Literature DB >> 6699681

Receptive field properties in the cat's area 17 in the absence of on-center geniculate input.

H Sherk, J C Horton.   

Abstract

Most neurons of area 17 in the cat respond to both light and dark stimuli, and it is often assumed that these responses originate from the on-center and off-center cells, respectively, of the lateral geniculate nucleus. This has not been demonstrated experimentally, however. Whether the on and off pathways make unique contributions to some of the response properties characteristic of visual cortex, such as orientation selectivity, is also unknown. The aim of these experiments was to investigate these questions by inactivating the retinogeniculate on pathway. In cats in which D,L-2-amino-4-phosphonobutyric acid (APB) had been injected into one eye, we found that, in the geniculate layers driven by that eye, there were no cells with on-center responses (Horton, J. C., and H. Sherk (1984) J. Neurosci. 4: 374-380). The on pathway appeared to have been inactivated. To see how cortical receptive fields were affected, we examined 184 binocular cells in area 17 contralateral to the injected eye. Each cell still had a normal receptive field in the ipsilateral eye, and we compared the cell's response properties in that eye with those in the eye injected with APB to assess the drug's effects. Overall responsiveness in the injected eye was severely reduced, and responses to the onset of stationary light stimuli were almost entirely abolished. Responses to moving light edges were weak or absent in most cells but still strong in a few; simple cells tended to have more vigorous light edge responses than complex cells. The general reduction in responsiveness, and the specific reduction in light edge responses, indicated that the on and off pathways both contribute (directly or indirectly) to the responses of most cells in area 17. The remaining responses to light edges we think originated mainly from the on-surrounds of off-center geniculate cells. Responses to moving dark edges were somewhat depressed compared to those in the normal eye. There was, however, no systematic change in direction selectivity and no reduction in specificity for orientation or length. In general, receptive field properties remained surprisingly normal despite the conspicuous reduction in responsiveness.

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Year:  1984        PMID: 6699681      PMCID: PMC6564909     

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


  12 in total

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2.  Subtraction inhibition combined with a spiking threshold accounts for cortical direction selectivity.

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Review 3.  Parallel information processing channels created in the retina.

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4.  Innervation patterns of single physiologically identified geniculocortical axons in the striate cortex of the tree shrew.

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5.  Visual orientation and directional selectivity through thalamic synchrony.

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Journal:  J Neurosci       Date:  2012-06-27       Impact factor: 6.167

6.  A model of direction-selective "simple" cells in the visual cortex based on inhibition asymmetry.

Authors:  P I Ruff; J P Rauschecker; G Palm
Journal:  Biol Cybern       Date:  1987       Impact factor: 2.086

7.  Rapid plasticity of visual responses in the adult lateral geniculate nucleus.

Authors:  Bartlett D Moore; Caitlin W Kiley; Chao Sun; W Martin Usrey
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8.  "Black" responses dominate macaque primary visual cortex v1.

Authors:  Chun-I Yeh; Dajun Xing; Robert M Shapley
Journal:  J Neurosci       Date:  2009-09-23       Impact factor: 6.167

9.  Genetic disruption of the On visual pathway affects cortical orientation selectivity and contrast sensitivity in mice.

Authors:  Rashmi Sarnaik; Hui Chen; Xiaorong Liu; Jianhua Cang
Journal:  J Neurophysiol       Date:  2014-03-05       Impact factor: 2.714

10.  Attentive and pre-attentive processes in change detection and identification.

Authors:  Howard C Hughes; Gideon Paul Caplovitz; Rebecca A Loucks; Robert Fendrich
Journal:  PLoS One       Date:  2012-08-16       Impact factor: 3.240

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