Literature DB >> 18775766

Responses of infragranular neurons in the rat primary somatosensory cortex to forepaw and hindpaw tactile stimuli.

K A Moxon1, L L Hale, J Aguilar, G Foffani.   

Abstract

Infragranular layers constitute the main output of the primary somatosensory cortex and represent an important stage of cortico-cortical and cortico-subcortical integration. We have previously used chronic multiple single-unit recordings to study the spatiotemporal structure of tactile responses of infragranular neurons within the forepaw cortical representation in rats [Tutunculer B, Foffani G, Himes BT, Moxon KA (2006) Structure of the excitatory receptive fields of infragranular forelimb neurons in the rat primary somatosensory cortex responding to touch. Cereb Cortex 16:791-810]. Here we extend our understanding of this structure by studying the overlap between the forepaw and hindpaw cortical representations. We recorded 204 responsive neurons in chronic experiments from eight anesthetized rats. Overall, only 23% of neurons responded exclusively to one paw, 52% of neurons responded to two paws, 19% of neurons responded to three paws, and 5% of neurons responded to all four paws. Quantitative measures of response magnitudes and latencies revealed the following main results. (1) The responses of forepaw neurons overall displayed greater magnitudes and shorter latencies than the responses of hindpaw neurons. (2) The responses to ipsilateral stimuli displayed smaller magnitudes, and longer-and more variable-latencies than the responses to contralateral stimuli. (3) The responses of forepaw neurons to hindpaw stimuli displayed smaller magnitudes and longer latencies than the responses to forepaw stimuli, whereas the responses of hindpaw neurons to forepaw stimuli displayed smaller magnitudes but similar latencies compared with the responses to hindpaw stimuli. These results show that the spatiotemporal structure of tactile responses of infragranular neurons extends across all four paws, and provide the basic architecture for studying physiological integration and pathophysiological reorganization of tactile information in the infragranular layers of the rat primary somatosensory cortex.

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Year:  2008        PMID: 18775766     DOI: 10.1016/j.neuroscience.2008.08.009

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  22 in total

1.  Functional role of exercise-induced cortical organization of sensorimotor cortex after spinal transection.

Authors:  T Kao; J S Shumsky; E B Knudsen; M Murray; K A Moxon
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2.  Bilateral Tactile Input Patterns Decoded at Comparable Levels But Different Time Scales in Neocortical Neurons.

Authors:  Clara Genna; Calogero M Oddo; Alberto Mazzoni; Anders Wahlbom; Silvestro Micera; Henrik Jörntell
Journal:  J Neurosci       Date:  2018-03-14       Impact factor: 6.167

Review 3.  Passive cycling in neurorehabilitation after spinal cord injury: A review.

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Journal:  J Spinal Cord Med       Date:  2016-11-14       Impact factor: 1.985

4.  Spinal cord injury immediately changes the state of the brain.

Authors:  Juan Aguilar; Desiré Humanes-Valera; Elena Alonso-Calviño; Josué G Yague; Karen A Moxon; Antonio Oliviero; Guglielmo Foffani
Journal:  J Neurosci       Date:  2010-06-02       Impact factor: 6.167

5.  Effect of spinal cord injury on neural encoding of spontaneous postural perturbations in the hindlimb sensorimotor cortex.

Authors:  Jaimie B Dougherty; Gregory D Disse; Nathaniel R Bridges; Karen A Moxon
Journal:  J Neurophysiol       Date:  2021-08-11       Impact factor: 2.714

6.  Exercise induces cortical plasticity after neonatal spinal cord injury in the rat.

Authors:  Tina Kao; Jed S Shumsky; Marion Murray; Karen A Moxon
Journal:  J Neurosci       Date:  2009-06-10       Impact factor: 6.167

7.  Encoding of temporal intervals in the rat hindlimb sensorimotor cortex.

Authors:  Eric B Knudsen; Robert D Flint; Karen A Moxon
Journal:  Front Syst Neurosci       Date:  2012-09-26

8.  Imaging the spatio-temporal dynamics of supragranular activity in the rat somatosensory cortex in response to stimulation of the paws.

Authors:  M L Morales-Botello; J Aguilar; G Foffani
Journal:  PLoS One       Date:  2012-07-19       Impact factor: 3.240

9.  Decoding hindlimb movement for a brain machine interface after a complete spinal transection.

Authors:  Anitha Manohar; Robert D Flint; Eric Knudsen; Karen A Moxon
Journal:  PLoS One       Date:  2012-12-27       Impact factor: 3.240

10.  Passive exercise of the hind limbs after complete thoracic transection of the spinal cord promotes cortical reorganization.

Authors:  Alessandro Graziano; Guglielmo Foffani; Eric B Knudsen; Jed Shumsky; Karen A Moxon
Journal:  PLoS One       Date:  2013-01-22       Impact factor: 3.240

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