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电生理运动单位数量估计(MUNE):测量小鼠后肢肌肉的复合肌肉动作电位(CMAP)

Electrophysiological Motor Unit Number Estimation (MUNE) Measuring Compound Muscle Action Potential (CMAP) in Mouse Hindlimb Muscles.

作者信息

Arnold W David, Sheth Kajri A, Wier Christopher G, Kissel John T, Burghes Arthur H, Kolb Stephen J

机构信息

Department of Neurology, The Ohio State University Wexner Medical Center; Department of Physical Medicine and Rehabilitation, The Ohio State University; Department of Neuroscience, The Ohio State University Wexner Medical Center;

Department of Neurology, The Ohio State University Wexner Medical Center.

出版信息

J Vis Exp. 2015 Sep 25(103):52899. doi: 10.3791/52899.

DOI:10.3791/52899
PMID:26436455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4676269/
Abstract

Compound muscle action potential (CMAP) and motor unit number estimation (MUNE) are electrophysiological techniques that can be used to monitor the functional status of a motor unit pool in vivo. These measures can provide insight into the normal development and degeneration of the neuromuscular system. These measures have clear translational potential because they are routinely applied in diagnostic and clinical human studies. We present electrophysiological techniques similar to those employed in humans to allow recordings of mouse sciatic nerve function. The CMAP response represents the electrophysiological output from a muscle or group of muscles following supramaximal stimulation of a peripheral nerve. MUNE is an electrophysiological technique that is based on modifications of the CMAP response. MUNE is a calculated value that represents the estimated number of motor neurons or axons (motor control input) supplying the muscle or group of muscles being tested. We present methods for recording CMAP responses from the proximal leg muscles using surface recording electrodes following the stimulation of the sciatic nerve in mice. An incremental MUNE technique is described using submaximal stimuli to determine the average single motor unit potential (SMUP) size. MUNE is calculated by dividing the CMAP amplitude (peak-to-peak) by the SMUP amplitude (peak-to-peak). These electrophysiological techniques allow repeated measures in both neonatal and adult mice in such a manner that facilitates rapid analysis and data collection while reducing the number of animals required for experimental testing. Furthermore, these measures are similar to those recorded in human studies allowing more direct comparisons.

摘要

复合肌肉动作电位(CMAP)和运动单位数量估计(MUNE)是可用于在体内监测运动单位池功能状态的电生理技术。这些测量方法能够深入了解神经肌肉系统的正常发育和退化情况。由于它们在人类诊断和临床研究中常规应用,所以这些测量方法具有明确的转化潜力。我们介绍了与人类所采用的类似的电生理技术,以便记录小鼠坐骨神经功能。CMAP反应代表在对周围神经进行超强刺激后,一块肌肉或一组肌肉的电生理输出。MUNE是一种基于CMAP反应改良的电生理技术。MUNE是一个计算值,代表供应受试肌肉或一组肌肉的运动神经元或轴突(运动控制输入)的估计数量。我们介绍了在小鼠坐骨神经受到刺激后,使用表面记录电极记录近端腿部肌肉CMAP反应的方法。描述了一种递增式MUNE技术,该技术使用次最大刺激来确定平均单个运动单位电位(SMUP)大小。MUNE通过将CMAP幅度(峰峰值)除以SMUP幅度(峰峰值)来计算。这些电生理技术允许在新生小鼠和成年小鼠中进行重复测量,其方式便于快速分析和数据收集,同时减少实验测试所需的动物数量。此外,这些测量结果与人类研究中记录的结果相似,从而能够进行更直接的比较。

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1
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PLoS One. 2014 Oct 27;9(10):e111428. doi: 10.1371/journal.pone.0111428. eCollection 2014.
2
Spinal muscular atrophy: diagnosis and management in a new therapeutic era.脊髓性肌萎缩症:新治疗时代的诊断与管理
Muscle Nerve. 2015 Feb;51(2):157-67. doi: 10.1002/mus.24497. Epub 2014 Dec 16.
3
Motor unit number estimation: a technology and literature review.
电信号与化学信号协同作用以及可生物降解支架在大鼠坐骨神经缺损修复中的应用
Bioact Mater. 2025 Mar 26;49:586-607. doi: 10.1016/j.bioactmat.2025.03.017. eCollection 2025 Jul.
4
Targeting senescence in Amyotrophic Lateral Sclerosis: senolytic treatment improves neuromuscular function and preserves cortical excitability in a TDP-43 mouse model.靶向肌萎缩侧索硬化症中的衰老:衰老细胞溶解疗法改善了TDP-43小鼠模型的神经肌肉功能并保留了皮质兴奋性
Res Sq. 2025 Mar 26:rs.3.rs-6081213. doi: 10.21203/rs.3.rs-6081213/v1.
5
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bioRxiv. 2025 Feb 6:2025.02.02.636117. doi: 10.1101/2025.02.02.636117.
6
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J Neurosci. 2025 Apr 9;45(15):e1279232025. doi: 10.1523/JNEUROSCI.1279-23.2025.
7
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8
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Bioengineering (Basel). 2024 Sep 10;11(9):904. doi: 10.3390/bioengineering11090904.
10
Neuromuscular junction dysfunction in Lafora disease.拉佛拉病中的神经肌肉接头功能障碍。
Dis Model Mech. 2024 Oct 1;17(10). doi: 10.1242/dmm.050905. Epub 2024 Oct 14.
运动单位数量估计:技术与文献综述
Muscle Nerve. 2014 Dec;50(6):884-93. doi: 10.1002/mus.24442.
4
VIP-expressing dendritic cells protect against spontaneous autoimmune peripheral polyneuropathy.表达血管活性肠肽的树突状细胞可预防自发性自身免疫性周围性多神经病。
Mol Ther. 2014 Jul;22(7):1353-1363. doi: 10.1038/mt.2014.77. Epub 2014 Apr 25.
5
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Ann Clin Transl Neurol. 2014 Jan 1;1(1):34-44. doi: 10.1002/acn3.23.
6
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7
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8
Electrophysiological and motor function scale association in a pre-symptomatic infant with spinal muscular atrophy type I.电生理和运动功能量表在无症状脊髓性肌萎缩症 I 型婴儿中的关联。
Neuromuscul Disord. 2013 Feb;23(2):112-5. doi: 10.1016/j.nmd.2012.09.006. Epub 2012 Nov 10.
9
Prospective cohort study of spinal muscular atrophy types 2 and 3.2 型和 3 型脊髓性肌萎缩症的前瞻性队列研究。
Neurology. 2012 Oct 30;79(18):1889-97. doi: 10.1212/WNL.0b013e318271f7e4. Epub 2012 Oct 17.
10
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Chin Med J (Engl). 2012 May;125(10):1760-6.