Department of Spine Surgery, Shenzhen People's Hospital, The Second Clinical Medical College, Jinan University, Shenzhen 518020, China; The First Affiliated Hospital, Jinan University, Guangzhou 510630, China.
Department of Spine Surgery, Shenzhen People's Hospital, The Second Clinical Medical College, Jinan University, Shenzhen 518020, China.
Bone. 2021 May;146:115886. doi: 10.1016/j.bone.2021.115886. Epub 2021 Feb 14.
Magnesium (Mg), as an essential mineral, supports and sustains the health and activity of the organs of the human body. Despite some clinical evidence on the association of Mg deficiency with muscle regeneration dysfunction and sarcopenia in older-aged individuals, there is no consensus on the action mode and molecular mechanism by which Mg influences aged muscle size and function. Here, we identified the appropriate Mg environment that promotes the myogenic differentiation and myotube hypertrophy in both C2C12 myoblast and primary aged muscle stem cell (MuSC). Through animal experiments, we demonstrated that Mg supplementation in aged mice significantly promotes muscle regeneration and conserves muscle mass and strength. Mechanistically, Mg stimulation activated the mammalian target of rapamycin (mTOR) signalling, inducing the myogenic differentiation and protein synthesis, which consequently offers protections against the age-related decline in muscle regenerative potential and muscle mass. These findings collectively provide a promising therapeutic strategy for MuSC dysfunction and sarcopenia through Mg supplementation in the elderly.
镁(Mg)作为一种必需矿物质,支持和维持着人体器官的健康和活动。尽管有一些临床证据表明镁缺乏与老年人肌肉再生功能障碍和肌肉减少症有关,但关于镁影响老年肌肉大小和功能的作用模式和分子机制尚无共识。在这里,我们确定了促进 C2C12 成肌细胞和原代老年肌肉干细胞(MuSC)成肌分化和肌管肥大的合适镁环境。通过动物实验,我们证明了在老年小鼠中补充镁可显著促进肌肉再生并保持肌肉质量和力量。在机制上,镁刺激激活了雷帕霉素靶蛋白(mTOR)信号通路,诱导成肌分化和蛋白质合成,从而对与年龄相关的肌肉再生潜力和肌肉质量下降提供保护。这些发现为通过在老年人中补充镁来治疗 MuSC 功能障碍和肌肉减少症提供了一种有前景的治疗策略。