Literature DB >> 7472377

Electrophysiological evidence for overlapping dominant and latent inputs to somatosensory cortex in squirrel monkeys.

C E Schroeder1, S Seto, J C Arezzo, P E Garraghty.   

Abstract

1. The pattern of reorganization in area 3b of adult primates after median or ulnar nerve section suggests that somatic afferents from the dorsum of the hand, carried by the radial nerve, have preferential access to the cortical territories normally expressing glabrous inputs carried by the median and ulnar nerves. A likely mechanism underlying preferential access is preexisting, but silent, radial nerve inputs to the glabrous region of cortex. 2. We tested this by comparing the effects of electrical stimulation of median or ulnar versus radial nerves, on responses in the hand representation of area 3b. Laminar current source density and multiunit activity profiles were sampled with the use of linear array multicontact electrodes spanning the laminae of area 3b. Data were obtained from three squirrel monkeys anesthetized during recording. 3. Compared with colocated median or ulnar nerve responses, the radial nerve response had 1) an initial short-latency response in the middle laminae that was subtle; there was a small transmembrane current flow component without a discernable multiunit activity correlate; and 2) a laminar sequence and distribution of activity that was similar to those of the median or ulnar nerve responses (i.e., initial activation of the middle, followed by upper and lower laminae), but the significant current flow and multiunit response to radial nerve stimulation occurs 12-15 ms later. 4. Normal corepresentation of nondominant dorsum hand (radial) inputs with the dominant (median or ulnar) inputs in the glabrous hand surface representation provides a clear vehicle for the biased patterns of reorganization occurring after peripheral nerve section. The initial, "subtle" activity phase in the nondominant response is believed to reflect intracortical inhibition, and the later "significant" response phase, a rebound excitation, possibly compounded by an indirect or extralemniscal input. The spatiotemporal pattern of nondominant input is proposed to play a role in normal somatosensory perception.

Mesh:

Year:  1995        PMID: 7472377     DOI: 10.1152/jn.1995.74.2.722

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  15 in total

1.  Ipsilateral hand input to area 3b revealed by converging hemodynamic and electrophysiological analyses in macaque monkeys.

Authors:  Michael L Lipton; Kai-Ming G Fu; Craig A Branch; Charles E Schroeder
Journal:  J Neurosci       Date:  2006-01-04       Impact factor: 6.167

2.  Receptor autoradiographic correlates of deafferentation-induced reorganization in adult primate somatosensory cortex.

Authors:  Preston E Garraghty; Lori L Arnold; Cara L Wellman; Todd M Mowery
Journal:  J Comp Neurol       Date:  2006-08-01       Impact factor: 3.215

3.  Short-term reorganization of input-deprived motor vibrissae representation following motor disconnection in adult rats.

Authors:  Gianfranco Franchi; Carlo Veronesi
Journal:  J Physiol       Date:  2006-05-11       Impact factor: 5.182

Review 4.  Top-down predictions in the cognitive brain.

Authors:  Kestutis Kveraga; Avniel S Ghuman; Moshe Bar
Journal:  Brain Cogn       Date:  2007-11       Impact factor: 2.310

5.  Reorganization of somatosensory cortical areas 3b and 1 after unilateral section of dorsal columns of the spinal cord in squirrel monkeys.

Authors:  Hui-Xin Qi; Li M Chen; Jon H Kaas
Journal:  J Neurosci       Date:  2011-09-21       Impact factor: 6.167

6.  Differences in AMPA and GABAA/B receptor subunit expression between the chronically reorganized cortex and brainstem of adult squirrel monkeys.

Authors:  Todd M Mowery; Rohini M Sarin; Polina V Kostylev; Preston E Garraghty
Journal:  Brain Res       Date:  2015-03-16       Impact factor: 3.252

7.  Interactions within the hand representation in primary somatosensory cortex of primates.

Authors:  Michael L Lipton; Mark C Liszewski; M Noelle O'Connell; Aimee Mills; John F Smiley; Craig A Branch; Joseph R Isler; Charles E Schroeder
Journal:  J Neurosci       Date:  2010-11-24       Impact factor: 6.167

8.  Spatiotemporal trajectories of reactivation of somatosensory cortex by direct and secondary pathways after dorsal column lesions in squirrel monkeys.

Authors:  Hui-Xin Qi; Feng Wang; Chia-Chi Liao; Robert M Friedman; Chaohui Tang; Jon H Kaas; Malcolm J Avison
Journal:  Neuroimage       Date:  2016-08-12       Impact factor: 6.556

9.  Microphysiology of epileptiform activity in human neocortex.

Authors:  Catherine A Schevon; Sau K Ng; Joshua Cappell; Robert R Goodman; Guy McKhann; Allen Waziri; Almut Branner; Alexandre Sosunov; Charles E Schroeder; Ronald G Emerson
Journal:  J Clin Neurophysiol       Date:  2008-12       Impact factor: 2.177

10.  Early withdrawal of axons from higher centers in response to peripheral somatosensory denervation.

Authors:  Alessandro Graziano; Edward G Jones
Journal:  J Neurosci       Date:  2009-03-25       Impact factor: 6.167

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