Literature DB >> 6151590

Functional role of GABA in cat primary somatosensory cortex: shaping receptive fields of cortical neurons.

R W Dykes, P Landry, R Metherate, T P Hicks.   

Abstract

Extracellular recordings of 209 neurons were obtained with carbon fiber-containing multibarrel micropipettes. The cells were isolated in the primary somatosensory cortex of cats anesthetized with barbiturate and classified according to the nature of their response to natural stimuli, the nature of the surrounding multiunit responses to the same stimuli, the response to thalamic stimulation, and their depth in the cortex. To study factors controlling the excitability of somatosensory neurons, their receptive fields were examined in the presence of iontophoretically administered gamma-aminobutyric acid (GABA), glutamate, and bicuculline methiodide (BMI). Even when the neurons were depolarized to perithreshold levels with glutamate, or when local inhibitory influences mediated by GABA were antagonized by BMI, the apparent specificity for one class of afferent input was maintained. Neurons responding to stimulation of either cutaneous or deep receptors maintained their modality specificity, and neurons in cutaneous rapidly adapting regions never took on slowly adapting properties. When ejected at currents that did not elicit action potentials, glutamate lowered the threshold for activation by cutaneous stimuli but did not enlarge the receptive field. With larger ejecting currents, the neurons developed an on-going discharge, but even at these higher doses, glutamate did not produce an increase in the receptive-field size. Some neurons in regions of cortex exhibiting slowly adapting multiunit responses were relatively insensitive to glutamate. These cells required four to five times more glutamate to evoke discharges than did most neurons. Other cells, previously unresponsive to somatic stimuli, could be shown to possess distinct cutaneous receptive fields when either glutamate or BMI was ejected in their vicinity. Iontophoretically administered BMI altered the firing pattern of somatosensory neurons, causing them to discharge in bursts of 3-15 impulses. BMI enlarged the receptive-field size of neurons in regions displaying rapidly adapting multiunit background discharges but not in those regions with slowly adapting multiunit discharges. This differential effect of BMI, suggesting that GABA controls receptive-field size in rapidly adapting regions, also indicates that neurons in rapidly adapting regions differ pharmacologically from those in other submodality regions. In all cortical regions, BMI blocked the poststimulus inhibitory period that normally followed thalamic stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6151590     DOI: 10.1152/jn.1984.52.6.1066

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


  55 in total

1.  Diverse types of interneurons generate thalamus-evoked feedforward inhibition in the mouse barrel cortex.

Authors:  J T Porter; C K Johnson; A Agmon
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

2.  Reorganization in primary motor cortex of primates with long-standing therapeutic amputations.

Authors:  C W Wu; J H Kaas
Journal:  J Neurosci       Date:  1999-09-01       Impact factor: 6.167

3.  Spatial and temporal structure of receptive fields in primate somatosensory area 3b: effects of stimulus scanning direction and orientation.

Authors:  J J DiCarlo; K O Johnson
Journal:  J Neurosci       Date:  2000-01-01       Impact factor: 6.167

4.  Differential depression at excitatory and inhibitory synapses in visual cortex.

Authors:  J A Varela; S Song; G G Turrigiano; S B Nelson
Journal:  J Neurosci       Date:  1999-06-01       Impact factor: 6.167

Review 5.  Thalamocortical control of feed-forward inhibition in awake somatosensory 'barrel' cortex.

Authors:  Harvey A Swadlow
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

6.  Activity of different classes of neurons of the motor cortex during locomotion.

Authors:  Irina N Beloozerova; Mikhail G Sirota; Harvey A Swadlow
Journal:  J Neurosci       Date:  2003-02-01       Impact factor: 6.167

7.  Second-order receptive fields reveal multidigit interactions in area 3b of the macaque monkey.

Authors:  Pramodsingh H Thakur; Paul J Fitzgerald; Steven S Hsiao
Journal:  J Neurophysiol       Date:  2012-03-28       Impact factor: 2.714

8.  GABAergic inhibition shapes temporal and spatial response properties of pyramidal cells in the electrosensory lateral line lobe of gymnotiform fish.

Authors:  C A Shumway; L Maler
Journal:  J Comp Physiol A       Date:  1989-01       Impact factor: 1.836

9.  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

10.  Presynaptic GABAB receptors modulate thalamic excitation of inhibitory and excitatory neurons in the mouse barrel cortex.

Authors:  James T Porter; Dalila Nieves
Journal:  J Neurophysiol       Date:  2004-07-14       Impact factor: 2.714

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