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丁螺环酮:一种新型抗焦虑药。

Buspirone: a new type of anxiolytic.

作者信息

Dommisse C S, DeVane C L

出版信息

Drug Intell Clin Pharm. 1985 Sep;19(9):624-8. doi: 10.1177/106002808501900903.

Abstract

Buspirone is a member of a new class of agents known as azaspirodecanediones, and represents the first nonbenzodiazepine anxiolytic to be introduced in the U.S. in recent years. It does not resemble the benzodiazepines or older anxiolytics such as meprobamate and the barbiturates in pharmacologic profile. Buspirone lacks anticonvulsant activity, interacts minimally with central nervous system depressants such as alcohol, and does not cause muscle relaxation. The drug is reported to have minimal sedating effect, to cause no impairment of driving-related skills, and to have no euphoriant effect or addictive potential. With this low side-effect profile, buspirone should not require Drug Enforcement Agency scheduling controls. Clinical trials indicate buspirone is efficacious in the treatment of mild to moderate anxiety disorders. Answers to questions of possible side effects related to dopaminergic intractions must await post-marketing experience. Buspirone is a suitable addition to drug formularies as its pre-marketing data suggest several advantages compared with anxiolytics currently available.

摘要

丁螺环酮是一类名为氮杂螺癸二酮的新型药物中的一员,是近年来在美国推出的首个非苯二氮䓬类抗焦虑药。在药理学特性上,它与苯二氮䓬类药物或诸如甲丙氨酯和巴比妥类等较老的抗焦虑药不同。丁螺环酮缺乏抗惊厥活性,与酒精等中枢神经系统抑制剂的相互作用极小,并且不会引起肌肉松弛。据报道,该药物的镇静作用极小,不会损害与驾驶相关的技能,也没有欣快感或成瘾潜力。鉴于其低副作用特征,丁螺环酮不应需要美国药品执法管理局的管制安排。临床试验表明,丁螺环酮在治疗轻至中度焦虑症方面有效。与多巴胺能相互作用相关的可能副作用问题的答案必须等待上市后经验。丁螺环酮适合添加到药物处方集,因为其上市前数据表明与目前可用的抗焦虑药相比有几个优点。

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