Literature DB >> 6655589

Spatio-temporal interaction in neurones of the cat's dorsal lateral geniculate nucleus.

J B Troy.   

Abstract

Temporal contrast sensitivities in the range 0.33-42 Hz for optimum spatial frequency grating stimuli were measured for large populations of XG and YG neurones. For fewer cells, complete spatial contrast sensitivity profiles were measured at a series of temporal frequencies and, in some cases, at a range of levels of retinal illumination too. Contrast sensitivities were measured from responses of cells reliably different from their maintained discharges. The cells' discharges were recorded extracellularly from the binocular segment of the A laminae of the cat's dorsal lateral geniculate nucleus. At their respective optimum spatial frequencies, YG cell were more sensitive on average than XG cells for most temporal frequencies, though the average temporal contrast sensitivity profiles of both cell classes had similar shapes. The optimum temporal frequency for both cell types was around 5 Hz. XG and YG cells seem to be relatively less sensitive to low temporal frequencies than their ganglion cell counterparts. At a retinal illumination of 230 cd/m2 (pupil, 3 mm2), increasing temporal frequency in the range 0.65-21 Hz produced a relative improvement in low spatial frequency contrast sensitivity in most XG and all YG cells studied. There were some XG cells, though, which showed little or no effect of temporal frequency on their spatial contrast sensitivity curves. At all temporal frequencies, the shapes of spatial contrast sensitivity curves and the cells' temporal contrast sensitivity profiles were not markedly dependent on the criterion level set to measure 'threshold' contrast. Reducing the level of retinal illumination in the range 230-0.007 cd/m2 (pupil, 3 mm2) produced a fall in contrast sensitivities for both XG and YG cells. The loss in sensitivity was more marked at high spatial and high temporal frequencies. The similar shapes of the temporal contrast sensitivity curves of XG and YG cells weakens the suggestion that the human counterparts of these cells would provide a suitable physiological substrate for the psychophysical sustained and transient channels. Although the behaviour of XG and YG cells parallels quite closely changes in cat and human psychophysical spatial contrast sensitivities with temporal frequency and retinal illumination, many problems remain for equating results from the two fields.

Entities:  

Mesh:

Year:  1983        PMID: 6655589      PMCID: PMC1193850          DOI: 10.1113/jphysiol.1983.sp014949

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


  25 in total

1.  The control of retinal ganglion cell discharge by receptive field surrounds.

Authors:  C Enroth-Cugell; P Lennie
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

2.  Spatial and temporal contrast sensitivity of striate cortical neurones.

Authors:  D J Tolhurst; J A Movshon
Journal:  Nature       Date:  1975-10-23       Impact factor: 49.962

3.  Adaptation and dynamics in X-cells and Y-cells of the cat retina.

Authors:  H G Jakiela; C Enroth-Cugell
Journal:  Exp Brain Res       Date:  1976-02-26       Impact factor: 1.972

4.  Temporal determinants of the form of the spatial contrast threshold MTF.

Authors:  L E Arend
Journal:  Vision Res       Date:  1976       Impact factor: 1.886

5.  Spatial frequency and orientation tuning curves of visual neurones in the cat: effects of mean luminance.

Authors:  S Bisti; R Clement; L Maffei; L Mecacci
Journal:  Exp Brain Res       Date:  1977-03-30       Impact factor: 1.972

6.  Adaptation and dynamics of cat retinal ganglion cells.

Authors:  C Enroth-Cugell; R M Shapley
Journal:  J Physiol       Date:  1973-09       Impact factor: 5.182

7.  Analysis of the response characteristics of optic tract and geniculate units and their mutual relationship.

Authors:  A M Coenen; H J Gerrits; A J Vendrik
Journal:  Exp Brain Res       Date:  1972-10-29       Impact factor: 1.972

8.  Separate channels for the analysis of the shape and the movement of moving visual stimulus.

Authors:  D J Tolhurst
Journal:  J Physiol       Date:  1973-06       Impact factor: 5.182

9.  Inhibitory interaction in the cat's lateral geniculate nucleus.

Authors:  W Singer; E Pöppel; O Creutzfeldt
Journal:  Exp Brain Res       Date:  1972       Impact factor: 1.972

10.  Dark adaptation and receptive field organisation of cells in the cat lateral geniculate nucleus.

Authors:  V Virsu; B B Lee; O D Creutzfeldt
Journal:  Exp Brain Res       Date:  1977-01-18       Impact factor: 1.972

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  9 in total

1.  Sluggish and brisk ganglion cells detect contrast with similar sensitivity.

Authors:  Ying Xu; Narender K Dhingra; Robert G Smith; Peter Sterling
Journal:  J Neurophysiol       Date:  2004-12-15       Impact factor: 2.714

2.  The variability of the maintained discharge of cat dorsal lateral geniculate cells.

Authors:  M W Levine; J B Troy
Journal:  J Physiol       Date:  1986-06       Impact factor: 5.182

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

Authors:  G Sclar
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

4.  Detection latencies of X and Y type cells of the cat's dorsal lateral geniculate nucleus.

Authors:  J B Troy; P Lennie
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

5.  Spatial contrast sensitivities of X and Y type neurones in the cat's dorsal lateral geniculate nucleus.

Authors:  J B Troy
Journal:  J Physiol       Date:  1983-11       Impact factor: 5.182

6.  A comparison of visual responses of cat lateral geniculate nucleus neurones with those of ganglion cells afferent to them.

Authors:  B G Cleland; B B Lee
Journal:  J Physiol       Date:  1985-12       Impact factor: 5.182

7.  Contrast sensitivity of cats and humans in scotopic and mesopic conditions.

Authors:  Incheol Kang; Rachel E Reem; Amy L Kaczmarowski; Joseph G Malpeli
Journal:  J Neurophysiol       Date:  2009-05-20       Impact factor: 2.714

8.  Temporal and spatial tuning of dorsal lateral geniculate nucleus neurons in unanesthetized rats.

Authors:  Balaji Sriram; Philip M Meier; Pamela Reinagel
Journal:  J Neurophysiol       Date:  2016-03-02       Impact factor: 2.714

9.  Spatiotemporal frequency responses of cat retinal ganglion cells.

Authors:  L J Frishman; A W Freeman; J B Troy; D E Schweitzer-Tong; C Enroth-Cugell
Journal:  J Gen Physiol       Date:  1987-04       Impact factor: 4.086

  9 in total

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