Post-Movement Beta Synchronization Induced by Speed Effects IHI from Ipsilateral to Contralateral Motor Cortex.

IF 2.7 3区 医学 Q3 NEUROSCIENCES eNeuro Pub Date : 2025-03-11 DOI:10.1523/ENEURO.0370-24.2025
Xiangzi Zhang, Shengyao Zhang, Haoyuan Zhang, Houmin Wang, Jinyi Long
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Abstract

Beta event-related spectral perturbation (ERSP), including bilateral movement-related beta desynchronization (MRBD) and post-movement beta synchronization (PMBS), can be evoked by unilateral speed movement. A potential correlation might exist between power (de)synchronization and interhemispheric coherence during movement execution. However, during the PMBS phase, the existence of interhemispheric coupling and the effect of speed on it are largely undiscovered. This study aimed to answer this question. In the present study, we investigated eight healthy, right-handed volunteers using a combination of electroencephalography (EEG), transcranial magnetic stimulation (TMS), and electromyography (EMG). We explored interhemispheric (directed) coherence during isotonic right index finger abduction movements at two speeds: ballistic and self-paced. We discovered that: (i) Compared to the MRBD period, interhemispheric coherence was greater during the PMBS period. Furthermore, ballistic movement induced a larger coherence during the PMBS period, but not during the MRBD period. (ii) In the MRBD phase, directed coherence from the contralateral motor cortex (CM1) to the ipsilateral motor cortex (IM1) was larger, with a reverse tendency observed during the PMBS period. Additionally, in ballistic movement, directed coherence from IM1 to CM1 was stronger and positively correlated with coherence, with no effect of speed on directed coherence detected in the MRBD phase. To advance the understanding of neural mechanisms and the causality of interhemispheric coherence during the PMBS period, we investigated the interhemispheric inhibition (IHI) from IM1 to CM1 at different speeds. A stronger IHI from IM1 to CM1 at PMBS peak time was demonstrated, which was enhanced during ballistic movement. Additionally, IHI was negatively correlated with PMBS, and movement speed was positively associated with interhemispheric coupling during the PMBS period and IHI from IM1 to CM1.Significance Statement The present study explored interhemispheric (directed)coherence during isotonic right index finger abduction movements at two speeds: ballistic and self-paced. We discovered a dominance of interhemispheric coherence during the PMBS period of ballistic movement. Furthermore, directed coherence from the CM1 to the IM1 was more predominant in the MRBD phase, with a reverse tendency observed during the PMBS period. Additionally, directed coherence from IM1 to CM1 was stronger and positively correlated with coherence in ballistic movement. Advanced exploration revealed a stronger IHI from IM1 to CM1 at PMBS peak time, which was enhanced during ballistic movement. Additionally, IHI was negatively correlated with PMBS, and movement speed was positively associated with interhemispheric coupling during the PMBS period and IHI.

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同侧至对侧运动皮层速度效应诱导的运动后β同步。
单侧快速运动可诱发双侧运动相关β去同步(MRBD)和运动后β同步(PMBS)等β事件相关谱摄动(ERSP)。在运动执行过程中,力量(去)同步和半球间相干之间可能存在潜在的相关性。然而,在PMBS阶段,半球间耦合的存在以及速度对其的影响在很大程度上尚未被发现。本研究旨在回答这个问题。在本研究中,我们使用脑电图(EEG)、经颅磁刺激(TMS)和肌电图(EMG)相结合的方法调查了8名健康的右撇子志愿者。我们在两种速度下探索了右食指外展运动的半球间(定向)一致性:弹道速度和自定速度。我们发现:(i)与MRBD期相比,PMBS期的半球间相干性更强。此外,弹道运动在PMBS期间引起了更大的相干性,而在MRBD期间则没有。(ii)在MRBD阶段,从对侧运动皮质(CM1)到同侧运动皮质(IM1)的定向相干性更大,在PMBS期间观察到相反的趋势。此外,在弹道运动中,从IM1到CM1的定向相干性更强,且与相干性呈正相关,而在MRBD阶段,速度对定向相干性没有影响。为了进一步了解PMBS期间脑间相干性的神经机制和因果关系,我们研究了不同速度下IM1到CM1的脑间抑制(IHI)。在PMBS峰值时间,从IM1到CM1的IHI更强,在弹道运动过程中增强。此外,IHI与PMBS呈负相关,运动速度与PMBS期间的半球间耦合和IM1到CM1的IHI呈正相关。本研究探讨了两种速度下右食指外展运动的半球间(定向)一致性:弹道速度和自定速度。我们发现在弹道运动的PMBS期间,半球间相干性占主导地位。此外,从CM1到IM1的定向相干性在MRBD阶段更为突出,在PMBS期间观察到相反的趋势。此外,从IM1到CM1的定向相干性更强,与弹道运动的相干性呈正相关。超前探测发现,PMBS峰值时IM1 - CM1的IHI较强,在弹道运动期间IHI增强。此外,IHI与PMBS呈负相关,运动速度与PMBS期间的半球间耦合和IHI呈正相关。
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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.
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