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老年骨骼肌无力:潜在机制

Skeletal muscle weakness in old age: underlying mechanisms.

作者信息

Brooks S V, Faulkner J A

机构信息

Institute of Gerontology, University of Michigan, Ann Arbor 48109-2007.

出版信息

Med Sci Sports Exerc. 1994 Apr;26(4):432-9.

PMID:8201898
Abstract

Maintenance of muscle mass and strength contributes to mobility which impacts on quality of life. Although muscle atrophy, declining strength, and physical frailty are generally accepted as inevitable concomitants of aging, the causes are unknown. Clarification of the mechanisms responsible for these changes would enhance our understanding of the degree to which they are preventable or treatable. The decline in muscle function between maturity and old age is similar for muscles of many different animals including human beings, and is typified by the decreases of approximately 35% in maximum force, approximately 30% in maximum power, and 20% in normalized force (kN.m-2) and power (W.kg-1) of extensor digitorum longus (EDL) muscles in old compared with adult mice. Much of the age-associated muscle atrophy and declining strength may be explained by motor unit remodeling which appears to occur by selective denervation of muscle fibers with reinnervation by axonal sprouting from an adjacent innervated unit. Muscles in old mice appear more susceptible to injury than muscles in young or adult mice and have a decreased capacity for recovery. The process of age-related denervation may be aggravated by an increased susceptibility of muscles in old animals to contraction-induced injury coupled with impaired capacity for regeneration.

摘要

维持肌肉质量和力量有助于保持身体活动能力,而这会对生活质量产生影响。虽然肌肉萎缩、力量下降和身体虚弱通常被认为是衰老不可避免的伴随现象,但其原因尚不清楚。阐明导致这些变化的机制将增进我们对它们在多大程度上可预防或可治疗的理解。包括人类在内的许多不同动物的肌肉,从成熟到老年的功能下降情况相似,其典型表现是,与成年小鼠相比,老年小鼠的趾长伸肌(EDL)最大力量下降约35%,最大功率下降约30%,归一化力量(kN.m-2)和功率(W.kg-1)下降20%。许多与年龄相关的肌肉萎缩和力量下降可能是由运动单位重塑来解释的,运动单位重塑似乎是通过对肌纤维进行选择性去神经支配,并由相邻受神经支配单位的轴突发芽进行再支配而发生的。老年小鼠的肌肉似乎比幼年或成年小鼠的肌肉更容易受伤,且恢复能力下降。老年动物的肌肉对收缩诱导损伤的易感性增加,同时再生能力受损,这可能会加剧与年龄相关的去神经支配过程。

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