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J Neurophysiol 89: 3328-3339, 2003. First published February 26, 2003; doi:10.1152/jn.01085.2002
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New Corticocuneate Cellular Mechanisms Underlying the Modulation of Cutaneous Ascending Transmission in Anesthetized Cats

Juan Aguilar1, Casto Rivadulla2, Cristina Soto1 and Antonio Canedo1

1Department of Physiology, Faculty of Medicine, 15705 Santiago de Compostela, Spain; and 2Department of Medicine, University of La Coruña, 15006 La Coruña, Spain

Submitted 3 December 2002; accepted in final form 25 February 2003

The ascending cutaneous transmission through the middle cuneate nucleus is subject to cortico-feedback modulation. This work studied the intracuneate cellular mechanisms underlying the corticocuneate influence. Single unit extracellular records combined with iontophoresis showed that the corticocuneate input activates cuneo-lemniscal (CL) and noncuneo-lemniscal (nCL) cells via N-methyl-D-aspartate (NMDA) and non-NMDA receptors as shown by the decrease of the cortical-induced activation on ejection of CNQX and APV, either alone or in combination. These results were confirmed by in vivo intracellular recordings. Two subgroups of nCL cells were distinguished according to their sensitivity to iontophoretic ejection of glycine and its antagonist, strychnine. Finally, the corticalevoked activation of CL cells was decreased by GABA and increased by glycine acting at a strychnine-sensitive site, indicating that glycine indirectly affects the cuneo-lemniscal transmission. A model is proposed whereby the cortex influences CL cells through three different mechanisms, producing 1) activation via non-NMDA and NMDA receptors, 2) inhibition through GABAergic nCLs, and 3) disinhibition via serial glycinergic-GABAergic nCL cells. These corticocuneate feedback effects serve to potentiate the activity of CL cells topographically aligned through direct activation and disinhibition, while inhibiting, via GABAergic cells, other CL neurons not topographically aligned.


Address for reprint requests: A. Canedo, Dept. of Physiology, Faculty of Medicine, 15705 Santiago de Compostela, Spain (E-mail: fsancala{at}usc.es).




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