阻力运动:一个强大的工具,适应,破坏,重建和调节骨骼肌的分子和结构环境。

Käthe Bersiner, So-Young Park, Kirill Schaaf, Woo-Hwi Yang, Christian Theis, Daniel Jacko, Sebastian Gehlert
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引用次数: 1

摘要

目的:骨骼肌通过维持或增加力量和肌肉质量来调节健康和表现。尽管抵抗运动(RE)的分子机制明显以蛋白质合成的激活为目标,但在RE刺激后,许多其他机制和结构必须参与协调通讯、修复和恢复稳态。实际上,RE可以通过强度、连续性和体积的变化来调节,这些变化会影响分子反应和骨骼肌适应。这些方面的知识对于训练计划的规划和评估RE训练对骨骼肌的影响是重要的。方法:在这篇叙述性综述中,我们介绍了适应RE的骨骼肌亚结构的一般方面。我们进一步强调了控制急性和重复RE时人类骨骼肌合成代谢、降解、修复和记忆的分子机制,并将这些方面与主要训练变量联系起来。结果:虽然RE是激活骨骼肌合成代谢的关键刺激,但它也会引起肌纤维损伤。然而,为了增加肌肉质量,同时对肌体环境的基本亚结构进行相应的适应,RE必须不断重复。这需要分子机制的永久参与,在每次re诱导的肌肉损伤后重建骨骼肌完整性。结论:多种分子调节因子协同控制急性反复RE后骨骼肌的适应性,并将其作用扩展到肌肉生长之外。关键阻力训练变量的变化可能会影响这些机制,而不会影响肌肉生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Resistance exercise: a mighty tool that adapts, destroys, rebuilds and modulates the molecular and structural environment of skeletal muscle.

Resistance exercise: a mighty tool that adapts, destroys, rebuilds and modulates the molecular and structural environment of skeletal muscle.

Resistance exercise: a mighty tool that adapts, destroys, rebuilds and modulates the molecular and structural environment of skeletal muscle.

Resistance exercise: a mighty tool that adapts, destroys, rebuilds and modulates the molecular and structural environment of skeletal muscle.

Purpose: Skeletal muscle regulates health and performance by maintaining or increasing strength and muscle mass. Although the molecular mechanisms in response to resistance exercise (RE) significantly target the activation of protein synthesis, a plethora of other mechanisms and structures must be involved in orchestrating the communication, repair, and restoration of homeostasis after RE stimulation. In practice, RE can be modulated by variations in intensity, continuity and volume, which affect molecular responses and skeletal muscle adaptation. Knowledge of these aspects is important with respect to planning of training programs and assessing the impact of RE training on skeletal muscle.

Methods: In this narrative review, we introduce general aspects of skeletal muscle substructures that adapt in response to RE. We further highlighted the molecular mechanisms that control human skeletal muscle anabolism, degradation, repair and memory in response to acute and repeated RE and linked these aspects to major training variables.

Results: Although RE is a key stimulus for the activation of skeletal muscle anabolism, it also induces myofibrillar damage. Nevertheless, to increase muscle mass accompanied by a corresponding adaptation of the essential substructures of the sarcomeric environment, RE must be continuously repeated. This requires the permanent engagement of molecular mechanisms that re-establish skeletal muscle integrity after each RE-induced muscle damage.

Conclusion: Various molecular regulators coordinately control the adaptation of skeletal muscle after acute and repeated RE and expand their actions far beyond muscle growth. Variations of key resistance training variables likely affect these mechanisms without affecting muscle growth.

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