卫星细胞中运动方式依赖的线粒体呼吸能力和培养肌管中条件血清诱导的反应。

IF 2.6 4区 医学 Q2 PHYSIOLOGY
Takanaga Shirai, Hayato Shinkai, Riku Tanimura, Kazuki Uemichi, Shunsuke Sugiyama, Kohei Takeda, Yu Kitaoka, Tohru Takemasa
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引用次数: 0

摘要

运动诱导的线粒体适应有助于肌肉功能和代谢健康。我们的目的是研究中强度游泳(MOD)和高强度间歇训练(HIIT)与运动条件血清处理的骨骼肌细胞线粒体功能的关系。雄性ICR小鼠(7-8周龄)被分配到久坐、MOD或HIIT组。MOD组进行5次60分钟的训练,HIIT组进行加权高强度间歇游泳。本研究评估了足底肌线粒体酶活性、分离卫星细胞线粒体呼吸能力以及运动衍生血清处理C2C12肌管的线粒体功能。在运动后立即和24小时分别获得血清,以评估急性效应和慢性适应性。与久坐组相比,MOD和HIIT组显示肌肉柠檬酸合成酶和细胞色素c氧化酶活性显著增加,但MOD和HIIT组之间无显著差异。与久坐组和HIIT组相比,MOD组的卫星细胞表现出更高的基础呼吸、ATP产生和最大呼吸能力。急性血清显著改善了HIIT组培养C2C12肌管的最大线粒体呼吸,而慢性训练血清改善了这些参数,但没有表现出模式特异性作用。MOD增强卫星细胞的线粒体呼吸功能,可能是由于持续的有氧代谢信号,而HIIT产生一种有效但短暂的全身反应,强烈增强肌肉细胞的线粒体功能。运动方式的不同影响强调了时间和运动方式在驱动特定线粒体适应中的重要性,从而为优化代谢健康的量身定制运动处方提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exercise modality-dependent mitochondrial respiratory capacity in satellite cells and conditioned serum-induced responses in cultured myotubes.

Exercise-induced mitochondrial adaptations contribute to muscle function and metabolic health. We aimed to investigate the association of moderate-intensity swimming (MOD) and high-intensity interval training (HIIT) with mitochondrial function in skeletal muscle cells treated with exercise-conditioned serum. Male ICR mice (7-8 weeks old) were assigned to the Sedentary, MOD or HIIT group. The MOD group underwent five sessions of 60 min. The HIIT group performed weighted high-intensity swimming intervals. This study assessed mitochondrial enzyme activity in the plantaris muscle, mitochondrial respiratory capacity in isolated satellite cells, and mitochondrial function in C2C12 myotubes treated with exercise-derived serum. Serum was obtained immediately and 24 h postexercise to assess acute effects and chronic adaptations, respectively. The MOD and HIIT groups demonstrated significantly increased muscle citrate synthase and cytochrome c oxidase activities compared with the Sedentary group, but with no significant differences between the MOD and HIIT groups. Satellite cells exhibited higher basal respiration, ATP production and maximal respiratory capacity in the MOD group than in the Sedentary and HIIT groups. Acute serum notably improved maximal mitochondrial respiration in cultured C2C12 myotubes in the HIIT group, whereas serum from chronic training improved those parameters but demonstrated no modality-specific effects. MOD enhances mitochondrial respiratory function in satellite cells, probably owing to sustained aerobic metabolic signalling, whereas HIIT produces a potent but transient systemic response that acutely boosts mitochondrial function in muscle cells. The differential effects of exercise modalities emphasize the importance of timing and exercise modality in driving specific mitochondrial adaptations, thereby providing valuable insights for tailored exercise prescriptions for optimizing metabolic health.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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