Literature DB >> 7143249

Analysis of orientation bias in cat retina.

W R Levick, L N Thibos.   

Abstract

1. Responses of cat retinal ganglion cells to a drifting sinusoidal grating stimulus were measured as a function of the grating orientation and spatial frequency.2. The response at fixed frequency and contrast varied with orientation in the manner of a cosine function. A new measure was introduced to quantify this orientation bias in the response domain on an absolute scale of 0-100%. Under experimental conditions designed to maximize the effect, the mean bias for 250 cells was 16% and the range was 0-46%. In 70% of cells there was significant bias.3. Orientation bias varied with spatial frequency and was maximal near the high-frequency limit. The majority of biassed cells preferred the same orientation at high and low frequencies but in some cells a reversal occurred: the orientation which gave maximum response at high frequencies gave minimum response at low frequencies. The greatest variation of cut-off frequency with orientation was (2/3) octave.4. Orientation bias was due to neural, not optical, factors. Nevertheless, the phenomenon could often be imitated by deliberately introduced optical astigmatism of up to 4 dioptres for brisk-sustained units and over 10 dioptres for brisk-transient units.5. The grating orientation preferred by cells varied systematically with position in the visual field. The central tendency was for the grating which yielded maximum response to lie parallel to the line joining the cell to the area centralis. This generalization failed for units within 2 degrees of the centre of the area centralis.6. Analysis of orientation bias indicates a functional asymmetry of receptive fields such that the centre mechanism, and sometimes also the surround mechanism, is elongated along the line joining cell to area centralis.

Mesh:

Year:  1982        PMID: 7143249      PMCID: PMC1224778          DOI: 10.1113/jphysiol.1982.sp014301

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


  18 in total

1.  Properties of cat retinal ganglion cells: a comparison of W-cells with X- and Y-cells.

Authors:  J Stone; Y Fukuda
Journal:  J Neurophysiol       Date:  1974-07       Impact factor: 2.714

2.  The morphological types of ganglion cells of the domestic cat's retina.

Authors:  B B Boycott; H Wässle
Journal:  J Physiol       Date:  1974-07       Impact factor: 5.182

3.  Brisk and sluggish concentrically organized ganglion cells in the cat's retina.

Authors:  B G Cleland; W R Levick
Journal:  J Physiol       Date:  1974-07       Impact factor: 5.182

4.  Cat retinal ganglion cells: size and shape of receptive field centres.

Authors:  P Hammond
Journal:  J Physiol       Date:  1974-10       Impact factor: 5.182

5.  Dendritic fields of the retinal ganglion cells in the cat.

Authors:  F M Honrubia; J H Elliott
Journal:  Arch Ophthalmol       Date:  1970-08

6.  A physiological mechanism for Hebb's postulate of learning.

Authors:  G S Stent
Journal:  Proc Natl Acad Sci U S A       Date:  1973-04       Impact factor: 11.205

7.  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

Review 8.  Form and function of cat retinal ganglion cells.

Authors:  W R Levick
Journal:  Nature       Date:  1975-04-24       Impact factor: 49.962

9.  Another tungsten microelectrode.

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

10.  Cat retinal ganglion cell dendritic fields.

Authors:  J E Brown; D Major
Journal:  Exp Neurol       Date:  1966-05       Impact factor: 5.330

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  59 in total

1.  Orientation sensitivity of ganglion cells in primate retina.

Authors:  Christopher L Passaglia; John B Troy; Lukas Rüttiger; Barry B Lee
Journal:  Vision Res       Date:  2002-03       Impact factor: 1.886

2.  The sensitivity of neurons in the lateral geniculate body of the cat to the orientation vectors of brightness gradients.

Authors:  N F Podvigin; E Poeppel; N B Kiseleva; I V Kozlov; E A Vershinina; M P Granstrem
Journal:  Neurosci Behav Physiol       Date:  2001 Nov-Dec

3.  Orientation selectivity in macaque V1: diversity and laminar dependence.

Authors:  Dario L Ringach; Robert M Shapley; Michael J Hawken
Journal:  J Neurosci       Date:  2002-07-01       Impact factor: 6.167

4.  Signals in macaque striate cortical neurons that support the perception of glass patterns.

Authors:  Matthew A Smith; Wyeth Bair; J Anthony Movshon
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

5.  Local sensitivity to stimulus orientation and spatial frequency within the receptive fields of neurons in visual area 2 of macaque monkeys.

Authors:  X Tao; B Zhang; E L Smith; S Nishimoto; I Ohzawa; Y M Chino
Journal:  J Neurophysiol       Date:  2011-11-23       Impact factor: 2.714

6.  Texture discrimination by cells in the cat lateral geniculate nucleus.

Authors:  H C Nothdurft
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

7.  Quantitative study of striate single unit responses in monkeys performing an orientation discrimination task.

Authors:  R Vogels; G A Orban
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

8.  Orientation bias of cat dorsal lateral geniculate cells: directional analysis of the major axis of the receptive field centre.

Authors:  B Ahmed; P Hammond
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

9.  Coarse-scale biases for spirals and orientation in human visual cortex.

Authors:  Jeremy Freeman; David J Heeger; Elisha P Merriam
Journal:  J Neurosci       Date:  2013-12-11       Impact factor: 6.167

10.  Subtype-dependent postnatal development of direction- and orientation-selective retinal ganglion cells in mice.

Authors:  Hui Chen; Xiaorong Liu; Ning Tian
Journal:  J Neurophysiol       Date:  2014-08-06       Impact factor: 2.714

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