Impact of Intranasal Insulin Administration On Na+/K+-Atpase and Са2+-Transporting System Components in Rat Cardiomyocytes with Type 1 Diabetes Mellitus

I. Sukhov, O. Chistyakova
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Abstract

Cardiovascular pathology is the main cause of morbidity among patients with diabetes mellitus. The development of a specific therapy aimed at either blunting the protein signals involved in pathological cardiomyocyte hypertrophy or upregulating the expression of cardioprotective pathways can support new strategies for treating diabetes-induced cardiac dysfunctions. The aim of the work was to study the impact of intranasal insulin administration (IIA) on the expression of genes encoding insulin-dependent signaling proteins and components of the Ca2+-transporting system, as well as on the activity of Na+/K+-ATPase in cardiomyocytes on the model of experimental type 1 diabetes mellitus (DM1) in rats. It was shown that IIA eliminates the uncoupling of molecular mechanisms involved in electromechanical coupling in rat cardiomyocytes that occurs under the conditions of mild DM1. This allowed us to recommend IIA as a therapeutic approach to the prevention and treatment of structural and functional myocardial disorders caused by diabetes.
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鼻内胰岛素对1型糖尿病大鼠心肌细胞Na+/K+- atp酶和Са2+-转运系统组分的影响
心血管病变是糖尿病患者发病的主要原因。一种特异性治疗的发展,旨在减弱病理性心肌细胞肥大的蛋白质信号或上调心脏保护通路的表达,可以支持治疗糖尿病引起的心功能障碍的新策略。本研究的目的是研究鼻内胰岛素给药(IIA)对实验性1型糖尿病(DM1)大鼠心肌细胞中胰岛素依赖信号蛋白和Ca2+转运系统成分编码基因表达的影响,以及Na+/K+- atp酶活性的影响。结果表明,IIA消除了在轻度DM1条件下发生的大鼠心肌细胞机电耦合分子机制的解耦。这使我们推荐IIA作为预防和治疗糖尿病引起的结构和功能性心肌疾病的治疗方法。
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