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Time‐dependent inhibition of CYP3A4 by sertraline, a selective serotonin reuptake inhibitor
Author(s) -
Masubuchi Yasuhiro,
Kawaguchi Yuki
Publication year - 2013
Publication title -
biopharmaceutics and drug disposition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 58
eISSN - 1099-081X
pISSN - 0142-2782
DOI - 10.1002/bdd.1857
Subject(s) - sertraline , cyp3a4 , pharmacology , chemistry , microsome , cytochrome p450 , serotonin reuptake inhibitor , metabolite , metabolism , reuptake inhibitor , drug metabolism , drug interaction , enzyme , pharmacokinetics , biochemistry , serotonin , antidepressant , endocrinology , biology , receptor , hippocampus
Drug–drug interactions associated with selective serotonin reuptake inhibitors (SSRIs) are widely known. A major interaction by SSRIs is the inhibition of cytochrome P450 (P450)‐mediated hepatic drug metabolism. The SSRI, sertraline, is also reported to increase the blood concentration of co‐administered drugs. The potency of sertraline directly to inhibit hepatic drug metabolism is relatively weak compared with the other SSRIs, implying that additional mechanisms are involved in the interactions. The study examined whether sertraline produces time‐dependent inhibition of CYP3A4 and/or other P450 enzymes. Incubation of human liver microsomes with sertraline in the presence of NADPH resulted in marked decreases in testosterone 6β‐hydroxylation activities, indicating that sertraline metabolism leads to CYP3A4 inactivation. This inactivation required NADPH and was not protected by glutathione. No significant inactivation was observed for other P450 enzymes. Spectroscopic evaluation revealed that microsomes with and without sertraline in the presence of NADPH gave a Soret peak at 455 nm, suggesting the formation of metabolic intermediate (MI) complexes of sertraline metabolite(s) with the reduced form of P450. This is the first report indicating that sertraline produced time‐dependent inhibition of CYP3A4, which may be associated with MI complex formation. Copyright © 2013 John Wiley & Sons, Ltd.