ArticlesAbstractPharmacognosy Research,2010,2,1,26-30.DOI:10.4103/0974-8490.60584Published:March 2010Type:Original ArticleAuthors:Nirmal K Bairwa, Neeraj K Sethiya, and SH Mishra Author(s) affiliations:Nirmal K Bairwa, Neeraj K Sethiya, SH Mishra Herbal Drug Technology Laboratory, Pharmacy Department, Faculty of Technology and Engineering, The Maharaja Sayajirao University of Baroda, Vadodara, Gujarat - 390 001, India Abstract:The present study reports protective activity of ethyl acetate fraction of methanol extract of stem bark of Ceiba pentandra against paracetamol-induced liver damage in rats. The ethyl acetate fraction (400 mg/kg) was administered orally to the rats with hepatotoxicity induced by paracetamol (3 gm/kg). Silymarin (100 mg/kg) was used as positive control. High performance thin layer chromatography (HPTLC) fingerprinting of ethyl acetate fraction revealed presence of its major chemical constituents. A significant (P < 0.05) reduction in serum enzymes GOT (ALT), aspartate aminotransferase (AST), GPT alkaline phosphatase (ALP), total bilirubin content and histopathological screening in the rats treated gave indication that ethyl acetate fraction of methanolic extract of Ceiba pentandra possesses hepatoprotective potential against paracetamol-induced hepatotoxicity in rats. Keywords:Ceiba pentandra, Hepatoprotective, Hepatotoxicity, ParacetamolView:PDF (1.14 MB) PDF Thumbnails Document Outline Search Document Find Toggle Sidebar Previous Next Page: Fullscreen Print Download Current View Zoom Out Zoom In Automatic Zoom Actual Size Fit Page Full Width 50% 75% 100% 125% 150% 200% More Information Less Information Close Click here to download the PDF file. Images Protective Effect of Stem Bark of Ceiba pentandra linn. against Paracetamol-induced Hepatotoxicity in Rats Keywords12‑epilycodoline N‑oxide15-lipoxygenase inhibitory activityCeiba pentandraHepatoprotectiveHepatotoxicityParacetamol ‹ In vitro Sun Protection Factor Determination of Herbal Oils used in Cosmetics up Effect of Dragon Fruit Extract on Oxidative Stress and Aortic Stiffness in Streptozotocin-induced Diabetes in Rats ›