European Journal of Clinical Pharmacology

, Volume 62, Issue 7, pp 497–502

Inhibitory effect of medroxyprogesterone acetate on human liver cytochrome P450 enzymes

  • Jiang-Wei Zhang
  • Yong Liu
  • Wei Li
  • Da-Cheng Hao
  • Ling Yang
Pharmacokinetics and Disposition

Abstract

Objective

Medroxyprogesterone acetate (MPA), frequently used in contraception and chemotherapy, was involved in a report of drug-drug interaction (DDI) when co-administrated with phenytoin, doxifluridine and cyclophosphamide. In order to clarify the mechanism of such interaction, an in vitro study was undertaken to evaluate MPA’s potential to inhibit cytochrome P450 (CYP) enzymes.

Methods

Inhibitory effects of MPA on seven CYPs, including CYP1A2, CYP2A6, CYP2C8, CYP2C9, CYP2D6, CYP2E1 and CYP3A4, were conducted in human liver microsomes. Time- and NADPH-dependent inhibitions were also tested. DDI potential was predicted according to the [I]/Ki value.

Results

MPA was found to inhibit CYP2C9 and CYP3A4; half inhibition concentration (IC50) was 16.1 μM and 31.5 μM, respectively. Slight inhibition was observed on CYP1A2, CYP2A6, CYP2C8 and CYP2D6 with IC50 of more than 100 μM. MPA exhibited activation rather than inhibition on CYP2E1. Further study revealed that MPA showed a noncompetitive inhibition on CYP2C9 and a competitive inhibition on CYP3A4 with Ki of 9.0 μM and 36 μM, respectively. In addition, MPA was not a mechanism-based inhibitor to any of seven isoforms tested. By using predicted concentration of MPA in liver, [I]/Ki was estimated to be 0.24 and 0.06 for CYP2C9 and CYP3A4, respectively. The concentration of phenytoin co-administrated with MPA was calculated to increase by 24%.

Conclusion

Based on our results, MPA can possibly cause clinically relevant DDI via the inhibition of CYP2C9.

Keywords

Cytochrome P450 CYP2C9 Drug-drug interaction Medroxyprogesterone acetate (MPA) Phenytoin 

Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  • Jiang-Wei Zhang
    • 1
    • 2
  • Yong Liu
    • 1
  • Wei Li
    • 1
    • 2
  • Da-Cheng Hao
    • 1
    • 2
  • Ling Yang
    • 1
  1. 1.Laboratory of Pharmaceutical Resource Discovery, Dalian Institute of Chemical PhysicsChinese Academy of SciencesDalianPeople’s Republic of China
  2. 2.Graduate School of Chinese Academy of SciencesBeijingPeople’s Republic of China

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