8周阻力训练对2型糖尿病雄性Wistar大鼠肌肉肌肉生长抑制素基因表达和胰岛素抵抗的影响

Majid Hassan Qomi, S. Arshadi, Abdolali Banayifar, Y. Kazemzadeh
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摘要

背景与目的:肌萎缩是糖尿病未控制的指标之一。本研究旨在探讨8周阻力训练(RT)对链脲佐菌素(STZ)诱导的糖尿病大鼠比目鱼肌肌肉生长抑制素基因表达和胰岛素抵抗的影响。材料与方法:一般选取体重200 ~ 250 g、8 ~ 10周龄Wistar雄性大鼠14只。然后将新制备的糖尿病STZ溶液腹腔注射给大鼠。实验动物随机分为对照组和抗阻训练组。阻力训练方案进行了十次重复,以100%的体重爬上梯子,持续八周,每周五天。最后一次训练后约48小时,取大鼠比目鱼肌,评估肌肉生长抑制素基因表达。统计学资料分析采用独立t检验,P <0.05为显著性水平。结果:独立t检验结果显示,阻力训练组大鼠比目鱼肌中肌生长抑制素蛋白基因的平均表达率显著低于对照组(P = 0.013)。与对照组相比,抗阻训练组血糖、胰岛素和胰岛素抵抗水平均显著降低(p值分别为0.001、0.005和0.001)。肌生长抑制素基因的平均表达量与血糖呈显著正相关(P = 0.012, r = 0.539),与胰岛素抵抗呈显著正相关(P = 0.015, r = 0.525)。结论:抗阻训练可降低2型糖尿病大鼠肌肉生长抑制素的表达,改善胰岛素抵抗。因此,靶向肌生长抑制素可能是治疗代谢性疾病如肥胖、糖尿病和代谢综合征的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Eight Weeks of Resistance Training on Muscle Myostatin Gene Expression and Insulin Resistance in Male Wistar Rats with Type 2 Diabetes
Background and Objectives: Muscular atrophy is one of the indicators of uncontrolled diabetes. The aim of the current study was to investigate effects of eight weeks of resistance training (RT) on myostatin gene expression in soleus muscles and insulin resistance in streptozotocin (STZ)-induced diabetic rats. Materials and Methods: In general, 14 Wistar male rats weighing 200–250 g and aging 8–10 weeks were selected for the study. Then, a newly prepared diabetic STZ solution was intraperitoneally injected to the rats. Animals were randomly divided into two groups of controls and resistance training diabetes. The resistance training protocol was carried out at ten repetitions as climbing up the ladder with 100% of the body weight for eight weeks, five days a week. Nearly 48 h after the last training session, soleus muscles of the rats were removed and the myostatin gene expression was assessed. Statistical data analysis was carried out using independent t-test at a significance level of P <0.05. Results: Results of the independent t-test showed that the mean expression rate of myostatin protein genes in rat soleus muscles of the resistance training group was significantly lower than that of the control group (P = 0.013). Furthermore, levels of glucose, insulin and insulin resistance were significantly lower in resistance training group, compared to those in control group (P-values of 0.001, 0.005 and 0.001, respectively). A significantly positive correlation was seen between the mean expression of myostatin protein gene and the blood glucose (P = 0.012, r = 0.539), as well as the expression of myostatin protein gene and the insulin resistance (P = 0.015, r = 0.525). Conclusions: Results of this study indicated that resistance training decreased myostatin expression and could improve insulin resistance in rats with type 2 diabetes. Hence, targeting myostatin might be a new therapeutic approach for the treatment of metabolic diseases such as obesity, diabetes and metabolic syndrome.
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