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[ATP敏感性钾通道及其影响物质]

[ATP-sensitive potassium channels and substances affecting them].

作者信息

Pospísilová Y

机构信息

II. interní klinika Fakultní nemocnice, Brno-Bohunice.

出版信息

Vnitr Lek. 1998 Jul;44(7):435-8.

PMID:9748883
Abstract

ATP-sensitive potassium channels are the site of action of the sulphonylurea derivatives that are used to treat non-insulin-dependent diabetes mellitus. These ATP-sensitive potassium channels are also found in myocardial cells and in vascular smooth muscle cells. The sulphonylurea derivatives have been reported to cancel the cardioprotective effects by blocking the opening of these channels in myocardium and vascular smooth muscles. A new sulphonylurea derivative, glimepiride, has been shown to be devoid of vascular ATP-sensitive potassium channel binding properties. The so called potassium-channel-openers, on the other hand, are expected to be used in the treatment of hypertension, ischemic heart disease and asthma bronchiale.

摘要

ATP敏感性钾通道是用于治疗非胰岛素依赖型糖尿病的磺酰脲类衍生物的作用位点。这些ATP敏感性钾通道也存在于心肌细胞和血管平滑肌细胞中。据报道,磺酰脲类衍生物通过阻断心肌和血管平滑肌中这些通道的开放来消除心脏保护作用。一种新的磺酰脲类衍生物格列美脲已被证明没有血管ATP敏感性钾通道结合特性。另一方面,所谓的钾通道开放剂有望用于治疗高血压、缺血性心脏病和支气管哮喘。

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