Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA; Department of Internal Medicine, The Neuroscience Program, Wake Forest School of Medicine, Winston-Salem, NC, USA; Department of Internal Medicine, The Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, USA; Department of Internal Medicine, The Sticht Center for Healthy Aging and Alzheimer's Prevention, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA; Department of Internal Medicine, The Sticht Center for Healthy Aging and Alzheimer's Prevention, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Ageing Res Rev. 2021 May;67:101305. doi: 10.1016/j.arr.2021.101305. Epub 2021 Feb 18.
Examining neural etiologic factors'role in the decline of neuromuscular function with aging is essential to our understanding of the mechanisms underlying sarcopenia, the age-dependent decline in muscle mass, force and power. Innervation of the skeletal muscle by both motor and sympathetic axons has been established, igniting interest in determining how the sympathetic nervous system (SNS) affect skeletal muscle composition and function throughout the lifetime. Selective expression of the heart and neural crest derivative 2 gene in peripheral SNs increases muscle mass and force regulating skeletal muscle sympathetic and motor innervation; improving acetylcholine receptor stability and NMJ transmission; preventing inflammation and myofibrillar protein degradation; increasing autophagy; and probably enhancing protein synthesis. Elucidating the role of central SNs will help to define the coordinated response of the visceral and neuromuscular system to physiological and pathological challenges across ages. This review discusses the following questions: (1) Does the SNS regulate skeletal muscle motor innervation? (2) Does the SNS regulate presynaptic and postsynaptic neuromuscular junction (NMJ) structure and function? (3) Does sympathetic neuron (SN) regulation of NMJ transmission decline with aging? (4) Does maintenance of SNs attenuate aging sarcopenia? and (5) Do central SN group relays influence sympathetic and motor muscle innervation?
研究神经病因因素在衰老过程中神经肌肉功能下降中的作用,对于理解导致肌肉减少症(随年龄增长而发生的肌肉质量、力量和功能下降)的机制至关重要。运动和交感神经轴突都支配骨骼肌,这激发了人们对确定交感神经系统(SNS)如何影响骨骼肌组成和功能的兴趣。心脏和神经嵴衍生 2 基因在外周 SNs 中的选择性表达增加了肌肉质量和力量,调节骨骼肌的交感神经和运动神经支配;提高乙酰胆碱受体稳定性和 NMJ 传递;预防炎症和肌原纤维蛋白降解;增加自噬;并可能增强蛋白质合成。阐明中枢 SNs 的作用将有助于确定内脏和神经肌肉系统对不同年龄生理和病理挑战的协调反应。本综述讨论了以下问题:(1)SNS 是否调节骨骼肌运动神经支配?(2)SNS 是否调节突触前和突触后神经肌肉接头(NMJ)结构和功能?(3)SN 对 NMJ 传递的调节是否随年龄增长而下降?(4)SNs 的维持是否能减轻衰老性肌肉减少症?以及(5)中枢 SN 群传递是否影响交感神经和运动肌肉支配?