Suppr超能文献

关于丁螺环酮作用机制的注释。

Notes on buspirone's mechanisms of action.

作者信息

Garattini S, Caccia S, Mennini T

出版信息

J Clin Psychiatry. 1982 Dec;43(12 Pt 2):19-24.

PMID:6130069
Abstract

Buspirone is a novel psychotropic drug with clear anxiolytic activity in man. There are a number of neurochemical differences between buspirone and both neuroleptics and benzodiazepines. Moreover, buspirone is extensively metabolized, and several metabolites are present in the brain together with the parent compound. One of these, 1-PP, is present in the brain at higher concentrations than the parent drug, particularly when the drug is given orally. On the basis of the reported experimental data, it can be postulated that buspirone's anticonflict activity in rats may be mediated, at least partially, through 1-PP, without involving any effect on the dopaminergic system. The possibility that buspirone and 1-PP may mimic the action of benzodiazepine on some sites in the complex benzodiazepine-GABA receptors is discussed.

摘要

丁螺环酮是一种新型精神药物,对人体具有明确的抗焦虑活性。丁螺环酮与抗精神病药物和苯二氮䓬类药物在神经化学方面存在许多差异。此外,丁螺环酮会被广泛代谢,几种代谢产物与母体化合物一起存在于大脑中。其中一种代谢产物1-PP在大脑中的浓度高于母体药物,尤其是口服给药时。根据已报道的实验数据,可以推测丁螺环酮在大鼠中的抗冲突活性可能至少部分通过1-PP介导,而不涉及对多巴胺能系统的任何影响。文中还讨论了丁螺环酮和1-PP可能在复杂的苯二氮䓬-GABA受体的某些位点模拟苯二氮䓬作用的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验