Ma Yuxia, Liu Yi, Zheng Jiachuang, Zheng Zhixia, Li Jingjing
Department of Geriatric Medicine, Longgang Central Hospital of Shenzhen, No.6082 Longgang Avenue, Longgang District, Shenzhen, 518116, Guangdong, China.
Cangzhou Prison, No.47 Hexi North Street, Cangzhou, 061001, Heibei, China.
Eur Geriatr Med. 2025 Mar 13. doi: 10.1007/s41999-025-01181-4.
In this study, 24-month-old (aged) mice were used as a naturally occurring model of aging-associated sarcopenia, while 2-month-old (young) mice served as the normal control. Six weeks of treadmill training was employed as an aerobic exercise intervention. The mRNA and protein levels of fibronectin type III domain-containing protein 5 (Fndc5/irisin), MuRF1, and Atrogin-1 in gastrocnemius muscles were analyzed using qRT-PCR and Western blot. Oxidative stress was assessed using relevant detection kits. Skeletal muscle function was evaluated through the four-paw hanging test, rotarod test, grip strength assay, and measurements of quadriceps, tibialis anterior, and gastrocnemius muscle mass.
Aerobic exercise interventions enhanced skeletal muscle function by increasing hanging time, maximum speed, grip strength, and increased quadriceps, gastrocnemius, and tibialis anterior muscle mass. On the other hand, aerobic exercise reduced MuRF1 and Atrogin-1 expression in the gastrocnemius muscles of sarcopenia mice, along with lower malondialdehyde levels, and higher superoxide dismutase activity, T-ATPase, and glutathione peroxidase activity. A decline in Fndc5/irisin expression was further detected in the gastrocnemius muscles with aging. In Fndc5-knockout aged mice, aerobic exercise failed to improve skeletal muscle function compared to wild-type aged mice, as evaluated by hanging time, grip strength, maximum speed, and quadriceps, gastrocnemius, and tibialis anterior muscle mass, further validating the involvement of Fndc5 in the improvement of aging-associated sarcopenia.
Aerobic exercise improves aging-associated sarcopenia in mice, with Fndc5/irisin playing a role in this process.
在本研究中,24月龄小鼠被用作与衰老相关的肌肉减少症的自然发生模型,而2月龄小鼠作为正常对照。采用六周的跑步机训练作为有氧运动干预。使用qRT-PCR和蛋白质免疫印迹法分析腓肠肌中含III型纤连蛋白结构域蛋白5(Fndc5/鸢尾素)、肌肉环指蛋白1(MuRF1)和肌肉萎缩F-box蛋白1(Atrogin-1)的mRNA和蛋白水平。使用相关检测试剂盒评估氧化应激。通过四爪悬挂试验、转棒试验、握力测定以及股四头肌、胫骨前肌和腓肠肌质量测量来评估骨骼肌功能。
有氧运动干预通过增加悬挂时间、最大速度、握力以及增加股四头肌、腓肠肌和胫骨前肌质量来增强骨骼肌功能。另一方面,有氧运动降低了肌肉减少症小鼠腓肠肌中MuRF1和Atrogin-1的表达,同时丙二醛水平降低,超氧化物歧化酶活性、T-ATP酶和谷胱甘肽过氧化物酶活性升高。随着衰老,在腓肠肌中进一步检测到Fndc5/鸢尾素表达下降。在Fndc5基因敲除的老年小鼠中,与野生型老年小鼠相比,通过悬挂时间、握力、最大速度以及股四头肌、腓肠肌和胫骨前肌质量评估,有氧运动未能改善骨骼肌功能,进一步证实了Fndc5参与改善与衰老相关的肌肉减少症。
有氧运动可改善小鼠与衰老相关的肌肉减少症,Fndc5/鸢尾素在此过程中发挥作用。