Identification of drugs inhibiting the in vitro metabolism of tacrolimus by human liver microsomes

Br J Clin Pharmacol. 1996 Mar;41(3):187-90. doi: 10.1111/j.1365-2125.1996.tb00181.x.

Abstract

1. Tacrolimus, an immunosuppressive macrolide, is metabolized by enzymes of the cytochrome P450 3A subfamily. In this study, 34 drugs were tested for their interactions with tacrolimus metabolism by human liver microsomes. 2. Fifteen drugs which inhibit the in vitro metabolism of tacrolimus were identified: bromocriptine, corticosterone, dexamethasone, ergotamine, erythromycin, ethinyloestradiol, josamycin, ketoconazole, miconazole, midazolam, nifedipine, omeprazole, tamoxifen, troleandomycin and verapamil.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bromocriptine / pharmacology
  • Corticosterone / pharmacology
  • Humans
  • In Vitro Techniques
  • Kinetics
  • Liver / drug effects
  • Liver / metabolism*
  • Microsomes / drug effects
  • Microsomes / metabolism*
  • Tacrolimus / metabolism*

Substances

  • Bromocriptine
  • Corticosterone
  • Tacrolimus