Literature DB >> 1541349

Cortical modulation of thalamo-cortical neurons relaying exteroceptive information: a microstimulation study in the guinea pig.

C Rapisarda1, A Palmeri, S Sapienza.   

Abstract

The nature and organization of cortical influences on somatosensory thalamic neurons were investigated in the guinea pig in order to ascertain if mechanisms subserving sensory-motor integration in the thalamus are as precise as has previously been demonstrated in the agranular frontal cortex (AGr) and granular parietal cortex (Gr). The study was carried out on 14 chronically-implanted awake animals. In each experiment one or two motor foci within AGr and Gr were identified according to the region of the movement evoked by intracortical microstimulation at the lowest threshold stimulation (usually 5-15 microA). Spontaneous activity of 182 thalamo-cortical single neurons was recorded in the nucleus ventralis thalami (VT). The neurons were also identified by their response to activation of cutaneous receptive fields (RFs) located in regions of vibrissae or limbs, and then tested for cortical stimulation with a pulse intensity equal to the threshold for evoking motor effects. During the cortico-thalamic tests, the duration of stimulating trains was reduced in order to avoid the appearance of limb or vibrissa movements which could activate somatosensory ascending pathways forwarding peripheral messages to VT. The cortical control on VT neurons appears to be organized in a very precise manner. It was seen that: 1) The influences on these neurons relaying exteroceptive signals specifically emanated from AGr and Gr areas which in turn received exteroceptive input. 2) The vibrissa units responded to stimulation of foci in either AGr or Gr but the reactivity was greater upon stimulation of Gr than AGr. The incidence of responses was very high when the vibrissa RF was overlapping or adjacent to the region of the cortically-evoked vibrissa movement. The response pattern was mostly excitatory. Responses were rarely observed when vibrissa RF lay distant from the vibrissa moved by cortical stimulation. 3) Neurons with limb RFs responded constantly to stimulation of Gr foci only when the RF was overlapping or adjacent to the region of the cortical motor target; in these two conditions the response pattern was excitatory and inhibitory, respectively. Inhibitions only concerned neurons with forelimb RFs. Responses to stimulation of AGr were rarely obtained. From a functional point of view, the excitatory nature of the cortical control on thalamo-cortical VT neurons suggests that a cortical signal inducing movement of a given body part is able to enhance the afferent transmission of somatosensory messages arising in the same body part.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1541349     DOI: 10.1007/bf02259135

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  33 in total

1.  Impulse transmission of thalamic somatosensory relay nuclei as modified by electrical stimulation of the cerebral cortex.

Authors:  K IWAMA; C YAMAMOTO
Journal:  Jpn J Physiol       Date:  1961-04-15

2.  Multiple representations of the body and input-output relationships in the agranular and granular cortex of the chronic awake guinea pig.

Authors:  C Rapisarda; A Palmeri; G Aicardi; S Sapienza
Journal:  Somatosens Mot Res       Date:  1990       Impact factor: 1.111

3.  Pyramidal tract control over cutaneous and kinesthetic sensory transmission in the cat thalamus.

Authors:  T Tsumoto; S Nakamura; K Iwama
Journal:  Exp Brain Res       Date:  1975-03-27       Impact factor: 1.972

4.  Spatial organization of thalamocortical and corticothalamic projection systems in the rat SmI barrel cortex.

Authors:  J Chmielowska; G E Carvell; D J Simons
Journal:  J Comp Neurol       Date:  1989-07-15       Impact factor: 3.215

5.  Mapping the effects of motor cortex stimulation on somatosensory relay neurons in the rat thalamus: direct responses and afferent modulation.

Authors:  H C Shin; J K Chapin
Journal:  Brain Res Bull       Date:  1990-02       Impact factor: 4.077

6.  Inhibition of afferent transmission in cuneate nucleus during voluntary movement in the cat.

Authors:  C Ghez; M Pisa
Journal:  Brain Res       Date:  1972-05-12       Impact factor: 3.252

7.  Corticofugal influence upon cat thalamic ventrobasal complex.

Authors:  J E Burchfiel; F H Duffy
Journal:  Brain Res       Date:  1974-04-26       Impact factor: 3.252

8.  A chronic unit study of the sensory properties of neurons in the forelimb areas of rat sensorimotor cortex.

Authors:  C F Sievert; E J Neafsey
Journal:  Brain Res       Date:  1986-08-27       Impact factor: 3.252

Review 9.  The physiology of excitatory amino acids in the vertebrate central nervous system.

Authors:  M L Mayer; G L Westbrook
Journal:  Prog Neurobiol       Date:  1987       Impact factor: 11.685

10.  Corticofugal influences of S1 cortex on ventrobasal thalamic neurons in the awake rat.

Authors:  B Yuan; T J Morrow; K L Casey
Journal:  J Neurosci       Date:  1986-12       Impact factor: 6.167

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  4 in total

1.  Changes in corticothalamic modulation of receptive fields during peripheral injury-induced reorganization.

Authors:  S A Chowdhury; K A Greek; D D Rasmusson
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-20       Impact factor: 11.205

2.  Coherence between motor cortical activity and peripheral discontinuities during slow finger movements.

Authors:  Elizabeth R Williams; Demetris S Soteropoulos; Stuart N Baker
Journal:  J Neurophysiol       Date:  2009-05-27       Impact factor: 2.714

3.  Corticothalamic influences on transmission of tactile information in the ventroposterolateral thalamus of the cat: effect of reversible inactivation of somatosensory cortical areas I and II.

Authors:  S Ghosh; G M Murray; A B Turman; M J Rowe
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

4.  Propofol suppresses synaptic responsiveness of somatosensory relay neurons to excitatory input by potentiating GABA(A) receptor chloride channels.

Authors:  Shui-Wang Ying; Peter A Goldstein
Journal:  Mol Pain       Date:  2005-01-14       Impact factor: 3.395

  4 in total

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