Literature DB >> 6726345

Cutaneous responsiveness in primary somatosensory (S-I) hindpaw cortex before and after partial hindpaw deafferentation in adult rats.

J T Wall, C G Cusick.   

Abstract

The hindpaw of the rat is normally innervated by the sciatic and saphenous nerves. In the present studies, the hindpaws of adult rats were partially deafferented by transection of the sciatic nerve for variable periods of time. The organization of the hindpaw representation in primary somatosensory (S-I) cortex was then studied with neurophysiological mapping techniques and compared to the organization seen in normal rats. The objective was to determine whether cutaneous responsiveness was recovered in the cortical area which lost normal cutaneous inputs from the sciatic nerve, and, if recovery occurred, to characterize the time course and spatial extent of this recovery. Normal rats were found to have a topographically organized representation of the hindpaw in S-I cortex. As determined by nerve recording and cortical mapping, approximately 85% of this representation is responsive to cutaneous inputs from the sciatic nerve, while the remaining 15% is responsive to inputs from the saphenous nerve. Following transection of the sciatic nerve, all hindpaw skin regions normally innervated by the sciatic nerve remained denervated. In cortex, the representation of cutaneous inputs from the saphenous nerve expanded into parts of the hindpaw region normally representing sciatic inputs and occupied an area about 3 times larger than the saphenous representation in normal rats. This expansion was initially observed 1 to 2 days after transection and was stably maintained with longer deafferentation times. However, even after chronic deafferentation of up to 5 months, this enlarged saphenous representation was still only half the size of the normal hindpaw representation in normal rats. These findings suggest that cortical representations of deafferented skin can become activated by substitute cutaneous inputs. The rapid time course for substitution suggests these changes are due to functional modifications in normally existing connections. With the deafferentation conditions used in the present study, input substitution was limited to only parts of the deprived cortex. A hypothesis is presented which suggests these changes are due to adjustments in the dominance of saphenous and sciatic inputs to specific regions of cortex.

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Year:  1984        PMID: 6726345      PMCID: PMC6564980     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  21 in total

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Authors:  G W Huntley; A L de Blas; E G Jones
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

2.  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
Journal:  J Neurophysiol       Date:  2011-08-24       Impact factor: 2.714

3.  A focal zone of thalamic plasticity.

Authors:  J L Parker; M L Wood; J O Dostrovsky
Journal:  J Neurosci       Date:  1998-01-01       Impact factor: 6.167

4.  Expansion of innervation territory by afferents involved in plasma extravasation after nerve regeneration in adult and neonatal rats.

Authors:  Z Wiesenfeld-Hallin; E Kinnman; H Aldskogius
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

5.  Peripheral nerve damage facilitates functional innervation of brain grafts in adult sensory cortex.

Authors:  F F Ebner; R S Erzurumlu; S M Lee
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

6.  Plasticity in the barrel cortex of the adult mouse: effects of peripheral deprivation on GAD-immunoreactivity.

Authors:  E Welker; E Soriano; H Van der Loos
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

7.  Large-scale expansion of the face representation in somatosensory areas of the lateral sulcus after spinal cord injuries in monkeys.

Authors:  Shashank Tandon; Niranjan Kambi; Leslee Lazar; Hisham Mohammed; Neeraj Jain
Journal:  J Neurosci       Date:  2009-09-23       Impact factor: 6.167

8.  Primary somatosensory cortex in rats with pain-related behaviours due to a peripheral mononeuropathy after moderate ligation of one sciatic nerve: neuronal responsivity to somatic stimulation.

Authors:  G Guilbaud; J M Benoist; A Levante; M Gautron; J C Willer
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

9.  Peripheral nerve injury induces immediate increases in layer v neuronal activity.

Authors:  Yang Han; Nan Li; Steven R Zeiler; Galit Pelled
Journal:  Neurorehabil Neural Repair       Date:  2013-04-18       Impact factor: 3.919

10.  Large-scale reorganization in the somatosensory cortex and thalamus after sensory loss in macaque monkeys.

Authors:  Neeraj Jain; Hui-Xin Qi; Christine E Collins; Jon H Kaas
Journal:  J Neurosci       Date:  2008-10-22       Impact factor: 6.167

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