Effects of blood flow restriction on motoneurons synchronization.

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neural Circuits Pub Date : 2025-05-01 eCollection Date: 2025-01-01 DOI:10.3389/fncir.2025.1561684
Mansour Taleshi, Franziska Bubeck, Leonardo Gizzi, Ivan Vujaklija
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Abstract

Blood flow restriction (BFR) is a peripheral intervention that induces transient and reversible physiological perturbations. While this intervention offers a unique model to explore neuromuscular responses in multiple contexts, its impact on neural input to motoneurons remains unclear. Here, the influence of BFR on muscle force control, behavior, and neural input to motoneurons during isometric-trapezoidal and isometric-sinusoidal little finger abduction precision tasks has been studied. Sixteen healthy participants performed the tasks under pre-BFR, during BFR, and at two post-BFR conditions. High-density surface electromyography (EMG) was recorded from the abductor digiti minimi muscle, and motor unit spike trains (MUST) were decomposed using blind source separation technique. Coherence between cumulative spike trains (CSTs) of identified motor units was calculated to assess common synaptic input in the delta and alpha frequency bands. As expected, during BFR application, participants reported higher level of discomfort and significant deterioration in force-tracking performance, as measured using root mean square error (RMSE). Following the BFR release, the level of discomfort, along with impaired neuromuscular performance were reduced to pre-BFR condition. Coherence analysis revealed a prominent peak in the alpha band. The mean z-score coherence in the alpha band showed a reduction of 27% for isometric-trapezoidal and 31% for isometric-sinusoidal conditions from pre-BFR to BFR, followed by a rebound post-BFR intervention with increases of 13% and 20%, respectively. In the delta band, coherence values were consistently higher during sinusoidal tasks compared to trapezoidal ones. These findings indicate that brief BFR application led to decrease in motoneuron synchronization and force control precision likely due to desensitization as shown by changes in coherence alpha band.

血流限制对运动神经元同步的影响。
血流限制(BFR)是一种外周干预,可引起短暂和可逆的生理扰动。虽然这种干预提供了一种独特的模型来探索多种情况下的神经肌肉反应,但其对运动神经元的神经输入的影响尚不清楚。本文研究了等距-梯形和等距-正弦小指外展精确任务中,BFR对肌肉力量控制、行为和运动神经元神经输入的影响。16名健康参与者在BFR前、BFR期间和两个BFR后条件下执行任务。采用盲源分离技术对小指外展肌的高密度表面肌电图(EMG)和运动单元尖峰序列(MUST)进行分解。计算已识别运动单元的累积尖峰序列(CSTs)之间的一致性,以评估δ和α频段的共同突触输入。正如预期的那样,在使用BFR期间,参与者报告了更高程度的不适,并且使用均方根误差(RMSE)测量了力跟踪性能的显着恶化。在BFR释放后,不适程度以及受损的神经肌肉功能降低到BFR前的状态。相干分析显示在α波段有一个显著的峰。alpha波段的平均z-score一致性显示,从BFR前到BFR前,等距-梯形条件降低了27%,等距-正弦条件降低了31%,BFR干预后出现反弹,分别增加了13%和20%。在delta波段,正弦任务的相干值始终高于梯形任务。这些发现表明,短时间使用BFR可能导致运动神经元同步和力控制精度下降,这可能是由于相干α带的变化所导致的脱敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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