Recurrent inhibition contribution to corticomuscular coherence modulation between contraction types

Abstract

Recent findings provided evidence that spinal regulatory mechanisms were involved in corticomuscular coherence (CMC) modulation between contraction types. Although their relative contributions could not be precisely identified, it was suggested that recurrent inhibition (RI) could modulate CMC by regulating the synchronization of spinal motoneuron activity. To confirm this hypothesis, concurrent modulations of RI and CMC for the soleus (SOL) were compared during submaximal isometric, shortening and lengthening plantar flexions. Submaximal contraction intensity was set at 50% of the maximal SOL EMG activity. CMC was computed in the time‐frequency domain between the Cz EEG electrode signal and the nonrectified SOL EMG signal. The RI was quantified through the paired Hoffmann (H) reflex technique by comparing the modulations of the test and conditioning H‐reflexes (H' and H1, respectively). Both beta‐band CMC and the ratio between H′ and H1 amplitudes were significantly lower in SOL during lengthening compared with isometric and shortening contractions. Furthermore, we observed a negative linear correlation between the RI and beta‐band CMC. Finally, a higher RI increase during lengthening contractions compared to either isometric or shortening ones was correlated with a larger decrease in CMC. Collectively, these novel findings provide robust evidence that the RI acts as a neural “filter” that contributes to the modulation of corticomuscular interactions between contraction types, possibly by disrupting the oscillatory muscle activation.