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首页> 外文期刊>BioMed research international >Shen-Fu Injection Preconditioning Inhibits Myocardial Ischemia-Reperfusion Injury in Diabetic Rats: Activation of eNOS via the PI3K/Akt Pathway
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Shen-Fu Injection Preconditioning Inhibits Myocardial Ischemia-Reperfusion Injury in Diabetic Rats: Activation of eNOS via the PI3K/Akt Pathway

机译:参附注射液预处理可抑制糖尿病大鼠心肌缺血-再灌注损伤:通过PI3K / Akt途径激活eNOS

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摘要

The aim of this paper is to investigate whether Shen-fu injection (SFI), a traditional Chinese medicine, could attenuate myocardial ischemia-reperfusion (MI/R) injury in diabetes. Streptozotocin-induced diabetic rats were randomly assigned to the Sham, I/R, SFI preconditioning, and SFI plus wortmannin (a phosphatidylinositol 3-kinase inhibitor) groups. After the treatment, hearts were subjected to 30 min of coronary artery occlusion and 2 h reperfusion except the Sham group. Myocardial infarct size and cardiomyocytes apoptosis were increased significantly in MI/R group as compared with the Sham group. SFI preconditioning significantly decreased infarct size, apoptosis, caspase-3 protein expression, MDA level in myocardial tissues, and plasma level of CK and LDH but increased p-Akt, p-eNOS, bcl-2 protein expression, and SOD activity compared to I/R group. Moreover, SFI-induced cardioprotection was abolished by wortmannin. We conclude that SFI preconditioning protects diabetic hearts from I/R injury via PI3K/Akt-dependent pathway.
机译:本文旨在研究中药参服注射液(SFI)能否减轻糖尿病患者的心肌缺血再灌注(MI / R)损伤。链脲佐菌素诱导的糖尿病大鼠随机分为Sham,I / R,SFI预处理和SFI加渥曼青霉素(一种磷脂酰肌醇3激酶抑制剂)组。治疗后,除假手术组外,对心脏进行30分钟的冠状动脉闭塞和2小时的再灌注。与假手术组相比,MI / R组心肌梗死面积和心肌细胞凋亡明显增加。与I相比,SFI预处理显着降低了梗死面积,细胞凋亡,caspase-3蛋白表达,心肌组织MDA水平以及血浆CK和LDH水平,但增加了p-Akt,p-eNOS,bcl-2蛋白表达和SOD活性。 / R组。此外,渥曼青霉素废除了SFI诱导的心脏保护作用。我们得出的结论是,SFI预处理可通过PI3K / Akt依赖性途径保护糖尿病心脏免受I / R损伤。

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