Buspirone And Anxiety Disorders: A Review With Pharmacological And Clinical Perspectives

F. Batool
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引用次数: 8

Abstract

The treatment of anxiety is one of the leading problems in medicine today. Buspirone, an azpirone derivative and a 5-HT-1A (5hydroxytryptamine-1A) partial agonist, is the first nonbenzodiazepine anxiolytic introduced into medicine for the treatment of generalized anxiety disorder (GAD). It has a strong affinity for the 5-HT-1A receptor and does not appear to interact at the benzodiazepine receptor complex. Buspirone's distinctive mechanism of action helps to avoid pharmacological properties ancillary to the treatment of anxiety and contributes towards an apparently superior safety profile with generally fewer and more tolerable adverse effects than benzodiazepines. This article provides a brief overview on the results of animals and clinical studies in which the potential for buspirone dependence or abuse and the effects of its withdrawal were assessed. The pharmacology of serotonin systems and its role in the management of anxiety, along with the review of the contemporary literature is also discussed.
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丁螺环酮与焦虑症:从药理学和临床角度综述
焦虑的治疗是当今医学的主要问题之一。丁螺环酮是一种阿兹吡酮衍生物和5-HT-1A(5羟色胺- 1a)部分激动剂,是第一个用于治疗广泛性焦虑症(GAD)的非苯二氮卓类抗焦虑药。它对5-HT-1A受体有很强的亲和力,并且似乎不与苯二氮卓类受体复合物相互作用。丁螺环酮独特的作用机制有助于避免辅助治疗焦虑的药理学特性,并且与苯二氮卓类药物相比,具有明显更好的安全性,通常副作用更少,更可容忍。本文简要概述了动物和临床研究的结果,其中评估了丁螺环酮依赖或滥用的可能性及其停药的影响。血清素系统的药理学及其在焦虑管理中的作用,以及对当代文献的回顾也进行了讨论。
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