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首页> 外文期刊>Gerontology: International Journal of Experimental and Clinical Gerontology >Apoptosis in skeletal myocytes: A potential target for interventions against sarcopenia and physical frailty - A mini-review
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Apoptosis in skeletal myocytes: A potential target for interventions against sarcopenia and physical frailty - A mini-review

机译:骨骼肌细胞凋亡:针对肌肉减少症和身体虚弱的干预措施的潜在目标-简述

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Background: Sarcopenia, the age-related loss of muscle mass and function, represents a relevant public health issue due to its high prevalence and detrimental consequences. While the exact mechanisms underlying the pathogenesis of sarcopenia are not clear, growing experimental evidence indicates that progressive myonuclear elimination over the course of aging via an apoptosis-like process may represent a converging mechanism through which muscle atrophy and loss of physical function develop. Notably, the proapoptotic environment taking place in aged muscle appears amenable to interventions. Objective: We aimed at providing (1) an overview of signaling pathways of apoptosis relevant to sarcopenia, and (2) a review of the literature supporting myocyte apoptosis as a target for interventions against muscle aging. Methods: We summarized findings from studies focused on skeletal myocyte apoptosis as a mechanism in the development of sarcopenia and reports supporting myonuclear apoptosis as a target for interventions against age-related muscle loss. Results: Advanced age is associated with increased signaling through extrinsic and intrinsic apoptotic pathways in skeletal myocytes. In contrast, downregulation of myocyte apoptosis through calorie restriction, exercise training, hormonal supplementation, drugs (e.g. angiotensin-converting enzyme inhibitors, acetaminophen, antimyostatin antibodies), nutraceuticals or genetic interventions (e.g. PGC-1α overexpression) is linked with preservation of muscle integrity and improved physical performance in late life. Preliminary data also indicate that skeletal myocyte apoptotic signaling may be downregulated by compounds, such as resveratrol, with calorie restriction-mimicking properties. Whether exercise mimetics exert a similar effect has not yet been investigated. Conclusions: Available evidence suggests that targeting myonuclear apoptosis might provide novel and effective therapeutic tools to combat sarcopenia. Further research is required to definitely establish if downregulating myonuclear apoptosis is effective in maintaining muscle mass and function in late life, identify the most relevant apoptotic pathway(s) to target, and determine the optimal timing for intervening.
机译:背景:肌肉减少症是与年龄相关的肌肉质量和功能丧失,由于其高患病率和有害后果,代表了相关的公共卫生问题。虽然肌肉少肌症发病机理的确切机制尚不清楚,但是越来越多的实验证据表明,在衰老过程中,通过凋亡样过程逐渐清除肌核,可能代表了肌肉萎缩和身体机能丧失的收敛机制。值得注意的是,在老年肌肉中发生的促凋亡环境似乎适合进行干预。目的:我们旨在提供(1)与少肌症相关的凋亡信号通路的概述,以及(2)支持将肌细胞凋亡作为干预肌肉衰老目标的文献综述。方法:我们总结了以骨骼肌细胞凋亡为机制的肌肉减少症研究的结果,并报道了支持肌核细胞凋亡作为干预与年龄相关的肌肉丢失的靶标。结果:高龄与骨骼肌细胞内在和内在凋亡途径的信号传导增加有关。相反,通过限制卡路里,运动训练,激素补充,药物(例如血管紧张素转换酶抑制剂,对乙酰氨基酚,抗肌生长抑制素抗体),营养保健品或遗传干预措施(例如PGC-1α过表达)来降低心肌细胞凋亡与维持肌肉完整性有关。并改善了晚年的体能表现。初步数据还表明,骨骼肌细胞凋亡信号可能被具有类似卡路里限制特性的化合物(例如白藜芦醇)下调。模拟运动是否发挥类似作用尚未进行调查。结论:现有证据表明,靶向肌核细胞凋亡可能为对抗少肌症提供新颖有效的治疗手段。需要进一步的研究来明确确定下调心肌细胞凋亡是否在维持生命后期肌肉质量和功能,确定最相关的凋亡途径以及确定干预的最佳时机方面是否有效。

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