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Autophagy contributes to retardation of cardiac growth in diabetic rats

机译:自噬有助于延缓糖尿病大鼠心脏的生长

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摘要

Diabetes mellitus is a major predictor of heart failure, although the mechanisms by which the disease causes cardiomyopathy are not well understood. The purpose of this study was to determine whether prolonged exposure of cardiomyocytes to high glucose concentrations induces autophagy and contributes to cardiomyopathy. Interestingly, there were no differences in the autophagic activation produced by different glucose concentrations. However, cell viability was decreased by high glucose. In the diabetic rats, we found a higher level of microtubule-associated protein light chain 3 (LC3) expression and a reduction in the size of the left ventricle (LV) (P<0.05) caused by growth retardation, suggesting activated autophagy. Our in vitro findings indicate that hyperglycemic oxidative stress induces autophagy, and our in vivo studies reveal that autophagy is involved in the progression of pathophysiological remodeling of the heart. Taken together, the studies suggest that autophagy may play a role in the pathogenesis of juvenile diabetic cardiomyopathy.
机译:糖尿病是心力衰竭的主要预测指标,尽管对该疾病引起心肌病的机制尚不清楚。这项研究的目的是确定心肌细胞长时间暴露于高葡萄糖浓度是否会诱导自噬并导致心肌病。有趣的是,不同葡萄糖浓度产生的自噬激活没有差异。但是,高葡萄糖会降低细胞活力。在糖尿病大鼠中,我们发现由生长迟缓引起的微管相关蛋白轻链3(LC3)的表达水平较高,并且左心室(LV)的大小减少(P <0.05),表明激活的自噬。我们的体外研究结果表明,高血糖氧化应激会诱导自噬,而我们的体内研究表明自噬与心脏的病理生理重塑有关。两者合计,研究表明自噬可能在青少年糖尿病性心肌病的发病机理中起作用。

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