Literature DB >> 1963252

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

H C Shin1, J K Chapin.   

Abstract

We have used single-unit recording techniques to map the spatial distribution of the primary somatosensory (SI) cortical influences on thalamic somatosensory relay nuclei in the rat. A total of 193 microelectrode penetrations were made to record single neurons in tracks through the medial and lateral ventroposterior (VPL and VPM), ventrolateral (VL), posterior (Po), and reticular (nRt) thalamic nuclei. Single units were classified according to their (1) location within the nuclei, (2) receptive fields, and (3) response to standardized microstimulation in deep layers of the SI cortical forepaw areas. The SI stimulation produced short-latency (1- to 7-msec) excitatory responses in different percentages of neurons recorded in the following thalamic nuclei: VPL, 42.0%; Po, 25.0%; nRt, 16.4%; VL, 13.6%; and VPM, 9.9%. Within the VPL, the highest proportion of responsive neurons was found in the anterior region. Although most of the VL region was unresponsive, the caudal subregion bordering the rostral VPL showed some responsiveness (13.6% of neurons). In general, the spatial pattern of corticothalamic influences appeared to reciprocate the known thalamocortical connection patterns, but with a heterogeneity that was unpredicted. The same parameters of SI cortical stimulation were used in studies of corticofugal modulation of afferent transmission through the VPL thalamus. A condition-test (C-T) paradigm was implemented in which the cortical stimulation (C) was delivered at a range of time intervals before test (T) mechanical vibratory stimulation was applied to digit 4 of the contralateral forepaw. The time course of cortical effects was analyzed by measuring the averaged evoked unit responses of thalamic neurons to the T stimuli, and plotting them as a function of C-T intervals from 5 to 50 msec. Of the 20 VPL neurons tested during SI stimulation, the average response to T stimulation was decreased a mean of 36%, with the suppression peaking (at 49% inhibition of the afferent response) about 15 msec after the C stimulus. Considerable rostrocaudal variation was observed, however. Whereas neurons in the rostral VPL (near VL) were strongly inhibited (-69%), neurons in the middle and caudal VPL exhibited facilitations at long and short C-T intervals, respectively. This study establishes a specific projection system from the forepaw region of SI cortex to different subregions of the VPL thalamus, producing specific temporal patterns of sensory modulation.

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Year:  1990        PMID: 1963252     DOI: 10.3109/08990229009144717

Source DB:  PubMed          Journal:  Somatosens Mot Res        ISSN: 0899-0220            Impact factor:   1.111


  5 in total

1.  Immediate thalamic sensory plasticity depends on corticothalamic feedback.

Authors:  D J Krupa; A A Ghazanfar; M A Nicolelis
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

2.  Response properties of neurons in primary somatosensory cortex of owl monkeys reflect widespread spatiotemporal integration.

Authors:  Jamie L Reed; Hui-Xin Qi; Zhiyi Zhou; Melanie R Bernard; Mark J Burish; A B Bonds; Jon H Kaas
Journal:  J Neurophysiol       Date:  2010-02-17       Impact factor: 2.714

3.  Cortex dynamically modulates responses of thalamic relay neurons through prolonged circuit-level disinhibition in rat thalamus in vivo.

Authors:  Lu Li; Ford F Ebner
Journal:  J Neurophysiol       Date:  2016-08-31       Impact factor: 2.714

Review 4.  Forebrain mechanisms of nociception and pain: analysis through imaging.

Authors:  K L Casey
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

5.  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

  5 in total

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