Abstract

Spinal interneurons play a critical role in motor output. A given interneuron may receive convergent input from several different sensory modalities and descending centers and relay this information to just as many targets. Therefore, there is a critical need to quantify populations of spinal interneurons simultaneously. Here, we quantify the functional connectivity of spinal neurons through the concurrent recording of populations of lumbar interneurons and hindlimb motor units in the in vivo cat model during activation of either the ipsilateral sural nerve or contralateral tibial nerve. Two microelectrode arrays were placed into lamina VII, one at L3 and a second at L6/7, while an electrode array was placed on the surface of the exposed muscle. Stimulation of tibial and sural nerves elicited similar changes in the discharge rate of both interneurons and motor units. However, these same neurons showed highly significant differences in prevalence and magnitude of correlated activity underlying these two forms of afferent drive. Activation of the ipsilateral sural nerve resulted in highly correlated activity, particularly at the caudal array. In contrast, the contralateral tibial nerve resulted in less, but more widespread correlated activity at both arrays. These data suggest that the ipsilateral sural nerve has dense projections onto caudal lumbar spinal neurons, while contralateral tibial nerve has a sparse pattern of projections.

Highlights

  • Long range monosynaptic projections to spinal motoneurons are relatively rare in the mammalian motor system

  • Recordings from interneurons and motor units were made to quantify the functional connectivity of spinal neurons

  • Despite interneuron and motor unit discharge patterns which, overall, were similar across modes of activation, the functional connectivity underlying this activation was different across nerves

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Summary

Introduction

Long range monosynaptic projections to spinal motoneurons are relatively rare in the mammalian motor system. Descending projections primarily terminate onto spinal interneurons in order to activate the spinal motoneurons—the classic exception to this are the cortical projections to motor pools which control distal muscles in phylogenetically advanced species (Lemon and Griffiths, 2005). Large diameter Ia afferents, which are exquisitely sensitive to vibration, have monosynaptic projections to nearly the entire homonymous motor pool (Mendell and Henneman, 1968). These specific cortical and reflex pathways are the minority of synaptic contacts on the spinal motoneuron and represent the exception, rather than the rule. Most synaptic contacts on the spinal motoneuron come from spinal interneurons.

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