Department of Physical Medicine and Rehabilitation, School of Medicine, Faculty of Health Sciences, Queen's University, Kingston, ON K7L 4X3, Canada; School of Kinesiology and Health Studies, Faculty of Arts and Sciences, Queen's University, Kingston, ON K7L 4X3, Canada.
School of Health and Exercise Science, University of British Columbia, Kelowna, BC V1V 1V7, Canada.
Exp Gerontol. 2021 Sep;152:111465. doi: 10.1016/j.exger.2021.111465. Epub 2021 Jul 2.
Human biological aging from maturity to senescence is associated with a gradual loss of muscle mass and neuromuscular function. It is not until very old age (>80 years) however, that these changes often manifest into functional impairments. A driving factor underlying the age-related loss of muscle mass and function is the reduction in the number and quality of motor units (MUs). A MU consists of a single motoneuron, located either in the spinal cord or the brain stem, and all of the muscle fibres it innervates via its peripheral axon. Throughout the adult lifespan, MUs are slowly, but progressively lost. The compensatory process of collateral reinnervation attempts to recapture orphaned muscle fibres following the death of a motoneuron. Whereas this process helps mitigate loss of muscle mass during the latter decades of adult aging, the neuromuscular system has fewer and larger MUs, which have lower quality connections between the axon terminal and innervated muscle fibres. Whether this process of MU death and degradation can be attenuated with habitual physical activity has been a challenging question of great interest. This review focuses on age-related alterations of the human neuromuscular system, with an emphasis on the MU, and presents findings on the potential protective effects of lifelong physical activity. Although there is some discrepancy across studies of masters athletes, if one considers all experimental limitations as well as the available literature in animals, there is compelling evidence of a protective effect of chronic physical training on human MUs. Our tenet is that high-levels of physical activity can mitigate the natural trajectory of loss of quantity and quality of MUs in old age.
从成熟到衰老,人类的生物衰老与肌肉质量和神经肌肉功能的逐渐丧失有关。然而,只有到非常老年(>80 岁)时,这些变化才常常表现为功能障碍。肌肉质量和功能随年龄下降的一个主要因素是运动单位(MUs)数量和质量的减少。一个 MU 由单个运动神经元组成,位于脊髓或脑干中,通过其外周轴突支配它所支配的所有肌肉纤维。在整个成年期,MUs 缓慢但逐渐减少。轴突侧支再支配的代偿过程试图在运动神经元死亡后重新支配失去的肌肉纤维。虽然这个过程有助于减轻成年后期衰老过程中肌肉质量的损失,但神经肌肉系统的 MU 数量更少,体积更大,轴突末端与支配的肌肉纤维之间的连接质量较低。习惯性的身体活动是否可以减轻 MU 的死亡和退化过程,一直是一个非常有趣的具有挑战性的问题。本综述重点介绍了与人类神经肌肉系统相关的年龄变化,强调了 MU,并介绍了终身身体活动对其潜在保护作用的研究结果。尽管在对大师运动员的研究中存在一些差异,但如果综合考虑所有实验限制以及动物的可用文献,就有令人信服的证据表明慢性身体训练对人类 MU 具有保护作用。我们的原则是,高水平的身体活动可以减轻 MU 数量和质量随年龄自然下降的趋势。