Metabolism of tacrolimus (FK 506) in rat liver microsomes. Effect of rifampin and dexamethasone

Res Commun Mol Pathol Pharmacol. 1997 Apr;96(1):107-10.

Abstract

The in vitro metabolism of tacrolimus (TAC, FK 506) was investigated in the liver microsomes prepared from normal rats as well as rats treated with dexamethasone (DEX) and rifampin (RIF). The rate of tacrolimus metabolism was similar in control and RIF treated rat liver microsomes, whereas it significantly increased in microsomes obtained from dexamethasone treated rats. Seven different possible metabolites were identified in the microsomal preparations from rats treated with rifampin or dexamethasone whereas the microsomes from the control rats failed to produce the mono-demethylated and monohydroxylated metabolite of TAC (TAC+2, m/z = 805.5). There was an apparent difference in the amount of individual metabolites formed in different groups. This indicates quantitative differences in the induction of cytochrome P450 3A, an enzyme sub family known to be primarily responsible for tacrolimus metabolism. Lack of induction of tacrolimus metabolism by rifampin can be attributed to the lack of effect of rifampin in inducing cytochrome P450 3A in rats.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Antitubercular Agents / pharmacology*
  • Aryl Hydrocarbon Hydroxylases*
  • Cytochrome P-450 CYP3A
  • Cytochrome P-450 Enzyme System / biosynthesis
  • Dexamethasone / pharmacology*
  • Dose-Response Relationship, Drug
  • Enzyme Induction / drug effects
  • Immunosuppressive Agents / metabolism*
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Mass Spectrometry
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism*
  • Oxidoreductases, N-Demethylating / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Rifampin / pharmacology*
  • Tacrolimus / metabolism*

Substances

  • Anti-Inflammatory Agents
  • Antitubercular Agents
  • Immunosuppressive Agents
  • Dexamethasone
  • Cytochrome P-450 Enzyme System
  • Aryl Hydrocarbon Hydroxylases
  • Cytochrome P-450 CYP3A
  • Oxidoreductases, N-Demethylating
  • Rifampin
  • Tacrolimus