Metabolism of FK 506 in differentially induced rat liver microsomes

Res Commun Chem Pathol Pharmacol. 1992 Oct;78(1):121-4.

Abstract

The in vitro hepatic metabolism of FK 506 was studied in microsomes prepared from control rats as well as in microsomes prepared from rats treated with the selective cytochrome P-450 isozyme inducers 3-methylcholanthrene (IA), phenobarbital (IIB), and dexamethasone (IIIA). The metabolism of FK 506 was similar for control microsomes and for microsomes prepared from phenobarbital and 3-methylcholanthrene induced animals. The percentage of FK 506 metabolized by these tissue preparations ranged from 21.7 to 32.7%. In contrast, the percentage of FK 506 metabolized by dexamethasone induced microsomes was 86.4%. The metabolism of FK 506 was not effected when the selective IA and IIB isozyme inhibitors alpha-naphthoflavone and orphenadrine were added to the incubations. However, the metabolism of FK 506 decreased by approximately 44% when the IIIA specific isozyme inhibitor troleandomycin was added to the dexamethasone induced microsomes. Therefore, the metabolism of FK 506 is apparently mediated primarily by the steroid inducible cytochrome P-450 IIIA isozyme.

MeSH terms

  • Animals
  • Cytochrome P-450 Enzyme Inhibitors
  • Cytochrome P-450 Enzyme System / biosynthesis*
  • Dexamethasone
  • Enzyme Induction
  • Enzyme Inhibitors / pharmacology
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / biosynthesis*
  • Male
  • Methylcholanthrene
  • Microsomes, Liver / enzymology*
  • Microsomes, Liver / metabolism
  • Phenobarbital
  • Rats
  • Rats, Sprague-Dawley
  • Tacrolimus / metabolism*

Substances

  • Cytochrome P-450 Enzyme Inhibitors
  • Enzyme Inhibitors
  • Isoenzymes
  • Methylcholanthrene
  • Dexamethasone
  • Cytochrome P-450 Enzyme System
  • Tacrolimus
  • Phenobarbital