Literature DB >> 3609203

Expression of "retinal" contrast gain control by neurons of the cat's lateral geniculate nucleus.

G Sclar.   

Abstract

This paper describes the temporal tuning of cells in the lateral geniculate nucleus of the cat (27 X cells, 51 Y cells) and how this changes with stimulus contrast. Drifting sinusoidal gratings of optimal spatial frequency were presented at 7 temporal frequencies (0.5, 1, 2, 4, 8, 16 and 32 Hz) and 4 contrasts (10, 20, 40, 80%). For some cells response growth at all temporal frequencies was proportional to changes in contrast. Thus, their temporal tuning functions, on log-log axes, were displaced vertically with increasing contrast. This shift also largely characterizes the response to low temporal frequencies of the other neurons studied. For these other cells, however, responses to high temporal frequencies grew disproportionately large with increasing contrast generally causing their tuning functions to change shape. Typically the peaks of these functions shifted to higher frequencies at higher contrasts. Most of the X cells studied displayed behavior of the first type, while Y cells usually followed the second pattern. This qualitative impression was confirmed quantitatively. Cubic spline functions were fit to the temporal tuning functions obtained at different contrast levels and the peaks of the curves were extracted. X and Y cells preferred similar temporal frequencies at low contrast levels (X mean = 8.1 Hz; Y mean = 8.4 Hz) but Y cell values were significantly higher at higher contrasts (80%) (X mean = 12.0 Hz; Y mean = 16.8 Hz).(ABSTRACT TRUNCATED AT 250 WORDS)

Mesh:

Year:  1987        PMID: 3609203     DOI: 10.1007/bf00270692

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


  25 in total

1.  Quantitative analysis of retinal ganglion cell classifications.

Authors:  S Hochstein; R M Shapley
Journal:  J Physiol       Date:  1976-11       Impact factor: 5.182

2.  A study of Golgi preparations from the dorsal lateral geniculate nucleus of the adult cat.

Authors:  R W Guillery
Journal:  J Comp Neurol       Date:  1966-09       Impact factor: 3.215

3.  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

4.  How the contrast gain control modifies the frequency responses of cat retinal ganglion cells.

Authors:  R M Shapley; J D Victor
Journal:  J Physiol       Date:  1981-09       Impact factor: 5.182

5.  The effect of contrast on the transfer properties of cat retinal ganglion cells.

Authors:  R M Shapley; J D Victor
Journal:  J Physiol       Date:  1978-12       Impact factor: 5.182

6.  Spatial properties of X and Y cells in the lateral geniculate nucleus of the cat and conduction veolcities of their inputs.

Authors:  Y T So; R Shapley
Journal:  Exp Brain Res       Date:  1979-08-01       Impact factor: 1.972

7.  The contrast gain control of the cat retina.

Authors:  R Shapley; J D Victor
Journal:  Vision Res       Date:  1979       Impact factor: 1.886

8.  Another tungsten microelectrode.

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

9.  The origin of the S (slow) potential in the mammalian lateral geniculate nucleus.

Authors:  E Kaplan; R Shapley
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

10.  The nonlinear pathway of Y ganglion cells in the cat retina.

Authors:  J D Victor; R M Shapley
Journal:  J Gen Physiol       Date:  1979-12       Impact factor: 4.086

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  9 in total

1.  Adaptation to temporal contrast in primate and salamander retina.

Authors:  D Chander; E J Chichilnisky
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

2.  Human ocular following responses are plastic: evidence for control by temporal frequency-dependent cortical adaptation.

Authors:  T Maddess; M R Ibbotson
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

3.  Distinct properties of stimulus-evoked bursts in the lateral geniculate nucleus.

Authors:  Henry J Alitto; Theodore G Weyand; W Martin Usrey
Journal:  J Neurosci       Date:  2005-01-12       Impact factor: 6.167

4.  Surround suppression and temporal processing of visual signals.

Authors:  Henry J Alitto; W Martin Usrey
Journal:  J Neurophysiol       Date:  2015-02-04       Impact factor: 2.714

5.  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

6.  Cortical contrast gain control in human spatial vision.

Authors:  P Bobak; I Bodis-Wollner; M S Marx
Journal:  J Physiol       Date:  1988-11       Impact factor: 5.182

7.  Factors governing the adaptation of cells in area-17 of the cat visual cortex.

Authors:  T Maddess; M E McCourt; B Blakeslee; R B Cunningham
Journal:  Biol Cybern       Date:  1988       Impact factor: 2.086

8.  Contrast gain control and retinogeniculate communication.

Authors:  Henry J Alitto; Daniel L Rathbun; Tucker G Fisher; Prescott C Alexander; W Martin Usrey
Journal:  Eur J Neurosci       Date:  2018-03-23       Impact factor: 3.386

9.  Stimulus Contrast and Retinogeniculate Signal Processing.

Authors:  Daniel L Rathbun; Henry J Alitto; David K Warland; W Martin Usrey
Journal:  Front Neural Circuits       Date:  2016-02-19       Impact factor: 3.492

  9 in total

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