Bufalin inhibits CYP3A4 activity in vitro and in vivo

Acta Pharmacol Sin. 2009 May;30(5):646-52. doi: 10.1038/aps.2009.42.

Abstract

Aim: To investigate the inhibitory interactions of bufalin and CYP3A4.

Methods: Recombinant human CYP3A4 was incubated with bufalin in vitro. Bufalin was administered ig and iv to Wistar rats to further estimate its impact on CYP3A4, and midazolam was given to index the activity of CYP3A4.

Results: The IC(50) of bufalin was 14.52 micromol/L. Bufalin affected CYP3A4 activity with increases in AUC(0-t) and t(1/2), and decreases in CL and the formation of 1-hydroxy-midazolam after ig or iv administration of midazolam (P<0.05). An increase in C(max) after ig bufalin administration (P<0.05) was observed.

Conclusion: Bufalin showed a modest but significant inhibition of CYP3A4 both in vitro and in vivo. The likelihood of an interaction between bufalin and the CYP3A4-metabolized drugs in human might not be negated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bufanolides / administration & dosage
  • Bufanolides / pharmacology*
  • Cytochrome P-450 CYP3A / administration & dosage
  • Cytochrome P-450 CYP3A Inhibitors*
  • Drug Interactions
  • Drugs, Chinese Herbal / pharmacology*
  • Humans
  • In Vitro Techniques
  • Male
  • Midazolam / pharmacokinetics
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / antagonists & inhibitors

Substances

  • Bufanolides
  • Cytochrome P-450 CYP3A Inhibitors
  • Drugs, Chinese Herbal
  • Recombinant Proteins
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human
  • Midazolam
  • bufalin