左西孟旦对缺血再灌注损伤及细胞凋亡的保护作用。

Patrick Scheiermann, Andres Beiras-Fernandez, Haitham Mutlak, Florian Weis
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引用次数: 13

摘要

左西孟旦是一种钙增敏剂,具有正性肌力和血管舒张特性。它增加肌钙蛋白C对钙的敏感性,打开三磷酸腺苷依赖性钾离子通道,抑制磷酸二酯酶III。左西孟旦被批准用于心力衰竭,但大型临床试验对左西孟旦是否优于β-肾上腺素能激动剂的长期生存率提出了质疑。尽管存在争议,但越来越多的证据表明,由于左西孟旦对K(+)通道的影响,左西孟旦对缺血/再灌注(I/R)损伤有有益的作用。因此,K(+)通道激动剂最近被授予专利,用于减少移植和创伤治疗中器官或组织的损伤。此外,实验研究和临床试验表明,左西孟旦能有效抑制心肌细胞凋亡。其潜在的分子机制目前尚不清楚。然而,由于左西孟旦对I/R损伤的有益作用,人们很容易认为左西孟旦抑制心肌细胞凋亡。然而,这两种现象之间的联系尚未得到很好的确定。本文综述了左西孟旦对I/R损伤和细胞凋亡作用的实验研究和临床试验,并对近期专利进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The protective effects of levosimendan on ischemia/reperfusion injury and apoptosis.

Levosimendan is a calcium sensitizer with positive inotropic and vasodilating properties. It increases the sensitivity of troponin C for calcium, opens adenosine triphosphate-dependent potassium K(+) channels and inhibits phosphodiesterase III. Levosimendan is approved for use in cardiac failure but large clinical trials have raised doubts whether levosimendan is superior to β-adrenergic agonists regarding long-term survival of patients. Despite this controversy, there is growing evidence of beneficial effects of levosimendan in ischemia/reperfusion (I/R) injury due to its effect on K(+) channels. As a consequence, patents on K(+) channel agonists have been granted recently for reducing injury in organs or tissue in transplants and trauma therapy. Moreover, experimental studies and clinical trials have shown that levosimendan effectively inhibits cardiomyocyte apoptosis. The underlying molecular mechanism is currently unclear. However, it is tempting to assume that levosimendan inhibits cardiomyocyte apoptosis due to its beneficial effect on I/R injury. However, the link between these two phenomena has not been well established. This review summarizes experimental studies and clinical trials on the effects of levosimendan in I/R injury and apoptosis also discussing recent patents.

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