@article {1150, title = {In-vitro Antioxidant and In-Vivo Hepatoprotective Activity of Ethenolic Extract of Tectona grandis Bark Against CCl4 Induced Liver Injury in Rats}, journal = {Pharmacognosy Journal}, volume = {12}, year = {2020}, month = {May 2020}, pages = {598-602}, type = {Research Article}, chapter = {598}, abstract = {

Objectives: The systematic screening of Tectona grandis bark with the purpose of discovering new bioactive compounds as a hepatoprotective agent and to establish the scientific basis for the therapeutic actions of traditional plant medicines. Methods: Tectona grandis bark ethenolic extract was studied for the hepatoprotective activity against CCl4 induced liver injury in rats. Serum enzymes level, total bilirubin and histopathological study of liver were performed. This extract{\textquoteright}s DPPH radical scavenging potential was also studied. Results: Oral administration of ethenolic extract of Tectona grandis bark (200 mg/kg) exhibited significant reduction (p\<0.05) in CCl4-induced increased levels of SGPT, SGOT, ALP and bilirubin (Total) concentration. Treatment with Liv 52 syrup also reversed the hepatotoxicity significantly (p\<0.05). Histopathological studies also provided supportive evidence for biochemical analysis. This extract also showed better activity in quenching DPPH radical. Conclusion: Tectona grandis bark ethenolic extract shown to have hepatoprotective and antioxidant action due to presence of quinones and tannin like phytoconstituents.

}, keywords = {Antioxidant, CCL4 induced hepatopathy, Hepatotoxicity, Histopathology, Quinones, Tectona grandis}, doi = {10.5530/pj.2020.12.89 }, author = {Rajkumar S Bagali and Sunil S Jalalpure and SS Patil} } @article {427, title = {Evaluation of in vitro Antioxidant and Anticancer Activity of Simarouba glauca Leaf Extracts on T-24 Bladder Cancer Cell Line}, journal = {Pharmacognosy Journal}, volume = {9}, year = {2017}, month = {September 2017}, pages = {906-912}, type = {Original Article}, chapter = {906}, abstract = {

Objective: Screening of preliminary phytochemicals, evaluation of in vitro antioxidant and in vitro anticancer activities of Simarouba glauca leaf extracts on T-24 Bladder cancer cell line. Materials and Methods: Herbal extraction was carried out by Soxhlet method using chloroform, ethylacetate, methanol, ethanol, aqueous and hydroalcohol. Phytochemical investigation was done using biochemical tests. Total phenolic content was estimated by Folin-Ciocalteu reagent (FCR) method. Antioxidant potential of leaf extracts was analyzed by Ferric ion reducing antioxidant power (FRAP) assay, Phosphomolybdenum (PM) assay and 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay. In vitro anticancer activity on T-24 bladder cancer cell line was assessed by MTT assay. Statistical analysis used: Statistical analysis of data was performed by analysis of variance (one-way ANOVA) and level of statistical significance between groups was carried out using GraphPad Prism version 5.0 for Windows (GraphPad Software, San Diego, CA, USA). Results: Phytochemical analysis revealed the presence of rich secondary metabolite present in all the solvent extracts. Hydroalcoholic extract showed highest presence of phenolic content (92.38\±0.29 mg/g) GAE. Ethanol and methanol extract showed highest antioxidant capacity in DPPH, FRAP and PM assay as compared to the other extracts based on the test performed. The results confirmed that ethanol extract significantly (p\<0.05) inhibited T-24 cell line with IC50 value (533.55\±25.02 \μg/mL) as compared to standard drug doxorubicin (0.16\μM/mL). Conclusions: The results of the present findings strengthen the potential property of Simarouba glauca as a resource for the discovery of novel antioxidant and anticancer agents.

}, keywords = {Antioxidant; Anticancer; Bladder Cancer; Phytochemical; Simarouba glauca.}, doi = {10.5530/pj.2017.6.142}, url = {http://fulltxt.org/article/195}, author = {Sridevi I Puranik and Shridhar C Ghagane and Rajendra B Nerli and Sunil S Jalalpure and Murigendra B. Hiremath} }