胰岛素和氯沙坦对糖尿病大鼠心脏水平胰岛素样生长因子1受体调节的影响

A. Bikhazi, Wael M Maharsy, Lina N. Kadi, N. Issa, Ghinwa M. Barakat, N. Nuwayri-Salti, G. Karam, O. Batal, K. Bitar
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引用次数: 1

摘要

本研究探讨胰岛素/血管紧张素- ii受体亚型-1阻滞剂(AR1B)氯沙坦治疗链脲佐菌素诱导的糖尿病大鼠心脏中胰岛素样生长因子-1受体(IGF-1R)的调节。雄性大鼠分为:正常(N)组、氯沙坦治疗的正常(NL)组、糖尿病(D)组、胰岛素治疗的糖尿病(di)组、氯沙坦治疗的糖尿病(DL)组和胰岛素/氯沙坦共治疗的糖尿病(DIL)组。治疗后30天,大鼠进行心脏灌注(i125)标记的IGF-1,以评估受体对冠状动脉内皮细胞(CE)和心肌细胞(CM)的结合亲和力。这表明IGF-1与受体在CE上的结合亲和力在所有组中都比N增加。在CM上,与N相比,D、DI和DL的结合亲和力增加,但在DIL中几乎归一化。Western blot分析和对心脏组织进行的免疫组织化学分析显示,与其他组相比,DIL组IGF-1R密度降低。这些结果表明胰岛素、血管紧张素- ii和IGF-1之间存在复杂的相互作用,并通过AR1B治疗对糖尿病状态下心肌重构的大规模阻断。
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Effect of Insulin and Losartan on Modulation of Insulin-Like Growth Factor 1 Receptor at Heart Level in Diabetic Rats
This study investigates insulin-like growth factor-1 receptor (IGF-1R) modulation in hearts of streptozotocin- induced diabetic rats treated with insulin/angiotensin-II receptor subtype-1 blocker (AR1B), losartan. Male rats were di- vided into: normal (N), losartan-treated normal (NL), diabetic (D), insulin-treated diabetic (DI), losartan-treated diabetic (DL), and insulin/losartan co-treated diabetic (DIL) groups. Thirty days post-treatment, rats underwent heart perfusion us- ing (I 125 )-labeled IGF-1 to assess receptor-binding affinity on coronary endothelial cells (CE) and cardiomyocytes (CM). This revealed an increase in binding affinity of IGF-1 to its receptor on CE in all groups compared to N. On CM, binding affinity increased in D, DI, and DL compared to N, but was almost normalized in DIL. Western blot analyses and immu- nohistochemistry done on heart tissues showed decrease in IGF-1R density in DIL versus remaining groups. These results demonstrate a complex interaction between insulin, angiotensin-II, and IGF-1, and mass blockade of myocardial remodel- ing by AR1B treatment in diabetic state.
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