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肌肉疲劳的分子机制。

Molecular Mechanisms of Muscle Fatigue.

机构信息

Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queen's Medical Centre, University of Nottingham Medical School, Nottingham NG7 2UH, UK.

出版信息

Int J Mol Sci. 2021 Oct 27;22(21):11587. doi: 10.3390/ijms222111587.

Abstract

Muscle fatigue (MF) declines the capacity of muscles to complete a task over time at a constant load. MF is usually short-lasting, reversible, and is experienced as a feeling of tiredness or lack of energy. The leading causes of short-lasting fatigue are related to overtraining, undertraining/deconditioning, or physical injury. Conversely, MF can be persistent and more serious when associated with pathological states or following chronic exposure to certain medication or toxic composites. In conjunction with chronic fatigue, the muscle feels floppy, and the force generated by muscles is always low, causing the individual to feel frail constantly. The leading cause underpinning the development of chronic fatigue is related to muscle wasting mediated by aging, immobilization, insulin resistance (through high-fat dietary intake or pharmacologically mediated Peroxisome Proliferator-Activated Receptor (PPAR) agonism), diseases associated with systemic inflammation (arthritis, sepsis, infections, trauma, cardiovascular and respiratory disorders (heart failure, chronic obstructive pulmonary disease (COPD))), chronic kidney failure, muscle dystrophies, muscle myopathies, multiple sclerosis, and, more recently, coronavirus disease 2019 (COVID-19). The primary outcome of displaying chronic muscle fatigue is a poor quality of life. This type of fatigue represents a significant daily challenge for those affected and for the national health authorities through the financial burden attached to patient support. Although the origin of chronic fatigue is multifactorial, the MF in illness conditions is intrinsically linked to the occurrence of muscle loss. The sequence of events leading to chronic fatigue can be schematically denoted as: trigger (genetic or pathological) -> molecular outcome within the muscle cell -> muscle wasting -> loss of muscle function -> occurrence of chronic muscle fatigue. The present review will only highlight and discuss current knowledge on the molecular mechanisms that contribute to the upregulation of muscle wasting, thereby helping us understand how we could prevent or treat this debilitating condition.

摘要

肌肉疲劳(MF)会随着时间的推移降低肌肉在恒定负荷下完成任务的能力。MF 通常是短暂的、可逆的,表现为疲劳或缺乏能量的感觉。导致短暂疲劳的主要原因与过度训练、训练不足/失健或身体损伤有关。相反,当与病理状态相关或在慢性暴露于某些药物或有毒复合物后,MF 可能会持续存在且更为严重。伴随着慢性疲劳,肌肉感觉松弛,肌肉产生的力量总是很低,导致个体一直感到虚弱。导致慢性疲劳发展的主要原因与衰老、固定不动、胰岛素抵抗(通过高脂肪饮食摄入或药理学介导的过氧化物酶体增殖物激活受体(PPAR)激动剂)介导的肌肉消耗有关,与全身性炎症相关的疾病(关节炎、败血症、感染、创伤、心血管和呼吸系统疾病(心力衰竭、慢性阻塞性肺疾病(COPD)))、慢性肾衰竭、肌肉萎缩症、肌肉肌病、多发性硬化症,以及最近的 2019 年冠状病毒病(COVID-19)。表现出慢性肌肉疲劳的主要结果是生活质量差。这种类型的疲劳对受影响的人以及国家卫生当局来说都是一个巨大的日常挑战,因为这给患者支持带来了经济负担。尽管慢性疲劳的起源是多因素的,但疾病状态下的 MF 与肌肉丧失的发生密切相关。导致慢性疲劳的事件序列可以示意性地表示为:触发(遗传或病理)->肌肉细胞内的分子结果->肌肉消耗->肌肉功能丧失->发生慢性肌肉疲劳。本综述仅将重点放在并讨论有助于理解肌肉消耗上调的分子机制的当前知识,这将有助于我们了解如何预防或治疗这种使人衰弱的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d29/8584022/608f39a26342/ijms-22-11587-g001.jpg

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