A single low-dimensional neural component of motor unit activity explains force generation across repetitive isometric tasks
Cabral, H. V.; Inglis, J. G.; Pourreza, E.; Dos Santos, M. A.; Cosentino, C.; O'Reilly, D.; Delis, I.; Negro, F.
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Previous studies suggest that low-dimensional control underlies motor unit activity, with low-frequency oscillations in common synaptic inputs serving as the primary determinant of muscle force production. In this study, we used principal component analysis (PCA) and factor analysis (FA) to investigate the relationship between low-dimensional motor unit components and force oscillations during repetitive isometric tasks with similar force profiles. We assessed the consistency of these components across trials in both individual (tibialis anterior; first dorsal interosseous) and synergistic muscles (vastus medialis, VM; vastus lateralis, VL). Participants performed 15 trials of a force-matching learning task. Three post-skill acquisition trials were selected for analysis to ensure high similarity in force profiles. Motor units were decomposed from high-density surface electromyograms, tracked across trials, and their smoothed discharge rates were decomposed into low-dimensional components using PCA and FA. Parallel analysis indicated that a single component could explain the smoothed discharge rates for the individual muscles and two components for VM-VL. Importantly, the first component explained most of the variance ([~]70%) in smoothed discharge rates across all muscles. The first motor unit component also showed significantly higher correlations with force oscillations than the second component and remained highly consistent across trials. These findings were further supported by a non-linear framework combining network- and information-theoretic tools, which revealed high motor unit network density in the first component of all muscles. Collectively, these results suggest that, during isometric contractions, motor unit activity is primarily controlled by a single dominant shared synaptic input that closely mirrors force oscillations.
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