Neural Filtering of Physiological Tremor Oscillations to Spinal Motor Neurons Mediates Short-Term Acquisition of a Skill Learning Task.

IF 2.7 3区 医学 Q3 NEUROSCIENCES
eNeuro Pub Date : 2024-07-17 Print Date: 2024-07-01 DOI:10.1523/ENEURO.0043-24.2024
Hélio V Cabral, Alessandro Cudicio, Alberto Bonardi, Alessandro Del Vecchio, Luca Falciati, Claudio Orizio, Eduardo Martinez-Valdes, Francesco Negro
{"title":"Neural Filtering of Physiological Tremor Oscillations to Spinal Motor Neurons Mediates Short-Term Acquisition of a Skill Learning Task.","authors":"Hélio V Cabral, Alessandro Cudicio, Alberto Bonardi, Alessandro Del Vecchio, Luca Falciati, Claudio Orizio, Eduardo Martinez-Valdes, Francesco Negro","doi":"10.1523/ENEURO.0043-24.2024","DOIUrl":null,"url":null,"abstract":"<p><p>The acquisition of a motor skill involves adaptations of spinal and supraspinal pathways to alpha motoneurons. In this study, we estimated the shared synaptic contributions of these pathways to understand the neural mechanisms underlying the short-term acquisition of a new force-matching task. High-density surface electromyography (HDsEMG) was acquired from the first dorsal interosseous (FDI; 7 males and 6 females) and tibialis anterior (TA; 7 males and 4 females) during 15 trials of an isometric force-matching task. For two selected trials (pre- and post-skill acquisition), we decomposed the HDsEMG into motor unit spike trains, tracked motor units between trials, and calculated the mean discharge rate and the coefficient of variation of interspike interval (COV<sub>ISI</sub>). We also quantified the post/pre ratio of motor units' coherence within delta, alpha, and beta bands. Force-matching improvements were accompanied by increased mean discharge rate and decreased COV<sub>ISI</sub> for both muscles. Moreover, the area under the curve within alpha band decreased by ∼22% (TA) and ∼13% (FDI), with no delta or beta bands changes. These reductions correlated significantly with increased coupling between force/neural drive and target oscillations. These results suggest that short-term force-matching skill acquisition is mediated by attenuation of physiological tremor oscillations in the shared synaptic inputs. Supported by simulations, a plausible mechanism for alpha band reductions may involve spinal interneuron phase-cancelling descending oscillations. Therefore, during skill learning, the central nervous system acts as a matched filter, adjusting synaptic weights of shared inputs to suppress neural components unrelated to the specific task.</p>","PeriodicalId":11617,"journal":{"name":"eNeuro","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11255391/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"eNeuro","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1523/ENEURO.0043-24.2024","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/1 0:00:00","PubModel":"Print","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

The acquisition of a motor skill involves adaptations of spinal and supraspinal pathways to alpha motoneurons. In this study, we estimated the shared synaptic contributions of these pathways to understand the neural mechanisms underlying the short-term acquisition of a new force-matching task. High-density surface electromyography (HDsEMG) was acquired from the first dorsal interosseous (FDI; 7 males and 6 females) and tibialis anterior (TA; 7 males and 4 females) during 15 trials of an isometric force-matching task. For two selected trials (pre- and post-skill acquisition), we decomposed the HDsEMG into motor unit spike trains, tracked motor units between trials, and calculated the mean discharge rate and the coefficient of variation of interspike interval (COVISI). We also quantified the post/pre ratio of motor units' coherence within delta, alpha, and beta bands. Force-matching improvements were accompanied by increased mean discharge rate and decreased COVISI for both muscles. Moreover, the area under the curve within alpha band decreased by ∼22% (TA) and ∼13% (FDI), with no delta or beta bands changes. These reductions correlated significantly with increased coupling between force/neural drive and target oscillations. These results suggest that short-term force-matching skill acquisition is mediated by attenuation of physiological tremor oscillations in the shared synaptic inputs. Supported by simulations, a plausible mechanism for alpha band reductions may involve spinal interneuron phase-cancelling descending oscillations. Therefore, during skill learning, the central nervous system acts as a matched filter, adjusting synaptic weights of shared inputs to suppress neural components unrelated to the specific task.

脊髓运动神经元对生理震颤振荡的神经过滤介导了技能学习任务的短期习得。
运动技能的习得涉及脊髓和脊髓上通路对α运动神经元的适应。在本研究中,我们估算了这些通路的共享突触贡献,以了解短期内获得新的力量匹配任务的神经机制。在进行 15 次等长力匹配任务时,我们从第一背侧骨间肌(FDI,7 名男性和 6 名女性)和胫骨前肌(TA,7 名男性和 4 名女性)采集了高密度表面肌电图(HDsEMG)。在选定的两次试验中(技能学习前和技能学习后),我们将 HDsEMG 分解为运动单位尖峰序列,在试验之间跟踪运动单位,并计算平均放电率和尖峰间期变异系数(CoVISI)。我们还量化了德尔塔、阿尔法和贝塔波段内运动单元相干性的后/前比率。两块肌肉的力匹配改善伴随着平均放电率的提高和 CoVISI 的降低。此外,α波段的曲线下面积减少了22%(TA)和13%(FDI),而δ或β波段没有变化。这些减少与力/神经驱动和目标振荡之间的耦合增加有显著关联。这些结果表明,短期力匹配技能的习得是由共享突触输入中生理震颤振荡的衰减介导的。在模拟的支持下,α波段减弱的一个合理机制可能涉及脊髓中间神经元相消降序振荡。因此,在技能学习过程中,中枢神经系统就像一个匹配滤波器,调整共享输入的突触权重,以抑制与特定任务无关的神经成分。 重要意义 前人的研究认为,只有运动神经元共享突触输入的低频振荡,包括与任务相关和任务无关的振荡,才是产生肌肉力量的原因。在我们的研究中,我们探讨了习得一项涉及精确发力的新运动任务是否需要这些共享突触输入的特定改变。我们的研究结果表明,对于手部肌肉和腿部肌肉来说,技能的掌握是由与所需的力量波动(即生理震颤带振荡)无关的共享突触振荡的减少所介导的。因此,在力量匹配任务学习过程中,中枢神经系统就像一个神经过滤器,调节共享输入的突触权重,以减弱与特定任务无关的神经成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信