Inactivation of hepatocyte protein kinase C by carbon tetrachloride: involvement of drug's metabolic activation and prooxidant effect

Biochem Biophys Res Commun. 1990 Sep 28;171(3):1353-60. doi: 10.1016/0006-291x(90)90835-b.

Abstract

The involvement of CCl4 biotransformation mechanism in decreasing the Protein Kinase C activity has been analyzed in hepatocytes isolated from phenobarbital-pretreated rats. A significant inhibition (55%) and an almost total disappearance (87%) of the enzyme activity were observed at 15 min and at 30 min incubation with CCl4, respectively. Cell preincubation with Trolox or desferrioxamine allowed a marked whilst not complete protection of both cytosolic and particulate Protein Kinase C activity. These results show that the CCl4 reactive metabolites play a primary role in hepatocyte Protein Kinase C impairment and suggest that besides lipid peroxidation other mechanisms -possibly a derangement of Ca2+ homeostasis- may be involved in this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Biotransformation
  • Carbon Tetrachloride / metabolism
  • Carbon Tetrachloride / pharmacology*
  • Cells, Cultured
  • Chromans / pharmacology
  • Kinetics
  • Liver / enzymology*
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism
  • Phenobarbital / pharmacology
  • Protein Kinase C / antagonists & inhibitors*
  • Rats
  • Rats, Inbred Strains

Substances

  • Antioxidants
  • Chromans
  • Carbon Tetrachloride
  • Protein Kinase C
  • 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid
  • Phenobarbital