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[血管解痉剂作用机制的实验。I. 硝普钠、硝酸甘油、普尼拉明和维拉帕米对离体冠状动脉钾停搏挛缩的影响]

[Experments on the mechanism of action of vascular spasmolytic agents. I. Effect nitroprusside sodium, nitroglycerine, prenylamine and verapamil on the arrested potassium contracture of isolated coronary arteries].

作者信息

Fermum R, Klinner U, Meisel P

出版信息

Acta Biol Med Ger. 1976;35(10):1347-58.

PMID:828374
Abstract

On the potassium contracture of isolated coronary arteries of cattle, the relaxation effected by calcium depletion can be blocked by lanthanum ions. The contracture persisting in calcium-free solution (arrested potassium contracture) is used to differentiate the sites of attack of spasmolytics. Verapamil and prenylamine are ineffective in this contracture model. By contrast, nitroprusside sodium and nitroglycerol as before act spasmolytically. Thus, both groups of drugs act through basically different sites. The findings are consistent with the hypothesis that the spasmolytic action of verapamil and prenylamine is based on a blockade of calcium influx. For nitroprusside sodium and nitroglycerol such a mechanism on the arrested potassium contracture has to be ruled out.

摘要

关于牛离体冠状动脉的钾挛缩,钙耗竭所产生的舒张作用可被镧离子阻断。在无钙溶液中持续存在的挛缩(停滞性钾挛缩)用于区分解痉药的作用部位。维拉帕米和普尼拉明在这种挛缩模型中无效。相比之下,硝普钠和硝酸甘油如前所述具有解痉作用。因此,这两组药物的作用部位基本不同。这些发现与以下假设一致,即维拉帕米和普尼拉明的解痉作用基于对钙内流的阻断。对于硝普钠和硝酸甘油,必须排除这种作用于停滞性钾挛缩的机制。

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