Mind over muscle? Time manipulation improves physical performance by slowing down the neuromuscular fatigue accumulation.

While physical performance has long been thought to be limited only by physiological factors, many experiments denote that psychological ones can also influence it. Specifically, the deception paradigm investigates the effect of psychological factors on performance by manipulating a psychological variable unbeknownst to the subjects. For example, during a physical exercise performed to failure, previous results revealed an improvement in performance (i.e., holding time) when the clock shown to the subjects was deceptively slowed down. However, the underlying neurophysiological changes supporting this performance improvement due to deceptive time manipulation remain unknown. Here, we addressed this issue by investigating from a neuromuscular perspective the effect of a deceptive clock manipulation on a single-joint isometric task conducted to failure in 24 healthy participants (11 females). Neuromuscular fatigue was assessed by pre- to post-exercise changes in quadriceps maximal voluntary torque (Tmax ), voluntary activation level (VAL), and potentiated twitch (TTW ). Our main results indicated a significant performance improvement when the clock was slowed down (Biased: 356 ± 118 s vs. Normal: 332 ± 112 s, p = .036) but, surprisingly, without any difference in the associated neuromuscular fatigue (p > .05 and BF < 0.3 for Tmax , VAL, and TTW between both sessions). Computational modeling showed that, when observed, the holding time improvement was explained by a neuromuscular fatigue accumulation based on subjective rather than actual time. These results support a psychological influence on neuromuscular processes and contribute significantly to the literature on the mind-body influence, by challenging our understanding of fatigue.

Recurrent inhibition contribution to corticomuscular coherence modulation between contraction types.

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.

Combined effect of contraction type and intensity on corticomuscular coherence during isokinetic plantar flexions.

During isometric contractions, corticomuscular coherence (CMC) may be modulated along with the contraction intensity. Furthermore, CMC may also vary between contraction types due to the contribution of spinal inhibitory mechanisms. However, the interaction between the effect of the contraction intensity and of the contraction type on CMC remains hitherto unknown. Therefore, CMC and spinal excitability modulations were compared during submaximal isometric, shortening and lengthening contractions of plantar flexor muscles at 25, 50, and 70% of the maximal soleus (SOL) EMG activity. CMC was computed in the time-frequency domain between the Cz EEG electrode signal and the SOL or medial gastrocnemius (MG) EMG signals. The results indicated that beta-band CMC was decreased in the SOL only between 25 and 50-70% contractions for both isometric and anisometric contractions, but remained similar for all contraction intensities in the MG. Spinal excitability was similar for all contraction intensities in both muscles. Meanwhile a divergence of the EEG and the EMG signals mean frequency was observed only in the SOL and only between 25 and 50-70% contractions, independently from the contraction type. Collectively, these findings confirm an effect of the contraction intensity on beta-band CMC, although it was only measured in the SOL, between low-level and high-level contraction intensities. Furthermore, the current findings provide new evidence that the observed modulations of beta-band CMC with the contraction intensity does not depend on the contraction type or on spinal excitability variations.

Specific modulation of corticomuscular coherence during submaximal voluntary isometric, shortening and lengthening contractions.

During voluntary contractions, corticomuscular coherence (CMC) is thought to reflect a mutual interaction between cortical and muscle oscillatory activities, respectively measured by electroencephalography (EEG) and electromyography (EMG). However, it remains unclear whether CMC modulation would depend on the contribution of neural mechanisms acting at the spinal level. To this purpose, modulations of CMC were compared during submaximal isometric, shortening and lengthening contractions of the soleus (SOL) and the medial gastrocnemius (MG) with a concurrent analysis of changes in spinal excitability that may be reduced during lengthening contractions. Submaximal contractions 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 unrectified SOL or MG EMG signal. Spinal excitability was quantified through normalized Hoffmann (H) reflex amplitude. The results indicate that beta-band CMC and normalized H-reflex were significantly lower in SOL during lengthening compared with isometric contractions, but were similar in MG for all three muscle contraction types. Collectively, these results highlight an effect of contraction type on beta-band CMC, although it may differ between agonist synergist muscles. These novel findings also provide new evidence that beta-band CMC modulation may involve spinal regulatory mechanisms.