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P物质、氨甲酰甲胆碱、4-氨基吡啶和钾可拮抗低频刺激、河豚毒素、普鲁卡因以及镁对豚鼠输精管场刺激的抑制作用。

Substance P, bethanechol, 4-aminopyridine, and potassium antagonize the depressing effects of low-frequency stimulation, tetrodotoxin, procaine, and of magnesium on the field-stimulated guinea-pig vas deferens.

作者信息

Zetler G, Sowoidnich T

出版信息

Arch Int Pharmacodyn Ther. 1980 Nov;248(1):50-68.

PMID:6163401
Abstract

The twitch-response enhancing potencies of (the agonists) substance P, bethanechol, 4-aminopyridine and of potassium chloride were compared in the field-stimulated guinea-pig vas deferens. The agonists were tested after the twitching activity of the isolated organ had been reduced to an equal extent by (the antagonists) tetrodotoxin, procaine, magnesium chloride, and by decreased stimulation frequency. Further experiments were performed in the functionally denervated organ. The potencies differed with the type of antagonism of the twitch-response. This pointed at different modes of action and/or sites of mechanism of the response-enhancing compounds. The pharmacological nature of agonists and antagonists as well as the results in the denervated organ indirectly suggested a predominantly neuronal point of mechanism of the agonists. This was most obvious for substance P.

摘要

在电场刺激的豚鼠输精管中,比较了(激动剂)P物质、氨甲酰甲胆碱、4-氨基吡啶和氯化钾增强抽搐反应的效能。在通过(拮抗剂)河豚毒素、普鲁卡因、氯化镁以及降低刺激频率使离体器官的抽搐活动同等程度降低后,对激动剂进行了测试。在功能去神经的器官中进行了进一步实验。效能因抽搐反应的拮抗类型而异。这表明反应增强化合物的作用方式和/或作用机制位点不同。激动剂和拮抗剂的药理性质以及去神经器官中的结果间接表明激动剂的作用机制主要在神经元。这对P物质最为明显。

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