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J Neurophysiol 96: 2995-3005, 2006. First published August 30, 2006; doi:10.1152/jn.00061.2006
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Intraspinal Microstimulation Excites Multisegmental Sensory Afferents at Lower Stimulus Levels Than Local {alpha}-Motoneuron Responses

R. A. Gaunt1, A. Prochazka1, V. K. Mushahwar1, L. Guevremont1 and P. H. Ellaway2

1Department of Biomedical Engineering and Center for Neuroscience, University of Alberta, Edmonton, Alberta, Canada; and 2 Division of Neuroscience and Mental Health, Imperial College London, London, United Kingdom

Submitted 19 January 2006; accepted in final form 26 August 2006

Microstimulation within the motor regions of the spinal cord is often assumed to activate motoneurons and propriospinal neurons close to the electrode tip. However, previous work has shown that intraspinal microstimulation (ISMS) in the gray matter activates sensory afferent axons as well as {alpha}-motoneurons (MNs). Here we report on the recruitment of sensory afferent axons and MNs as ISMS amplitudes increased. Intraspinal microstimulation was applied through microwires implanted in the dorsal horn, intermediate region and ventral horn of the L5–L7 segments of the spinal cord in four acutely decerebrated cats, two of which had been chronically spinalized. Activation of sensory axons was detected with electroneurographic recordings from dorsal roots. Activation of MNs was detected with electromyographic (EMG) recordings from hindlimb muscles. Sensory axons were nearly always activated at lower stimulus levels than MNs irrespective of the stimulating electrode location. EMG response latencies decreased as ISMS stimulus intensities increased, suggesting that MNs were first activated transsynaptically and then directly as intensity increased. ISMS elicited antidromic activity in dorsal root filaments with entry zones up to 17 mm rostral and caudal to the stimulation sites. We posit that action potentials elicited in localized terminal branches of afferents spread antidromically to all terminal branches of the afferents and transsynaptically excite MNs and interneurons far removed from the stimulation site. This may help explain how focal ISMS can activate many MNs of a muscle even though they are distributed in long thin columns.


Address for reprint requests and other correspondence: R. A. Gaunt, Dept. of Biomedical Engineering and Center for Neuroscience, University of Alberta, 507 HMRC, University of Alberta, Edmonton AB, T6G 2S2, Canada (E-mail: rgaunt{at}ualberta.ca)




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