Interaction of methadone with substrates of human hepatic cytochrome P450 3A4

  • Iribarne C
  • Dréano Y
  • Bardou L
 et al. 
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Abstract

Methadone, a synthetic drug, is one of the most widely used drugs for opiate dependency treatment. This drug has been demonstrated to be extensively metabolized by cytochrome P450 3A4 in human liver microsomes. Thus, the aim of this in vitro study was to determine if methadone is an inhibitor of other P450s characterized by their specific catalytic activities. Enzymatic activities specific to P450 2E1, P450 1A, P450 2B and P450 2C were not inhibited by methadone. Conversely, nifedipine oxidation, mediated by cytochrome P450 3A4, was potently inhibited by methadone by a mixed-type inhibition mechanism with a Ki of 100 μM. Fluvoxamine, a new antidepressant, was shown to be a potent mixed-type inhibitor of methadone N-demethylation with a Ki of 7 μM. Finally, methadone appears to be a mixed-type inhibitor and not a suicide inhibitor of cytochrome P450 3A family. Accordingly, caution should be advised in the clinical use of methadone when other drugs are administered that are able to induce or inhibit P450 3A4, such as rifampicin or nifedipine, diazepam and fluvoxamine.

Author-supplied keywords

  • 2-ethylidene-1,5-dimethyl-3,3-diphenyl pyrrolidine
  • 4-NP
  • 4-nitrophenol hydroxylation
  • 6-dimethylamino-4,4-diphenyl-3-heptanone
  • CHZ
  • Catalytic activities
  • Cytochrome P450
  • Cytochrome P450 (EC 1.14.14.1), P450 or CYP
  • EROD
  • Fluvoxamine
  • In vitro inhibition
  • M 1
  • MROD
  • Meth or methadone
  • Methadone
  • NADPH
  • NIF
  • P450 3A4
  • PROD
  • TOLB
  • TST
  • chlorzoxazone 6-hydroxylation
  • ethoxyresorufin O-deethylation
  • individual forms of P450 designed according to the
  • methoxyresorufin O-demethylation
  • nicotamide adenine diphosphate reduced
  • nifedipine oxidation
  • pentoxyresorufin O-depentylation
  • testosterone 6β-hydroxylation
  • tolbutamide hydroxylation

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Authors

  • C. Iribarne

  • Y. Dréano

  • L.G. Bardou

  • J.F. Ménez

  • F. Berthou

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