Time-course effects of ethanol pretreatment on hepatic necrosis and fat accumulation induced by aflatoxin B1 in the rat

Toxicol Lett. 1991 Jan;55(1):1-9. doi: 10.1016/0378-4274(91)90021-w.

Abstract

Effect of ethanol pretreatment on acute hepatotoxicity and hepatic fat accumulation induced by aflatoxin B1 (AFB1) was followed up to 120 h in male Wistar rats. Pretreatment with 4 oral doses of ethanol (4.0 g/kg body wt. each) at 48, 45, 24 and 21 h prior to AFB1 (2.0 mg/kg body wt.) single intraperitoneal administration caused a significant increase in the activity of plasma glutamic oxaloacetic transaminase (PGOT, 2.4-fold), plasma glutamic pyruvic transaminase (PGPT, 2.8-fold), liver triglycerides (2.3-fold) and the severity of liver necrosis at 72 h after AFB1 administration. The effect of ethanol pretreatment on an increase in the accumulation of liver cholesterol and cholesterol esters induced by AFB1 is additive in nature. In a time-course study, it was shown that liver necrosis and triglyceride, cholesterol and cholesterol ester accumulation occurred simultaneously in both groups of rats treated with AFB1 and ethanol-AFB1. These results suggest that fat accumulation per se is not a primary cause of liver necrosis induced by AFB1 and ethanol-AFB1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Brown / metabolism*
  • Administration, Oral
  • Aflatoxin B1
  • Aflatoxins / toxicity*
  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Carcinogens / toxicity*
  • Cholesterol / metabolism
  • Drug Interactions
  • Ethanol / administration & dosage
  • Ethanol / pharmacology*
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Rats
  • Rats, Inbred Strains
  • Time Factors
  • Triglycerides / metabolism

Substances

  • Aflatoxins
  • Carcinogens
  • Triglycerides
  • Ethanol
  • Cholesterol
  • Aflatoxin B1
  • Aspartate Aminotransferases
  • Alanine Transaminase