耐力运动训练对糖尿病大鼠主动脉内皮损伤生物标志物的影响

IF 3.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Mahtab Fouladi, Maryam Mahmoudabady, Zahra Gholamnezhad, Sadegh Shabab, Saeed Niazmand, Hossein Salmani
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引用次数: 0

摘要

鉴于缺乏运动会增加糖尿病相关心血管事件的风险,本研究调查了链脲佐菌素(STZ)诱导的糖尿病大鼠血管损伤的分子机制。目的是阐明不同运动(间歇训练和持续训练)和二甲双胍对生化指标、主动脉损伤、氧化应激和炎症的影响,为糖尿病相关血管并发症的潜在治疗干预提供见解。雄性 Wistar 大鼠接受单剂量 STZ(60 毫克/千克)诱导糖尿病。糖尿病大鼠接受间歇训练或持续训练(40 分钟/天,5 天/周,6 周)、二甲双胍(300 毫克/千克)或二甲双胍与运动相结合的训练。6 周后,评估血清中的生化指标、氧化应激标记物以及主动脉组织中内皮一氧化氮合酶(eNOS)、凝集素样氧化低密度脂蛋白受体-1(LOX-1)和细胞间粘附分子-1(ICAM-1)的 mRNA 表达。与糖尿病组相比,所有治疗组的血清空腹血糖 (FBS)、甘油三酯 (TG)、总胆固醇 (TC)、低密度脂蛋白 (LDL)、TG/HDL、TC/HDL 和 LDL/HDL 比率均显著降低。与糖尿病组相比,两种运动、二甲双胍和运动+二甲双胍组合都能通过降低丙二醛(MDA)和提高主动脉组织的抗氧化状态来显著降低氧化应激。此外,与糖尿病组相比,运动组、二甲双胍组和组合组中 eNOS 的表达明显升高,而 LOX-1 和 ICAM-1 的表达则明显降低。在大多数情况下,运动与二甲双胍联合使用(尤其是间歇训练)比单独使用更有效。看来,在服用二甲双胍的同时进行运动可作为一种治疗方法,通过改善高血糖和高脂血症,减少氧化应激和血管炎症反应,从而改善与实验性糖尿病内皮损伤相关的生物标志物功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Impact of Endurance Exercise Training on Biomarkers of Aortic Endothelial Damage in Diabetic Rats

Impact of Endurance Exercise Training on Biomarkers of Aortic Endothelial Damage in Diabetic Rats

Given the heightened risk of diabetes-related cardiovascular events associated with inactivity, this study investigates the molecular mechanisms of vascular damage in streptozotocin (STZ)-induced diabetic rats. The aim is to elucidate the impact of different exercises (interval and continuous training) and metformin on biochemical parameters, aortic injury, oxidative stress, and inflammation to provide insights into potential therapeutic interventions for diabetes-associated vascular complications. Male Wistar rats were administered a single dose of STZ (60 mg/kg) to induce diabetes. Diabetic rats underwent either interval training or continuous training (40 min/day, 5 days/week, 6 weeks), received metformin (300 mg/kg), or a combination of metformin and exercise. After 6 weeks, biochemical parameters in serum and oxidative stress markers and mRNA expression of endothelial nitric oxide synthase (eNOS), lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), and intercellular adhesion molecule-1 (ICAM-1) in aorta tissue were assessed. Serum levels of fasting blood sugar (FBS), triglyceride (TG), total cholesterol (TC), low-density lipoprotein (LDL), TG/HDL, TC/HDL, and LDL/HDL ratios were significantly reduced in all treatment groups compared to the diabetes group. Both types of exercises, metformin, and exercise+metformin combinations, significantly reduced oxidative stress by decreasing malondialdehyde (MDA) and enhancing the antioxidant status in the aortic tissue compared to the diabetic group. In addition, in exercise groups, metformin, and combination groups, the expression of eNOS was significantly elevated, while LOX-1 and ICAM-1 expression significantly decreased compared to the diabetic group. In most cases, the combination of exercise and metformin (especially interval training) was more effective than exercise alone. It seems that exercise along with taking metformin can be considered as a therapeutic method by improving hyperglycemia and hyperlipidemia and reducing oxidative stress and vascular inflammatory responses, leading to ameliorating biomarkers function related to endothelial damage in experimental diabetes conditions.

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来源期刊
Cardiovascular Therapeutics
Cardiovascular Therapeutics 医学-心血管系统
CiteScore
5.60
自引率
0.00%
发文量
55
审稿时长
6 months
期刊介绍: Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged. Subject areas include (but are by no means limited to): Acute coronary syndrome Arrhythmias Atherosclerosis Basic cardiac electrophysiology Cardiac catheterization Cardiac remodeling Coagulation and thrombosis Diabetic cardiovascular disease Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF) Hyperlipidemia Hypertension Ischemic heart disease Vascular biology Ventricular assist devices Molecular cardio-biology Myocardial regeneration Lipoprotein metabolism Radial artery access Percutaneous coronary intervention Transcatheter aortic and mitral valve replacement.
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