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本文引用的文献

1
Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice.自愿转轮运动伴有或不伴有卵泡抑素过表达可改善 C57BL/6J 小鼠老年期的 NMJ 传递,但不能减少运动单位丧失。
Neurobiol Aging. 2021 May;101:285-296. doi: 10.1016/j.neurobiolaging.2021.01.012. Epub 2021 Feb 5.
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Impairment Mechanisms and Intervention Approaches for Aged Human Neuromuscular Junctions.老年人神经肌肉接头的损伤机制与干预方法
Front Mol Neurosci. 2020 Nov 16;13:568426. doi: 10.3389/fnmol.2020.568426. eCollection 2020.
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The TOR Pathway at the Neuromuscular Junction: More Than a Metabolic Player?神经肌肉接头处的TOR信号通路:仅是一个代谢参与者吗?
Front Mol Neurosci. 2020 Aug 28;13:162. doi: 10.3389/fnmol.2020.00162. eCollection 2020.
4
Putative Cut-Points in Sarcopenia Components and Incident Adverse Health Outcomes: An SDOC Analysis.疑似肌少症成分的切点与不良健康结局的发生:SDOC 分析。
J Am Geriatr Soc. 2020 Jul;68(7):1429-1437. doi: 10.1111/jgs.16517. Epub 2020 Jul 7.
5
Rodent Model of Muscular Atrophy for Sarcopenia Study.用于少肌症研究的肌肉萎缩啮齿动物模型。
J Bone Metab. 2020 May;27(2):97-110. doi: 10.11005/jbm.2020.27.2.97. Epub 2020 May 31.
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Maintaining Muscle Function Across the Lifespan: The State of Science.维持整个生命周期中的肌肉功能:科学现状。
Am J Phys Med Rehabil. 2020 Dec;99(12):1171-1176. doi: 10.1097/PHM.0000000000001429.
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Sarcopenia Definition: The Position Statements of the Sarcopenia Definition and Outcomes Consortium.肌肉减少症定义:肌肉减少症定义和结局共识联盟的立场声明。
J Am Geriatr Soc. 2020 Jul;68(7):1410-1418. doi: 10.1111/jgs.16372. Epub 2020 Mar 9.
8
Neuromuscular junction transmission failure is a late phenotype in aging mice.神经肌肉接头传递失败是衰老小鼠的晚期表型。
Neurobiol Aging. 2020 Feb;86:182-190. doi: 10.1016/j.neurobiolaging.2019.10.022. Epub 2019 Nov 5.
9
Nutrition and Muscle Strength, As the Key Component of Sarcopenia: An Overview of Current Evidence.营养与肌肉力量:肌少症的关键组成部分——当前证据概述。
Nutrients. 2019 Dec 3;11(12):2942. doi: 10.3390/nu11122942.
10
Sex differences in body composition but not neuromuscular function following long-term, doxycycline-induced reduction in circulating levels of myostatin in mice.长期使用强力霉素降低循环中肌肉生长抑制素水平后,小鼠的身体成分存在性别差异,但神经肌肉功能没有差异。
PLoS One. 2019 Nov 21;14(11):e0225283. doi: 10.1371/journal.pone.0225283. eCollection 2019.

剖析与年龄相关的肌肉无力和萎缩:神经肌肉接头传递作为与年龄相关身体机能衰退的驱动因素。

Profiling age-related muscle weakness and wasting: neuromuscular junction transmission as a driver of age-related physical decline.

作者信息

Padilla Carlos J, Harrigan Markus E, Harris Hallie, Schwab Jan M, Rutkove Seward B, Rich Mark M, Clark Brian C, Arnold W David

机构信息

Division of Neuromuscular Diseases, Department of Neurology, The Ohio State University Wexner Medical Center, 1060 Carmack Road, Room 207, Columbus, OH, 43210, USA.

Belford Center for Spinal Cord Injury, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

出版信息

Geroscience. 2021 Jun;43(3):1265-1281. doi: 10.1007/s11357-021-00369-3. Epub 2021 Apr 24.

DOI:10.1007/s11357-021-00369-3
PMID:33895959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8190265/
Abstract

Pathological age-related loss of skeletal muscle strength and mass contribute to impaired physical function in older adults. Factors that promote the development of these conditions remain incompletely understood, impeding development of effective and specific diagnostic and therapeutic approaches. Inconclusive evidence across species suggests disruption of action potential signal transmission at the neuromuscular junction (NMJ), the crucial connection between the nervous and muscular systems, as a possible contributor to age-related muscle dysfunction. Here we investigated age-related loss of NMJ function using clinically relevant, electrophysiological measures (single-fiber electromyography (SFEMG) and repetitive nerve stimulation (RNS)) in aged (26 months) versus young (6 months) F344 rats. Measures of muscle function (e.g., grip strength, peak plantarflexion contractility torque) and mass were assessed for correlations with physiological measures (e.g., indices of NMJ transmission). Other outcomes also included plantarflexion muscle contractility tetanic torque fade during 1-s trains of stimulation as well as gastrocnemius motor unit size and number. Profiling NMJ function in aged rats identified significant declines in NMJ transmission stability and reliability. Further, NMJ deficits were tightly correlated with hindlimb grip strength, gastrocnemius muscle weight, loss of peak contractility torque, degree of tetanic fade, and motor unit loss. Thus, these findings provide direct evidence for NMJ dysfunction as a potential mechanism of age-related muscle dysfunction pathogenesis and severity. These findings also suggest that NMJ transmission modulation may serve as a target for therapeutic development for age-related loss of physical function.

摘要

与年龄相关的骨骼肌力量和质量的病理性丧失会导致老年人身体功能受损。促进这些状况发展的因素仍未完全明确,这阻碍了有效且特异性的诊断和治疗方法的开发。跨物种的不确定证据表明,神经肌肉接头(NMJ)处动作电位信号传递的破坏,即神经和肌肉系统之间的关键连接,可能是与年龄相关的肌肉功能障碍的一个促成因素。在这里,我们使用临床相关的电生理测量方法(单纤维肌电图(SFEMG)和重复神经刺激(RNS)),在老年(26个月)与年轻(6个月)的F344大鼠中研究了与年龄相关的NMJ功能丧失。评估肌肉功能(如握力、足底屈曲峰值收缩扭矩)和质量的测量值与生理测量值(如NMJ传递指标)之间的相关性。其他结果还包括在1秒刺激序列中足底屈曲肌肉收缩强直扭矩的衰减,以及腓肠肌运动单位的大小和数量。对老年大鼠的NMJ功能进行分析发现,NMJ传递的稳定性和可靠性显著下降。此外,NMJ缺陷与后肢握力、腓肠肌重量、峰值收缩扭矩丧失、强直衰减程度和运动单位丧失密切相关。因此,这些发现为NMJ功能障碍作为与年龄相关的肌肉功能障碍发病机制和严重程度的潜在机制提供了直接证据。这些发现还表明,NMJ传递调节可能作为与年龄相关的身体功能丧失的治疗开发靶点。