Decreased Cardiac NOX4 and SIRT-1 Protein Levels Contribute to Decreased Angiogenesis in the Heart of Diabetic Rats: Rescue Effects of IGF-1 and Exercise.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY Advanced pharmaceutical bulletin Pub Date : 2023-01-01 Epub Date: 2022-01-03 DOI:10.34172/apb.2023.039
Shiva Roshan Milani, Bagher Pourheydar, Saman Daneshfar, Leila Chodari
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Abstract

Purpose: Reduced angiogenesis in the heart tissue is a primary risk factor for heart disease in the diabetes condition. This study was aimed to evaluate the changes of two main angiogenesis mediators, NADPH oxidase 4 (NOX4) and sirtuin 1 (SIRT-1) protein levels in the heart of diabetic rats and the impact of Insulin-like growth factor 1 (IGF-1) and exercise on these proteins. Methods: Injection of 60 mg/kg of streptozotocin in 40 male Wistar rats led to the induction of type 1 diabetes. Angiogenesis was detected in the hearts by immunostaining for PECAM-1/ CD31 after 30 days of treatment with IGF-1 (2 mg/kg/day) and exercise. ELISA technique was utilized to establish the expression levels of NOX4 and SIRT-1 within the heart. Results: The results revealed a significant increase in HbA1c and a significant decrease in SIRT1, NOX4 levels and angiogenesis grade in the heart of diabetes group compared to control group. Meanwhile, IGF-1 and exercise alone or in combination completely masked these effects. Additionally, synergistic effect on SIRT-1, HbA1c levels and angiogenesis grade is evident when IGF-1 and exercise are applied simultaneously. Conclusion: Our findings suggest that reduction in angiogenesis in the heart of diabetic rats may be mediated by down expression of NOX4 and SIRT-1 protein levels. It was also displayed that IGF-1 and exercise as novel therapies increase NOX4 and SIRT-1 protein levels within the hearts of diabetic rats.

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心脏 NOX4 和 SIRT-1 蛋白水平降低导致糖尿病大鼠心脏血管生成减少:IGF-1和运动的拯救作用。
目的心脏组织血管生成减少是糖尿病患者患心脏病的主要风险因素。本研究旨在评估糖尿病大鼠心脏中两种主要血管生成介质--NADPH氧化酶4(NOX4)和sirtuin 1(SIRT-1)蛋白水平的变化,以及胰岛素样生长因子1(IGF-1)和运动对这些蛋白的影响。研究方法向 40 只雄性 Wistar 大鼠注射 60 毫克/千克链脲佐菌素,诱发 1 型糖尿病。IGF-1(2 毫克/公斤/天)和运动治疗 30 天后,通过免疫染色法检测 PECAM-1/ CD31 在心脏中的血管生成。利用 ELISA 技术确定心脏中 NOX4 和 SIRT-1 的表达水平。结果显示结果显示,与对照组相比,糖尿病组的HbA1c明显升高,SIRT1、NOX4水平和血管生成等级明显降低。与此同时,IGF-1 和运动单独或联合使用完全掩盖了这些影响。此外,同时应用 IGF-1 和运动时,对 SIRT-1、HbA1c 水平和血管生成等级的协同作用也很明显。结论我们的研究结果表明,糖尿病大鼠心脏血管生成的减少可能是由 NOX4 和 SIRT-1 蛋白水平的表达下降介导的。研究还显示,IGF-1 和运动作为新型疗法可提高糖尿病大鼠心脏中 NOX4 和 SIRT-1 蛋白水平。
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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