The protective action of thymol against carbon tetrachloride hepatotoxicity in mice

Pharmacol Res. 1999 Aug;40(2):159-63. doi: 10.1006/phrs.1999.0472.

Abstract

The protective action of thymol (paramethyl-isopropyl-phenol) was investigated against carbon tetrachloride (CCl(4))-induced hepatotoxicity in male Swiss albino mice. The CCl(4)at a dose of 20 microl kg(-1)produced damage to liver cells and was followed by the significant increase (P<0.001) in serum alanine aminotransferase (ALT) activity and hepatic lipid peroxidation after 24 h. The hepatocellular necrosis was further confirmed by histopathological examination of liver section. Oral administration of thymol in a single dose (300 mg kg(-1)) resulted in significant (P<0.05) amelioration of CCl(4)-induced hepatotoxicity. Thymol also inhibited lipid peroxidation induced by CCl(4)in vivo. The protection offered by thymol was also evident from histopathology photomicrograph. In a separate in vitro assay, thymol inhibited the non-enzymatic lipid peroxidation of normal mice liver homogenate induced by Fe(3+)-ascorbate. The present study suggests that thymol protects the liver against CCl(4)-induced toxicity and the protection may be mediated through its ability to inhibit lipid peroxidation. However, other interactions between thymol and CCl(4)remains to be elucidated. 1999 Academic Press.

MeSH terms

  • Alanine Transaminase / blood
  • Alanine Transaminase / drug effects
  • Animals
  • Anti-Infective Agents / pharmacology*
  • Antioxidants / pharmacology
  • Butylated Hydroxytoluene / pharmacology
  • Carbon Tetrachloride / toxicity*
  • Chemical and Drug Induced Liver Injury
  • Lipid Peroxidation / drug effects
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Liver Diseases / prevention & control*
  • Male
  • Mice
  • Thymol / pharmacology*

Substances

  • Anti-Infective Agents
  • Antioxidants
  • Butylated Hydroxytoluene
  • Thymol
  • Carbon Tetrachloride
  • Alanine Transaminase