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在肌萎缩侧索硬化症中找出进行性的PIC改变。

PICking out progressive PIC alterations in amyotrophic lateral sclerosis.

作者信息

Deutsch Andrew J

机构信息

Department of Biomedical, Industrial, and Human Factors Engineering, College of Engineering and Computer ScienceWright State UniversityDaytonOhioUnited States.

出版信息

J Neurophysiol. 2024 May 1;131(5):822-824. doi: 10.1152/jn.00482.2023. Epub 2024 Mar 27.

DOI:10.1152/jn.00482.2023
PMID:38533934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11383380/
Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that causes motoneuron death. Alterations to motoneuron excitability in ALS are suspected to contribute to motoneuron degeneration. Therefore, mechanisms underlying changes in motoneuron excitability are being thoroughly investigated. A recent publication from Trajano et al. (Trajano GS, Orssatto LB, McCombe PA, Rivlin W, Tang L, Henderson RD. 601: 4723-4735, 2023) examined temporal changes to persistent inward currents (PICs) in ALS patients. They show that delta frequency (ΔF, an estimate of PICs) has opposite temporal trends in stronger and weaker muscles of ALS patients. This study is very important to aid in the understanding of disease mechanisms. This Neuro Forum article explores some important considerations for interpreting the results of this study, including treatment effects, potential sex differences, and a lack of comparison to healthy individuals.

摘要

肌萎缩侧索硬化症(ALS)是一种导致运动神经元死亡的致命性神经退行性疾病。ALS中运动神经元兴奋性的改变被怀疑与运动神经元变性有关。因此,正在深入研究运动神经元兴奋性变化的潜在机制。特拉贾诺等人最近发表的一篇文章(特拉贾诺GS、奥尔萨托LB、麦科姆PA、里夫林W、唐L、亨德森RD。601:4723 - 4735,2023)研究了ALS患者持续性内向电流(PICs)的时间变化。他们发现,δ频率(ΔF,PICs的一种估计值)在ALS患者较强和较弱的肌肉中呈现相反的时间趋势。这项研究对于帮助理解疾病机制非常重要。这篇神经论坛文章探讨了一些解释这项研究结果的重要注意事项,包括治疗效果、潜在的性别差异以及缺乏与健康个体的比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/367b/11383380/7a907a2a1d2e/jn-00482-2023r01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/367b/11383380/7a907a2a1d2e/jn-00482-2023r01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/367b/11383380/7a907a2a1d2e/jn-00482-2023r01.jpg

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引用本文的文献

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本文引用的文献

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J Physiol. 2023 Nov;601(21):4723-4735. doi: 10.1113/JP285181. Epub 2023 Sep 28.
2
Estimates of persistent inward currents in lower limb motoneurons are larger in females than in males.下肢运动神经元中持续内向电流的估计值在女性中大于男性。
J Neurophysiol. 2023 Jun 1;129(6):1322-1333. doi: 10.1152/jn.00043.2023. Epub 2023 Apr 25.
3
Motoneuron excitability dysfunction in ALS: Pseudo-mystery or authentic conundrum?
肌萎缩侧索硬化症中的运动神经元兴奋性障碍:似是而非的谜团还是真正的难题?
J Physiol. 2022 Nov;600(22):4815-4825. doi: 10.1113/JP283630. Epub 2022 Oct 19.
4
Time Course of Alterations in Adult Spinal Motoneuron Properties in the SOD1(G93A) Mouse Model of ALS.肌萎缩侧索硬化症 SOD1(G93A)小鼠模型中成年脊髓运动神经元特性改变的时间进程。
eNeuro. 2021 Mar 22;8(2). doi: 10.1523/ENEURO.0378-20.2021. Print 2021 Mar-Apr.
5
Spinal motoneurones are intrinsically more responsive in the adult G93A SOD1 mouse model of amyotrophic lateral sclerosis.成年 G93A SOD1 肌萎缩侧索硬化症小鼠模型中的脊髓运动神经元内在地更敏感。
J Physiol. 2020 Oct;598(19):4385-4403. doi: 10.1113/JP280097. Epub 2020 Sep 4.
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Neuroscience. 2017 Oct 24;362:33-46. doi: 10.1016/j.neuroscience.2017.08.041. Epub 2017 Aug 24.
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C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis.C9orf72 扩增对以脊髓起病的肌萎缩侧索硬化症男性的影响存在差异。
J Neurol Neurosurg Psychiatry. 2017 Apr;88(4):281. doi: 10.1136/jnnp-2016-314093. Epub 2016 Sep 23.
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