Repeated oral benzene exposure alters enzymes involved in benzene metabolism

J Toxicol Environ Health. 1996 Aug 9;48(5):439-51.

Abstract

Benzene is a known carcinogen and hematopoietic toxin in humans and experimental animals. The effect of acute, high-dose exposure to benzene on hepatic bioactivation and detoxication enzymes has been defined, while little is known about the effect of repeated, low-dose benzene exposure on these enzymes. Our objective was to determine whether repeated, oral benzene exposure alters enzymes involved in benzene metabolism. Specifically, we were concerned with cytochrome P-450-2E1, a bioactivation enzyme, and glutathione transferase and aldehyde dehydrogenase, two detoxifying enzymes. Female CD-1 mice were treated by gavage for 3 wk with benzene doses of 5 mg/kg (0.064 mmol/kg) or 50 mg/kg (0.646 mmol/kg) in corn oil. These doses of benzene produced 0.048 and 0.236 mumol muconic acid/d, respectively. We found that repeated exposure to 50 mg benzene/kg/d decreased P-450-2E1 activity by 34% and induced glutathione transferase activity by 30% without affecting aldehyde dehydrogenase activity. These changes in enzyme activities may serve a protective role against repeated exposure to benzene.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Administration, Oral
  • Aldehyde Dehydrogenase / drug effects*
  • Animals
  • Benzene / administration & dosage
  • Benzene / metabolism
  • Benzene / toxicity*
  • Body Weight / drug effects
  • Cytochrome P-450 Enzyme System / drug effects*
  • Enzyme Induction
  • Female
  • Glutathione Transferase / drug effects*
  • Liver / drug effects
  • Liver / enzymology*
  • Mice
  • Organ Size / drug effects
  • Phenobarbital / pharmacology
  • Sorbic Acid / analogs & derivatives
  • Sorbic Acid / analysis

Substances

  • muconic acid
  • Cytochrome P-450 Enzyme System
  • Aldehyde Dehydrogenase
  • Glutathione Transferase
  • Benzene
  • Sorbic Acid
  • Phenobarbital