Selective Serotonin Reuptake Inhibitors and Cytochrome P-450 Mediated Drug-Drug Interactions: An Update

氟西汀 药理学 CYP2D6型 5-羟色胺再摄取抑制剂 氟伏沙明 再摄取抑制剂 药物相互作用 药品 帕罗西汀 西酞普兰 细胞色素P450 CYP3A4型 舍曲林 CYP2C19型 代谢物 化学 医学 抗抑郁药 血清素 内科学 新陈代谢 受体 海马体
作者
Alex Hemeryck,Frans M. Belpaire
出处
期刊:Current Drug Metabolism [Bentham Science Publishers]
卷期号:3 (1): 13-37 被引量:346
标识
DOI:10.2174/1389200023338017
摘要

The selective serotonin reuptake inhibitors (SSRIs) have become the most prescribed antidepressants in many countries. Although the SSRIs share a common mechanism of action, they differ substantially in their chemical structure, metabolism, and pharmacokinetics. Perhaps the most important difference between the SSRIs is their potential to cause drug-drug interactions through inhibition of cytochrome-P450 (CYP) isoforms. This paper provides an update on both the in vitro and in vivo evidence with respect to CYP-mediated drug-drug interactions with this class of antidepressants. The available evidence clearly indicates that the individual SSRIs display a distinct profile of cytochrome P450 inhibition. Fluvoxamine is a potent CYP1A2 and CYP2C19 inhibitor, and a moderate CYP2C9, CYP2D6, and CYP3A4 inhibitor. Fluoxetine and paroxetine are potent CYP2D6 inhibitors, whereas fluoxetines main metabolite, norfluoxetine, has a moderate inhibitory effect on CYP3A4. Sertraline is a moderate CYP2D6 inhibitor citalopram appears to have little effect on the major CYP isoforms. Fluoxetine deserves special attention as inhibitory effects on CYP-activity can persist for several weeks after fluoxetine discontinuation because of the long half-life of fluoxetine and its metabolite norfluoxetine. Drug combinations with SSRIs should be assessed on an individual basis. Knowledge regarding the CYP-isoforms involved in the metabolism of the co-administered drug may help clinicians to anticipate and avoid potentially dangerous drug-drug interactions. Anticipated interactions can usually be managed by appropriate dose adjustment and titration of the object drug. In some cases, therapeutic drug monitoring can be useful. Equally well, an SSRI with limited interaction potential may be selected to treat depression in patients that receive other medications. Keywords: Serotonin Reuptake Inhibitors, cytochrome-P450 (CYP), Alprazolam, Carbamazepine, Venlafaxine, Midazolam, Fluoxetine, Sertraline, Citalopram, CYP-isoform
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