Hepple Russell T, Rice Charles L
Department of Kinesiology & Physical Education, McGill University, Montreal, Québec, Canada.
McGill Research Centre for Physical Activity and Health, Montreal, Québec, Canada.
J Physiol. 2016 Apr 15;594(8):1965-78. doi: 10.1113/JP270561. Epub 2015 Dec 21.
Changes in the neuromuscular system affecting the ageing motor unit manifest structurally as a reduction in motor unit number secondary to motor neuron loss; fibre type grouping due to repeating cycles of denervation-reinnervation; and instability of the neuromuscular junction that may be due to either or both of a gradual perturbation in postsynaptic signalling mechanisms necessary for maintenance of the endplate acetylcholine receptor clusters or a sudden process involving motor neuron death or traumatic injury to the muscle fibre. Functionally, these changes manifest as a reduction in strength and coordination that precedes a loss in muscle mass and contributes to impairments in fatigue. Regular muscle activation in postural muscles or through habitual physical activity can attenuate some of these structural and functional changes up to a point along the ageing continuum. On the other hand, regular muscle activation in advanced age (>75 years) loses its efficacy, and at least in rodents may exacerbate age-related motor neuron death. Transgenic mouse studies aimed at identifying potential mechanisms of motor unit disruptions in ageing muscle are not conclusive due to many different mechanisms converging on similar motor unit alterations, many of which phenocopy ageing muscle. Longitudinal studies of ageing models and humans will help clarify the cause and effect relationships and thus, identify relevant therapeutic targets to better preserve muscle function across the lifespan.
运动神经元丢失导致运动单位数量减少;去神经-再支配的重复循环引起纤维类型分组;神经肌肉接头不稳定,这可能是由于维持终板乙酰胆碱受体簇所需的突触后信号机制逐渐紊乱,或者是由于涉及运动神经元死亡或肌纤维创伤性损伤的突发过程。在功能上,这些变化表现为力量和协调性下降,这在肌肉质量下降之前出现,并导致疲劳受损。姿势肌中的规律性肌肉激活或通过习惯性体育活动可以在一定程度上减轻衰老过程中的一些结构和功能变化。另一方面,高龄(>75岁)时的规律性肌肉激活会失去其功效,至少在啮齿动物中可能会加剧与年龄相关的运动神经元死亡。由于许多不同机制会导致相似的运动单位改变,其中许多表现出与衰老肌肉相似的现象,因此旨在确定衰老肌肉中运动单位破坏潜在机制的转基因小鼠研究尚无定论。对衰老模型和人类的纵向研究将有助于阐明因果关系,从而确定相关治疗靶点,以在整个生命周期中更好地保持肌肉功能。