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首页> 外文期刊>Basic Research in Cardiology: Official Journal of the German Association of Cardiovascular Research >The effects of curcumin post-treatment against myocardial ischemia and reperfusion by activation of the JAK2/STAT3 signaling pathway
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The effects of curcumin post-treatment against myocardial ischemia and reperfusion by activation of the JAK2/STAT3 signaling pathway

机译:姜黄素治疗后通过激活JAK2 / STAT3信号通路对心肌缺血和再灌注的影响

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摘要

In this study, we evaluated the effect of curcumin (Cur) post-treatment on isolated perfused rat hearts that had been subjected to a protocol of ischemia and reperfusion injury. We also examined whether the Janus kinase 2 and signal transducer and activator 3 of transcription (JAK2/STAT3) signaling pathway plays a role in the cardioprotective effects of Cur post-treatment. Isolated perfused rat hearts were subjected to 60 min of ischemia, followed by 60 min of reperfusion. The hearts were exposed to 1-lM Cur during the first 10 min of reperfusion in the absence or presence of the JAK kinase-specific inhibitor AG490 (AG, 1 lM). The Cur treatment conferred a cardioprotective effect, and the treated hearts demonstrated an improved post-ischemic cardiac functional recovery, a decreased myocardial infarct size and decreased lactate dehydrogenase release in the coronary flow, a reduced number of apoptotic cardiomyocytes, up-regulation of the anti-apoptotic protein Bcl2 and downregulation of the pro-apoptotic protein Caspase3. AG blocked the Cur-mediated cardioprotection by inhibiting the JAK2/STAT3 signaling pathway, as reflected by the abrogation of the Cur-induced up-regulation of Bcl2 and down-regulation of Caspase3. The results suggest that Cur post-treatment can attenuate IR injury through the activation of the JAK2/STAT3 signaling pathway, which transmits a survival signal to the myocardium.
机译:在这项研究中,我们评估了姜黄素(Cur)后处理对已经遭受缺血和再灌注损伤的离体灌流大鼠心脏的影响。我们还检查了Janus激酶2以及转录的信号转导和激活剂3(JAK2 / STAT3)信号通路是否在Cur后处理的心脏保护作用中起作用。离体的灌流大鼠心脏进行60分钟的缺血,然后再灌注60分钟。在不存在或存在JAK激酶特异性抑制剂AG490(AG,1 lM)的情况下,在再灌注的前10分钟内,将心脏暴露于1-lM Cur。 Cur治疗具有心脏保护作用,治疗后的心脏表现出改善的缺血后心脏功能恢复,心肌梗塞面积减少,冠状动脉血流中乳酸脱氢酶释放减少,凋亡性心肌细胞减少,抗氧化剂的上调-凋亡蛋白Bcl2和促凋亡蛋白Caspase3的下调。 AG通过抑制JAK2 / STAT3信号传导通路来阻断Cur介导的心脏保护作用,这是由Cur诱导的Bcl2上调和Caspase3下调的取消所反映的。结果表明,Cur后处理可通过激活JAK2 / STAT3信号通路来减轻IR损伤,该通路将生存信号传递至心肌。

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