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M1毒蕈碱拮抗剂哌仑西平对空间学习的阻断作用。

Blockade of spatial learning by the M1 muscarinic antagonist pirenzepine.

作者信息

Hagan J J, Jansen J H, Broekkamp C L

机构信息

Scientific Development Group, Organon International B.V., Oss, The Netherlands.

出版信息

Psychopharmacology (Berl). 1987;93(4):470-6. doi: 10.1007/BF00207237.

Abstract

Two experiments were conducted to determine the effects of the M1 muscarinic receptor antagonist pirenzepine on place navigation in a water maze. In the first experiment rats were required to learn the location of a hidden platform following intracerebroventricular injections of equimolar doses of pirenzepine or scopolamine methylbromide. Both drugs dose-dependently impaired spatial learning according to both escape latency data and transfer test analysis. Pirenzepine was approximately 3 times less potent than scopolamine, a potency ratio which suggests M1 receptor mediation of the impairment. In the second experiment pirenzepine (1 approximately 92.3 micrograms/rat ICV) was injected prior to training on a simultaneous place discrimination task in the water maze. Impairments of choice accuracy were found with a dose of 20 micrograms/rat in the absence of any marked increases in either errors of omission or choice latency. These data suggest that M1 receptor blockade impairs processes which are involved in spatial learning.

摘要

进行了两项实验以确定M1毒蕈碱受体拮抗剂哌仑西平对水迷宫中位置导航的影响。在第一项实验中,大鼠在脑室内注射等摩尔剂量的哌仑西平或甲基溴东莨菪碱后,需要学习隐藏平台的位置。根据逃避潜伏期数据和转移测试分析,两种药物均剂量依赖性地损害空间学习。哌仑西平的效力约为东莨菪碱的三分之一,这种效力比表明损伤是由M1受体介导的。在第二项实验中,在水迷宫中进行同时位置辨别任务训练之前,注射哌仑西平(1至约92.3微克/大鼠,脑室内注射)。在剂量为20微克/大鼠时发现选择准确性受损,而遗漏错误或选择潜伏期均未显著增加。这些数据表明,M1受体阻断会损害空间学习所涉及的过程。

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