Abstract

This article provides a perspective on major innovations over the past century in research on the spinal cord and, specifically, on specialized spinal circuits involved in the control of rhythmic locomotor pattern generation and modulation. Pioneers such as Charles Sherrington and Thomas Graham Brown have conducted experiments in the early twentieth century that changed our views of the neural control of locomotion. Their seminal work supported subsequently by several decades of evidence has led to the conclusion that walking, flying, and swimming are largely controlled by a network of spinal neurons generally referred to as the central pattern generator (CPG) for locomotion. It has been subsequently demonstrated across all vertebrate species examined, from lampreys to humans, that this CPG is capable, under some conditions, to self-produce, even in absence of descending or peripheral inputs, basic rhythmic, and coordinated locomotor movements. Recent evidence suggests, in turn, that plasticity changes of some CPG elements may contribute to the development of specific pathophysiological conditions associated with impaired locomotion or spontaneous locomotor-like movements. This article constitutes a comprehensive review summarizing key findings on the CPG as well as on its potential role in Restless Leg Syndrome, Periodic Leg Movement, and Alternating Leg Muscle Activation. Special attention will be paid to the role of the CPG in a recently identified, and uniquely different neurological disorder, called the Uner Tan Syndrome.

Highlights

  • GROSS ANATOMY OF THE SPINAL CORD The Central Pattern Generator (CPG) for locomotion could hardly be introduced properly without describing first the spinal cord itself as well as the supraspinal and peripheral systems associated with its physiological basis

  • The role of primary afferent inputs during locomotor activity is incompletely understood. It makes no doubt, in non-pathological cases, that the control system requires those inputs for successful progression in real life conditions. This said, results obtained from spinal cord transected (TX) and deafferented animal models have clearly shown that the spinal cord is capable of generating rhythmic locomotor-like output and corresponding movements in the absence of descending and peripheral signals (Grillner, 1981)

  • Increased fos-immunoreactive levels were found as soon as at 2.5 h post-trauma in sublesional segments of high-thoracic or cervical TX rats (Ruggiero et al, 1997). Because these same lumbar cord segments ( L1–L2 in mice) have been shown to contain critical CPG elements (Nishimaru et al, 2000) and, given that immediate early genes (IEGs) are well-known for their role in central nervous system (CNS) development and plasticity (Ginty et al, 1992), spontaneous changes in IEG expression (i.e., c-fos and nor-1) in L1–L2 segments may possibly be considered as among the first cellular events associated with cell property changes and increased CPG excitability post-spinal cord injury (SCI)

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Summary

Introduction

GROSS ANATOMY OF THE SPINAL CORD The Central Pattern Generator (CPG) for locomotion could hardly be introduced properly without describing first the spinal cord itself as well as the supraspinal and peripheral systems associated with its physiological basis. Experiments conducted in our laboratory using a simple and reliable semi-quantitative assay (ACOS, Guertin, 2005) and a mouse model (a complete low-thoracic TX) with no assistance or additional stimuli (e.g., no training, no tail stimulation, no sexual organ pinching, and no weight-support assistance to avoid unspecific non-drug-induced effects) have contributed to identify clearly a subset of transmembranal receptors involved in pharmacologically elicited, CPG-mediated locomotor-like movements in the lower extremities.

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