首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Cardioprotective Effects of 3-Phosphoinositide-Dependent Protein Kinase-1 on Hypoxic Injury in Cultured Neonatal Rat Cardiomyocytes and Myocardium in a Rat Myocardial Infarct Model
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Cardioprotective Effects of 3-Phosphoinositide-Dependent Protein Kinase-1 on Hypoxic Injury in Cultured Neonatal Rat Cardiomyocytes and Myocardium in a Rat Myocardial Infarct Model

机译:3-磷酸​​肌醇依赖性蛋白激酶-1对大鼠心肌梗死模型中新生大鼠心肌细胞和心肌缺氧性损伤的保护作用

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摘要

3-Phosphoinositide-dependent protein kinase-1 (PDK1) is involved in numerous cellular responses. In this study, we investigated the protective effects of PDK1 gene expression against hypoxic conditions in cultured rat CMCs (rCMCs) and in a rat myocardial infarction (MI) model using the lentiviral vector (LeV) system. LeV-PDKl transfer effectively reduced the apoptotic cell death caused by hypoxic injury as compared to LeV-GFP transfer in rCMCs the expression of survival proteins increased in the LeV-PDKl group, whereas apoptosis signaling decreased in the rCMCs and in infarcted hearts treated with LeV-PDKl. LeV-PDKl transfer also reduced apoptosis and infarct size and attenuated myocardial wall thinning and ventricular remodeling in a rat MI model. These findings suggest that PDK1 has a protective role in the injured ischemic myocardium via overexpression of the cell survival pathway in CMCs. Hence PDK1 can be used as a treatment strategy for myocardial salvage inin hypoxic injury.
机译:3-磷酸​​肌醇依赖性蛋白激酶-1(PDK1)参与许多细胞反应。在这项研究中,我们使用慢病毒载体(LeV)系统研究了PDK1基因表达对培养的大鼠CMC(rCMC)和大鼠心肌梗塞(MI)模型中低氧条件的保护作用。与rCMC中的LeV-GFP转移相比,LeV-PDK1转移有效地减少了由低氧损伤引起的凋亡细胞死亡,LeV-PDK1组中存活蛋白的表达增加,而在rCMC和经LeV治疗的梗死心脏中凋亡信号降低-PDKl。在大鼠MI模型中,LeV-PDK1转移还减少了细胞凋亡和梗塞大小,并减弱了心肌壁变薄和心室重构。这些发现表明PDK1通过在CMCs中过度表达细胞存活途径在受损的缺血心肌中具有保护作用。因此,PDK1可作为缺氧性心肌损伤的抢救治疗策略。

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