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大鼠中毒扁豆碱刺激的药理学特征

Pharmacological characterization of the physostigmine stimulus in rats.

作者信息

Jung M, Perio A, Worms P, Soubrie P

机构信息

Sanofi Recherche, rue du Professeur J.-Blayac, Montpellier, France.

出版信息

Psychopharmacology (Berl). 1988;95(4):553-5. doi: 10.1007/BF00172975.

Abstract

Rats were trained to discriminate 0.10 mg/kg SC physostigmine from saline in a two-lever food-reinforced task. There was generalization to the acetylcholine esterase inhibitor THA as well as to the muscarinic receptor agonists arecoline, oxotremorine and RS 86, but not to neostigmine or nicotine. The physostigmine cue was blocked by SC scopolamine hydrobromide and by ICV pirenzepine, but not by scopolamine methylbromide or by mecamylamine. These antagonism studies suggest that the discriminative cue elicited by physostigmine might be mainly mediated by central M1 receptors.

摘要

在一项双杠杆食物强化任务中,训练大鼠区分皮下注射0.10 mg/kg毒扁豆碱与生理盐水。对乙酰胆碱酯酶抑制剂他克林以及毒蕈碱受体激动剂槟榔碱、氧化震颤素和RS 86存在泛化,但对新斯的明或尼古丁不存在泛化。毒扁豆碱线索被皮下注射氢溴酸东莨菪碱和脑室内注射哌仑西平阻断,但不被甲基溴东莨菪碱或美加明阻断。这些拮抗研究表明,毒扁豆碱引发的辨别线索可能主要由中枢M1受体介导。

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