Literature DB >> 6473083

The representation of contrast and other stimulus parameters by single neurons in area 17 of the cat.

C Y Li, O Creutzfeldt.   

Abstract

The responses of neurons in area 17 were tested as a function of various stimulus parameters. The thresholds of individual cortical neurons were at contrasts between 0.01 and 0.1 (increment of 0.5 X 10(-1) cd/m-2 on a background of 3 cd/m-2), the dynamic ranges were 1.0-2.0 log units of increment, and all cells showed a response decrease at increments above a certain maximum (supersaturation response). The averaged contrast/response curve for all neurons was S-shaped in the logarithmic plot, had a dynamic range of 2.5 log units, reached its maximum at a contrast of 0.75 and supersaturated above this level. The contrast/sensitivity curves changed their slope under different stimulus conditions. They became flatter when the non-dominant eye was stimulated as compared to dominant eye stimulation or when the stimulation was done at a non-optimal orientation or direction, and they became steeper when both eyes were stimulated. But the maximum was reached at the same contrast and supersaturation was seen above maximum contrast no matter whether a cell was strongly (e.g. binocular stimulation at optimal orientation) or weakly excited (non-dominant or non-optimal orientation stimulation). After normalization, the averaged population contrast/response curves were virtually identical at all stimulus conditions. It was concluded, that range as well as maximum and supersaturation of cortical contrast/response curves are determined before the input reaches the cortex, and that the cortical cells summate, essentially, linearly. The findings furthermore demonstrate that the supersaturation of the cortical input must be due to subtractive inhibition, and that the same is true for the orientation sensitive inhibition in the cortex itself. Both, the peripheral contrast and the cortical orientation dependent inhibition cannot be explained by multiplicative inhibition. The fact, that the responses of neurons depend on many variables relativates their significance for feature representation.

Mesh:

Year:  1984        PMID: 6473083     DOI: 10.1007/bf00582601

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  29 in total

1.  Variability of the relative preference for stimulus orientation and direction of movement in some units of the cat visual cortex (areas 17 and 18).

Authors:  I M Donaldson; J R Nash
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

2.  Inhibitory mechanisms influencing complex cell orientation selectivity and their modification at high resting discharge levels.

Authors:  A M Sillito
Journal:  J Physiol       Date:  1979-04       Impact factor: 5.182

3.  An intracellular analysis of visual cortical neurones to moving stimuli: response in a co-operative neuronal network.

Authors:  O D Creutzfeldt; U Kuhnt; L A Benevento
Journal:  Exp Brain Res       Date:  1974       Impact factor: 1.972

4.  Scotopic and mesopic light adaptation in the cat's retina.

Authors:  B Sakmann; O D Creutzfeldt
Journal:  Pflugers Arch       Date:  1969       Impact factor: 3.657

5.  S-potential and dark adaptation in fish.

Authors:  K I Naka; W A Rushton
Journal:  J Physiol       Date:  1968-01       Impact factor: 5.182

6.  Linear signal transmission from prepotentials to cells in the macaque lateral geniculate nucleus.

Authors:  B B Lee; V Virsu; O D Creutzfeldt
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

7.  Orientation selectivity in the cat's striate cortex is invariant with stimulus contrast.

Authors:  G Sclar; R D Freeman
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

8.  Decreased post-synaptic inhibition in the visual cortex during flicker stimulation.

Authors:  U Kuhnt; O D Creutzeldt
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1971-01

9.  The dependence of response amplitude and variance of cat visual cortical neurones on stimulus contrast.

Authors:  D J Tolhurst; J A Movshon; I D Thompson
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

10.  Modification of orientation sensitivity of cat visual cortex neurons by removal of GABA-mediated inhibition.

Authors:  T Tsumoto; W Eckart; O D Creutzfeldt
Journal:  Exp Brain Res       Date:  1979-01-15       Impact factor: 1.972

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  23 in total

1.  Motion opponency in visual cortex.

Authors:  D J Heeger; G M Boynton; J B Demb; E Seidemann; W T Newsome
Journal:  J Neurosci       Date:  1999-08-15       Impact factor: 6.167

2.  Membrane potential and firing rate in cat primary visual cortex.

Authors:  M Carandini; D Ferster
Journal:  J Neurosci       Date:  2000-01-01       Impact factor: 6.167

3.  How noise contributes to contrast invariance of orientation tuning in cat visual cortex.

Authors:  D Hansel; C van Vreeswijk
Journal:  J Neurosci       Date:  2002-06-15       Impact factor: 6.167

4.  The relative contribution of retinal and cortical mechanisms to simultaneous contrast.

Authors:  B Lange-Malecki; J Poppinga; O D Creutzfeldt
Journal:  Naturwissenschaften       Date:  1990-08

5.  Stimulus dependency and mechanisms of surround modulation in cortical area MT.

Authors:  Xin Huang; Thomas D Albright; Gene R Stoner
Journal:  J Neurosci       Date:  2008-12-17       Impact factor: 6.167

6.  Selective tuning for contrast in macaque area V4.

Authors:  Ilaria Sani; Elisa Santandrea; Ashkan Golzar; Maria Concetta Morrone; Leonardo Chelazzi
Journal:  J Neurosci       Date:  2013-11-20       Impact factor: 6.167

7.  A multiplicative model for spatial interaction in the human visual cortex.

Authors:  Xian Zhang; Jason C Park; Jennifer Salant; Sonya Thomas; Joy Hirsch; Donald C Hood
Journal:  J Vis       Date:  2008-06-03       Impact factor: 2.240

8.  Linearity and normalization in simple cells of the macaque primary visual cortex.

Authors:  M Carandini; D J Heeger; J A Movshon
Journal:  J Neurosci       Date:  1997-11-01       Impact factor: 6.167

9.  Contrast response functions in the visual wulst of the alert burrowing owl: a single-unit study.

Authors:  Pedro Gabrielle Vieira; João Paulo Machado de Sousa; Jerome Baron
Journal:  J Neurophysiol       Date:  2016-07-27       Impact factor: 2.714

10.  Contrast adaptation contributes to contrast-invariance of orientation tuning of primate V1 cells.

Authors:  Lionel G Nowak; Pascal Barone
Journal:  PLoS One       Date:  2009-03-10       Impact factor: 3.240

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