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丁螺环酮:全球最新进展。

Buspirone: a worldwide update.

作者信息

Napoliello M J, Domantay A G

机构信息

Bristol-Myers Squibb Company, Princeton, NJ 08543-4000.

出版信息

Br J Psychiatry Suppl. 1991 Sep(12):40-4.

PMID:1840762
Abstract

Buspirone is an anxiolytic drug from the azapirone family of molecules. It differs chemically and pharmacologically from the benzodiazepines. Although its profile of efficacy is comparable with that of benzodiazepines, it produces less drowsiness, less psychomotor impairment, less alcohol potentiation, and has less potential for addiction or abuse. Buspirone also appears to have efficacy in major depressive disorders, in comparison with placebo, but its activity in panic disorders is less impressive. It may diminish alcohol dependence both in animals and in chronic alcoholics. Clinical studies in the elderly show no important difference from younger patients in safety and efficacy profile, pharmacokinetics, and dosage requirement. The drug appears to be well tolerated in primary care settings and to be free of adverse clinical interactions with many drugs that might be used concomitantly. However, because its pharmacology differs from that of conventional anxiolytics, patients need to be informed about both its gradual onset of action and absence of euphoria and immediate sedation.

摘要

丁螺环酮是一种来自氮杂螺环酮分子家族的抗焦虑药物。它在化学和药理学上与苯二氮䓬类药物不同。尽管其疗效与苯二氮䓬类药物相当,但它引起的嗜睡、精神运动损害、酒精增强作用较少,成瘾或滥用的可能性也较小。与安慰剂相比,丁螺环酮在重度抑郁症中似乎也有疗效,但其在惊恐障碍中的活性不太显著。它在动物和慢性酗酒者中都可能减轻酒精依赖。针对老年人的临床研究表明,在安全性和疗效、药代动力学及剂量需求方面,与年轻患者相比没有重要差异。该药物在初级保健环境中似乎耐受性良好,并且与许多可能同时使用的药物没有不良临床相互作用。然而,由于其药理学与传统抗焦虑药不同,需要告知患者其起效缓慢,且不会产生欣快感和即时镇静作用。

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