8周耐力训练对2型糖尿病大鼠心肌中FOXO3a和Beclin-1蛋白含量的影响

M. Jokar, M. S. Moghadam, F. Daryanoosh
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引用次数: 0

摘要

背景FOXO3a/Beclin-1通路是自噬的重要通路,在易患心肌病的糖尿病患者中可能受损。目的探讨8周耐力训练对2型糖尿病大鼠心肌组织FOXO3a和Beclin-1蛋白含量的影响。方法对12只平均体重270±20g的2月龄雄性Sprague-Dawley大鼠进行实验研究。在链脲佐菌素和烟酰胺诱导糖尿病后,将大鼠随机分为糖尿病运动组(n=6)和糖尿病对照组(n=6)。糖尿病锻炼组每周接受4天的干预,每次以10-30米/米的速度进行42分钟的干预,持续8周,而对照组没有接受任何训练计划。研究期间,大鼠未接受任何胰岛素治疗。收集的数据采用独立t检验进行分析,显著性水平为P≤0.05。结果与干预后的对照组相比,训练组的FOXO3a(P=0.12)和Beclin-1(P=0.34)蛋白含量没有观察到显著变化。结论耐力训练不影响FOXO3a和Beclin-1蛋白的含量。因此,耐力训练似乎不会影响2型糖尿病患者心肌中的自噬信号。A B S T R A C T
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of an 8-Week Endurance Training Program on the Content of FOXO3a and Beclin-1 Proteins in Heart Muscle of Rats With Type 2 Diabetes
Background The FOXO3a/Beclin-1 pathway is an important pathway in autophagy that can be impaired in diabetic patients who are prone to cardiomyopathy. Objective The aim of this study was to investigate the effect of an 8-week endurance training program on the content of FOXO3a and Beclin-1 proteins in the heart muscle tissue of rats with type 2 diabetes. Methods This experimental study was conducted on 12 male two-month-old Sprague Dawley rats with a mean weight of 270±20 g. After diabetic induction by streptozotocin and nicotinamide, rats were randomly assigned into two groups of diabetic-exercise (n=6) and diabetic-control (n=6). The diabeticexercise group received intervention 4 days per week, each session for 42 minutes at a speed of 10-30 m/m for 8 weeks, while the control group received no any training program. The rats did not receive any insulin treatment during the study. Collected data were analyzed using independent t-test at a significance level of P≤0.05. Findings No significant changes were observed in the content of FOXO3a (P=0.12) and Beclin-1 (P=0.34) proteins in the training group compared to the control group after intervention. Conclusion The endurance training can not affect the content of FOXO3a and Beclin-1 proteins. Therefore, it seems that endurance training may not affect autophagy signaling in the heart muscle of type 2 diabetic patients. A B S T R A C T
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