心力衰竭
自噬
骨骼肌
心肌细胞
内科学
医学
糖尿病
内分泌学
肌肉萎缩
免疫印迹
下调和上调
细胞凋亡
有氧运动
蛋白激酶B
链脲佐菌素
心脏病学
化学
生物化学
基因
作者
Alan Christhian Bahr,Naira Bohrer Scherer,Elizama de Gregório,Lucas Kieling,Alexandre Luz de Castro,Alex Sander da Rosa Araújo,Patrick Türck,Pedro Dal Lago
出处
期刊:Authorea - Authorea
日期:2024-06-11
标识
DOI:10.22541/au.171808585.50400712/v1
摘要
Introduction : Heart failure (HF) and type 2 diabetes mellitus (DM2) are global health problems that often lead to muscle atrophy. These conditions are associated with increased autophagy and apoptosis in the muscle cells, resulting in decreased muscle mass. Materials and methods: Male rats were assigned to one of four groups: control (CT), HF+DM (disease model), exercise+HF+DM (EX+HF+DM), and EX+HF+DM+photobiomodulation (EX+HF+DM+PBM). To induce DM2, we administered streptozotocin (0.25 ml/kg, i.p.). HF was induced by coronary ligation. One week post-induction, an eight-week aerobic exercise and PBM protocol was initiated. Western blot analysis was used to measure the expression of apoptosis-related proteins and autophagy. Results: The EX+HF+DM+PBM group showed a substantial increase in Nrf2, p-AKT, and LC3-I levels compared to the HF+DM group. Conclusion: These findings suggest that physical exercise combined with PBM can upregulate proteins that promote myocyte survival in rats with HF and DM2.
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