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Cardioprotective Effects of Salvianolic Acid A on Myocardial Ischemia-Reperfusion Injury In Vivo and In Vitro

机译:丹酚酸A对体内和体外心肌缺血再灌注损伤的保护作用

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摘要

Salvianolic acid A (SAA), one of the major active components of Danshen that is a traditional Chinese medicine, has been reported to possess protective effect in cardiac diseases and antioxidative activity. This study aims to investigate the cardioprotection of SAA in vivo and in vitro using the model of myocardial ischemia-reperfusion in rat and hydrogen peroxide (H2O2)-induced H9c2 rat cardiomyoblasts apoptosis. It was found that SAA significantly limited infarct size of ischemic myocardium when given immediately prior to reperfusion. SAA also significantly suppressed cellular injury and apoptotic cell death. Additionally, the results of western blot and phospho-specific antibody microarray analysis showed that SAA could up-regulate Bcl-2 expression and increase the phosphorylation of proteins such as Akt, p42/p44 extracellular signal-related kinases (Erk1/2), and their related effectors. The phosphorylation of those points was related to suppress apoptosis. In summary, SAA possesses marked protective effect on myocardial ischemia-reperfusion injury, which is related to its ability to reduce myocardial cell apoptosis and damage induced by oxidative stress. The protection is achieved via up-regulation of Bcl-2 expression and affecting protein phosphorylation. These findings indicate that SAA may be of value in cardioprotection during myocardial ischemia-reperfusion injury, which provide pharmacological evidence for clinical application.
机译:丹参酸A(SAA)是丹参的主要活性成分之一,是传统中药,据报道对心脏疾病具有保护作用,并具有抗氧化活性。本研究旨在利用大鼠心肌缺血再灌注模型和过氧化氢(H2O2)诱导的H9c2大鼠心肌成纤维细胞凋亡,研究SAA在体内和体外的心脏保护作用。发现当在再灌注前立即给予时,SAA显着限制了缺血性心肌的梗塞面积。 SAA还显着抑制细胞损伤和凋亡细胞死亡。此外,蛋白质印迹和磷酸化特异性抗体微阵列分析的结果表明,SAA可以上调Bcl-2表达并增加Akt,p42 / p44细胞外信号相关激酶(Erk1 / 2)等蛋白的磷酸化。它们的相关效应子。这些点的磷酸化与抑制细胞凋亡有关。总之,SAA对心肌缺血-再灌注损伤具有显着的保护作用,这与其降低心肌细胞凋亡和氧化应激诱导的损伤的能力有关。通过上调Bcl-2表达并影响蛋白质磷酸化来实现保护。这些发现表明,SAA可能在心肌缺血再灌注损伤期间的心脏保护中具有价值,这为临床应用提供了药理学证据。

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