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Spinal control of locomotion before and after spinal cord injury
Preprint   Open access

Spinal control of locomotion before and after spinal cord injury

Simon M Danner, Courtney T Shepard, Casey Hainline, Natalia A Shevtsova, Ilya A Rybak and David S K Magnuson
bioRxiv : the preprint server for biology
24 Mar 2023
DOI: https://doi.org/10.1101/2023.03.22.533794
PMID: 36993490
url
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055332View
Preprint (Author's original)Open Access (License Unspecified),  Open

Abstract

Thoracic spinal cord injury affects long propriospinal neurons that interconnect the cervical and lumbar enlargements. These neurons are crucial for coordinating forelimb and hindlimb movements in a speed-dependent manner. At the same time, recovery from spinal cord injury is usually studied over a very limited range of speeds. To overcome this limitation, we investigated overground locomotion in rats over the full range of speeds pre-injury and after recovery from thoracic hemisection or contusion injuries. Intact rats expressed a speed-dependent continuum of alternating (walk and trot) and non-alternating (canter, gallop, half-bound gallop, and bound) gaits. After a lateral hemisection injury, rats recovered the ability to locomote over a wide range of speeds but lost the ability to move using the highest-speed gaits (half-bound gallop and bound) and predominantly used the limb contralateral to injury as lead during canter and gallop. A moderate contusion injury resulted in a greater reduction in maximal speed, loss of non-alternating gaits, and emergence of novel alternating gaits. Analysis of the gait structure in phase space and the variability of limb coupling suggests substantial reorganization of intraspinal pathways mediating interlimb coordination following recovery of locomotion after lateral hemisection or midline contusion injuries. This reorganization appears as an increased reliance on local enlargement circuitry and suggests that speed-dependent gait changes in the forelimbs rely on ascending information from the lumbar circuitry that is impaired post-injury. These observations highlight how investigating the full repertoire of locomotor speeds can reveal otherwise hidden aspects of spinal circuitry and post-injury reorganization.

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