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抗抑郁药的药代动力学相互作用。

Pharmacokinetic interactions of antidepressants.

作者信息

Richelson E

机构信息

Department of Psychiatry and Pharmacology, Mayo Medical School, Rochester, Minn, USA.

出版信息

J Clin Psychiatry. 1998;59 Suppl 10:22-6.

PMID:9720479
Abstract

Seven of the newest antidepressants are the serotonin selective reuptake inhibitors (fluoxetine, sertraline, paroxetine, and fluvoxamine [currently approved in the United States for obsessive-compulsive disorder only]), a serotonin norepinephrine reuptake inhibitor (venlafaxine), a postsynaptic serotonin antagonist/presynaptic serotonin reuptake inhibitor (nefazodone), and presynaptic/postsynaptic noradrenergic/serotonergic receptor antagonist (mirtazapine). Many of these drugs are potent inhibitors of the cytochrome P450 (CYP) enzymes of the liver. The CYP enzymes most relevant to the use of antidepressants and for which the most thorough data are available are the CYP1A2, CYP2D6, and CYP3A4. These 3 CYP isoenzymes are discussed in relation to some of the drugs they metabolize, and appropriate cautions are recommended for concurrent administration of these new antidepressants and other drugs frequently prescribed to elderly patients.

摘要

七种最新的抗抑郁药包括5-羟色胺选择性再摄取抑制剂(氟西汀、舍曲林、帕罗西汀和氟伏沙明[目前在美国仅被批准用于强迫症])、一种5-羟色胺去甲肾上腺素再摄取抑制剂(文拉法辛)、一种突触后5-羟色胺拮抗剂/突触前5-羟色胺再摄取抑制剂(奈法唑酮)以及一种突触前/突触后去甲肾上腺素能/5-羟色胺能受体拮抗剂(米氮平)。这些药物中有许多是肝脏细胞色素P450(CYP)酶的强效抑制剂。与抗抑郁药使用最相关且有最全面数据的CYP酶是CYP1A2、CYP2D6和CYP3A4。将针对它们代谢的某些药物讨论这三种CYP同工酶,并针对这些新型抗抑郁药与老年患者常用的其他药物联合使用提出适当的注意事项。

相似文献

1
Pharmacokinetic interactions of antidepressants.抗抑郁药的药代动力学相互作用。
J Clin Psychiatry. 1998;59 Suppl 10:22-6.
2
Pharmacokinetic drug interactions of new antidepressants: a review of the effects on the metabolism of other drugs.新型抗抑郁药的药代动力学药物相互作用:对其他药物代谢影响的综述
Mayo Clin Proc. 1997 Sep;72(9):835-47. doi: 10.4065/72.9.835.
3
Venlafaxine: in vitro inhibition of CYP2D6 dependent imipramine and desipramine metabolism; comparative studies with selected SSRIs, and effects on human hepatic CYP3A4, CYP2C9 and CYP1A2.文拉法辛:体外对细胞色素P450 2D6依赖性丙咪嗪和地昔帕明代谢的抑制作用;与选定的选择性5-羟色胺再摄取抑制剂的比较研究,以及对人肝细胞色素P450 3A4、细胞色素P450 2C9和细胞色素P450 1A2的影响。
Br J Clin Pharmacol. 1997 Jun;43(6):619-26. doi: 10.1046/j.1365-2125.1997.00591.x.
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Interactions between tamoxifen and antidepressants via cytochrome P450 2D6.他莫昔芬与通过细胞色素 P450 2D6 的抗抑郁药的相互作用。
J Clin Psychiatry. 2009 Dec;70(12):1688-97. doi: 10.4088/JCP.08r04856blu.
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Clinically relevant pharmacology of selective serotonin reuptake inhibitors. An overview with emphasis on pharmacokinetics and effects on oxidative drug metabolism.选择性5-羟色胺再摄取抑制剂的临床相关药理学。重点关注药代动力学及对药物氧化代谢影响的综述。
Clin Pharmacokinet. 1997;32 Suppl 1:1-21. doi: 10.2165/00003088-199700321-00003.
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Venlafaxine and nefazodone, two pharmacologically distinct antidepressants.文拉法辛和奈法唑酮,两种药理特性不同的抗抑郁药。
Pharmacotherapy. 1997 May-Jun;17(3):511-30.
7
Antidepressant use in the elderly. Current status of nefazodone, venlafaxine and moclobemide.老年人使用抗抑郁药。奈法唑酮、文拉法辛和吗氯贝胺的现状。
Drugs Aging. 1997 Aug;11(2):119-31. doi: 10.2165/00002512-199711020-00004.
8
Clinically relevant pharmacokinetic drug interactions with second-generation antidepressants: an update.第二代抗抑郁药的临床相关药代动力学药物相互作用:最新进展
Clin Ther. 2008 Jul;30(7):1206-27. doi: 10.1016/s0149-2918(08)80047-1.
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New antidepressants and the cytochrome P450 system: focus on venlafaxine, nefazodone, and mirtazapine.新型抗抑郁药与细胞色素P450系统:聚焦于文拉法辛、奈法唑酮和米氮平。
Depress Anxiety. 1998;7 Suppl 1:24-32.
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Newer antidepressants and the cytochrome P450 system.新型抗抑郁药与细胞色素P450系统
Am J Psychiatry. 1996 Mar;153(3):311-20. doi: 10.1176/ajp.153.3.311.

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Third-generation antidepressants: do they offer advantages over the SSRIs?第三代抗抑郁药:它们比选择性5-羟色胺再摄取抑制剂(SSRI)更具优势吗?
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