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胆碱能药物对恒河猴延迟样本匹配行为的影响。

Effects of cholinergic drugs on delayed match-to-sample performance of rhesus monkeys.

作者信息

Penetar D M, McDonough J H

出版信息

Pharmacol Biochem Behav. 1983 Dec;19(6):963-7. doi: 10.1016/0091-3057(83)90399-4.

Abstract

Three adult rhesus monkeys were trained to stable performance baselines on a delayed match-to-sample (DMS) procedure. Subject-initiated trials resulted in brief presentations of a sample color stimulus (red, green, or blue) with matching performance tested after retention intervals of 0, 4, 8, and 16 seconds. The effects of graded doses of atropine SO4, benactyzine HCl and physostigmine salicylate on performance were studied. Only atropine produced a clear interaction between drug and retention interval with the greatest impairments being observed at the longest delays. Benactyzine only affected overall error rates, while physostigmine did not disrupt matching accuracy. The two highest doses of each compound produced reliable elevations in session times and drug-specific changes in the pattern of performance. The results with atropine confirm and extend previously reported work with scopolamine indicating a critical role for cholinergic mechanisms in short-term memory.

摘要

三只成年恒河猴在延迟匹配样本(DMS)程序上被训练至稳定的表现基线。由受试者发起的试验会短暂呈现一个样本颜色刺激(红色、绿色或蓝色),并在0、4、8和16秒的保持间隔后测试匹配表现。研究了不同剂量的硫酸阿托品、盐酸苯那嗪和水杨酸毒扁豆碱对表现的影响。只有阿托品在药物和保持间隔之间产生了明显的相互作用,在最长延迟时观察到最大的损伤。苯那嗪只影响总体错误率,而毒扁豆碱没有破坏匹配准确性。每种化合物的两个最高剂量导致会话时间可靠延长以及表现模式的药物特异性变化。阿托品的结果证实并扩展了先前关于东莨菪碱的报道工作,表明胆碱能机制在短期记忆中起关键作用。

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