运动素和肌肉减少症:揭示运动诱导线粒体稳态背后的机制。

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Metabolites Pub Date : 2025-01-16 DOI:10.3390/metabo15010059
Jiayin Wang, Dandan Jia, Zhiwang Zhang, Dan Wang
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引用次数: 0

摘要

背景/目的:肌肉减少症以肌肉质量和力量的逐渐减少为特征,与身体残疾、代谢功能障碍和死亡风险增加有关。运动疗法目前被认为是解决肌肉减少症的可行方法。然而,运动训练或体育活动背后的分子机制仍然知之甚少。线粒体稳态的破坏与肌少症的发病机制有关。运动训练通过显著维持线粒体稳态,包括促进线粒体自噬、改善线粒体生物发生、平衡线粒体动力学和维持线粒体氧化还原,有效延缓肌肉减少症的发生。运动因子(如脂肪因子、肌肉因子、肝因子和骨因子)是运动训练后释放的信号分子,可能通过改善线粒体稳态、减少炎症和调节蛋白质合成来促进骨骼肌代谢,从而防御肌肉减少症。方法:在这篇综述中,我们对运动诱导的运动进行了详细的总结,并阐述了它们的益处,特别关注了它们对肌肉减少症患者线粒体稳态的影响。结果:运动诱导骨骼肌的大量适应,包括增加肌肉质量,改善肌肉再生和肥大,提高激素释放,增强线粒体功能。越来越多的研究强调,运动因子具有调节线粒体自噬、线粒体生物发生、动力学、自噬和氧化还原平衡等过程的潜力。这些机制有助于维持线粒体稳态,从而支持骨骼肌代谢和线粒体健康。结论:通过对线粒体内分子机制的全面研究,本文揭示了运动因子作为对抗肌肉减少症的关键运动保护传感器的潜力的新见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis.

Background/Objectives: Sarcopenia, characterized by the progressive loss of muscle mass and strength, is linked to physical disability, metabolic dysfunction, and an increased risk of mortality. Exercise therapy is currently acknowledged as a viable approach for addressing sarcopenia. Nevertheless, the molecular mechanisms behind exercise training or physical activity remain poorly understood. The disruption of mitochondrial homeostasis is implicated in the pathogenesis of sarcopenia. Exercise training effectively delays the onset of sarcopenia by significantly maintaining mitochondrial homeostasis, including promoting mitophagy, improving mitochondrial biogenesis, balancing mitochondrial dynamics, and maintaining mitochondrial redox. Exerkines (e.g., adipokines, myokines, hepatokines, and osteokines), signaling molecules released in response to exercise training, may potentially contribute to skeletal muscle metabolism through ameliorating mitochondrial homeostasis, reducing inflammation, and regulating protein synthesis as a defense against sarcopenia. Methods: In this review, we provide a detailed summary of exercise-induced exerkines and confer their benefit, with particular focus on their impact on mitochondrial homeostasis in the context of sarcopenia. Results: Exercise induces substantial adaptations in skeletal muscle, including increased muscle mass, improved muscle regeneration and hypertrophy, elevated hormone release, and enhanced mitochondrial function. An expanding body of research highlights that exerkines have the potential to regulate processes such as mitophagy, mitochondrial biogenesis, dynamics, autophagy, and redox balance. These mechanisms contribute to the maintenance of mitochondrial homeostasis, thereby supporting skeletal muscle metabolism and mitochondrial health. Conclusions: Through a comprehensive investigation of the molecular mechanisms within mitochondria, the context reveals new insights into the potential of exerkines as key exercise-protective sensors for combating sarcopenia.

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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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