Effects of valproate on xenobiotic biotransformation in rat liver. In vivo and in vitro experiments

Pharm Weekbl Sci. 1992 Jun 19;14(3A):127-31. doi: 10.1007/BF01962703.

Abstract

Male Wistar rats were in vivo exposed for 2 weeks to 100 micrograms/ml sodium valproate by subcutaneous implantation of osmotic pumps and hepatocytes were isolated. As an in vitro model co-cultures of rat hepatocytes with epithelial cells were daily treated with valproate (25, 50, 100, 200 micrograms/ml) for 2 weeks. In both models the cytochrome P-450 content and the enzymatic activities of 7-ethoxycoumarin O-deethylase, aldrin epoxidase and glutathione S-transferase were determined in valproate-treated hepatocytes, in controls and in phenobarbital-induced cells. It appeared that in both systems the cytochrome P-450 content and the 7-ethoxycoumarin O-deethylase activity increased significantly after valproate treatment. On the other hand, the activities of aldrin epoxidase and glutathione S-transferase decreased. A cDNA probe, encoding rat P450IIB2 was used to determine whether mRNAs encoding the P450IIB subfamily were induced by valproate. It became clear that the inducing effect of valproate was even more pronounced in vitro than in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 7-Alkoxycoumarin O-Dealkylase / metabolism
  • Animals
  • Biotransformation / drug effects
  • Cells, Cultured
  • Cytochrome P-450 Enzyme System / metabolism
  • Glutathione Transferase / metabolism
  • Liver / cytology
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Mixed Function Oxygenases / metabolism
  • RNA, Messenger / analysis
  • Rats
  • Rats, Inbred Strains
  • Valproic Acid / pharmacology*
  • Xenobiotics / pharmacokinetics*

Substances

  • RNA, Messenger
  • Xenobiotics
  • Valproic Acid
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • aldrin epoxidase
  • 7-Alkoxycoumarin O-Dealkylase
  • Glutathione Transferase