首页> 外文期刊>Frontiers in Pharmacology >Aldehyde Dehydrogenase 2 Has Cardioprotective Effects on Myocardial Ischaemia/Reperfusion Injury via Suppressing Mitophagy
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Aldehyde Dehydrogenase 2 Has Cardioprotective Effects on Myocardial Ischaemia/Reperfusion Injury via Suppressing Mitophagy

机译:醛脱氢酶2对抑制心肌线粒体的心肌缺血/再灌注损伤具有保护作用

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Mitophagy, a selective form of autophagy, is excessively activated in myocardial ischemia/reperfusion (I/R). The study investigated whether aldehyde dehydrogenase 2 (ALDH2) exerted its cardioprotective effect by regulating mitophagy. Myocardial infarct size and apoptosis after I/R in rats were ameliorated by Alda-1, an ALDH2 activator, and aggravated by ALDH2 inhibition. Both in I/R rats and hypoxia/reoxygenation H9C2 cells, ALDH2 activation suppressed phosphatase and tensin homolog-induced putative kinase 1 (PINK1)/Parkin expression, regulating mitophagy, by preventing 4-hydroxynonenal, reactive oxygen species and mitochondrial superoxide accumulation. Furthermore, the effect was enhanced by ALDH2 inhibition. Thus, ALDH2 may protect hearts against I/R injury by suppressing PINK1/Parkin–dependent mitophagy.
机译:线粒体吞噬是自噬的一种选择性形式,在心肌缺血/再灌注(I / R)中被过度激活。该研究调查了醛脱氢酶2(ALDH2)是否通过调节线粒体来发挥其心脏保护作用。通过ALDH2激活剂Alda-1改善大鼠I / R后的心肌梗塞大小和细胞凋亡,并通过抑制ALDH2加剧心肌梗塞的大小和细胞凋亡。在I / R大鼠和缺氧/复氧H9C2细胞中,ALDH2激活均可通过阻止4-羟基壬醛,活性氧和线粒体超氧化物的积累来抑制磷酸酶和张力蛋白同源推定的激酶1(PINK1)/ Parkin的表达,从而调节线粒体。此外,ALDH2抑制作用增强了该作用。因此,ALDH2可以通过抑制PINK1 / Parkin依赖性线粒体来保护心脏免受I / R损伤。

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