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本文引用的文献

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Hypothalamic Sirt1 protects terminal Schwann cells and neuromuscular junctions from age-related morphological changes.下丘脑 Sirt1 可保护末端雪旺细胞和神经肌肉接头免受与年龄相关的形态变化。
Aging Cell. 2018 Aug;17(4):e12776. doi: 10.1111/acel.12776. Epub 2018 May 30.
2
Therapeutic electrical stimulation of injured peripheral nerve tissue using implantable thin-film wireless nerve stimulators.使用可植入薄膜无线神经刺激器对受伤的周围神经组织进行治疗性电刺激。
J Neurosurg. 2018 Feb 9;130(2):486-495. doi: 10.3171/2017.8.JNS163020. Print 2019 Feb 1.
3
The Scaffolding Protein, Grb2-associated Binder-1, in Skeletal Muscles and Terminal Schwann Cells Regulates Postnatal Neuromuscular Synapse Maturation.支架蛋白Grb2相关结合蛋白-1在骨骼肌和终末施万细胞中调节出生后神经肌肉突触成熟。
Exp Neurobiol. 2017 Jun;26(3):141-150. doi: 10.5607/en.2017.26.3.141. Epub 2017 Jun 16.
4
Inflammatory response during slow- and fast-twitch muscle regeneration.慢肌和快肌再生过程中的炎症反应。
Muscle Nerve. 2017 Mar;55(3):400-409. doi: 10.1002/mus.25246. Epub 2016 Nov 30.
5
The multicellular complexity of peripheral nerve regeneration.周围神经再生的细胞复杂性。
Curr Opin Neurobiol. 2016 Aug;39:38-46. doi: 10.1016/j.conb.2016.04.005. Epub 2016 Apr 26.
6
Serial assessment of functional recovery following nerve injury using implantable thin-film wireless nerve stimulators.使用植入式薄膜无线神经刺激器对神经损伤后的功能恢复进行连续评估。
Muscle Nerve. 2016 Dec;54(6):1114-1119. doi: 10.1002/mus.25153. Epub 2016 Oct 6.
7
Age-related fragmentation of the motor endplate is not associated with impaired neuromuscular transmission in the mouse diaphragm.与年龄相关的运动终板碎片化与小鼠膈肌神经肌肉传递受损无关。
Sci Rep. 2016 Apr 20;6:24849. doi: 10.1038/srep24849.
8
A robust neuromuscular system protects rat and human skeletal muscle from sarcopenia.一个强健的神经肌肉系统可保护大鼠和人类骨骼肌免受肌肉减少症的影响。
Aging (Albany NY). 2016 Apr;8(4):712-29. doi: 10.18632/aging.100926.
9
Neuregulin1 displayed on motor axons regulates terminal Schwann cell-mediated synapse elimination at developing neuromuscular junctions.运动轴突上显示的神经调节蛋白1在发育中的神经肌肉接头处调节终末施万细胞介导的突触消除。
Proc Natl Acad Sci U S A. 2016 Jan 26;113(4):E479-87. doi: 10.1073/pnas.1519156113. Epub 2016 Jan 11.
10
Macrophage-Induced Blood Vessels Guide Schwann Cell-Mediated Regeneration of Peripheral Nerves.巨噬细胞诱导的血管引导雪旺细胞介导的周围神经再生。
Cell. 2015 Aug 27;162(5):1127-39. doi: 10.1016/j.cell.2015.07.021. Epub 2015 Aug 13.

正常是什么?神经损伤后的神经肌肉接头再支配。

What is Normal? Neuromuscular junction reinnervation after nerve injury.

机构信息

Division of Plastic Surgery, Department of Surgery, Washington University School of Medicine, St Louis, Missouri.

Department of Neurosurgery, Washington University School of Medicine, St Louis, Missouri.

出版信息

Muscle Nerve. 2019 Nov;60(5):604-612. doi: 10.1002/mus.26654. Epub 2019 Aug 23.

DOI:10.1002/mus.26654
PMID:31408210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7092387/
Abstract

INTRODUCTION

In this study we present a reproducible technique to assess motor recovery after nerve injury via neuromuscular junction (NMJ) immunostaining and electrodiagnostic testing.

METHODS

Wild-type mice underwent sciatic nerve transection with repair. Hindlimb muscles were collected for microscopy up to 30 weeks after injury. Immunostaining was used to assess axons (NF200), Schwann cells (S100), and motor endplates (α-bungarotoxin). Compound motor action potential (CMAP) amplitude was used to assess tibialis anterior (TA) function.

RESULTS

One week after injury, nearly all (98.0%) endplates were denervated. At 8 weeks, endplates were either partially (28.3%) or fully (71.7%) reinnervated. At 16 weeks, NMJ reinnervation reached 87.3%. CMAP amplitude was 83% of naive mice at 16 weeks and correlated with percentage of fully reinnervated NMJs. Morphological differences were noted between injured and noninjured NMJs.

DISCUSSION

We present a reproducible method for evaluating NMJ reinnervation. Electrodiagnostic data summarize NMJ recovery. Characterization of wild-type reinnervation provides important data for consideration in experimental design and interpretation.

摘要

简介

本研究通过神经肌肉接头(NMJ)免疫染色和电诊断测试,提供了一种可重现的评估神经损伤后运动功能恢复的技术。

方法

野生型小鼠进行坐骨神经切断修复。损伤后 30 周内采集后肢肌肉进行显微镜检查。免疫染色用于评估轴突(NF200)、施万细胞(S100)和运动终板(α-银环蛇毒素)。使用复合运动动作电位(CMAP)幅度评估胫前肌(TA)功能。

结果

损伤后 1 周,几乎所有(98.0%)终板均失神经支配。8 周时,终板部分(28.3%)或完全(71.7%)再支配。16 周时,NMJ 再支配率达到 87.3%。16 周时,CMAP 幅度为正常小鼠的 83%,与完全再支配 NMJ 的百分比相关。损伤和未损伤 NMJ 之间存在形态差异。

讨论

我们提出了一种可重现的评估 NMJ 再支配的方法。电诊断数据总结了 NMJ 的恢复情况。野生型再支配的特征为实验设计和解释提供了重要数据。