Treadmill exercise alleviates diabetic cardiomyopathy by suppressing plasminogen activator inhibitor expression and enhancing eNOS in streptozotocin-induced male diabetic rats.

OBJECTIVE

To investigate the biological mechanism of the effect of different intensity exercises on diabetic cardiomyopathy.

METHODS

87 raise specific pathogen SPF healthy 6-week-old male Sprague-Dawley rats, fed 6 weeks with high-fat diet for rats were used, and a diabetic model was established by intraperitoneal injection of streptozotocin - randomly selected 43 rats were divided into Diabetic control group (DCG,  = 10), Diabetic exercise group 1 (DEG1,  = 11), Diabetic exercise group 2 (DEG2,  = 11) and Diabetic exercise group 3 (DEG3,  = 11). The rats in DEG1 were forced to run on a motorized treadmill, the exercise load consisted of running at a speed of 10 m/min, the exercise load of the rats in DEG2 were running at a speed of 15 m/min, the exercise load of the rats in DEG3 were running at a speed of 20 m/min, for one hour once a day for 6 weeks. After 6 weeks of exercise intervention, glucose metabolism-related indexes in rats such as blood glucose (FBG), glycosylated serum protein (GSP) and insulin (FINS); cardiac fibrinolytic system parameters such as PAI-1 (plasminogen activator inhibitor 1), Von Willebrand factor (vWF), protein kinase C (PKC) and diacylglycerol (DAG); and serum level of NO, eNOS and T-NOS were measured.

RESULT

Compared with DCG, fasting blood glucose and GSP were decreased, while insulin sensitivity index and insulin level were increased in all rats of the three exercise groups. FBG decrease was statistically significant ( < 0.01), only GSP decrease was statistically significant ( < 0.05) in DEG1 and DEG2, PAI-1 in three exercise groups were significantly reduced ( < 0.05), plasma vWF levels in the three exercise groups were significantly lower than those in the DCG group ( < 0.01); PKC levels decreased dramatically in the three exercise groups and DAG levels decrease slightly ( < 0.05), but with no significant difference. Compared with DCG, the serum level of NO was significantly higher ( < 0.05), and eNOS level was significantly elevated ( < 0.05). T-NOS elevation was statistically significant in DEG1 ( < 0.05).

CONCLUSIONS

Low- and moderate-intensity exercise can better control blood glucose level in diabetic rats; myocardial PAI-1 in DEG1, DEG2 and DEG3 rats decreased significantly ( < 0.05), serum NO increased ( < 0.05) and eNOS increased ( < 0.05) significantly. Therefore, it is inferred that exercise improves the biological mechanism of diabetic cardiomyopathy by affecting the levels of PAI-1 and eNOS, and there is a dependence on intensity.