Literature DB >> 8187856

Non-dominant suppression in the dorsal lateral geniculate nucleus of the cat: laminar differences and class specificity.

C Wang1, B Dreher, W Burke.   

Abstract

Binocular non-dominant suppression (NDS) in the dorsal lateral geniculate nucleus (LGNd) of the cat was studied by recording from single neurons in the LGNd of anaesthetized, paralysed cats while stimulating the non-dominant eye with a moving light bar. The maintained discharge rate of LGNd neurons was varied by stimulating the dominant eye in various ways: by varying the size or contrast of a flashed spot, by varying the inner diameter of a flashed annulus of large outer diameter, by varying the velocity of a moving light bar, and by covering the eye. Non-dominant suppression was quantified either as the decrease in the maintained discharge rate (the "dip"), expressed as spikes per second, or as the ratio of the dip to the maintained discharge rate (the "dip ratio"). At low maintained discharge rates the dip, although low in value, frequently approached the maintained rate, i.e. the dip ratio approached unity. As the maintained discharge rate increased the dip value also increased, but more slowly than the maintained discharge rate, i.e. the dip ratio decreased. At maintained discharge rates above about 30 spikes/s, in many neurons the dip appeared to be approaching a constant value. This strong dependence of NDS on the maintained discharge rate of the LGNd neuron suggests that the inhibitory input to the cell arises from a region of the brain that receives an input both from the non-dominant eye and from the LGNd cell. Reasons are given for thinking that this region is the perigeniculate nucleus. Because of the strong dependence of dip and dip ratio on the maintained discharge rate, it was necessary to adopt stringent criteria when comparing NDS in two different sets of neurons or of the same set of neurons in different conditions. We recognized a significant difference in NDS between two classes of neurons or between two states only if: (1) there was no significant difference between the maintained discharge rates, and (2) there was a significant difference for both dip and dip ratio between the two classes or states. Using these criteria we found: (1) no difference between non-lagged X (XNL) and non-lagged Y (YNL) cells, (2) no difference between on-centre and off-centre cells for either XNL or YNL cells, (3) no difference between XNL cells and lagged X (XL) cells.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 8187856     DOI: 10.1007/bf00241539

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


  62 in total

1.  Binocular inhibition in the lateral geniculate body.

Authors:  E F VASTOLA
Journal:  Exp Neurol       Date:  1960-06       Impact factor: 5.330

2.  Spatial and temporal response properties of lagged and nonlagged cells in cat lateral geniculate nucleus.

Authors:  A B Saul; A L Humphrey
Journal:  J Neurophysiol       Date:  1990-07       Impact factor: 2.714

3.  Segregation of form, color, and stereopsis in primate area 18.

Authors:  D H Hubel; M S Livingstone
Journal:  J Neurosci       Date:  1987-11       Impact factor: 6.167

4.  Neuronal dynamics in the visual corticothalamic pathway revealed through binocular rivalry.

Authors:  F J Varela; W Singer
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

5.  Residual eye movements in receptive-field studies of paralyzed cats.

Authors:  R W Rodieck; J D Pettigrew; P O Bishop; T Nikara
Journal:  Vision Res       Date:  1967-01       Impact factor: 1.886

6.  Sustained and transient neurones in the cat's retina and lateral geniculate nucleus.

Authors:  B G Cleland; M W Dubin; W R Levick
Journal:  J Physiol       Date:  1971-09       Impact factor: 5.182

7.  Two classes of single-input X-cells in cat lateral geniculate nucleus. II. Retinal inputs and the generation of receptive-field properties.

Authors:  D N Mastronarde
Journal:  J Neurophysiol       Date:  1987-02       Impact factor: 2.714

8.  Coexistence of glutamic acid decarboxylase- and somatostatin-like immunoreactivity in neurons of the feline nucleus reticularis thalami.

Authors:  W H Oertel; A M Graybiel; E Mugnaini; R P Elde; D E Schmechel; I J Kopin
Journal:  J Neurosci       Date:  1983-06       Impact factor: 6.167

9.  Receptive fields of cat's non-relay lateral geniculate and perigeniculate neurons.

Authors:  A Wróbel; R Tarnecki
Journal:  Acta Neurobiol Exp (Wars)       Date:  1984       Impact factor: 1.579

10.  The binocular input to cells in the feline dorsal lateral geniculate nucleus (dLGN).

Authors:  P C Murphy; A M Sillito
Journal:  J Physiol       Date:  1989-08       Impact factor: 5.182

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  4 in total

1.  Binocular interactions and disparity coding in area 21a of cat extrastriate visual cortex.

Authors:  C Wang; B Dreher
Journal:  Exp Brain Res       Date:  1996-03       Impact factor: 1.972

2.  Binocular combination of luminance profiles.

Authors:  Jian Ding; Dennis M Levi
Journal:  J Vis       Date:  2017-11-01       Impact factor: 2.240

3.  Synaptic organization of thalamocortical axon collaterals in the perigeniculate nucleus and dorsal lateral geniculate nucleus.

Authors:  Martha E Bickford; Haiyang Wei; Michael A Eisenback; Ranida D Chomsung; Arkadiusz S Slusarczyk; Aygul B Dankowsi
Journal:  J Comp Neurol       Date:  2008-05-10       Impact factor: 3.215

4.  Binocular neurons in parastriate cortex: interocular 'matching' of receptive field properties, eye dominance and strength of silent suppression.

Authors:  Phillip A Romo; Natalie Zeater; Chun Wang; Bogdan Dreher
Journal:  PLoS One       Date:  2014-06-13       Impact factor: 3.240

  4 in total

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