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阿扑芬、阿托品和东莨菪碱的行为效应与毒扁豆碱行为效应拮抗作用的关系。

Relationship of the behavioral effects of aprophen, atropine and scopolamine to antagonism of the behavioral effects of physostigmine.

作者信息

Genovese R F, Elsmore T F, Witkin J M

机构信息

Department of Medical Neurosciences, Walter Reed Army Institute of Research, Washington, DC 20307-5100.

出版信息

Pharmacol Biochem Behav. 1990 Sep;37(1):117-22. doi: 10.1016/0091-3057(90)90051-i.

Abstract

Behavioral effects of aprophen, atropine and scopolamine, in rats, were examined under a multiple schedule of food presentation and at different injection-test times. The effects of the varied treatments were compared to the ability of the drugs, under identical conditions, to prevent the behavioral effects of the anticholinesterase, physostigmine. Potencies of the antagonists to decrease response rates varied across three log units. All three antagonists produced dose-related attenuation of the response suppressant effects of physostigmine. In general, aprophen was a better antagonist than scopolamine or atropine. It blocked behavioral effects of physostigmine across a wider range of doses than the other compounds, and did so with less behavioral disruption. Although substantial differences between the three antagonists were observed, the behavioral effects of all three antagonists (when administered alone) were positively correlated with their efficacy as antagonists of the response suppressant effects of physostigmine.

摘要

在食物呈现的多重时间表下以及不同的注射-测试时间,研究了阿普罗芬、阿托品和东莨菪碱对大鼠的行为影响。将不同处理的效果与这些药物在相同条件下预防抗胆碱酯酶药物毒扁豆碱行为效应的能力进行了比较。拮抗剂降低反应率的效力在三个对数单位范围内变化。所有三种拮抗剂均产生了与剂量相关的毒扁豆碱反应抑制作用的减弱。总体而言,阿普罗芬是比东莨菪碱或阿托品更好的拮抗剂。与其他化合物相比,它在更宽的剂量范围内阻断了毒扁豆碱的行为效应,并且这样做时行为干扰较少。尽管观察到三种拮抗剂之间存在显著差异,但所有三种拮抗剂(单独给药时)的行为效应与它们作为毒扁豆碱反应抑制效应拮抗剂的效力呈正相关。

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