<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vimala Yerramilli</style></author><author><style face="normal" font="default" size="100%">Mahendra Singh</style></author><author><style face="normal" font="default" size="100%">Ishwar Singh</style></author><author><style face="normal" font="default" size="100%">Laxman Nagar</style></author><author><style face="normal" font="default" size="100%">Jitendra Singh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepato-restorative Activity of Methanolic Extracts of Coccinia grandis L. Voigt. in CCl4 - Intoxicated Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Callus</style></keyword><keyword><style  face="normal" font="default" size="100%">CCl4</style></keyword><keyword><style  face="normal" font="default" size="100%">Coccinia grandis</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Liver</style></keyword><keyword><style  face="normal" font="default" size="100%">Silymarin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1096-1102</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Coccinia grandis&lt;/em&gt; has pharmacological activities such as antioxidant, anti-ulcer, antiinflammatory, anti-hypersensitive, anti-hyperglycaemic, anti-cancer and hepatoprotective.&lt;strong&gt; Objective: &lt;/strong&gt;This work is aimed to investigate an alternative low-cost green drug with hepatoprotective potential from methanolic extract of the leaf, stem and their corresponding calli of &lt;em&gt;Coccinia grandis&lt;/em&gt;. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Using 42 Albino Wistar rats divided into seven groups each group containing 6 rats. 1.5ml/kg bw of CCl&lt;sub&gt;4&lt;/sub&gt; diluted in olive oil was orally injected for fourteen days and methanolic extracts of parent plant parts, callus and silymarin, and on the last day of treatment, experimental rats were anesthetized, blood and organ removed for the biochemical and histopathological analysis.&lt;strong&gt; Results:&lt;/strong&gt; This work is aimed to investigate an alternative low-cost green drug with hepatoprotective potential. Liver damage was induced by CCl&lt;sub&gt;4&lt;/sub&gt; (1.5 ml/kg body weight) in Wistar albino rats and recovery was noted by treating with Silymarin (100mg/kg bw), a known standard herbal drug and by treating with crude methanolic extract of leaf and stem parts of &lt;em&gt;Coccinia grandis&lt;/em&gt; and their corresponding calli (leaf callus and stem callus at 180mg/kg bw) in terms of marked decrease in CCl&lt;sub&gt;4-&lt;/sub&gt; increased SGOT (Serum glutamic oxaloacetic transaminase), SGPT (Serum glutamic pyruvic transaminase), ALP (Alkaline phosphatase), TB (Total bilirubin) and rise in TP (Total protein) compared to untreated control group. Histopathological studies of hepatocytes provide evidence of the centrilobular vacuolar degeneration and recovery by Silymarin or treatment with plant and callus extracts. &lt;strong&gt;Conclusion:&lt;/strong&gt; Biochemical and histopathological examination proved the hepatoprotective potential of calli and parent plant parts (leaf, stem) of &lt;em&gt;Coccinia grandis&lt;/em&gt;.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1096</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Vimala Yerramilli&lt;sup&gt;1*&lt;/sup&gt;, Mahendra Singh&lt;sup&gt;1&lt;/sup&gt;,Ishwar Singh&lt;sup&gt;2&lt;/sup&gt;, Laxman Nagar&lt;sup&gt;3&lt;/sup&gt;, Jitendra Singh&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1,2&lt;/sup&gt;,Department of Botany, Chaudhary Charan Singh, University, Meerut, 250004-INDIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1, 3,4&lt;/sup&gt;Department of Microbiology, Chaudhary Charan Singh, University, Meerut, 250004-INDIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Priyanka Godara</style></author><author><style face="normal" font="default" size="100%">Bunty Kumar Dulara</style></author><author><style face="normal" font="default" size="100%">Neelam Barwer</style></author><author><style face="normal" font="default" size="100%">Navneet Singh Chaudhary</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative GC-MS Analysis of Bioactive Phytochemicals from Different Plant Parts and Callus of Leptadenia reticulata Wight and Arn.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Callus</style></keyword><keyword><style  face="normal" font="default" size="100%">Fatty Acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Root</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem</style></keyword><keyword><style  face="normal" font="default" size="100%">Steroids</style></keyword><keyword><style  face="normal" font="default" size="100%">Terpenoids</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">129-140</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Aim:&lt;/strong&gt; The aim of this study is identification and comparative analysis of bioactive phytochemicals present in methanol and ethyl acetate extracts of different plant organs and callus of &lt;em&gt;Leptadenia reticulata&lt;/em&gt; by GC–MS technique. &lt;strong&gt;Methodology:&lt;/strong&gt; The shade dried plant samples (leaves stem and root) and callus produced from leaf of&lt;em&gt; L. reticulata&lt;/em&gt; were powdered and then sequentially extracted in methanol and ethyl acetate solvents. Total eight extracts were prepared which were Methanolic Leaf Extract (MLE), Methanolic Stem Extract (MSE), Methanolic Root Extract (MRE), Methanolic Callus Extract (MCE), Ethyl Acetate Leaf Extract (EALE), Ethyl Acetate Root Extract (EARE), Ethyl Acetate Stem Extract (EASE) and Ethyl Acetate Callus Extract (EACE). Then, each of the extracts was further subjected to Gas Chromatography– Mass Spectrometry (GC–MS) analysis. &lt;strong&gt;Results:&lt;/strong&gt; The GC–MS analysis of the eight extracts revealed the presence of 77 different types of high and low molecular weight phytochemicals and bioactive compounds in varying quantities. Some of the phytochemicals detected for first time in &lt;em&gt;L. reticulata&lt;/em&gt; are γ-sitosterol, Campesterol, Pristane, Hexahydrofarnesol, Stearic acid, Arachidic acid, Coniferyl alcohol, n-Tetracosanol-1, Ascorbic acid 2,6-dihexadecanoate, (2S,3S)-3,7,4’-Trihydroxy-5-methoxy-6-methylflavanone etc. These chemical compounds are considered biologically active and pharmacologically important. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study gives a detailed comparison of detection and identification of various bioactive phytochemicals from different plant parts (leaves, stem and root) and callus of&lt;em&gt; L. reticulata.&lt;/em&gt; This provides a basis for the biological and biochemical characterization of some newly detected biologically and pharmacologically important phytochemical components from this plant.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">129</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Priyanka Godara, Bunty Kumar Dulara, Neelam Barwer, Navneet Singh Chaudhary&lt;sup&gt;* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Botany, University of Rajasthan, JLN Marg, Jaipur-302004, Rajasthan, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Choudhary D</style></author><author><style face="normal" font="default" size="100%">Shekhawat JK</style></author><author><style face="normal" font="default" size="100%">Kataria V</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">GC-MS Analysis of Bioactive Phytochemicals in Methanol Extract of Aerial Part and Callus of Dipterygium glaucum Decne</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Callus</style></keyword><keyword><style  face="normal" font="default" size="100%">Campesterol</style></keyword><keyword><style  face="normal" font="default" size="100%">Capparidaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Fatty Acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Stigmasterol</style></keyword><keyword><style  face="normal" font="default" size="100%">Terpenoids</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1055-1063</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;This study was designed to evaluate the phytocomponents present in aerial part and &lt;em&gt;in vitro &lt;/em&gt;induced callus methanol extracts of &lt;em&gt;Dipterygium glaucum&lt;/em&gt; by Gas Chromatography-Mass Spectrometry (GC-MS) technique. &lt;strong&gt;Methods: &lt;/strong&gt;GC-MS analysis of aerial part sample and callus produced from leaf of &lt;em&gt;D. glaucum &lt;/em&gt;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. &lt;strong&gt;Results: &lt;/strong&gt;This study was carried out to identified and comparative analysis of bioactive phytochemicals from aerial part extract and callus extract of&lt;em&gt; D. glaucum&lt;/em&gt;. 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. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study represents the detection and identification of different phytochemical compounds from aerial part and callus extract of&lt;em&gt; D. glaucum&lt;/em&gt;. Thus, due to the presence of various important bioactive phytocomponents this plant is recommended as a pharmaceutically important plant.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1055</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Choudhary D, Shekhawat JK, Kataria V*&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Biotechnology Unit, Department of Botany (UGC-Centre of Advanced Study), Jai Narain Vyas University, New Campus, Jodhpur 342001, Rajasthan, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ruchi Singh</style></author><author><style face="normal" font="default" size="100%">Preeti Chaturvedi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Characterization of Rhizome, Fruit, Leaf and Callus of Rheum emodi Wall. using GC-MS</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Callus</style></keyword><keyword><style  face="normal" font="default" size="100%">Fruit</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaf</style></keyword><keyword><style  face="normal" font="default" size="100%">Rheum emodi</style></keyword><keyword><style  face="normal" font="default" size="100%">Rhizome</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">617-623</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Rheum emodi&lt;/em&gt; is an immensely useful medicinal herb of Himalaya having remarkable antidiabetic and anticancerous activities reported mainly from rhizomatous portion of the plant. The present study reports Gas Chromatographic- Mass spectroscopic characterization of both the conventionally used part i.e., the rhizome as well as other parts of &lt;em&gt;R. emodi&lt;/em&gt; including callus to exploit the nonconventional parts for future use. &lt;strong&gt;Objective:&lt;/strong&gt; To explore the bioactive constituents in the methanol extract of rhizome, fruit, leaf and callus of &lt;em&gt;R. emodi&lt;/em&gt;. &lt;strong&gt;Methods:&lt;/strong&gt; Phytochemical characterization of the plant extracts was performed by using GC-MS QP 2010 Plus. Various constituents were identified after matching their mass fragmentation pattern with data available in GC-MS library of National Institute of Standards Technology (NIST) and Wiley Registry of Mass Spectral Data’s, New York (Wiley). &lt;strong&gt;Results: &lt;/strong&gt;Total of 95 bioactive compounds were obtained in methanol extract of &lt;em&gt;R. emodi&lt;/em&gt; out of which rhizome, fruit, leaf and callus revealed 31, 38, 27 and 47 compounds respectively. Two anthraquinones, chrysophanol (43.97%) and physcion (3.23%) were obtained from rhizome whereas fruit possessed only physcion (4.66%). &lt;strong&gt;Conclusion:&lt;/strong&gt; The present findings characterizes and helps to supplement the chemical profile of the plant for its futuristic role in nutritional, pharmaceutical and therapeutic industries.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Short Communication</style></work-type><section><style face="normal" font="default" size="100%">617</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ruchi Singh*, Preeti Chaturvedi &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Biological Sciences, College of Basic Sciences and Humanities (CBSH), G. B. Pant University of Agriculture and Technology, Pantnagar, Udham Singh Nagar-263145, Uttarakhand, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aswathy Jayasree Madanakumar</style></author><author><style face="normal" font="default" size="100%">Greeshma Murukan</style></author><author><style face="normal" font="default" size="100%">Bosco Lawarence</style></author><author><style face="normal" font="default" size="100%">Murugan Kumaraswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation, Purification of Quercetin from in vitro Cell Suspension Culture of Caesalpinia pulcherrima and its Analysis by HPLC-DAD and NMR</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Caesalpinia pulcherrima</style></keyword><keyword><style  face="normal" font="default" size="100%">Callus</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell suspension culture</style></keyword><keyword><style  face="normal" font="default" size="100%">Elicitors; growth hormones</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/380</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s44-s51</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Caesalpinia pulcherrima&lt;/em&gt;, belongs to Caesapiniaceae, is a known medicinal plant widely distributed in India and is used in traditional medicine for the treatment of various ailments. Many phytochemicals are reported from the plant as potential source of crude drug. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; An efficient and simple reproducible protocol was developed for callus production using leaf explants of &lt;em&gt;C. pulcherrima&lt;/em&gt;. The combination of 2, 4-D, kin and BA, was used for the callus induction. Subsequently, cell suspension culture and quercetin synthesis from &lt;em&gt;in vitro&lt;/em&gt; callus was attempted. Role of effect of elicitors (Sucrose, ABA and salicylic acid) in cell suspension culture was carried in MS medium containing 2,4-D + BA + kinetin. Flavonoids was purified, fractionated by HPLC-DAD and NMR.&lt;strong&gt; Results:&lt;/strong&gt; 2, 4-D (2.5 mg/L), BA (2.5 mg/L) + kin (1 mg/mL) was effective for maximum callus induction from leaf explants. Significant cell suspension culture was noticed with liquid MS medium containing 2,4-D (2 mg/L)+ BA (1mg/L)+ kinetin (1.5 mg/L). Sucrose, ABA and salicylic acid (SA) at different concentrations influenced cell biomass and quercetin accumulation. The addition of ABA/SA along with sucrose was found to have no remarkable effect on cell biomass and also quercetin synthesis. However, cells cultured in the medium fortified with 45 g/L sucrose without ABA/ SA showed the highest quercetin content (16.5 mg/g). Flavonoids was purified, fractionated by HPLC-DAD and NMR revealed the presence of 9 components such as quercetin, isoquercetin, quercetrin, rutin, quercetin 3-O-&amp;beta;-D-xyloside, quercetin 3-Oarabinopyranoside, quercetin 3-O- &amp;alpha;-arabinopyranosyl (1&amp;rarr;2) &amp;beta;-galactopyranoside, isorhamnetin 3-O-rutinoside and an unknown compound. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;C. pulcherima&lt;/em&gt; reveals significant synthesis of quercetin. Quercetin content recorded in cell suspension culture was significantly higher compared with &lt;em&gt;in vivo&lt;/em&gt; plants grown in fields and the compounds were identified by NMR.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s44</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aswathy Jayasree Madanakumar, Greeshma Murukan, Bosco Lawarence, Murugan Kumaraswamy* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Plant Biochemistry and Molecular Biology Laboratory, University College, Trivandrum, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record></records></xml>