Rapid, substrate-specific, and dose-dependent deactivation of liver cytosolic glutathione S-transferases in vivo by 1,1-dichloroethylene

Res Commun Chem Pathol Pharmacol. 1985 Jan;47(1):59-72.

Abstract

Administration of 200 mg 1,1-dichloroethylene (1,1-DCE)/kg to fasted male rats rapidly decreased liver cytosolic glutathione (GSH) S-transferase activities by half within 1 hr. This early decrease was not associated with increased serum activities of this soluble enzyme and is considered due to enzyme deactivation. The early decrease in enzyme activities was concomitant with a three-fourths depletion of cytosolic GSH and preceded changes in cytochrome P-450 and the onset of liver cytotoxicity, both of which occurred abruptly between 2 and 3 hr. Substantial changes in GSH S-transferase activities at 4 hr were produced only by severely hepatotoxic doses of 1,1-DCE. The early decrease in hepatic GSH S-transferase activities was selective for substrates dichloronitrobenzene, chlorodinitrobenzene and 1,2-epoxy-3-(p-nitrophenoxy)-propane with apparent sparing of activity towards ethacrynic acid. The rapid, selective and dose-dependent deactivation of the hepatic GSH S-transferases could be relevant to the catastrophic hepatotoxicity of 1,1-DCE.

Publication types

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

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Cytochrome P-450 Enzyme System / metabolism
  • Cytosol / enzymology
  • Dichloroethylenes / pharmacology*
  • Glutathione Transferase / antagonists & inhibitors*
  • Hydrocarbons, Chlorinated / pharmacology*
  • Kinetics
  • Liver / enzymology*
  • Male
  • Rats
  • Rats, Inbred Strains
  • Substrate Specificity

Substances

  • Dichloroethylenes
  • Hydrocarbons, Chlorinated
  • vinylidene chloride
  • Cytochrome P-450 Enzyme System
  • Glutathione Transferase
  • Aspartate Aminotransferases
  • Alanine Transaminase