Document Type : Research Paper I Open Access I Released under CC BY-NC 4.0 license

Authors

1 PhD of Exercise Physiology, Faculty of Sport Sciences, Urmia University, Urmia, Iran

2 Assistant Professor of Exercise Physiology, Faculty of Sport Sciences, Urmia University, Urmia, Iran

3 Associate Professor of Physiology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran

Abstract

Diabetes, as a chronic metabolic disorder with a high prevalence, highlights the importance of ongoing research and the need for new methods to prevent and treat this epidemic disease.The aim of this study was to evaluate the changes in fibrosis and apoptosis of heart tissue in diabetic rats following two aerobic and interval training methods with astaxanthin supplementation. 35 Wistar male rats were randomly divided into7groups after induction of diabetes, including diabetic control, diabetes sham, diabetes+aerobic exercise+supplement. Diabetes+ intervalexercise + supplement, diabetes + interval, diabetes + aerobic, diabetes + supplement were included. Interval training for 8 weeks with 5 sessions per week with an intensity of 80% vo2max and aerobic training with an intensity of about 65 to 75% Vo2max was performed on the treadmill.The protein content of Cas3, COL4a1 and fibronectin were measured by Western blotting. COL4a1 protein content in both training and combination groups and supplement group showed a significant decrease with the control group. Also, the content of Cas3 and fibronectin protein in the combined and aerobic groups was significantly reduced compared to the control group, but there was no significant difference in the content of these proteins between the supplement and interval groups compared to the control group. It seems that the synergistic effects of exercise with different intensities along with astaxanthin supplementation prevent the upward trend of apoptosis and fibrosis in the heart tissue of diabetic rats and its subsequent complications such as diabetic cardiomyopathy.

Keywords

Main Subjects

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