Protective effect of cornuside against carbon tetrachloride-induced acute hepatic injury

Biosci Biotechnol Biochem. 2011;75(4):656-61. doi: 10.1271/bbb.100739. Epub 2011 Apr 22.

Abstract

This study elucidated the effects of cornuside on carbon tetrachloride (CCl₄)-induced hepatotoxicity. Rats were treated intraperitoneally with 0.5 mL/kg of CCl₄. Sixteen h after CCl₄ treatment, the levels of serum aminotransferases, tumor necrosis factor-α (TNF-α), and lipid peroxidation were significantly elevated, whereas the hepatic antioxidative enzyme activities were decreased. These changes were attenuated by cornuside. Histological studies also indicated that cornuside inhibited CCl₄-induced liver damage. Furthermore, the contents of hepatic nitrite, inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2) were elevated after CCl₄ treatment, while cytochrome P450 2E1 (CYP2E1) expression was suppressed. Cornuside treatment inhibited the formation of liver nitrite, and reduced the overexpression of iNOS and COX-2 proteins, but restored the liver CYP2E1 content as compared with the CCl₄-treated rats. Our data indicate that cornuside protects the liver from CCl₄-induced acute hepatotoxicity, perhaps due to its ability to restore the CYP2E1 function and suppress inflammatory responses, in combination with its capacity to reduce oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Carbon Tetrachloride / toxicity*
  • Chemical and Drug Induced Liver Injury / blood
  • Chemical and Drug Induced Liver Injury / metabolism
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Cyclooxygenase 2 / metabolism
  • Cytochrome P-450 CYP2E1 / metabolism
  • Cytoprotection / drug effects*
  • Gene Expression Regulation, Enzymologic / drug effects
  • Glucosides / pharmacology*
  • Lipid Peroxidation / drug effects
  • Liver / drug effects
  • Liver / enzymology
  • Liver / metabolism
  • Liver / pathology
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Nitrites / metabolism
  • Pyrans / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Transaminases / blood
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Antioxidants
  • Glucosides
  • Nitrites
  • Pyrans
  • Tumor Necrosis Factor-alpha
  • cornuside
  • Carbon Tetrachloride
  • Cytochrome P-450 CYP2E1
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2
  • Transaminases