Mansour Taleshi, Franziska Bubeck, Leonardo Gizzi, Ivan Vujaklija
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引用次数: 0
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.
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.