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奈法唑酮与苯二氮䓬类药物的联合使用:III. 与阿普唑仑的药代动力学相互作用研究。

Coadministration of nefazodone and benzodiazepines: III. A pharmacokinetic interaction study with alprazolam.

作者信息

Greene D S, Salazar D E, Dockens R C, Kroboth P, Barbhaiya R H

机构信息

Department of Metabolism, Bristol-Myers Squibb Company, Princeton, New Jersey 08543-4000, USA.

出版信息

J Clin Psychopharmacol. 1995 Dec;15(6):399-408. doi: 10.1097/00004714-199512000-00003.

Abstract

This study was conducted to determine the potential for an interaction between nefazodone, a new antidepressant, and alprazolam after single- and multiple-dose administration in a randomized, double-blind, parallel-group, placebo-controlled study in 48 healthy male volunteers. A group of 12 subjects received either placebo twice daily, 1 mg of alprazolam twice daily, 200 mg of nefazodone twice daily, or the combination of 1 mg of alprazolam and 200 mg of nefazodone twice daily for 7 days. Serial blood samples were collected after dosing on day 1 and day 7 and before the morning dose on days 4, 5, and 6 for the determination of alprazolam and its metabolites alpha-hydroxyalprazolam (AOH) and 4-hydroxyalprazolam (4OH) and nefazodone and its metabolites hydroxynefazodone (HO-nefazodone), m-chlorophenylpiperazine (mCPP), and a triazole dione metabolite (dione) by validated high-performance liquid chromatography methods. Steady-state levels in plasma were reached by day 4 for alprazolam, 4OH, nefazodone, HO-nefazodone, mCPP, and dione. Noncompartmental pharmacokinetic analysis showed that at steady state, alprazolam Cmax and AUCtau values significantly increased approximately twofold and 4OH Cmax and AUCtau values significantly decreased by 40 and 26%, respectively, when nefazodone was coadministered with alprazolam. There was no effect of alprazolam on the single-dose or steady-state pharmacokinetics of nefazodone, HO-nefazodone, or dione after the coadministration of alprazolam and nefazodone. However, the mean steady-state mCPP Cmax and AUCtau significantly increased by approximately threefold and t1/2 values significantly increased by approximately twofold after the coadministration of alprazolam and nefazodone in comparison to those when nefazodone was given alone. Competitive inhibition between alprazolam and nefazodone metabolism at cytochrome P450 3A4 may be responsible for the pharmacokinetic interaction when alprazolam and nefazodone were coadministered. No adjustment of nefazodone dosage is required when nefazodone and alprazolam are coadministered. Because alprazolam concentrations in plasma are increased in the presence of nefazodone, a reduction in alprazolam dosage is recommended when the two agents are coadministered.

摘要

本研究旨在通过一项随机、双盲、平行组、安慰剂对照试验,在48名健康男性志愿者中确定新型抗抑郁药奈法唑酮与阿普唑仑单剂量及多剂量给药后的相互作用潜力。一组12名受试者每日两次接受安慰剂、每日两次接受1毫克阿普唑仑、每日两次接受200毫克奈法唑酮,或每日两次接受1毫克阿普唑仑与200毫克奈法唑酮的组合,共7天。在第1天和第7天给药后以及第4、5、6天晨服前采集系列血样,通过经验证的高效液相色谱法测定阿普唑仑及其代谢物α-羟基阿普唑仑(AOH)和4-羟基阿普唑仑(4OH)以及奈法唑酮及其代谢物羟基奈法唑酮(HO-奈法唑酮)、间氯苯哌嗪(mCPP)和一种三唑二酮代谢物(二酮)。阿普唑仑、4OH、奈法唑酮、HO-奈法唑酮、mCPP和二酮在第4天达到血浆稳态水平。非房室药代动力学分析表明,在稳态时,奈法唑酮与阿普唑仑合用时,阿普唑仑的Cmax和AUCtau值显著增加约两倍,4OH的Cmax和AUCtau值分别显著降低40%和26%。阿普唑仑与奈法唑酮合用时,阿普唑仑对奈法唑酮、HO-奈法唑酮或二酮的单剂量或稳态药代动力学没有影响。然而,与单独给予奈法唑酮相比,阿普唑仑与奈法唑酮合用时,平均稳态mCPP的Cmax和AUCtau显著增加约三倍,t1/2值显著增加约两倍。阿普唑仑与奈法唑酮合用时,细胞色素P450 3A4处阿普唑仑与奈法唑酮代谢之间的竞争性抑制可能是药代动力学相互作用的原因。奈法唑酮与阿普唑仑合用时无需调整奈法唑酮剂量。由于奈法唑酮存在时血浆中阿普唑仑浓度会升高,因此两种药物合用时建议降低阿普唑仑剂量。

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