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Galactosamine-induced hepatotoxic effect and hepatoprotective role of a protein isolated from the herb Cajanus indicus L in vivo

✍ Scribed by Prasenjit Manna; Mahua Sinha; Parames C. Sil


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
409 KB
Volume
21
Category
Article
ISSN
1095-6670

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✦ Synopsis


Abstract

dd(+)‐Galactosamine is a well‐known experimental hepatotoxin. The present study was conducted to determine the protective role of a 43‐kD protein isolated from the leaves of the herb Cajanus indicus L against dd(+)‐galactosamine (GalN) induced liver damage in mice. Both preventive and curative effects of the protein have been investigated in the study. The protein was administered intraperitoneally at a dose of 2 mg/kg body weight for 4 days before and after GalN intoxication at a dose of 800 mg/kg body weight for 3 days. The increased activities of serum marker enzymes, alanine aminotransferase, and alkaline phosphatase because of GalN administration, were significantly reduced by the protein treatment. The protein also normalized the altered activities of antioxidant enzymes superoxide dismutase, catalase, glutathione reductase, and glutathione‐S‐transferase as well as the levels of cellular metabolites, reduced glutathione, glutathione disulfide, and total thiols. In addition, the enhanced hepatic lipid peroxidation because of GalN intoxication was also effectively inhibited by the protein treatment. Results suggest that GalN caused hepatic damages via oxidative insult and that the protein provided protection through its antioxidant mechanism. © 2007 Wiley Periodicals, Inc. J Biochem Mol Toxicol 21:13–23, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.20154


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✍ Sarmistha Datta; Swati Sinha; Prantosh Bhattacharyya 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 59 KB 👁 2 views

A herbal protein, CI-1 purified from a leguminous plant Cajanus indicus, showed dose dependent (1.5-6.0 mg/kg  7 days) protective activity on isolated hepatocytes (ex vivo) against b-galactosamine HCl induced hepatic damage in rats. It enhanced the percent viability of the hepatocytes following bga