Literature DB >> 7320898

The relationship between response amplitude and contrast for cat striate cortical neurones.

A F Dean.   

Abstract

1. The activity of forty-three neurones in the cat's striate cortex in response to laterally moving sinusoidal gratings of various contrasts was recorded, in order to examine the relationship between response amplitude and contrast. 2. Neurones seemed to exhibit contrast thresholds: stimuli of very low contrast failed to evoke a change in the response amplitude from the concurrent levels of spontaneous activity. 3. The suprathreshold portion of the response-contrast relation was found to be monotonic. Typically, the relation was adequately described as linear up to contrasts of about 0.3, above which, varying degrees of saturation were evident. 4. The response-contrast relation had a higher threshold and a shallower slope when the spatial frequency was not optimal for the neurone. 5. The slope, or gain, of the response-contrast relation for a stimulus of optimal orientation and spatial frequency varied considerably from neurone to neurone. The gains of special complex cells were significantly greater than those of either standard complex cells or simple cells. 6. The distributions of contrast threshold and contrast gain were examined for their dependence on optimal spatial frequency. Contrast threshold was significantly positively correlated with optimal spatial frequency, while contrast gain was significantly negatively correlated with optimal spatial frequency. This behaviour is consistent with an optical contribution to the measured response properties of striate cortical neurones.

Mesh:

Year:  1981        PMID: 7320898      PMCID: PMC1245500          DOI: 10.1113/jphysiol.1981.sp013875

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  25 in total

1.  The outer disinhibitory surround of the retinal ganglion cell receptive field.

Authors:  H Ikeda; M J Wright
Journal:  J Physiol       Date:  1972-10       Impact factor: 5.182

2.  Repetitive impulses generated in fast and slow pyramidal tract cells by intracellularly applied current steps.

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3.  The visual cortex as a spatial frequency analyser.

Authors:  L Maffei; A Fiorentini
Journal:  Vision Res       Date:  1973-07       Impact factor: 1.886

4.  Orientation specificity and response variability of cells in the striate cortex.

Authors:  G H Henry; P O Bishop; R M Tupper; B Dreher
Journal:  Vision Res       Date:  1973-09       Impact factor: 1.886

5.  Glass-coated platinum-plated tungsten microelectrodes.

Authors:  E G Merrill; A Ainsworth
Journal:  Med Biol Eng       Date:  1972-09

6.  Hypercomplex cells in the cat's striate cortex.

Authors:  B Dreher
Journal:  Invest Ophthalmol       Date:  1972-05

7.  Application of Fourier analysis to the visibility of gratings.

Authors:  F W Campbell; J G Robson
Journal:  J Physiol       Date:  1968-08       Impact factor: 5.182

8.  Three factors limiting the reliable detection of light by retinal ganglion cells of the cat.

Authors:  H B Barlow; W R Levick
Journal:  J Physiol       Date:  1969-01       Impact factor: 5.182

9.  Another tungsten microelectrode.

Authors:  W R Levick
Journal:  Med Biol Eng       Date:  1972-07

10.  Optical and retinal factors affecting visual resolution.

Authors:  F W Campbell; D G Green
Journal:  J Physiol       Date:  1965-12       Impact factor: 5.182

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  35 in total

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3.  Linear systems analysis of functional magnetic resonance imaging in human V1.

Authors:  G M Boynton; S A Engel; G H Glover; D J Heeger
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4.  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

5.  The effects of contrast on the linearity of spatial summation of simple cells in the cat's striate cortex.

Authors:  D J Tolhurst; A F Dean
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

6.  Scaling of perceptual errors can predict the shape of neural tuning curves.

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7.  A retinal source of spatial contrast gain control.

Authors:  Benjamin Scholl; Kenneth W Latimer; Nicholas J Priebe
Journal:  J Neurosci       Date:  2012-07-18       Impact factor: 6.167

8.  Contrast adaptation and representation in human early visual cortex.

Authors:  Justin L Gardner; Pei Sun; R Allen Waggoner; Kenichi Ueno; Keiji Tanaka; Kang Cheng
Journal:  Neuron       Date:  2005-08-18       Impact factor: 17.173

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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