.131}, author = {Kalaivani Selvaraj and Girija Sivakumar and Aruthra Arumugam Pillai and Vishnu Priya Veeraraghavan and Srinivasa Rao Bolla and Geetha Royapuram Veeraraghavan and Gayathri Rengasamy and Joel P Joseph and Janardhana PB} } @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 {804, title = {Preparation of Triphala Churna using the Ingredients Obtained from Local Market and Comparative Standardization}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {January 2019}, pages = {102-111}, type = {Original Article}, chapter = {102}, abstract = {

Introduction: In the recent years there has been rapid growth in the field of herbal medicine most of the tradition systems of medicine are accepted universally after standardization only. it very important to develop an essential techniques to standardization of herbal related drugs. The present study standardization of Triphala Churna majorly focused on that area under WHO guidelines. Method: This polyherbal Churna used treat the constipation and other gastric disorders. In this study a prepared Thriphala Churna was comparatively standardized with the reference obtained from market. For the standardization of the above formulations were done by evaluating the macroscopical, microscopical, powder flow properties, extractive values, Physicochemical characters, heavy metal content detection, qualitavte and quantitive determination of tannins and alkaloids, TLC finger print, in-vitro anti-oxidant activity and cytotoxic activity to assess the quality and safety and therapeutic activity of formulation. Results: The above parameters for the both formulation complies with the strands. The flow properties are poor. From the preliminary phytochemical test revealed the presence of various bioactive constituents. Majorly the concentration of tannins and flavonoids are high in water extract and also the water extract having the good anti-oxidant and in vitro cytotoxic activity. Hence the Triphala extracts may be used for various Ayurvedic preparations to chronic diseases like cancer.

}, keywords = {Cytotoxic activity, in-vitro anti-oxidant activity, standardization, Thriphala Churna, TLC finger print}, doi = {10.5530/pj.2019.1.18}, author = {Gunji Venkateswarlu and Seru Ganapaty and Akula Murali Sri Sudhakar} } @article {853, title = {Protective Effect of Terminalia catappa Leaves and Terminalia chebula Fruits on the Enzymatic and Non-enzymatic Anti-oxidant Levels in the Doxorubicin Induced Toxicity Rats}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {February 2019}, pages = {346-349}, type = {Original Article}, chapter = {346}, abstract = {

Background: Oxidative stress plays an important role in chronic complications of diabetes, cancer, liver disorder etc. The free radicals such as superoxide anions, hydrogen peroxides are causing the oxidative stress and it involves the cellular damage. Evidences recommended that the natural medicines from plant sources are treated to overcome the oxidative stress complications. Objective: The aim of the present is to find the antioxidant activity of the ethanolic extract of Terminalia catappa leaves and Terminalia chebula fruits in the doxorubicin (DOX) induced toxicity rats. Methods: Oxidative stress is induced with a single dose of doxorubicin and then the animals were treated with a dose of various concentration of ethanolic extract of T. catappa leaves and T. chebula fruits (200, 300 mg/kg/b.w) for 21 days. After the treatment, lipid peroxide (LPO), reduced glutathione (GSH), vitamin C, vitamin E, glutathiones- transferase (GST), glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase levels are determined. Propranolol 25mg/kg is used as standard drug. Results: In the present study, after the treatment of doxorubicin the levels of SOD, CAT, GSH, GST, GPX, vitamin C, vitamin E levels are decreased and LPO level is increased. After the treatment of T. catappa leaves and T. chebula fruits the levels were returned to the normal level. Conclusion: The results proved that the ethanolic extract of T. catappa leaves and T. chebula fruits may protects the cells from oxidative stress induced by the doxorubicin induced toxicity rats.

}, keywords = {Doxorubicin, Enzymatic antioxidant, Non-enzymatic antioxidant, Oxidative stress, Termianlia catappa, Terminalia chebulla.}, doi = {10.5530/pj.2019.11.51}, author = {Panneerselvam Punniyakotti and Rengasamy Lakshminarayanan Rengarajan and Shanmugam Velayuthaprabhu and Kalaiyarasan Vijayakumar and Ramasamy Manikandan and Arumugam Vijaya Anand} } @article {948, title = {Screening In vitro Anticancer Activity of Alseodaphne semecarpifolia Nees Stem Bark Extracts against some Cancer Cell lines}, journal = {Pharmacognosy Journal}, volume = {11}, year = {2019}, month = {September 2019}, pages = {884-888}, type = {Original Article}, chapter = {884}, abstract = {

Introduction: Cancer is considered as the prime lethal disease that affects different organs of the body. Even with the rapid developments in the medical sciences, there are no proper medicines to cure specific kind of cancer without side effects. The inhibition of tumour cell growth without side effects either by the use herbal or synthetic drugs is considered as an important target in cancer therapy. In traditional medicinal system A. semecarpifolia stem bark is the prime source of herbal drug to treat lymphatic and skin cancers. Objective: The purpose of this study is to evaluate the anticancer potential of A. semecarpifolia stem bark extracts against some cancer cell lines. Methods: The in vitro anticancer activity was evaluated against DLA, EAC, HeLa, HepG2 and L929 cell lines by trypan blue dye exclusion assay and SRB assay. Results: The results of the anticancer activity revealed that, when compared to standard drug Cyclophosphamide, SBPEE and SBCE of A. semecarpifolia showed significant anticancer activity against DLA and EAC cell lines, without causing any toxicity to the normal mouse fibroblast cells L929. Whereas, none of the three extracts showed cytotoxicity against HeLa, HepG2 and L929 cell lines. Conclusion: The present study suggested that, SBPEE and SBCE possesses significant cytotoxic activity against DLA and EAC cell lines, which confirms the traditional medicinal claim of A. semecarpifolia as a potent anticancer plant against lymphatic and skin cancer.

}, keywords = {Alseodaphne semecarpifolia, Carcinoma, Cell lines, Cell viability, Cytotoxicity, Lymphoma}, doi = {10.5530/pj.2019.11.141}, author = {Chethankumara Ganadhal Puttaramaiah and Krishna Venkatarangaiah and Nagaraj Kakanahalli} } @article {507, title = {Anthelmintic Activity of Fruit Extract and Fractions of Piper longum L. In vitro}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {333-340}, type = {Original Article}, chapter = {333}, abstract = {

The present study was aimed to assess the in vitro ovicidal, larvicidal and adulticidal activity of methanolic extract and its fractions from fruits of Piper longum against strongyle ova, larvae and adult amphistomes respectively. The fruits of P. longum was identified and the accession number 006 was obtained. The phytochemical analysis revealed the presence of tannins, flavonoids, glycosides, phenolics, diterpenes and triterpenes in extract and fractions of P. longum. The extract and fractions were diluted serially in 6.25 per cent tween 80 to obtain concentrations of 500, 250, 125, 62.5, 31.25, 15.63, 7.81, 3.91 and 1.95 mg/mL. Ivermectin and thiabendazole at 10 \μg/mL acted as positive controls and 6.25 per cent tween 80 as negative control. The methanolic extract was highly active against ova with IC50 of 0.026 mg/mL. The n-hexane fraction was potent in inducing larval mortality with IC50 of 1.383 mg/mL while chloroform fraction inhibited larval migration with IC50 of 1.796 mg/mL. Amphistomes were highly sensitive for methanolic extract of P. longum which possessed IC50 of 5.493 mg/mL Based on IC50 values, the methanolic extract was found to be most potent while chloroform fraction was effective against ova, larvae and also adults. GCMS analysis of potent methanolic extract revealed the presence of piperidinone, hydrocinnamic acid, ethylhexahydro azepine, methyleugenol, hexadecanoic acid and caryophyllene oxide which may have contributed for the anthelmintic activity. The acute oral toxicity study revealed mild vascular changes in liver. From the present study, it can be concluded that chloroform fraction of P. longum possessed maximum broad spectrum anthelmintic activity comparable to controls.

}, keywords = {Adulticidal, GCMS, IC50, Larvicidal, Ovicidal, Piper longum.}, doi = {10.5530/pj.2018.2.57}, url = {http://fulltxt.org/article/487}, author = {Krishnaprasad Ganapati Koorse and Sujith Samraj and Preethy John and Priya Manakkulaparambil Narayanan and Devi SS and Usha PTA and Surya Sunilkumar and Gleeja VL} } @article {745, title = {Antibacterial Property and Molecular Docking Studies of Leaf Calli Phytochemicals of Bridelia scandens Wild.}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1221-1229}, type = {Original Article}, chapter = {1221}, abstract = {

Background: Bridelia scandens Wild. (Euphorbiaceae) leaves are widely used to cure asthma, bronchitis pleurisy, exudation, sores in mouth and genital cancers. Objective: To evaluate antibacterial activity of the leaf calli methanol extract (LCME). Materials and Methods: Mass production of leaf calli was established on MS medium supplemented with 0.5 mg/L BAP and 0.5 mg/L 2, 4-D. Methanol extract of the dried calli was subjected to HR-LCMS analysis, antibacterial screening of the extract was carried out against human pathogenic clinical isolates. Molecular docking study of HR-LCMS identified compounds was performed by docking with bacterial enzyme DNA gyrase. Results: HR-LCMS analysis of LCME shows that the compounds azaperone bifonazole, fusidic acid, lasalocid and quinine as the major constituents. The antibacterial screening of LCME against clinical pathogens showed significant bactericidal activity against the strains Staphylococcus aureus (17.67\±0.88 mm.d.), Streptococcus pneumonia (13.67\±0.33), Pseudomonas aeruginosa (16.33\±0.67), Salmonella typhi (17.67\±0.33), and Vibrio cholera (15.33\±0.33) as compared to the standard drug ciprofloxacin. The molecular docking of lasalocid against the bacterial enzyme DNA gyrase exhibited good binding affinity of -4.9 kcal/mol, good drug likeness (2.5589), 2 hydrogen bonds and hydrophobic interaction with 7 amino acid residues, so that lasalocid processes good inhibitor as compared to other 4 compounds. Conclusion: LCME of Bridelia scandens showed significant antibacterial activity against Staphylococcus aureus and Salmonella typhi. Lasalocid is the major phytocomponent of LCME which exhibited good inhibitory activity against bacterial enzyme DNA gyrase. This investigation supported traditional claim of LCME as potential antibacterial drug.\ 

}, keywords = {ADMET, Antibacterial, Bridelia scandens, DNA Gyrase, Molecular docking}, doi = {10.5530/pj.2018.6.209}, author = {Ravikumar Shivakumar and Krishna Venkatarangaiah and Sudhesh Shastri and Ravishankara Burladinni Nagaraja and Ajith Sheshagiri} } @article {562, title = {Antimicrobial Potential of Crude Extracts of Thespesia populnea L. Flower on Multiple Drug Resistant Opportunistic Pathogens in HIV/AIDS}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {590-597}, type = {Original Article}, chapter = {590}, abstract = {

Background: Thespesia populnea L. commonly known as tulip tree or \‘portia\’ tree has been traditionally used for different illnesses. Thespesia populnea L. is considered to have high tannin content and have high therapeutic value. Purpose: The antifungal and antibacterial potential of T. populnea L. should be checked on multiple drug resistant opportunistic pathogens Pseudomonas aeruginosa and Candida albicans in HIV/AIDS patients. Methods: In order to check the effect of antibiotics antibiogram was studied with antibiotic sensitivity discs. To study the major factor affecting resistance test on formation of biofilm was done by tube and plate methods. The dried flower powder was subjected to sauxlaut hot extraction and the crude extract was analysed by Gas Chromatography and Mass Spectrophotoscopy. Antimicrobial potential of the ethyl acetate extract of the flower was checked by well agar diffusion, UV Spectrometry for growth rate and docking of selected compounds on the microbes of our study by the application of a software. Results: The tested extracts and the selected compounds have showed significant results in the antimicrobial activities against the opportunistic pathogens in human. Higher the concentration of the extracts better is the inhibition of microbes. Conclusion: The study provides a scientific rationale for the traditional use in the management of opportunistic pathogens which are multidrug resistant.

}, keywords = {Antibiogram, Antimicrobial, Biofilm, Docking, Inhibition, Multidrug Resistant, Opportunistic Pathogens}, doi = {10.5530/pj.2018.3.97}, url = {http://fulltxt.org/article/530}, author = {Jancy Varghese and S. Rajamani and Betty Daniel} } @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 {575, title = {Bactericidal Kinetics and Antibiofilm Efficacy of Pimarane-Type Diterpenes from Viguiera arenaria Against Cariogenic Bacteria}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {429-434}, type = {Original Article}, chapter = {429}, abstract = {

Background: Dental caries is an infectious disease related to biofilm formation. Among the microorganisms presents in the oral microbiota, Streptococcus mutans can form biofilm on the tooth surface in the presence of dietary carbohydrates. This study aimed to evaluate the bactericidal kinetics and antibiofilm efficacy of ent-pimara-8(14),15-dien-19-oic acid (compound 1) and ent-8(14),15-pimaradien-3\β-ol (compound 2) obtained from Viguiera arenaria against oral pathogens; this study also aimed to determine the effect of these compounds on the morphology and architecture of the S. mutans biofilm by scanning electron microscopy (SEM). Materials and Methods: The bactericidal kinetics revealed different results depending on the tested bacteria. Compound 1 eliminated the viable bacteria within 24 hs of incubation. In the antibiofilm assay, compound 1 displayed promising results against S. mitis (ATCC 49456 and clinical isolate) and L. casei (clinical isolate), whereas compound 2 was not active at the evaluated concentrations. Conclusion: Compound 1 is an important metabolite in the search for new antibacterial agents against cariogenic bacteria both in the sessile and planktonic modes. The SEM image of Streptococcus mutans in the presence of compound 1 suggested that this metabolite acts by disrupting the bacterial membrane disrupting the bacterial membrane and/or cell wall and causing microrganism death.

}, keywords = {Antibacterial activity, Bactericidal kinetics, Scanning electron microscopy, Streptococcus mutans, Viguiera arenaria}, doi = {10.5530/pj.2018.3.70}, url = {http://fulltxt.org/article/503}, author = {Juarez Henrique Ferreira and Rafael Martinez Garcia and Fariza Abr{\~a}o and Yadira Arnet Fernandez and Regina Helena Pires and S{\'e}rgio Ricardo Ambr{\'o}sio and Rodrigo Cassio Sola Veneziani and Carlos Henrique Gomes Martins} } @article {577, title = {Detection and Quantification of Major Phytochemical Markers for Standardization of Talinum Portulacifolium, Gomphrena Serrata, Alternanthera Sessilis and Euphorbia Heterophylla by HPLC}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {March 2018}, pages = {439-446}, type = {Original Article}, chapter = {439}, abstract = {

Background: High-performance liquid chromatography is one of the major analytical techniques used in the quality control of phytochemicals. Objective: This research article presents the development of HPLC method to detect and quantify the major marker components, kaempferol, and quercetin from four plant species. Materials and Methods: HPLC method was developed for the qualitative and quantitative analysis of plant extracts by using orthophosphoric acid and methanol (95:5) at 370 nm for kaempferol, methanol and orthophosphoric acid (60:40) at 262nm for quercetin. Results: Kaempferol was detected from the hydro alcoholic extracts of Talinum portulacifolium leaves (RT 13.720, concentration 1.08 mg/ml) and flowers of Gomphrena serrata (RT 13.758, concentration 2.13mg/ml). Kaempferol was reported for the first time from Gomphrena serrata. Quercetin was separated and identified from the hydro alcoholic extracts Alternanthera sessilis stems (RT 6.503, concentration 0.01mg/ml). The hydroalcoholic extract of Euphorbia heterophylla stems (RT 6.588, concentration 0.01mg/ml) was also evaluated for the presence of quercetin. Conclusion: The method developed is very useful tool for qualifying and quantifying the plant specimens as well as their extracts.

}, keywords = {Extracts., HPLC, Kaempferol, Marker, Plant specimens, Quality control, Quercetin}, doi = {10.5530/pj.2018.3.72}, url = {http://fulltxt.org/article/505}, author = {Mamillapalli Vani and Shaik Abdul Rahaman and Avula Prameela Rani} } @article {486, title = {Effects of Leucaena leucocephala (Lam.) de Wit Leaves Extracts in Culture of Human Umbilical Vein Cells}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {148-153}, type = {Original Article}, chapter = {148}, abstract = {

Oxidative stress can induce vascular endothelial dysfunction in diabetic and hyperlipidemia patients. Leucaena leucocephala (Lam.) de Wit has been reported of possessing antioxidant, antidiabetic and anticholiesterase activity; as well as the toxic substance called mimosine. Aims: To determine antioxidant effects of Leucaena leucocephala (Lam.) de Wit Leave extracts in oxidative stress induced vascular endothelial function. Methods and Material: Leave extracts were determined for antioxidant activity. Either or both of oxidized low density lipoprotein (oxLDL) and glucose were applied to induce oxidative stress condition in human umbilical vein cultured (HUVCs) to observe superoxide dismutase (SOD) activity, nitric oxide (NO) level and morphological changes. Results: Total polyphenol and flavonoid were 51.04 \± 0.91 mg GAE/g and 0.13 \± 0.01 mg catechin/g of dried weight (DW), respectively. Free radical reduction efficiency of crude extract observed by 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay showed IC50 value of 329.6 \μg of vitamin C equivalent/mg of extracts. Frap value was showed 428.54 \± 15.32 mM FeII equivalent/g of DW. The result observing in HUVCs showed that comparing to the control, SOD activity, NO and MDA level were maintained in 0.05 mg/mL of L. leucocephala treated group, but NO and MDA level were lowered when comparing with oxLDL and glucose-induced oxidative stress. No change was observed in 0.05 mg/mL of L. leucocephala treated group, comparing with control group. Conclusion: This study has been performed to exhibit the antioxidant activity of L. leucocephala in endothelium functions and has been found to have an appropriate concentration at 0.05 mg/mL in reducing oxidative stress condition in impaired fasting blood glucose patients. Nevertheless, the optimal level for toxic activity in inhibition of cancer angiogenesis should be further investigated.

}, keywords = {antioxidant activity, De Wit, Leucaena leucocephala (Lam.), Nitric oxide, Superoxide dismutase, Vascular endothelial.}, doi = {10.5530/pj.2018.1.25}, url = {http://fulltxt.org/article/411}, author = {Ratikorn Chatchanayuenyong and Patcharawan Sujayanont and Auranut Vuttivirojana} } @article {626, title = {Evaluation of Modulatory Effect of Combination of Spondias Pinnata and Whey Preparation on Intestinal Antioxidants and Inflammatory Markers in Etoposide Induced Rat Model for Mucositis}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {640-644}, type = {Original Article}, chapter = {640}, abstract = {

Background: Etoposide is an important chemotherapeutic agent that is used to treat a wide spectrum of human cancers. The efficacy of this drug is often limited due to severe sideeffects such as mucositis, anorexia, myelosupperssion, alopecia. At present there are no anti-mucositic agents without side effects. To combat these side effects of cancer treatment, innovative and specific nutritional interventions are needed. The experimental procedure included an oral treatment with combination of Spondias pinnata and whey preparation (100 mg/kg b.w).on etoposide induced mucositis. Methods: Study was conducted at Central Research Laboratory, Kasturba Medical College. Rats were sacrificed by cervical dislocation and duodenum collected for estimation of biochemical parameters. Estimation was carried out for assessing the levels of TAO, GSH, LPO, NO and activity of MPO. Correlation analysis was performed by one-way Anova using graph pad prism to find the relation between control and test. Result: The antioxidant (TAO and GSH) were found to be significantly high in the rats which received the combination compared to the individual Spondias pinnata and whey treated groups. Administration Spondias pinnata and whey in combination shows significant decrease in the TBARS, NO and MPO levels. Conclusion: Spondias pinnata and whey preparation supplementation in combination have shown mucoprotective effects in rat model. Hence it can be considered as anti-mucositis therapeutic agents which can be safely administered during chemotherapy and can reverse mucositis.

}, keywords = {Etoposide, Lipid peroxidation (LPO), Mucositis, Myeloperoxidase (MPO), Nitric Oxide (NO), Spondias pinnata, Whey preparation}, doi = {10.5530/pj.2018.4.105}, url = {http://fulltxt.org/article/643}, author = {Vyshnavi, Gayathri Rao and Shyamala Nayak and Beena Shetty} } @article {494, title = {GC MS/MS analysis of Bioactive Compounds in Alcoholic Seed Extract of Gauzuma ulmifolia Lam}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {December 2017}, pages = {194-197}, type = {Original Article}, chapter = {194}, abstract = {

Introduction: Gauzuma ulmifolia Lam. (GU) belonging to the family Malvaceae, commonly called Bastard Cedar is native to tropical American countries. It was introduced into India more than 100 years ago. Methods: In the present study, alcoholic seed extract of Gauzuma ulmifolia Lam. was subjected to GC MS/MS analysis and chemical compounds were characterized. Results: Totally sixteen compounds were characterized. Chemical analysis of the extract showed that it includes bioactive compounds like D-Asarinin (65.02 \%), 2,6-Bis (3,4-methylenedioxyphenyl)-3,7-dioxabicyclo (3.3.0) octane (20.12 \%), 1-Dodecanone, 2-(imidazol- 1-yl)-1-(4-methoxyphenyl) (7.54 \%) and o-Anisic acid, tridec-2-ynyl ester (3.33 \%) as major constituents. Minor components such as Vitamin E, \γ \– Tocopherol, Ergost-5-en-3-ol, (3\β), Hexadecanoic acid, methyl ester is also present. Conclusion: Based on the above results, the seeds of this plant could posse\’s oxygen (92.27 \%), hydrocarbon (0.19 \%) and nitrogen (7.54 \%) derivatives of volatile principle. This is the first-time report on the composition of seed of GU.

}, keywords = {Alcoholic extract, D-Asarinin, Gauzuma ulmifolia, GC MS/MS analysis, Vitamin E.}, doi = {10.5530/pj.2018.1.33}, url = {http://fulltxt.org/article/419}, author = {Sivakami Sundari Ponnusamy and Shanaz Banu and Murugan Vedigounder and Dhanashree Narayanswamy} } @article {509, title = {High Antioxidant and Phenolic Contents Related to Antibacterial Activity against Gastrointestinal Pathogenic Bacteria of Some Thai Medicinal Plants}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {341-348}, type = {Original Article}, chapter = {341}, abstract = {

Objective: Thai medicinal plants were used as the traditional medicines and as part of everyday plants diet. Plants contain a mixture of phytochemical and exhibit a lot of functional food and medicinal properties. This project aims to investigate the potential of selected Thai medicinal plants according to the properties of their antioxidant and antibacterial activities. Methods: The eighteen plants were extracted using maceration method with 95\% ethanol. The antioxidant activity was evaluated by DPPH and FRAP assay. The total phenolic content was evaluated by Folin-Ciocalteu phenol reagent. The antibacterial activity was evaluated by agar disc diffusion method. The extract which exhibited high antioxidant and antibacterial activity was selected to observe morphological changes by the scanning electron microscope (SEM). Results: The extract of Caesalpinia sappan showed the highest activities on both antioxidant assayed by FRAP method and total phenolic contents, however, exhibited high antioxidant assayed by DPPH compared to Bauhinia strychnifolia extract. Moreover, the extract of C. sappan showed the excellent antibacterial activities against six pathogenic bacteria in Gastro-intestinal tract. The morphological change by SEM was selected for further investigation antibacterial activities of C. sappan extract. The results showed that the inhibitory effect to those bacterial strains could be caused by the disruption of the cell membrane and decrease biofilm formation after treatment with the extract. Conclusion: The ethanol extract of C. sappan exhibited strong antioxidant and antibacterial activities against the six pathogenic bacteria. This result suggested that C. sappan could be applied to use for medicinal purpose and functional products.

}, keywords = {Antibacterial activity, antioxidant activity, Caesalpinia sappan, Scanning electron microscope, total phenolic content}, doi = {10.5530/pj.2018.2.58}, url = {http://fulltxt.org/article/488}, author = {Parichat Phalanisong and Kanit Vichitphan and Jaehong Han and Sukanda Vichitphan} } @article {680, title = {Improved Bioactive Metabolite Production by Saccharopolyspora halotolerans VSM-2 Using Response Surface Methodology and Unstructured Kinetic Modelling}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {833-840}, type = {Original Article}, chapter = {833}, abstract = {

Background: This study targets to optimize and analyse the interactive effects of process variables for improved bioactive metabolite production using RSM and unstructured kinetic modelling by S. halotolerans VSM 2. Materials and Methods: RSM was applied to optimize the interactive effects of five variables, viz., time of incubation, pH, temperature, concentration of maltose and meat extract on bioactive metabolite production and its effect against the five responses viz., S. flexneri, S. marcescens, P. vulgaris, P. aeruginosa and E. coli. Models of Logistic and Luedeking-Piret were used to simulate the cellular increase and bioactive metabolite production. Results: RSM optimal conditions for the bioactive metabolite production recorded were incubation time (12days), pH (8), and temperature (250C), concentrations of maltose and meat extract (1 \% w/v) (each). The effect of the bioactive metabolite produced (zone of inhibition) against the responses were found to be 17 mm for S. flexneri, 17 mm for S. marcescens, 16 mm for P. vulgaris, 17 mm for P. aeruginosa and 18 mm for E coli. The data obtained from experimental values are in close agreement with the predicted values of RSM. Model adequacy was evaluated using ANOVA variance where the quadratic effect of p\<0.0001 which imply the significance of the model. The unstructured-, mathematical- kinetic models provided a better approximation of profiles of S. halotolerans VSM 2 growth, optimized media utilization and bioactive metabolite production. Conclusion: Optimization of the independent variables for the production of the bioactive metabolite using RSM by S. halotolerans VSM 2 and its effect against the five responses were documented. The predicted values are in good agreement with the experimental values. Unstructured models provided a better approximation of kinetic profiles for bioactive metabolite production by S. halotolerans VSM 2.

}, keywords = {Bioactive metabolites, Kinetic Modelling, Optimization, Response Surface Methodology, Saccharopolyspora halotolerans}, doi = {10.5530/pj.2018.5.142}, author = {Ushakiranmayi Managamuri and Muvva Vijayalakshmi and Mani Deepa Indupalli and Venkat Siva Rama Krishna Ganduri and Satish Babu Rajulapati and Sudhakar Poda} } @article {514, title = {Isolation, Characterization and in vitro Pharmacological Activities of Tagetes Erectus Linn}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {384-393}, type = {Original Article}, chapter = {384}, abstract = {

Tagetes erectus (family: Asteraceae), commonly known as \‘African marigold\’, is an ornamental plant widely distributed in India. The plant has been used in traditional medicines in India and elsewhere in the treatment of cold, bronchitis, rheumatism and inflammation. The flavonoid quercetin has been isolated from the methanol extract of the plant by column chromatography and identified by co-TLC, comparison of its melting point, UV, IR and NMR spectra. Quercetin content has been estimated as 1.22 (\±0.26) \% in the methanol extract of Tageteserectus whole plant based on HPTLC method using the solvent systemchloroform: methanol (8.5:1.5). The essential oil was isolated by hydrodistillation (oil yield 0.04\% v/w) and 25 compounds comprising 93.9\% of the constituents were identified by GC-MS analysis. Monoterpenoids Predominated the oil (78.5\%), with piperitone as the major compound (40.1\%) followed by terpinolene (12.7\%) and limonene (12.0\%). The in vitro antioxidant assays of the methanol extract showed moderate activity with IC50 values 109.45 (\±1.22) g/ml for DPPH radical scavenging assay and 201.53 (\±4.48) g/ml for superoxide scavenging assay and the marker compound quercetin showed IC50 values 26.40(\±1.75) and 13.87 (\±0.54) g/ml respectively. Reducing power assay also showed moderate activity. Antibacterial activity of the methanol extract and the essential oil against gram positive and gram-negative bacteria were done using disc diffusion method. The essential oil showed remarkable activity against the tested organisms, while the extract showed only moderate activity.

}, keywords = {Antibacterial activity, Disc diffusion method, DPPH radical scavenging assay, Flavonoids, Quercetin, Terpinolene}, doi = {10.5530/pj.2018.2.64}, url = {http://fulltxt.org/article/495}, author = {Resmi S and Divya V Nair and Athulya Subhash and Rose Jose and Vishnu V and Subin Mary Zachariah} } @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 {619, title = {Neuroprotective Activity of Sesbania grandifolara Seeds Extract Against Celecoxib Induced Amnesia in Mice}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {May 2018}, pages = {747-752}, type = {Original Article}, chapter = {747}, abstract = {

Background: Sesbania grandiflora are characterized by their high anti-oxidant properties. The degeneration of neurons in Alzheimer disease mainly occurs because of high production of free radicals. However, the impact of Sesbania grandiflora on cholinergic system and oxidative stress parameter has not been investigated. Aim: The present study was designed to evaluate the neuroprotective effect of ethanolic extract of Sesbania grandiflora seeds in mice. Material and method: The seeds of Sesbania grandiflora were powdered and subjected to successive extraction in Soxhlet apparatus. The different doses of ethanolic extract of Sesbania grandiflora seeds were evaluated for its neuroprotective activity against celecoxib induced amnesia in mice. Result and Conclusion: Phytochemical analysis of various extracts of Sesbania grandiflora revealed the presence of steroid, saponin, flavonoid, tannins and phenolic compounds. The ethanolic extract of Sesbania grandiflora significantly improves the memory of mice and reestablishes the amnesia induced by celecoxib. In addition to improvement in memory the extract treatment also decreases the activity of AchE and MDA and restore the antioxidant anzyme SOD, GSH and catalase in experimental animals. The results of our study showed that ethanolic extract of Sesbania grandiflora improve the cognition dysfunction in celecoxib treated mice through the modification in cholinergic system or by the blockage of oxidative stress and inhibition of AchE enzyme.

}, keywords = {Acetylcholine, Celecoxib, Free radical, Morris water maze, Sesbania grandiflora}, doi = {10.5530/pj.2018.4.125}, url = {http://fulltxt.org/article/663}, author = {Bhupesh Chander Semwal and Madhuri Verma and Yogesh Murti and Harlokesh Narayan Yadav} } @article {764, title = {Peels of Citrus Fruits: A Potential Source of Anti-inflammatory and Anti-nociceptive Agents}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {November 2018}, pages = {s172-s178}, type = {Original Article}, chapter = {s172}, abstract = {

Introduction: The present study was contemplated to evaluate the anti-inflammatory and analgesic potentials in peels of some commercially grown Citrus fruits of South India viz, Lime (Citrus aurantifolia), Orange (Citrus reticulata), Sour Orange (Citrus aurantium), Pomello (Citrus grandis) and Citron (Citrus medica). Methods: The peel of the fruits were separated and subjected to cold extraction using 70\% alcohol. The extracts obtained were screened for the presence of phytoconstituents by qualitative phytochemical analysis; the anti-inflammatory activity of extracts at 250 and 500mg/Kg body weight concentrations were assessed by in vivo Carrageenan induced rat paw edema model and in vitro HRBC membrane stabilization assay whereas Tail immersion and Hot plate methods have been used to evaluate their analgesic property. Results: The results revealed that, all extracts treated animals have shown significant decrease in paw edema volume at 3rd and 4th hour of treatment and increase in reaction time in tail immersion and hot plate readings at 120 and 150 min and are comparable to the standards. From the results it was evident that Citron peel extract exhibited significant antiinflammatory and analgesic property in all models. Preliminary phytochemical investigation revealed that extracts were bestowed with presence of flavonoids, terpenoids, steroids, glycosides, alkaloids, carotenoids and phenolic compounds which might be responsible for the antinociceptive and anti-inflammatory activities. Conclusion: From the results it was evident that all citrus fruits have prominent activity in terms of parameters assessed in a dose dependent manner and are more effective in the later phase. The study thus documents that Citrus peels are good sources of anti-inflammatory and anti-nociceptive agents.

}, keywords = {Carrageenan, Citrus peel, Hot plate, HRBC, Phytochemicals, Tail immersion}, doi = {10.5530/pj.2018.6s.30}, author = {Pallavi Malleshappa and Ramesh Chapeyil Kumaran and Krishna Venkatarangaiah and Sameera Parveen} } @article {656, title = {Pharmacognostic Study of Leaves of Hedeoma patens}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {July/2018}, pages = {73-76}, type = {Original Article}, chapter = {73}, abstract = {

Introduction: Oregano is a plant consumed as a spice and used to a lesser extent as a medicinal plant for the treatment of respiratory and stomach diseases, among others. Oregano is made up of a large number of species and is currently under study for its antimicrobial, antioxidant, anti-inflammatory and hypoglycemic properties. However, pharmacognostic studies of some wild species are lacking. Methods: The present research aims to identify taxonomically and to evaluate the morphological characteristics of Hedeoma patens, a plant used as oregano in Mexico. Results: The specimens were identified as Hedeoma patens J. and their main morphological features were trichome-pelted sites for synthesis of essential oils. Conclusion: The plant used in Badiraguato, Sinaloa is Hedeoma patens J. and the structures that synthesize phenolic compounds and essential oils could suggest a potential use of this plant and will form a basis for future research.

Key words: Essential oils, Bioactives, Hedeoma patens J, Oregano, Pharmacognostic, Chemical/ Nutraceutical Industries.

}, doi = {10.5530/pj.2017.3.14}, author = {Laura Aracely Contreras-Angulo and Denisse Vega-Gaxiola and Alexis Emus-Medina and Jose Basilio Heredia} } @article {677, title = {Pharmacognostic Study of Leaves of Hedeoma patens}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {921-924}, type = {Original Article}, chapter = {921}, abstract = {

Introduction: Oregano is a plant consumed as a spice and used to a lesser extent as a medicinal plant for the treatment of respiratory and stomach diseases, among others. Oregano is made up of a large number of species and is currently under study for its antimicrobial, antioxidant, anti-inflammatory and hypoglycemic properties. However, pharmacognostic studies of some wild species are lacking. Methods: The present research aims to identify taxonomically and to evaluate the morphological characteristics of Hedeoma patens, a plant used as oregano in Mexico. Results: The specimens were identified as Hedeoma patens J. and their main morphological features were trichome-pelted sites for synthesis of essential oils. Conclusion: The plant used in Badiraguato, Sinaloa is Hedeoma patens J. and the structures that synthesize phenolic compounds and essential oils could suggest a potential use of this plant and will form a basis for future research.

}, keywords = {Bioactives, Chemical/ Nutraceutical Industries, Essential oils, Hedeoma patens J, Oregano, Pharmacognostic}, doi = {10.5530/pj.2018.5.155}, author = {Laura Aracely Contreras-Angulo and Denisse Vega-Gaxiola and Alexis Emus-Medina and Jose Basilio Heredia} } @article {521, title = {Pharmacognostical and Phytochemical Analysis on Leaves of Homalium ceylanicum (Gardn.) Benth.}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {272-277}, type = {Original Article}, chapter = {272}, abstract = {

Objective: Kakhara, Dhanimari or Kakhda is one of the folklore plant of Odisha, which has been identified as Homalium ceylanicum (Gardn.) Benth. (Syn. H. zeylanicum) belonging to family Salicaceae (Flacourtiaceae). The leaves and bark of the plant is used in rheumatism, diabetes and wound healing. Review of literature revealed that the scientific evaluation on various parts of the plants has not been carried out, hence the present study has been designed to study leaves of Homalium ceylanicum Benth. For its morphology, anatomy, physiochemical and phytochemical aspects. Methods: The leaves samples were collected from Gandhamardana hills, Odisha, in month of September 2016, herbarium was provided with herbarium reference no. phm/6216/2016-17 and also certified by BSI Kolkata. Macroscopic observations were made with naked eyes and centimeter scale was used to measure the leaf size. Microscopy of leaf, Stomatal index and powder microscopy was done as per standard protocol. Physicochemical and qualitative analysis were done following standard API protocols. Results: Leaves are simple, alternate, with crenate margin and petiole is pubescent. T.S. of petiole shows boat shaped with two protruding arms supported by 2 meristele. The schematic diagram of T.S. of petiole shows somewhat orbicular to boat shaped with two arms protruding supporting two meristele in each arm. Stomatal index is 15.94-16.91, powder is bitter with leafy aroma, microscopic shows paracyctic stomata key character of genus. LOD is 8.66 \± 0.72 and carbohydrates are present in both extracts. Conclusion: the anatomical characters and values obtained from analytical study can help in standardization.

}, keywords = {Anukta Dravya, Flacourtiaceae, Homalium ceylanicum, Leaf, Salicaceae}, doi = {10.5530/pj.2018.2.48}, url = {http://fulltxt.org/article/478}, author = {Acharya Rabinarayan and Jani Switu and Chinappa Rudrappa and Shukla Vinay} } @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 {628, title = {Protective Effect of Dietary Curcumin and Capsaicin on LPS-Induced Inflammation in Mice}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {June 2018}, pages = {725-729}, type = {Original Article}, chapter = {75}, abstract = {

Objective: The current study aimed to evaluate the anti-inflammatory potency of combined curcumin and capsaicin against lipopolysaccharide (LPS) induced organ damage in mice. Methods: Adult male albino mice were distributed into five experimental groups for treatment with olive oil, LPS, curcumin, capsaicin and their combination, respectively, for 7 days prior to LPS induced inflammation. At the end of the experiment, blood samples were collected and used for the analysis of serum non-specific enzymes including serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase (ALP), total bilirubin (TB), urea, creatinine and sugar, while the organ homogenates were subjected for the evaluation of antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutothione S transferase (GST), nitric oxide (NO); lipid peroxidation (LPO) and it was further confirmed by histopathological study of different organs. Results and Conclusion: Curcumin, capsaicin and their combination had shown significant restoration of non-specific serum enzymes, antioxidant enzymes and attenuated inflammatory cells infiltration thereby preventing tissue/organ damage in LPS-challenged mice. However, the protective effect was found to be more when the two compounds were fed in combination. This beneficial potency of combined spice treatment is may be due to the contribution of diversified active moieties of curcumin and capsaicin in combination compared to individual molecules.

}, keywords = {Capsaicin, Curcumin, Lipid peroxidation, LPS, Septic shock, Superoxide dismutase}, doi = {10.5530/pj.2018.4.121}, url = {http://fulltxt.org/article/659}, author = {Thriveni Vasanthkumar and Manjunatha Hanumanthappa and Prabhakar BT} } @article {500, title = {Review on Ethnomedical Uses, Pharmacological Activity and Phytochemical Constituents of Samanea Saman(jacq.) Merr. Rain Tree}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {January 2018}, pages = {202-209}, type = {Review Article}, chapter = {202}, abstract = {

Medicinal plants have been used as therapeutic drug throughout the world. But, a very few of them have been scientifically validated. Samanea Saman belongs to the Leguminosae family commonly known as rain tree and is native to tropical America. S.saman tree has different parts like a leaf, fruits, pods, seeds, and wood. S.saman is currently studied for the production of biogas which is easily obtained in the urban and rural areas. S.saman has been used in traditional medicine as a remedy for the treatment of different diseases. The phytochemical screening of the plant revealed the presence of alkaloids\–C8H17ON and C17H36ON3 pithecolobine and saponin (samarin). Natural products are mainly derived from medicinal plants, which are tested in vitro and in vivo models and used to investigate the mechanism of action of drugs with potential biological properties. Additionally, S.saman were recommended as the suitable tree for planting in the urban environment as this species can reduce the outdoor temperature for all types of ground covers. This review is mainly focused on antioxidant, antibacterial, anti-diabetic potential, insecticidal, antifungal, analgesic, anti-ulcer and cytotoxic activities. However, this study helps to develop new strategies for the designing of novel drugs to treat various diseases related to human race.

}, keywords = {Chemical constituents, Gas production, Nanoparticles, Pharmacological activities, Samanea saman}, doi = {10.5530/pj.2018.2.35}, url = {http://fulltxt.org/article/465}, author = {Shanmugam Vinodhini and Devi Rajeswari V} } @article {738, title = {Virtual Screening of Indonesian Herbal Database as Murine Double Minute-2 (MDM2) Inhibitor}, journal = {Pharmacognosy Journal}, volume = {10}, year = {2018}, month = {August 2018}, pages = {1184-1189}, type = {Original Article}, chapter = {1184}, abstract = {

Background: Murine Double Minute-2 (MDM2) overexpression causes the p53 deficiency, so the role p53 as a cell regulator does not work in the case of cancer. Methods: In this study, virtual screening of Indonesian herbal database to discover MDM2 inhibitors was carried out. Autodock and Autodock Vina validated with Directory of Useful Decoy-Enhanced (DUD-E). Validation parameters were performed with Enrichment Factor, Receiver Operating Characteristics, and Area Under Curve. Results: The validation with the grid box 70x70x70 on Autodock resulting AUC value 0.72, while in Autodock Vina 0.43. Autodock Vina did not fulfilll the standard value but still used for comparison. Based on the virtual screening result, top ten compounds from Autodock are Nimolicinol, Jacoumaric acid, Isoarborinol, Lantic acid, Diosgenin, Theasaponin E1, Taraxasterol, Leucadenone C, Simiarenol, and Alpha-Amyrin were found to have strong interaction with MDM2, with binding energy (\ΔG) ranging from -8.83 to -9.65 kcal/mol. The Autodock Vina screening resulted in the identification of Yuehchukene, Morusin, Cyanidin, Leucadenone C, Roxburghine-B, Ocidentoside, Beta-sitosterol, Curine, Withangulatin, and Jacoumaric acid as potential inhibitors with binding energy (\ΔG) ranging from -8.7 to -9.4 kcal/mol. Conclusion: Jacoumaric acid and Leucadenone C were shown to interact with the active site in MDM2 at residues Leu54, Ile61, Met62, and Ile99.

}, keywords = {Cancer, Docking, Indonesian Herbal, Inhibitor, MDM2, Virtual Screening}, doi = {10.5530/pj.2018.6.203}, author = {Alexander Victory and Rezi Riadhi Syahdi and Arry Yanuar} } @article {412, title = {Bioactive Propensity of Macroalgae from the Andaman \& Nicobar Islands}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {815-820}, type = {Original Article}, chapter = {815}, abstract = {

Aims: Marine macroalgae are the rich source of biologically active metabolites and potential source for development of novel biotechnological products. The present study was made to explore the metabolically active compounds from the macroalgae of the Andaman \& Nicobar Islands. Methods and Material: Different solvents such as methanol (MeOH), ethyl acetate (EtoAc), butanol (BuOH) and aqueous (H2O) extracts of nine macroalgae were tested for antimicrobial, antibiofilm and cytotoxicity (brine shrimp larvae). Results: Out of the 36 extracts 27 extracts showed antimicrobial activity against the human pathogens and 14 extracts revealed antibiofilm activities. The three EtoAc extracts of Sargassum ilicifolium, MeOH extract of Sargassum sp. and MeOH extract of Padina tetrastromatica showed inhibition against 8 pathogenic bacteria. Also, aqueous extract of Padina tetrastromatica (71.82 \%) and BuOH extract of Dictyosphaeria cavernosa (71.58 \%) exhibited higher antibiofilm nature. The highest cytotoxic effect was exhibited by species Actinotrichia fragilis and all its four extracts significantly (P\<0.01) inhibited the brine shrimp larvae, among this aqueous extract showed the lowest LC50 value, 31.7 \μg/ml, followed by EtoAc extract, 89.33 \μg/ml. Conclusion: It was observed that different species have different kind of bioactive nature.

}, keywords = {Antibiofilm, Antifouling, Antimicrobial, Bioactivity, Cytotoxic Effect, Marine Macro Algae.}, doi = {10.5530/pj.2017.6.127}, url = {http://fulltxt.org/article/180}, author = {Sivadasan Deepa and Pitchiah Venkateshwaran and Nambali Valsalan Vinithkumar and Ramalingam Kirubagaran} } @article {269, title = {Botanical Pharmacognosy of Holostemma ada-kodien Schult}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {February 2017}, pages = {163-170}, type = {Original Article}, chapter = {1463}, abstract = {

Background: Holostemma ada-kodien Schult. is a perennial, twinning, laticiferous climbing herb belongs to the family Asclepiadaceae. It is an important medicinal plant with rejuvenate properties, used in Ayurveda for promoting vitality and life. The roots are sweet, ophthalmic, emollient, aphrodisiac, expectorant and galactagogue. It is highly specialized for the richness of a diverse array of aminoacids such as alanine, aspartic acid, glycine, serine, thereonine, valine, and terpenoid sugars. Aim: The present study was performed with the objectives of elaborating the macroscopic and histo-morpho diagnostic profile of Holostemma ada-kodien and analyse the quantitative, and powder microscopic peculiarities to support its pharmacognostic characterization. Materials and Methods: microscopic evaluation, quantitative standards and powder microscopy were carried out using the stem, root tuber, root and leaves. Results: Distribution of uniseriate, tricellular clothing trichomes in the epidermal tissues of the midrib, entire leaf margin with campylodromous major venation pattern, amphistomatic epidermis with anisocytic stomata, dorsiventral differentiation of mesophyll, small palisade ratio, small stomatal index, and the vascular system with several free collateral bundles in the petiole were features characteristic of the species. Gelatinous fibers distributed as concentric \‘white rings\’ in the cortical tissues of the stem as distinct groups, deposition of druses crystals of calcium oxalate in the epidermal tissues of the lamina, ground tissues of petiole, cortical tissues of stem, root, root tubers and parenchymatous pith of the stem. Secondary xylem appeared fissured as radial and tangential strips, like the spokes of a wheel in cross section of the root tuber. Xylem core seemed irregular and wedge shaped in the mature root, with more axial and radial parenchyma and less xylem fibers also features characteristic of the taxon.

}, keywords = {Anisocytic stomata, compound starch grains, druses crystals, gelatinous fibres, stone cells}, doi = {10.5530/pj.2017.2.27}, url = {http://phcogj.com/fulltext/294}, author = {Sudhakaran Madathilparambil Vasu} } @article {374, title = {Chemical Constituents of Dracontomelon Dao (Blanco) Merr. et Rolfe}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {July 2017}, pages = {654-656}, type = {Original Article}, chapter = {654}, abstract = {

Introduction: The leaves, twigs and flowers of Dracontomelon dao (Blanco) Merr. et Rolfe, an indigenous Philippine tree were investigated for their chemical constituents. Methods: The compounds were isolated by silica gel chromatography and their structures were identified by NMR spectroscopy. Results: Chemical investigation of D. dao led to the isolation of cardol (1), \β-sitosteryl-3\β-glucopyranoside-6, O-fatty acid esters (2), \β-sitosteryl fatty acid esters (3), and a mixture of \β-sitosterol (4a) and stigmasterol (4b) from the petiole; 1, a mixture of 4a and 4b, anacardic acid (5), triacylglycerols (6), monoacylglycerol (7), long-chain fatty acid esters (8), and linoleic acid (9) from the twigs; and a mixture of 4a and 4b, 5, 6, 8, long-chain fatty alcohols (10), and long- chain hydrocatbons (11) from the flowers of D. dao.The structures of 1 and 5 were elucidated by extensive 1D and 2D NMR spectroscopy, while those of 2-4 and 6-11 were identified by NMR spectroscopy. Conclusion: This is the first report on the isolation of 1, 4b and 6-9 from D. dao.

}, keywords = {3-Alkylphenols, Anacardaceae, Anacardic Acid, B-Sitosteryl Fatty Acid Esters, B-Sitosteryl-3β-Glucopyranoside-6{\textquoteright}-O-Fatty Acid Esters, Cardol, Dracontomelon dao (Blanco) merr. Et Rolfe}, doi = {10.5530/pj.2017.5.103}, url = {/files/pj-9-5/10.5530pj.2017.5.103/index.html}, author = {Consolacion Y. Ragasa and Tyson C. Batarra and Julius Leonard A. Vivar and Mariquit M. De Los Reyes and Chien-Chang Shen} } @article {423, title = {Cytotoxicity and Oral Acute Toxicity Studies of Litsea glutinosa C. B (ROB) Stem Bark Ethanol Extract}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {880-886}, type = {Original Article}, chapter = {880}, abstract = {

Background: Litsea glutinosa (Lauraceae) stem bark is widely used in folk medicine as a hepatoprotective, anti-diarrheal and anti-dysenteric drug but there is a lack of information about its toxicity. Objective: To evaluate cytotoxicity and acute toxicity of the stem bark ethanol extract (BEE). Materials and Methods: In vitro cytotoxicity of BEE was measured against breast adenocarcinoma, prostate, and colon carcinoma cell lines. In the acute toxicity tests, rats received oral doses of BEE as 1000, 2000, and 3000 mg/kg body weight. Mortality, signs of toxicity, body weight, food consumption, and gross findings were observed for 14 days. Blood samples were collected from anesthetized animals and used for hematological and biochemical parameters. Histopathological study was performed using liver and kidney samples. Results: The BEE does not show significant cytotoxic effect against the tested cell lines up to the range from 5 to 320 \μg/ml. In acute toxicity study, also lethality was not observed up to 3000 mg/kg b.w. No significant differences were noticed in body and organ weights and histopathology examinations between the control and treated groups. Conclusion: This study authenticates stem BEE may contain bioactive compounds of potential therapeutic significance which are relatively safe from toxic effects, and evidences the medicinal use of this plant in folk medicine.

}, keywords = {Acute toxicity, Breast adenocarcinoma cell line, Haematology., Litsea glutinosa, MTT Assay}, doi = {10.5530/pj.2017.6.138}, url = {http://fulltxt.org/article/191}, author = {Arunodaya Hosahalli Sumithregowda and Krishna Venkatarangaiah and Kumaraswamy Malleshappa Honnenahally and Vinaykumar Nagenahalli Manjunath} } @article {237, title = {Differentiation of Five Commercially Available Triphala churnas of an Ayurvedic Formulation by Elemental Fingerprint}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {November 2016}, pages = {117-122.}, type = {Original Article}, chapter = {117}, abstract = {

Introduction:Triphala churna (TPC) is one of the well known Ayurvedic powdered preparations of Indian System of Medicine and is used in the treatment of various diseases. Elemental pattern of TPC was developed in order to investigate the identity and quality of commercial TPC drugs. Method: Inductively coupled plasma mass spectrometry (ICP-MS) was used for the quantitative determination of ten essential and trace elements in five marketed samples of Triphala churna. The concentration patterns of these elements were deciphered by multivariate statistical analysis such as hierarchical cluster analysis (HCA), fuzzy c-means (FCM) and k-means (KM) cluster analysis. Results: The elemental concentrations ranged from 1.3 mg/kg (Cr, TPC3) to 14220 mg/kg (K, TPC4). The elemental fingerprint of Triphala churna was established based on three churnas viz. TPC1, TPC3 and TPC5, which were found in one cluster with a very high degree of similarity by KM, FCM and HCA techniques. Conclusion: Based on the results, the graphical pattern of elements detected in these samples can be considered as elemental fingerprint of Triphala churna and can be used for authentication and/or to determine the quality of commercial TPC drugs.\ 

}, keywords = {Ayurvedic Drugs, Elemental Fingerprint, Fuzzy c-Means, Hierarchical Cluster Analysis, Inductively Coupled Plasma Mass Spectrometry, k-Means, Triphala churna}, doi = {10.5530/pj.2017.1.20}, author = {Venkata Siva Satyanarayana Kantamreddi and V. Thirumala Veni and Murali Krishna Malasani and Boddana Simhachalam} } @article {330, title = {Evaluation of in-vitro Anthelmintic Activity of Ximenia americana, Hopea ponga and Vitex leucoxylon}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {367-371}, type = {Original Article}, chapter = {367}, abstract = {

Objective: Evaluating Anthelmintic activity of Ximenia americana, Hopea ponga and Vitex leucoxylon extracts by using in vitro assay. Methods: The serial exhaustive extraction was carried out with a series of solvents: chloroform, ethyl acetate, methanol, ethanol and water with increasing polarity using Soxhlet apparatus. The concentrated and dried extracts were evaluated for anthelmintic activity by employing standard in vitro method (Pheretima Posthuma model). Results: In vitro anthelmintic study shows that in case of Ximenia americana chloroform extract showed higher anthelmintic activity where as incase of Hopea ponga and Vitex leucoxylon methanol extract exhibited significant activity when compared to other solvent extracts. Conclusion: Results confirm that methanol extract of Hopea ponga exhibited highest anthelmintic activity among all tested extracts. This study provides scientific evidence that the leaves of Ximenia americana, Hopea ponga and Vitex leucoxylon have anthelmintic efficacy. However further comprehensive chemical and pharmacological investigation should be carried out to isolate the active compounds and appropriate elucidation of its mechanism of action and it helps in the development of new pharmaceuticals to treat Helminthiasis.

}, keywords = {Hopea ponga, in vitro anthelmintic activity, Pheretima Posthuma model, Vitex leucoxylon, Ximenia americana}, doi = {10.5530/pj.2017.3.62}, url = {/files/PJ-9-3/10.5530pj.2017.3.62}, author = {Arun Kashivishwanath Shettar and Ankala Basappa Vedamurthy} } @article {351, title = {An examination of the Antimicrobial and Anticancer Properties of Khaya senegalensis (Desr.) A. Juss. Bark Extracts}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {May 2017}, pages = {504-518}, type = {Original Article}, chapter = {504}, abstract = {

Background: Khaya senegalensis (Desr.) A. Juss. is a common component of the pharmacopeia\’s of multiple African groupings which inhabit the areas in which it grows. Amongst these groups there is a myriad of medicinal uses in the treatment of a wide variety of bacterial, fungal and protozoal infections, as well as in the treatment of cancers. This study was undertaken to test K. senegalensis bark extracts for the ability to inhibit microbial and cancer cell growth, and thus to validate traditional African medicinal usage of this plant in treating a variety of diseases. Materials and Methods: K. senegalensis bark powder was extracted by both solvent maceration and subcritical fluid extraction (SFE). The extracts were tested for the ability to inhibit bacterial and G. duodenalis growth. Inhibition of Caco-2 and HeLa cancer cells was evaluated using MTS-based colorimetric cell proliferation assays. Toxicity was evaluated using an Artemia franciscana nauplii bioassay and GC-MS headspace analysis was used to identify phytochemical components. Results: K. senegalensis bark extracts displayed strong inhibitory activity against bacterial triggers of several autoimmune inflammatory diseases. The growth inhibitory activity of the methanolic and subcritical extracts was particularly noteworthy against P. mirabilis (MIC values of 185 and 211\μg/mL, respectively against the reference strains). These extracts were similarly potent growth inhibitors of K. pneumoniae and A. baylyi\ and were moderate inhibitors (MIC \>1000\μg/mL) of P. aeruginosa and S. pyogenes growth. The methanolic and subcritical K. senegalensis extracts were also potent inhibitors of G. duodenalis (187 and 328\μg/mL, respectively), as well as Caco-2 (268 and 470\μg/mL, respectively) and HeLa carcinomas (155 and 174\μg/mL, respectively). GC-MS analysis of the SFE extract revealed relative abundances of a variety of mono- and sesquiterpenoids. Furthermore, all K. senegalensis bark extracts were non-toxic in the Artemia franciscana toxicity assay, indicating their safety for therapeutic use. Conclusion: These studies validate traditional African therapeutic usage of K. senegalensis in the treatment of microbial infections, autoimmune inflammatory diseases and some cancers.

}, keywords = {African mahogany, Anti bacterial activity, Anti-cancer activity, Anti-proliferative activity, Giardia duodenalis, Meliaceae, Sub-critical fluid extraction, Terpenoid.}, doi = {10.5530/pj.2017.4.82}, url = {/files/PJ-9-4/10.5530pj.2017.4.82}, author = {Camille Rabadeaux and Lou Vallette and Joseph Sirdaarta and Craig Davis and Ian Edwin Cock} } @article {431, title = {Extracellular L-Asparaginase from Streptomyces labedae VSM-6: Isolation, Production and Optimization of Culture Conditions Using RSM}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {932-941}, type = {Original Article}, chapter = {932}, abstract = {

Objective: The present study was intended to isolate actinomycetes VSM-6 from deep sea sediment samples of Bay of Bengal that is potent to produce L - asparaginase. Materials and Methods: The identification of the isolate was executed by polyphasic taxonomy. Optimization was carried out one factor at a time (O-F-A-T) for the production of the L - asparaginase. RSM was pledged to optimize the L - asparaginase production by S.labedae VSM-6. Central composite design was applied to study the influence of the variables and their interactive effects on the production of L - asparaginase. Unstructured Kinetic modelling for L - asparaginase production was adopted using Leudeking-Piret (LILP) and Logistic Incorporated Modified Leudeking-Piret (LIMLP) models. Results: Optimization using One-Factor-At-A-time registered a turnout of 8.92 IU/ml of L - asparaginase production. But results obtained from the statistical design are in agreement with the experimental results. The model followed the second order polynomial equation and the model adequacy was determined by the P value (\<0.0001), Coefficient determination (R2) with a value of 0.9942 and the adjusted R2 = 0.9087 which determines that the model was significant. The experimental values are in compliance with the model anticipated values and catalogued an escalation in yield of L - asparaginase (10.17 IU/ml) by RSM. Unstructured Kinetic modelling for L - asparaginase production adopting Leudeking-Piret (LILP) and Logistic Incorporated Modified Leudeking-Piret (LIMLP) models showed L - asparaginase production of (10.17 IU/ml), closer to model anticipated value (10.23 IU/ml) so unstructured models provided a better approximation for L - asparaginase production by S.labedae VSM-6. Conclusion: From our study we have reported for the first time the production of L - asparaginase from S.labedae VSM-6 using central composite design and kinetic modelling.

}, keywords = {Central Composite Design, Kinetic Modelling, L - asparaginase, Optimization, Response Surface Methodology, Statistical Analysis., Streptomyces labedae}, doi = {10.5530/pj.2017.6.146}, url = {http://fulltxt.org/article/199}, author = {Ushakiranamayi Mangamuri and Muvva Vijayalakshmi and Venkat Siva Rama Krishna Ganduri and Satish Babu Rajulapati and Sudhakar Poda} } @article {433, title = {Hepatoprotective Effect of Curcumin and Capsaicin against Lipopolysaccharide Induced Liver Damage in Mice}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {947-951}, type = {Original Article}, chapter = {947}, abstract = {

Objective: The present study was undertaken to evaluate the possible ameliorative role of curcumin, capsaicin and their combination against lipopolysaccharide (LPS) induced hepatic toxicity in mice. Methods: Animals were distributed into five experimental groups: Normal control, vehicle control, curcumin, capsaicin and combined curcumin and capsaicin treatment groups respectively, for 7 days prior to LPS induced liver toxicity (3 mg/kg b.w. in saline). Hepatoprotective effect of individual and combined spice principles were evidenced by the measurement of serum marker enzyme activities such as, SGPT, ALP and TB and it was further confirmed by histopathological observation of liver tissue section. Results: The administration of LPS increased serum nonspecific enzymes (SGOT; 174.2\±3.79 IU/L, SGPT; 124.0\±3.14 IU/L, ALP; 320.15\±3.88 IU/L and total bilirubin level; 2.32\±1.23 mg/dL), however dietary curcumin and capsaicin decreased the activities of these non\–specific serum enzymes including total bilirubin indicating amelioration of the severe LPS induced hepatotoxicity, while the combined spice principles were more significant as shown by the levels of enzymes activities SGOT; 89.9\±1.39 IU/L, SGPT; 85.9\±1.83 IU/L, ALP; 138.4\±2.05 IU/L including total bilirubin level; 0.86\±0.03 mg/dL. Conclusion: Dietary curcumin and capsaicin individually are protective to LPS induced hepatotoxicity, the beneficial effect was found to be more when the two compounds were fed in combination.

}, keywords = {ALP., Capsaicin, Curcumin, Hepatoprotective activity, Lipopolysaccharide, SGOT, SGPT}, doi = {10.5530/pj.2017.6.148}, url = {http://fulltxt.org/article/201}, author = {Thriveni Vasanthkumar and Manjunatha Hanumanthappa and Prabhakar BT and Santhosh Kondajji Hanumanthappa} } @article {400, title = {Mosquito Larvicidal and Pupicidal Activity of Tephrosia purpurea Linn. (Family: Fabaceae) and Bacillus sphaericus against, Dengue Vector, Aedes aegypti}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {737-742}, type = {Original Article}, chapter = {737}, abstract = {

Objective: The bio-efficacy of Tephrosia purpurea leaf extract and bacterial insecticide, Bacillus sphaericus larvicidal activity was assessed against the first to fourth instars larvae of Aedes aegypti, under the laboratory conditions. Methods: The plant material was shade dried at room temperature and powdered coarsely. T. purpurea and B. sphaericus show the various concentrations of larvicidal and pupicidal activity against various instars larvae of A. aegypti. Results: The LC50 of T. purpurea against the first to fourth instars larvae were 139.24, 176.24, 219.28, 256.27, and 326.29 ppm and the 480.72, 541.21, 580.34, 672.20, and 762.80 ppm, respectively. B. sphaericus against the first to fourth instars larvae the LC50 values were 46.16, 56.23, 69.82, 80.81 and 96.12 ppm and the LC90 values 141.68, 172.46, 184.21, 193.31 and 218.16 ppm, respectively. However, the combined treatment of T. purpurea + B. sphaericus (1:2) material shows highest larvicidal activity of the LC50 values 80.08, 82.21, 88.00, 92.21 and 98.16 ppm; The LC90 values of 108.39, 118.71, 136.75, 149.02 and 153.24 ppm, against A. aegypti in all the tested concentrations than the individuals and clearly established that there is a substantial amount of synergist act. Conclusion: The present study reported that both T. purpurea and B. sphaericus materials could serve as a potential larvicidal agent. Since, A. aegypti is a container breeder vector mosquito this user and eco-friendly and low-cost vector control strategy could be a viable solution to the existing dengue disease burden. Therefore, this study provides first report on the mosquito larvicidal activity the combined effect of T. purpurea leaf extract and B. sphaericus against as target species of A. aegypti.

}, keywords = {Aedes aegypti, Bacillus sphaericus, Dengue vector, Larvicidal activity., Tephrosia purpurea}, doi = {10.5530/pj.2017.6.116}, url = {http://fulltxt.org/article/169}, author = {Ramesh Venkadachalam and Vijayakumar Subramaniyan and Manogar Palani and Mahadevan Subramaniyan and Prabhu Srinivasan and Murugan Raji} } @article {435, title = {Neuroprotective Effect of Pedalium murex Linn. Leaf against Lipopolysaccharide Induced Behavioural Disorders in Rats}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {957-962}, type = {Original Article}, chapter = {957}, abstract = {

Introduction: Effective treatment is necessary to minimize the neuronal damage and oxidative stress. Traditional medicines offer potent pharmacological activity with minimal side effects compared to synthetic drugs to treat such chronic disorders. There is no renowned remedy for arrest or rescuing infection or inflammation-induced brain damage. The present study was aimed to evaluate the neuroprotective effect of ethanol extract of Pedalium murex Linn. (EEPM) leaves against lipopolysaccharide (LPS)-induced endotoxemia. Methods: Neurodegeneration was induced in rats with a single intraperitoneal injection of LPS (1 mg/kg). The induced endotoxemia constantly linked with battery of behavioural tests viz., choice reaction time task (CRT), 8-arm radial maze (RAM) and water maze test (WMT). At the end of the study, rats were sacrificed, brain hippocampal region was removed and biochemical parameters were measured. Results: In WMT swimming length (cm) was increased in LPS-treated rats when compared to control animals, the swimming length (EEPM; 400 mg/kg) was found to be significant; in RAM, different doses of EEPM at 100, 200 and 400 mg/kg decreased the number of errors in entry 4.00\±0.36, 4.16\±0.16and 3.33\±2.79 respectively when compared with control animals (2.66\± 0.21). EEPM at 400 mg/kg showed significant activity, in CRT apparatus increased incorrect lever pressing was observed in LPS-treated rats when compared to control animals. Incorrect lever pressing was minimized by EEPM at 400 mg/kg (43.5\±2.40). Conclusions: Our results showed that EEPM is a hopeful aspirant for hindrance of infection and inflammation induced brain damage by LPS.

}, keywords = {Behavioural studies, Learning, Memory, Neuroprotective, Oxidative stress, Pedalium murex.}, doi = {10.5530/pj.2017.6.150}, author = {Swaminathan Gomathi and Rajagopal Shanmuga Sundaram and Vellaichamy Muthupandi Annapandian and Manickam Vijayabaskaran} } @article {397, title = {Phytochemical and Quality Assessment of Acacia nilotica Linn and Acacia leucophloea willd Flowers}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {721-724}, type = {Original Article}, chapter = {721}, abstract = {

Objective: The quality criteria for herbal drugs are based on a clear scientific definition of the raw material. Even though global herbal resources have a great potential as natural drugs and are of great commercial importance, they are very often procured and processed without any scientific evaluation, and launched onto the market without any mandatory safety and toxicology studies. On that basis, an attempt was made on a well-known herbal drug A.nilotica flower and A.leucophloea flower by evaluation of phytochemical and toxicological parameters like heavy metals, aflatoxins, total microbial load and pesticide residues. Method: The procedures recommended in AOAC, ASTA were followed to determine analysis of heavy metals, aflatoxins, microbial load and pesticide residues. Thin layer chromatographic technique was used to separate the chemical compounds present in the drug. Result and Conclusion: Results obtained during this experiment revealed that heavy metals, aflatoxins, total microbial load and pesticidal residues were variable but found within the prescribed limits. Phytochemical evaluation revealed that the catechin phytoconstituents is absent in A.leucophloea flowers when compared with A.nilotica flowers. Hence, there is an urgent need for mandatory evaluation of these parameters in every crude drug before further processing to ensure safety and efficacy of Indian medicinal plants for better acceptance at International platform. The study revealed specific identities for the particular crude drug which will be useful in identification and control to adulterations of the raw drug.

}, keywords = {A. leucophloea, A. nilotica flowers, Phytochemical, TLC and Catechin}, doi = {10.5530/pj.2017.6.113}, url = {http://fulltxt.org/article/166}, author = {Raju Ilavarasan and Leela Vadivelu} } @article {332, title = {A Quantitative Approach to Estimate both Essential and Non-essential Elements in Some Commercial Samples of Triphala churna by using WD-XRF Spectrometry}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {April 2017 }, pages = {378-381}, type = {Original Article}, chapter = {378}, abstract = {

Introduction: The need for quality control of herbal drugs is in demand in order to ensure the purity, safety and efficacy of herbal products. A total of 19 elements including essential and non-essential elements were characterized in five commercial samples of Triphala churna using WD-XRF spectrometry. Method: The WD-XRF method was validated for each element by a pre-calibrated program using five Chinese certified reference materials of vegetable standards (NCS ZC73012, NCS ZC73013, NCS ZC73017, NCS ZC85006 and NCS DC73348). Results: The following elements were detected in all the samples out of 19 elements tested with increasing order of concentrations (mg/kg): Cr (3) \< Cu (7) \< Ba (24) \< Zn (31) \< Pb (46) \< Mn (57) \< S (700) \< Na (1064) \< Mg (1250) \< Fe (1329) \< P (1400) \< Cl (2960) \< Ca (3110) \< Si (4350) \< K (15130). Lead (41-46 mg/kg), a nonessential element was found above its PDE limit (\≤ 10 mg/kg). Conclusion: WD-XRF method was found simple, rapid, reliable and non-destructive technique to investigate the elemental concentrations in herbal drugs.

}, keywords = {Ayurveda, Elemental analysis, ICP-MS, ISM, Triphala churna, WD-XRF}, doi = {10.5530/pj.2017.3.64}, url = {/files/PJ-9-3/10.5530pj.2017.3.64}, author = {Venkata Siva Satyanarayana Kantamreddi and V. Thirumala Veni and G. Y. S. K. Swamy} } @article {170, title = {Acetaminophen Induced Oxidative and Histopathological Alterations in Hepatic Tissue: Protective Effects of Alstonia Scholaris Leaf Extracts}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {June/2016}, pages = {385-391}, type = {Original Article}, chapter = {385}, abstract = {

Introduction: Alstonia scholaris Linn. is the common ingredients of various herbal formulation. Objectives: Present study was aimed to evaluate the oxidative and histopathological alterations in acetaminophen (APAP) induced hepatotoxicity and protective mechanisms of different leaf extracts of A. scholaris. Methods: Forty two wistar rats were randomly divided into seven groups with six rats in each and subjected to different treatments. Alterations in total oxidant status (TOS), total antioxidant status (TAS), oxidative stress index (OSI), total thiols (TTH), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione-s-transferase (GST), malondialdehyde (MDA) levels and histopathological alterations in hepatic tissue were analyzed to assess the extent of hepatic damage induced by APAP and the protection imparted against it by aqueous or ethanolic leaf extract of A. scholaris. Results: Single high oral dose of APAP administration increased (p\<0.05) hepatic levels of TOS, OSI and MDA and reduced TAS, TTH, SOD, CAT, GPx and GST activities indicating alteration in antioxidant system of hepatic tissue. The histopathological studies showed severe hepatic degeneration, vacuolization and granulation in cytoplasm, fragmentation of nuclei and membranes and infiltration of mononuclear cells on APAP treatment. Pre and post-treatments of aqueous or ethanolic extract following APAP administration restored TTH, reduced MDA and TOS and increased TAS compared to APAP treatment alone. Conclusions: Observations of histopathological and antioxidant parameters indicates that restoration of TAS and TTH levels by leaf extracts may be the primary protective mechanism in APAP induced hepatotoxicity. Further treatments with ethanolic extract showed more hepatoprotective potential than the aqueous extract of A. scholaris.

}, keywords = {Acetaminophen, Alstonia scholaris, Malondialdehyde., Super oxide dismutase, Total antioxidant status, Total thiols}, doi = {10.5530/pj.2016.4.12}, author = {Pawan Kumar Verma and Rajinder Raina and Mudasir Sultana and Maninder Singh and Pawan Kumar} } @article {102, title = {The Anticancer Potential of Pavonia odorata extract on Human Breast (MD-MB-231), Prostate (PC-3) and Lung (Calu-6) Cancer cell lines}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {28-30}, type = {Original Article}, chapter = {28}, abstract = {

Introduction: A huge reservoir of bioactive compounds exists in many species of plants, only a small percentage of which have been examined and continued to be an important source of anticancer agents. Worldwide effects are ongoing to identify new anticancer compounds from plants. With the current decline in the number of new molecular entities from the pharmaceutical industry, novel anticancer agents are being sought from traditional medicines. Objective: In the present study we investigated the efficacy of methanol extracts of Pavonia odorata, for its clonogenic inhibition on Human Breast cancer (MD-MB-231), Prostate cancer (PC-3) and Lung cancer (Calu-6) cell lines. Materials and Methods: The cytotoxic effect was evaluated by MTT assay. Results: The methanol extract of P. odorata showed significant cytotoxicity against MD-MB-231 and Calu-6, when compared to PC-3cells. Conclusion: The methanol extracts of P. odorata, showed effective cytotoxic activities in a dose dependent manner. Future work will be interesting to know the chemical composition and also better understanding the mechanism of action will help in developing it as drug for therapeutic application.

}, keywords = {Alternative medicine, Anti-cancer, Drugs, Indian Medicinal plants, Inhibition.}, doi = {10.5530/pj.2016.1.6}, author = {Girish H V and Vinod A B and Dhananjaya B L and Satish Kumar D and Senthil Duraisamy} } @article {167, title = {Anti-inflammatory activity of BCM-95 (bio-enhanced formulation of turmeric with increased bioavailabilty) compared to Curcumin in Wistar rats}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {June/2016}, pages = {380-384}, type = {Original Article}, chapter = {380}, abstract = {

Objective: To evaluate anti-inflammatory activity of bioenhanced turmeric formulation (BCM-95) compared to commercial Curcumin formulation (Curcuminoids 95\%) in Carrageenan-induced acute inflammatory model. Materials and Methods: Thirty six Wistar rats were divided into six groups-Normal control (2 ml of vehicle), Standard control (Indomethacin 10 mg/kg), 2 doses of BCM 95 (10 and 20 mg/kg) and Curcuminoids 95\% (10 and 20 mg/kg). Paw volume was measured using a digital plethysmometer. Vehicle or test drugs were given to rats 30 min before carrageenan administration. Baseline paw volume reading (V0) was noted just prior to administration of 0.1 ml of 1\% carrageenan to right hind paw of the rat. Test paw volume readings (Vt) were measured at 30, 60, 120, 180, 240, 300 and 360 min, after carrageenan injection. Oedema expressed as increased paw volume (vt-v0) was noted and percentage inhibition of oedema was calculated for all treatment groups. Statistical analysis: Difference between groups were analyzed with ANOVA followed by Tukey test. Results: All treatment groups demonstrated significant (p\<0.05) anti-inflammatory activity (oedema suppression) compared to normal control. Anti-inflammatory activity of BCM 95 treated groups were comparable to standard control group except at certain time points, whereas the same activity at all-time points with Curcuminoid 95\% treated groups were significantly less than standard control group. Percentage inhibition of paw oedema was maximum with standard control group followed by BCM 95 treated groups followed by Curcuminoid 95\% treated groups. Conclusion: BCM 95 treated groups showed significant anti-inflammatory activity compared to Curcuminoid 95\% treated groups.

}, keywords = {Anti-Inflammatory agents, Bioavailability, Curcumin, Inflammation, Wistar rats.}, doi = {10.5530/pj.2016.4.11}, author = {Sayeli Vinaykumar and Urval Pundarik Rathnakar and Ullal Sheetal Dinkar and Kamath Priyanka and Tiwary Gaurav and Shenoy Ashok Kudgi and Revappala Sekhar Nishith} } @article {193, title = {Callus Induction and Elicitation of Total Phenolics in Callus Cell Suspension Culture of Celastrus paniculatus {\textendash} willd, an Endangered Medicinal Plant in India}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {471-475}, type = {Original Article}, chapter = {471}, abstract = {

Celastrus paniculatus - Willd belonging to the family Celastraceae is a vulnerable medicinal plant in India. It has been employed as a stimulant, nervine tonic, rejuvenant, sedative, tranquilizer and diuretic. It is also used in the treatment of leprosy, leucoderma, rheumatism, gout, paralysis and asthma. Because of its high pharmaceutical application, this plant species were over exploited and now considered under threatened species. So the highlight of the present investigation is the induction of callus by using different concentration of various phytohormones such as 2, 4-D (0.5 - 3.0 mg/l) and NAA (0.5 - 2.5 mg/l). In order to ensure the presence of the bioactive compounds preliminary phytochemical screening of the various extracts of callus were performed. Finally elicitation of total phenolics were done in callus cell suspension cultures by using elicitors such as jasmonic acid, salicylic acid and copper sulphate. Among the applied elicitors jasmonic acid showed superiority. To our knowledge, this is the first report of the elicitation of secondary metabolites especially total phenolics from callus cell suspension cultures of Celastrus Paniculatus.

}, keywords = {Bioactive constituents, Callogenesis, Celastrus paniculatus, Elicitors, Total phenolics.}, doi = {10.5530/pj.2016.5.10}, author = {Anusha T S and Joseph M V and Elyas K K} } @article {207, title = {Physicochemical Evaluation and Pharmacognostical Standardization of Pellionia heyneana Wedd. Leaf}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {September 2016}, pages = {551-556}, type = {Original Article}, chapter = {551}, abstract = {

Introduction: Pellionia heyneana Wedd. Leaves have long been employed as a traditional remedy by the Cholanaikan tribe of South India to treat various ailments. Methods: Pharmacological and physicochemical evaluation of P. heyneana leaf has been carried out to determine its macro and microscopic characters, and also some of its quantitative characters as per standard procedures. Results: The pharmacognostical evaluation of P. heyneana leaves revealed the presence of characteristic microscopic features of the crude drug like cystoliths in upper epidermis, helicocytic stomata in lower epidermis, large number of peculiar shaped, huge (200-400 m) foliar sclereids, absence of palisade tissue in the lamina etc. Powder microscopy showed the presence of calcium oxalate crystals, stone cells, multicellular trichomes, resinous blocks, spiral vessels, xylem fibre, starch grains, simple fibre etc. Conclusions: All the parameters evaluated in the study will aid to identify the authenticity of P. heyneana leaf even from the crushed or powdered form.

}, keywords = {Cholanaikan tribe, Fluorescence analysis, Helicocytic stomata, Pharmacognosy, Powder microscopy.}, doi = {10.5530/pj.2016.6.6}, author = {Vilash V and Suja SR and Latha PG and Aneesh Kumar AL and Ragesh R Nair and S Rajasekharan} } @article {156, title = {Phytochemical and Antidiabetic Evaluation of the Methanolic Stem Bark Extract of Spathodea campanulata (P. Beauv.) Bignoniaceae}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Jan/2016}, pages = {243-249}, type = {Original Article}, chapter = {243}, abstract = {

Background: Spathodea campanulata (P. Beauv.) Bignoniaceae extract\ (SCE) is one of many herbal medicines\ used widely in Ugandan traditional\ medicine for various ailments. Generally most of these herbal\ medicines\ are yet to be standardized or have their phytochemical content characterized.\ Method: This study identified the secondary metabolites in the stem bark\ methanolic extract and quantified them. The same extract was subjected\ to serial solvent fractionation, TLC characterization and antidiabetic testing.\ Results: The secondary metabolites were found to comprise of 7.5\% alkaloids,\ 10\% flavonoids, 13\% tannins and 17\% saponins per gram of plant material.\ The TLC characteristics of the fractions (hexane (HX), ethylacetate (EA)\ and methanol (ME)) viewed under UV light revealed spots with the following\ Rf values; the hexane partition gave HX7EA3 (0.96 and 0.68) HX9EA1\ (0.68 and 0.3), EA1ME9 (0.86 and 0.58), EA3ME7 (0.87), EA7ME3 (0.85)\ and EA9ME1 (0.85). The ethylacetate partition gave the following HX1EA9 (0.53, 0.34 and 0.18), HX3EA7 (0.59, 0.40 and 0.26). Discussion: All the\ fractions produced nominal reduction of hyperglycemia. Except hexane\ fraction at 50 mg/kg and ethylacetate fraction at 200 mg/kg all the fractions\ had percentage reductions of glucose greater than that of the control at\ the experimental doses. Although the values of percentage reductions of\ hyperglycemia by the hexane fraction were apparently dose-dependent,\ the greatest margin of reduction of hyperglycemia was observed in the\ residual aqueous fraction. Conclusion: It was found that SCE contains\ valuable phytochemicals in appreciable quantities which are antidiabetic.\ The residual aqueous fraction is the most potent antihyperglycemic of the\ solvent fractions.

}, keywords = {Flavonoids, Saponins, Spathodea campanulata (P. Beauv.) Bignoniaceae, TLC Tannins, Uganda.}, doi = {10.5530/pj.2016.3.12}, author = {Tanayen Julius Kihdze and Ajayi Abayomi Mayowa and Oloro Joseph and Ezeonwumelu Joseph OC and Tanayen Grace Ghaife and Adzu Bulus and Arthur van Aerschot and Gert Laekeman and Agaba Amon Ganafa} } @article {113, title = {Role of Plant Based Lectins in Identifying Rare Bombay Blood Group}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {09/2015}, pages = {70-71}, type = {Original Article}, chapter = {70}, abstract = {

Background: Lectins are proteins found in a diversity of plants and organisms. They possess the ability to agglutinate erythrocytes with known carbohydrate specificity. Methods: A lectin named Anti H is used in identification of a very rare and important blood group named Bombay blood group is extracted from the plant Ulex europaeus. Our study was done to calculate the prevalence of Bombay blood group in our Indian population using the plant based extract lectin anti H. Blood grouping was done using the tube technique using commercially available antisera. Results: Out of the total 11,512 blood samples collected and analysed, two samples were identified to be Bombay blood group. The prevalence of Bombay blood group in our study is .017\%. The prevalence of the Bombay blood group varied slightly among different regions in parts of India. Conclusion: Anti H Lectin helped in identifying Bombay Blood Group which would otherwise have been missed in routine blood grouping. Plant based lectins will perform an important role in the field of transfusion medicine in near future.

}, keywords = {Blood grouping, Bombay phenotype, H antigen, Lectin, Ulex Europaeus.}, doi = {10.5530/pj.2016.1.15}, author = {Raj Bharath Rudrappan and Krishnan Veeran} } @article {196, title = {Triterpenes from Hoya paziae Kloppenb.}, journal = {Pharmacognosy Journal}, volume = {8}, year = {2016}, month = {Oct 2016}, pages = {487-489}, type = {Original Article}, chapter = {487}, abstract = {

Chemical investigation of the dichloromethane extracts of the stems of Hoya paziae Kloppenb. led to the isolation of taraxerol (1), taraxeryl acetate (2), and a mixture \α-amyrin acetate (3), and \β-amyrin acetate (4) in about 2.5:1 ratio. The structures of 1\–4 were identified by comparison of their NMR data with those reported in the literature.

}, keywords = {Apocynaceae, Hoya paziae, taraxerol, taraxeryl acetate, α-amyrin acetate, β-amyrin acetate}, doi = {10.5530/pj.2016.5.13}, author = {Melissa Borlagdan and Fernando B. Aurigue and Ian A. Van Altena and Consolacion Y. Ragasa} } @article {35, title = {Comparative analysis of phenolic contents and total antioxidant capacity of Moringa oleifera Lam}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {01/2015}, pages = {44-51}, type = {Original Article}, chapter = {44}, abstract = {

Introduction: Accumulation of reactive species higher than permissible limits in biological systems may lead to various degenerative disorders due to oxidative damage. Materials and Methods: Oxidation is a serious concern faced by the food industry causing deterioration of shelved-food quality. Antioxidant compounds like polyphenolics scavenge such free radicals and thus protect against oxidative stress. Consumption of polyphenol-rich plants as dietary component confers protection against such cellular damage. Results: Present study explores antioxidant capacity, total phenolic content (TPC) and total flavonoid content (TFC) of different extracts prepared from various parts of Moringa oleifera Lam. Higher TPC, TFC and antioxidant activity was shown by methanolic extracts followed by aqueous, petroleum benzene and chloroform extracts.The present study suggests that all the extracts might act as radical scavengers to certain extent possibly due to presence of polyphenolic compounds. Conclusion: M. oleifera exhibits strong antioxidant activity and could serve as prospective source of natural antioxidants to food and health industries.

}, keywords = {antioxidant activity, oxidation., sequential extract, total flavonoid content, total phenolic content}, doi = {10.5530/pj.2015.7.5}, author = {Swati Vyas and Sumita Kachhwaha and S. L. Kothari} } @article {1452, title = {GC-MS Analysis of Phytocomponents in, Pet Ether Fraction of Wrightia tinctoria Seed.}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {29th Apr, 2015}, pages = {249-253}, type = {Original Article}, chapter = {249}, abstract = {

Introduction:Wrightia tinctoria R.Br. (Family: Apocynaceae) commonly called \“Indrajau\” is well known in Indian traditional system for its traditional uses. Materials and Methods: The present investigation was carried out to determine the possible bioactive components of plant seed ethanolic extract, pet ether fraction using GC-MS analysis. 22 components were identified from pet ether fraction obtained from elution of ethanolic extract packed in silica column. Results: The prevailing compounds from fraction F6to F9 were [1,1\&$\#$39;-Bicyclopropyl]-2-octanoic acid, 2\&$\#$39;-hexyl-, methyl ester (21.39\%) , Trilinolein (7.74\%), 2-Myristynoyl pantetheine (18.07\%), 9-Octadecen-12-ynoic acid, methyl ester (4.46\%), 1Hexadecanol,2-methyl (3.77\%), Cyclopropane tetradecanoic acid, 2-octyl-, methyl ester (2.36\%), 1b, 4a-Epoxy-2H-cyclopenta [3,4] cyclopropa [8,9]cycloundec [1,2-b]oxiren-5 (6H)-one, 7-(acetyloxy) decahydro-2,9,10-trihydroxy-3,6,8,8,10a-pentamethyl (38.91\%), Geranyl isovalerate (23.58\%), cis-13-Octadecenoic acid (5.91\%), Quassin (3.82\%), cis-10-Heptadecenoic acid (3.08\%), 9,12,15-Octadecatrienoic acid 2-phenyl-1, 3-dioxan-5-yl ester (31.50\%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)-2,3-dihydroxypropyl ester (14.35\%), Cyclopropanebutanoic acid, 2-[ [2-[ [2- [(2-pentylcyclopropyl) methyl] cyclopropyl] methyl] cyclopropyl] methyl]-, methyl ester (10.13\%), 6,9,12,15-Docosatetraenoic acid, methyl ester (3.39\%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, trans-( 2.73\%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, cis-(4.34\%), Ursodeoxycholic acid (7.14\%), Bufa-20,22-dienolide, 3-(acetyloxy)-14,15-epoxy-16-hydroxy-, (3\á,5\á,15\á,16\á)-(4.75\%), 5H-Cyclopropa [3,4] benz [1,2-e]azulen-5-one, 9a (acetyloxy)-1,1a,1b,4,4a,7a,7b,8,9,9a-de cahydro-4a,7b,9-trihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-,[1aR-(1a\à,1b\á,4a\á,7a\à,7b\à,8\à,9\á,9a\à)]-(6.59\%), Docosahexaenoic acid, 1,2,3-propanetriyl ester (10.86\%), Olean-12-ene-3,15,16,21,22,28-hexol, (3\á,15\à,16\à,21\á,22\à)-( 4.40\%) found as the major components. Conclusion: It could be concluded that, Wrightia tinctoria contains various bioactive compounds. So it is recommended as a plant of phytopharmaceutical importance.

Key words: Bioactive components, Ethanolic extract, GC-MS, Indrajau, Wrightia tinctoria.

}, keywords = {Bioactive components, Ethanolic extract, GC-MS, Indrajau, Wrightia tinctoria.}, author = {Rajani Srivastava and Alok Mukerjee and Amita Verma} } @article {62, title = {GC-MS Analysis of Phytocomponents in, Pet Ether Fraction of Wrightia tinctoria Seed}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2015}, month = {Jul-Aug 2015}, pages = {249-253}, type = {Original Article}, chapter = {249}, abstract = {

Introduction: Wrightia tinctoria R.Br. (Family: Apocynaceae) commonly called \“Indrajau\” is well known in Indian traditional system for its traditional uses. Materials and Methods: The present investigation was carried out to determine the possible bioactive components of plant seed ethanolic extract, pet ether fraction using GC-MS analysis. 22 components were identified from pet ether fraction obtained from elution of ethanolic extract packed in silica column. Results: The prevailing compounds from fraction F6to F9 were [1,1\&$\#$39;-Bicyclopropyl]-2-octanoic acid, 2\&$\#$39;-hexyl-, methyl ester (21.39\%) , Trilinolein (7.74\%), 2-Myristynoyl pantetheine (18.07\%), 9-Octadecen-12-ynoic acid, methyl ester (4.46\%), 1Hexadecanol,2-methyl (3.77\%), Cyclopropane tetradecanoic acid, 2-octyl-, methyl ester (2.36\%), 1b, 4a-Epoxy-2H-cyclopenta [3,4] cyclopropa [8,9]cycloundec [1,2-b]oxiren-5 (6H)-one, 7-(acetyloxy) decahydro-2,9,10-trihydroxy-3,6,8,8,10a-pentamethyl (38.91\%), Geranyl isovalerate (23.58\%), cis-13-Octadecenoic acid (5.91\%), Quassin (3.82\%), cis-10-Heptadecenoic acid (3.08\%), 9,12,15-Octadecatrienoic acid 2-phenyl-1, 3-dioxan-5-yl ester (31.50\%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)-2,3-dihydroxypropyl ester (14.35\%), Cyclopropanebutanoic acid, 2-[ [2-[ [2- [(2-pentylcyclopropyl) methyl] cyclopropyl] methyl] cyclopropyl] methyl]-, methyl ester (10.13\%), 6,9,12,15-Docosatetraenoic acid, methyl ester (3.39\%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, trans-( 2.73\%), 9,12-Octadecadienoic acid, (2-phenyl-1,3-dioxolan-4-yl) methyl ester, cis-(4.34\%), Ursodeoxycholic acid (7.14\%), Bufa-20,22-dienolide, 3-(acetyloxy)-14,15-epoxy-16-hydroxy-, (3\á,5\á,15\á,16\á)-(4.75\%), 5H-Cyclopropa [3,4] benz [1,2-e]azulen-5-one, 9a (acetyloxy)-1,1a,1b,4,4a,7a,7b,8,9,9a-de cahydro-4a,7b,9-trihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-,[1aR-(1a\à,1b\á,4a\á,7a\à,7b\à,8\à,9\á,9a\à)]-(6.59\%), Docosahexaenoic acid, 1,2,3-propanetriyl ester (10.86\%), Olean-12-ene-3,15,16,21,22,28-hexol, (3\á,15\à,16\à,21\á,22\à)-( 4.40\%) found as the major components. Conclusion: It could be concluded that, Wrightia tinctoria contains various bioactive compounds. So it is recommended as a plant of phytopharmaceutical importance

}, keywords = {Bioactive components, Ethanolic extract, GC-MS, Indrajau, Wrightia tinctoria}, doi = {10.5530/pj.2015.4.7}, author = {Rajani Srivastava and Amita Verma}, editor = {Alok Mukerjee} } @article {1553, title = {Antistaphylococcal Activity of Xanthium cavanillesii Lactones}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, pages = {39-42}, type = {Original Article}, chapter = {39}, abstract = {

Objective: The genus Xanthium L., of the Asteraceae Dum. family, (tribe Heliantheae) comprises 30 species of cosmopolitan distribution, many of which, as X. spinosum and X. strumarium are used as medicinal plants. This genus has been the object of numerous phytochemical investigations being sesquiterpene lactones with guaiane or secoguaiane frameworks the main secondary metabolites. Several sesquiterpene lactones have been demonstrated to have antimicrobial activity, in particular against Gram+ bacteria and in Uruguay the infusion of Xanthium cavanillesii Show (common name \“Abrojo\” or \“Abrojo grande\”) which grows wild, is used as antiseptic in popular medicine. In this work we present the results of the antibacterial analysis of several extracts, fractions and pure compounds from X. cavanillesii against both sensitive and resistant strains of Staphylococcus aureus. Materials and Methods: Compounds were isolated from X. cavanillesii aerial parts by several chromatographic and spectroscopic methods antimicrobial analysis were performed according to Clinical and Laboratory Standards Institute guidelines. Results: The minimum inhibitory concentration (MIC) found were high for the sensitive 6538p strain when compared with common antibiotics. For the resistant strains, the pure compounds activity clearly outperformed the antibiotics, especially in the case of the multiresistant 700,699 strain with MICs of 31, 236 and 356 \μg/mL for the Xanthium compounds, gentamicin and oxacillin respectively.

Key words: Antimicrobial, abrojo, methicillin-resistant Staphylococcus aureus, sesquiterpene lactones

}, keywords = {abrojo, Antimicrobial, methicillin-resistant Staphylococcus aureus, sesquiterpene lactones}, author = {Cristina Olivaro and Nicole Paris and M. P{\'\i}a Cerdeiras and Alvaro V{\'a}zquez} } @article {1517, title = {Comparative analysis of phenolic contents and total antioxidant capacity of Moringa oleifera Lam.}, journal = {Pharmacognosy Journal}, volume = {7}, year = {2014}, month = {27th Nov, 2014}, pages = {44-51}, type = {Original Article}, chapter = {44}, abstract = {

Introduction: Accumulation of reactive species higher than permissible limits in biological systems may lead to various degenerative disorders due to oxidative damage. Materials and Methods: Oxidation is a serious concern faced by the food industry causing deterioration of shelved-food quality. Antioxidant compounds like polyphenolics scavenge such free radicals and thus protect against oxidative stress. Consumption of polyphenol-rich plants as dietary component confers protection against such cellular damage. Present study explores antioxidant capacity, total phenolic content (TPC) and total flavonoid content (TFC) of different extracts prepared from various parts of Moringa oleifera Lam. Results: Higher TPC, TFC and antioxidant activity was shown by methanolic extracts followed by aqueous, petroleum benzene and chloroform extracts. The present study suggests that all the extracts might act as radical scavengers to certain extent possibly due to presence of polyphenolic compounds. Conclusion: M. oleifera exhibits strong antioxidant activity and could serve as prospective source of natural antioxidants to food and health industries.

Key words:\  Antioxidant activity, total phenolic content, total flavonoid content, sequential extract, oxidation.

}, keywords = {antioxidant activity, oxidation, sequential extract, total flavonoid content, total phenolic content}, author = {Swati Vyas and Sumita Kachhwah and S.L. Kothari} } @article {1502, title = {Estrogenic Activity of Bauhinia racemosa extract in Female albino rats: An Investigational Study}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {3rd Sept, 2014}, pages = {5-9}, type = {Original Article}, chapter = {5}, abstract = {

Objective: To evaluate the effect of petroleum ether, ethanol and water extract of Bauhinia racemosa in female albino rats. Methods: Plant extracts were tested for their estrogenic activity by using ovariectomised method at two dose level: 200 mg/kg and 400mg/kg respectively. Further, Plant extracts and Standard drug Ethinyl estradiol (1\µg/kg) combination were tested for synergistic estrogenic activity. Results:In-vivo investigation revealed that ethanol extract at dose of 200 mg/kg and 400 mg/kg shows significance increase 325.23\±5.23, 328.84\±4.56 and 3.252\±0.47, 3.288\±0.27 in uterine wet weight and uterine weight ratio respectively in female albino rat as compared to control and petroleum ether and water extracts. Simultaneous administration of standard drug Ethinyl estradiol (1\µg/kg) with ethanol extract at dose of 200 mg/kg and 400 mg/ kg potentiates (327.36 \± 5.78, 330.95 \± 6.21 and 3.273 \± 0.64, 3.309 \± 0.49 uterine wet weight and uterine weight ratio respectively in female albino rat) the estrogenic activity as compared to individual administration of ethanol extract as a synergistic effect. Conclusion: It was observed that ethanol extract of Bauhinia racemosa produced significance estrogenic activity.

Key words:Bauhinia racemosa, estrogenic activity, Ethinyl estradiol, ovariectomy.

}, keywords = {Bauhinia racemosa, Estrogenic activity, Ethinyl estradiol, ovariectomy.}, author = {Gautam P. Vadnere and Aslam R. Pathan and Abhay K. Singhai} } @article {1503, title = {High-Performance Thin-Layer Chromatography Fingerprinting of Ethnopharmacological Important Seeds of Wrightia tinctoria}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {3rd Sept, 2014}, pages = {10-14}, type = {Original Article}, chapter = {10}, abstract = {

Introduction:Wrightia tinctoria R. Br. belongs to family Apocynaceae commonly called as sweet Indrajao, Pala indigo plant, Dyer\’s Oleander. \“Jaundice curative tree\” in south India. Materials and Methods: A method has been developed for different extracts of W. tinctoria for high-performance thin-layer chromatography (HPTLC) fingerprinting analysis for identification and quantification of the marker compound. Result: The satisfactory resolution was obtained in the solvent system toluene:ethyl acetate v/v (8:2) for petroleum ether extract, toluene:ethyl acetate v/v (7:3) for chloroform extract and toluene:ethyl acetate:formic acid v/v (7:3:0.1) for alcoholic extract. Conclusion: The HPTLC fingerprinting profile developed for different extracts of W. tinctoria will help in proper identification and quantification of the marker compound.

Key words: High-performance thin-layer chromatography fingerprinting, Wrightia tinctoria, petether extract, chloroform extract, alcoholic extract.

}, keywords = {Alcoholic extract, chloroform extract, High-performance thin-layer chromatography fingerprinting, petether extract, Wrightia tinctoria}, author = {Rajani Srivastava and Alok Mukerjee and Amita Verma} } @article {1523, title = {Isolation of Phytochemicals From Anticancer Active Extracts of Syzygium alternifolium Walp. Leaf}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {26th May 2014}, pages = {83-85}, type = {Research Article}, abstract = {

Objective: The aim of the present study was to isolate the phyto molecules from the leaf of endemic medicinal pant, Syzygium alternifolium. The phytochemical investigation of the leaf of the plant yielded a flavonoid Eucalyptin 1 and a triterpinoid Epibetulinic acid 2 in pure state. Results: The compound 1 is being reported for the first time from this plant. The anti-cancer activity showed leaf hexane extract (IC50 values 8.177 and 2.687 \µg/ml) was significantly active, when compared to extracts and compounds, against human cancer cell lines MCF-7 and DU-145. Also, hexane extract potentially inhibited the growth of DU-145 cell lines when compared with the reference compound doxorubicin. Amongst the isolated compounds, 1 was better cytotoxic than 2. Conclusion: The hexane extract of leaves of S. alternifolium yielded compounds 1 and 2 and the structure elucidation, based on spectroscopy, revealed them as Eucalyptin and Epibetulinic acid respectively. The compound 1 is being reported for the first time from this plant. The anti-cancer activity showed leaf hexane extract (IC50 values 8.177 and 2.687 mg/mL) was significantly active, when compared to extracts and compounds, against human cancer cell lines MCF-7 and DU-145. Also, hexane extract potentially inhibited the growth of DU-145 cell lines when compared with the reference compound doxorubicin. Amongst the isolated compounds, 1 was better cytotoxic than 2.

Key Words: Syzygium alternifolium, Myrtaceae, Eucalyptin, Epibetulinic acid, anticancer activity.

}, keywords = {Anticancer activity, Epibetulinic acid, Eucalyptin, Myrtaceae, Syzygium alternifolium}, author = {B. Komuraiah and Srinivas Chinde and A. Niranjana Kumar and K.V.N. Satya Srinivas and Ch. Venu and J. Kotesh Kumar and K.P. Sastry and Paramjit Grover} } @article {1526, title = {Physico Chemical Characterization and Anti Inflammatory Activity of Stem Extracts Of Berberis aristata DC and Cosinium fenestratum Linn in Carrageenan Induced Wistar Rats}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {26th May 2014}, pages = {72-77}, type = {Research Article}, abstract = {

An initial study on the physico-chemical properties of Berberis aristata and Cosinium fenestratum, both used as Daruharidra by the Ayurvedic drug industry, recorded all the tested parameters within the limits of Ayurvedic Pharmacopeia of India. Also, analysis of secondary metabolite of the plants was carried out focusing on the presence and quantification of berberine in the samples. Further, the potential difference in the anti-inflammatory activity of the aqueous and methanolic stem extracts of the two species was compared using carrageenan induced Wistar rats model. At a dose of 25 mg/kg, the aqueous and methanolic crude extracts of both the plant species showed significant inhibition of rat paw edema at various time intervals viz.,0, 30, 60, 120 and 240 minutes as against the control standard drug indomethacin (p\<0.01, p\<0.001).

Key words: antiinflammation, Berberine, Berberis aristata, Cosinium fenestratum, Physico-chemical analysis.

}, keywords = {Antiinflammation, Berberine, Berberis aristata, Cosinium fenestratum, Physico-chemical analysis}, author = {S.Tamilselvi and Padma Venkatasubramanian and N.S. Vasanthi} } @article {1497, title = {Role of Boswellia ovalifoliolata Bal. Henry extract on high fat diet induced hypercholesterolemia}, journal = {Pharmacognosy journal}, volume = {6}, year = {2014}, month = {8th April 2014}, pages = {108-116}, type = {Original Article}, abstract = {

Objective: To evaluate the Antihypercholesterolemic effect of Boswellia ovalifoliolata Bal. Henry extract by performing in vivo studies and to check out its effects by evaluating parameters like food consumption, weight gain, fecal fat excretion, serum and liver lipid \&biochemical profiles. Even the study includes confirmation of activity by the histopathological studies. Methods: Animals were fed with cholesterol rich high fat diet. Food intake, Body weight and fecal fat excretion were measured. Serum and liver samples were analyzed for the estimation of lipid profiles and other biochemical parameters by using different kits. Histopathological study on liver, aorta, heart and adipose tissue was done to ensure the activity. Results: The animal group administered with methanolic extract of the plant has shown decreased levels of TC, LDL, VLDL, TG, HDL+VLDL, VLDL+LDL, LDL/TC, AI, SGOT, SGPT and elevated levels of HDL, HDL/TC in a dose dependent manner significantly (p\<0.01 \& p\<0.05). The evaluation of liver tissue of animal groups treated with herbal extract and standard had shown increased levels of SOD, GSH and Catalase, whereas levels of SGOT, SGPT, Total glucose, HMG-CoA, lipase, amylase and percentage of monaldehyde were decreased when compared with high fat diet fed rats. Body weight and Food intake in treated groups were significantly lower than that in model control. Conclusion: It can be confered from the present studies that the Boswellia ovalifoliolata Bal. Henry extract have strong activity against hypercholesterolemia and obesity suggesting a potential benefit as antihypercholesterolemic agent.

key words: Boswellia ovalifoliolata Bal. Henry, High fat diet, Lipid profile, Histopathological studies.

}, keywords = {Boswellia Ovalifoliolata Bal. Henry, High Fat Diet, lipid profile}, author = {D. Sathis Kumar, and David Banji, and A. Harani, and Ch. Pavan Kumar, and JN. Ravi Varma} }