Goreau, V. | bioRxiv Science

bioRxiv2026

Disrupted Inhibitory-Excitatory Balance Underlies Spinal Motoneuron Dysfunction in Incomplete Spinal Cord Injury

Incomplete spinal cord injury disrupts voluntary movement, in part through motoneuron dysfunction, yet the mechanisms underlying this dysfunction remain poorly understood. Using a non-invasive approach to decode the spiking activity of large populations of spinal motoneurons, we quantified the relative contributions of excitatory, inhibitory, and neuromodulatory inputs to motoneuron rate coding after chronic incomplete spinal cord injury. Eighteen participants with incomplete spinal cord injury and 18 age- and sex-matched control participants performed submaximal isometric plantar flexion tasks while high-density surface electromyography was recorded from the soleus and gastrocnemius medialis muscles. Motoneuron firing behaviour was analysed to estimate neuromodulatory drive and the balance between inhibitory and excitatory inputs. Participants with incomplete spinal cord injury exhibited lower rate coding, characterised by lower firing rates at recruitment, lower firing rate modulation, and lower peak firing rates compared with healthy controls. Although estimates of neuromodulatory drive did not differ between groups, individuals with spinal cord injury showed a shift in the inhibition-excitation balance toward greater inhibition compared with controls. Furthermore, increasing inhibitory input through muscle length changes and antagonist tendon vibration modulated motoneuron firing in controls, but not in individuals with incomplete spinal cord injury. Together, these findings suggest that impaired rate coding after incomplete spinal cord injury arises from an altered inhibitory-excitatory balance rather than reduced neuromodulatory drive. Taking advantage of methodological advances to decode spinal motor neuron activity during voluntary contraction, this study identified excessive inhibitory input to spinal motoneurons as a key neural mechanism contributing to muscle weakness and impaired motor function in individuals with incomplete spinal cord injury.

neuroscience↗

bioRxiv2023

Estimates of persistent inward currents in lower limb muscles are not different between inactive, resistance-trained and endurance-trained young individuals

Persistent inward currents (PICs) increase the intrinsic excitability of -motoneurons. The main objective of this study was to determine whether estimates of -motoneuronal PIC magnitude is influenced by chronic endurance and resistance training. We also aimed to investigate whether there is a relationship in the estimates of -motoneuronal PIC magnitude between muscles. Estimates of PIC magnitude were obtained in three groups of young individuals: resistance-trained (n=12), endurance-trained (n=12), and inactive (n=13). We recorded high-density surface electromyography (HDsEMG) signals from tibialis anterior, gastrocnemius medialis, soleus, vastus medialis, and vastus lateralis. Then, signals were decomposed with convolutive blind source separation to identify motor units spike trains. Participants performed triangular isometric contractions to a peak of 20% of their maximum voluntary contraction. A paired-motor-unit analysis was used to calculate {Delta}F, which is assumed to be proportional to PIC magnitude. Despite the substantial differences in physical training experience between groups, we found no differences in {Delta}F, regardless of the muscle. Significant correlations of estimates of PICs magnitude were found between muscles of the same group (VL-VM, SOL-GM). Only one correlation (out of 8) between muscles of different groups was found (GM and TA). Overall, our findings suggest that estimates of PIC magnitude in the lower limb muscles are not influenced by physical training experience in healthy young individuals. They also suggest muscle-specific and muscle group-specific regulations of the diffuse monoamine inputs.

neuroscience↗