肌萎缩
骨骼肌
内分泌学
肌萎缩性肥胖
内科学
有氧运动
体内
脂肪团
发病机制
肥胖
医学
生物
体外
肌肉团
减肥
衰老
心肌细胞
动物研究
机制(生物学)
化学
转基因小鼠
分解代谢
脂质代谢
脂肪组织
老化
蛋白质分解代谢
双重角色
炎症
脂毒性
作者
Danni Wang,Xinyue Zheng,Zhu Yang,Wen Zhang,Sujuan Liu,Yanmei Niu
标识
DOI:10.1093/gerona/glaf271
摘要
Sarcopenic obesity (SO), a dual condition characterized by the coexistence of sarcopenia and obesity, elevates the risk of metabolic disorders, disability, and mortality to magnitudes exceeding the combined risks of both conditions individually, demonstrating a "super-additive impairment" effect on health. Therefore, this study aims to investigate the mechanisms underlying the pathogenesis and progression of SO. We utilized natural aging mice fed high-fat diets (HFD) to simulate the progression of muscle mass decline observed in geriatric populations and high-calorie diets prevalent in modern societies, creating an SO animal model with exceptional clinical relevance. Our study demonstrates that HFD exacerbates age-related reductions in muscle mass, accompanied by decreased physical performance and increased lipid accumulation. Importantly, HFD-induced lipid infiltration emerges as a significant contributor to the further decline in skeletal muscle mass in SO mice, and the Nrf2/Prdx6 pathway is a mechanism regulating this factor. Aerobic exercise, a safe and reliable means for older adults, is particularly effective for fat loss and muscle maintenance. In our study, aerobic exercise effectively alleviated the detrimental effects of HFD on muscle health in aging mice. Mechanistic studies revealed that Nrf2 and Prdx6 protein expression was significantly suppressed in vivo by HFD and in vitro following palmitic acid (PA) exposure. Conversely, overexpression of Nrf2 and Prdx6 in vitro was able to mimic the protective effects of aerobic exercise. Our results indicate that the Nrf2/Prdx6 pathway plays a crucial role in counteracting muscle mass loss induced by HFD and may underlie beneficial effects of aerobic exercise on skeletal muscle.
科研通智能强力驱动
Strongly Powered by AbleSci AI