伊洛前列素对家兔心肌缺血的保护作用可与其通过KATP(+)通道开放介导的血管扩张作用分离。

A Vesper, K Schrör
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引用次数: 6

摘要

研究了伊洛前列素阻断K(+)通道对兔缺血心脏保护作用的影响。格列本脲是一种atp依赖性K(+)通道阻滞剂,可阻止由拟前列环素伊洛前列素介导的冠状动脉舒张。相比之下,伊洛前列素的心脏保护作用是通过预防缺血引起的左心室舒张压升高和细胞内肌钙蛋白T的损失来确定的,而格列本脲不影响心脏缺血2小时。由此可见,伊洛前列素的心脏保护作用可与开放KATP(+)通道介导的冠状动脉血管扩张作用分离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The cardioprotective actions of iloprost in myocardial ischemia of the rabbit can be separated from its vasodilatory effects mediated by KATP(+)-channel opening.

The modification of cardioprotective actions of iloprost by K(+)-channel blockade was studied in ischemic rabbit hearts. Glibenclamide, a blocker of ATP-dependent K(+)-channels, prevented coronary vasodilation mediated by the prostacyclin mimetic iloprost. In contrast, the cardioprotective effects of iloprost which were determined from prevention of ischemia induced rise in left ventricular enddiastolic pressure and loss of cytosolic troponin T in hearts made globally ischemic for two hours were not affected by glibenclamide. It is concluded that the cardioprotective action of iloprost can be separated from ist coronary vasodilator effect mediated by opening KATP(+)-channels.

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