Functional contribution of mesencephalic locomotor region nuclei to locomotor recovery after spinal cord injury.

Cell Rep Med

Centre de Recherche du CHU de Québec, CHUL-Neurosciences, 2705 Boul. Laurier, Québec, QC G1V 4G2, Canada; Faculty of Medicine, Department of Psychiatry and Neurosciences, Université Laval, Québec, QC G1V 4G2, Canada. Electronic address:

Published: February 2023

AI Article Synopsis

  • Spinal cord injury (SCI) disrupts communication between the brain and spinal cord, affecting locomotion.
  • Electrical stimulation of the mesencephalic locomotor region (MLR) has shown potential for promoting recovery in rodent models of SCI, but there's ongoing debate about the best anatomical targets for therapy.
  • Our research identifies glutamatergic neurons in the cuneiform nucleus as beneficial for improving walking speed and rhythm, suggesting they are key targets for future treatments in SCI recovery.

Article Abstract

Spinal cord injury (SCI) results in a disruption of information between the brain and the spinal circuit. Electrical stimulation of the mesencephalic locomotor region (MLR) can promote locomotor recovery in acute and chronic SCI rodent models. Although clinical trials are currently under way, there is still debate about the organization of this supraspinal center and which anatomic correlate of the MLR should be targeted to promote recovery. Combining kinematics, electromyographic recordings, anatomic analysis, and mouse genetics, our study reveals that glutamatergic neurons of the cuneiform nucleus contribute to locomotor recovery by enhancing motor efficacy in hindlimb muscles, and by increasing locomotor rhythm and speed on a treadmill, over ground, and during swimming in chronic SCI mice. In contrast, glutamatergic neurons of the pedunculopontine nucleus slow down locomotion. Therefore, our study identifies the cuneiform nucleus and its glutamatergic neurons as a therapeutical target to improve locomotor recovery in patients living with SCI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975330PMC
http://dx.doi.org/10.1016/j.xcrm.2023.100946DOI Listing

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