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丁螺环酮会对空间导航产生剂量相关的损害。

Buspirone produces a dose-related impairment in spatial navigation.

作者信息

McNaughton N, Morris R G

机构信息

Department of Psychology, University of Otago, Dunedin, New Zealand.

出版信息

Pharmacol Biochem Behav. 1992 Sep;43(1):167-71. doi: 10.1016/0091-3057(92)90653-w.

Abstract

Classical anxiolytic drugs and hippocampal lesions have common behavioural effects that include loss of place navigation in the water maze. The novel anxiolytic drug buspirone, unlike classical anxiolytic drugs, does not interact with GABA and is not muscle relaxant, sedative, hypnotic, anticonvulsant, or addictive. Buspirone affects hippocampal electrophysiology in a similar fashion to classical anxiolytics and so we predicted it would have similar effects on spatial navigation. Rats injected with buspirone (0.1-10.0 mg/kg, IP) showed a loss of acquisition of spatial navigation in the water maze that has a similar dose dependence to that reported for the effects of buspirone on the hippocampus. This finding demonstrates that the effects of anxiolytics on spatial navigation are not due to their side effects and supports the view that changes in hippocampal function may underlie some components of clinical anxiolytic action.

摘要

经典抗焦虑药物和海马损伤具有共同的行为效应,包括在水迷宫中空间导航能力丧失。新型抗焦虑药物丁螺环酮与经典抗焦虑药物不同,它不与GABA相互作用,也不是肌肉松弛剂、镇静剂、催眠剂、抗惊厥药或成瘾性药物。丁螺环酮对海马电生理的影响与经典抗焦虑药物相似,因此我们预测它对空间导航会有类似的影响。注射丁螺环酮(0.1 - 10.0毫克/千克,腹腔注射)的大鼠在水迷宫中空间导航能力的获得出现丧失,其剂量依赖性与报道的丁螺环酮对海马的影响相似。这一发现表明抗焦虑药物对空间导航的影响并非因其副作用,并支持海马功能变化可能是临床抗焦虑作用某些成分基础的观点。

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