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  4. Blood flow restriction modulates common drive to motor units and force precision
 
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Blood flow restriction modulates common drive to motor units and force precision

Other Title
implications for neuromuscular coordination
Journal
European Journal of Applied Physiology
Date Issued
2026-02-01
Author(s)
YI-CHING CHEN  
DOI
10.1007/s00421-025-05974-0
URI
https://www.scopus.com/pages/publications/105016586420
https://scholars.csmu.edu.tw/handle/123456789/24404
Abstract
Purpose: Blood flow restriction (BFR) is a resistance training technique that enhances muscle adaptation and strength gains under hypoxic conditions. However, its impact on motor unit (MU) coordination remains unclear. This study investigated how BFR influences intra- and inter-muscular common drives to MUs in two functional agonists during a static precision pinch task. Methods: Eighteen adults (23.9 ± 1.3 years; nine men, nine women) performed a thumb–index finger precision pinch under BFR and non-BFR conditions, while force fluctuation dynamics and MU activities in the flexor pollicis brevis (FPB) and first dorsal interosseous (FDI) were analyzed. Results: The results revealed a significant reduction in maximal voluntary contraction following BFR application (p = 0.003). In addition, BFR significantly increased force fluctuations (p = 0.007), potentiated discharge variability (p = 0.018), and strengthened force–discharge coupling specifically in the FPB (p = 0.010). BFR increased the mean recruitment threshold of motor units in the FDI (p < 0.001), but not in the FPB (p > 0.05) during finger precision pinch. Intra-muscular common drive increased within the FDI (p < 0.001) and FPB (p < 0.001), whereas inter-muscular common drive between agonist MUs decreased (p < 0.001). Conclusion: BFR application disrupts force precision stability and neuromuscular coordination between functional agonists during precision pinch. It increases global discharge variability and intra-muscular MU synchrony. However, the resulting force fluctuations are only partially compensated by reduced inter-muscular MU synchrony, offering limited coordination flexibility among agonists.
Type
journal article
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