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通过两种小鼠体内实验方法评估中枢与外周抗胆碱能活性。

Central versus peripheral anticholinergic activity as assessed by two in vivo procedures in mice.

作者信息

Malick J B, Barnett A

出版信息

J Pharm Sci. 1975 Jun;64(6):1066-8. doi: 10.1002/jps.2600640650.

Abstract

The activity of tertiary and quaternary anticholinergic drugs was compared in two different test procedures designed to measure cholinolytic activity in mice. The four drugs utilized were atropine sulfate, atropine methylnitrate, scopolamine hydrobromide, and scopolamine methylnitrate. The results led to the conclusion that one of these test procedures, the induction of mydriasis (increase in pupil size), primarily measures peripheral anticholinergic activity whereas the other procedure, inhibition of physostigmine lethality, primarily measures anticholinergic activity in the CNS. These two test procedures can be utilized to characterize the nature of the cholinolytic properties of prospective therapeutic drug candidates.

摘要

在旨在测量小鼠胆碱能溶解活性的两种不同测试程序中,比较了叔胺和季铵抗胆碱能药物的活性。所使用的四种药物为硫酸阿托品、硝酸甲基阿托品、氢溴酸东莨菪碱和硝酸甲基东莨菪碱。结果得出结论,这些测试程序之一,即瞳孔散大(瞳孔大小增加)的诱导,主要测量外周抗胆碱能活性,而另一种程序,即抑制毒扁豆碱致死率,主要测量中枢神经系统中的抗胆碱能活性。这两种测试程序可用于表征潜在治疗药物候选物的胆碱能溶解特性的性质。

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