Literature DB >> 7131312

Response latency of brisk-sustained (X) and brisk-transient (Y) cells in the cat retina.

J Bolz, G Rosner, H Wässle.   

Abstract

1. Several methods for evaluating light-evoked response latency and its variability in brisk-sustained (X) and brisk-transient (Y) retinal ganglion cells were tested. The most accurate procedure proved to be that described by Levick (1973), in which the time of the occurrence of the fourth impulse after stimulus onset is taken as an estimate of the latency.2. The shortest response latencies are obtained when the stimuli are the same size as the receptive field centre. At medium and high response amplitudes (> 150 impulses/sec) the response of brisk-transient (Y) cells to these optimal stimuli is 10-15 msec faster than that of adjacent brisk-sustained (X) cells.3. The response latency of brisk-sustained (X) cells for stimuli larger than the receptive field centre increases, whereas that of brisk-transient (Y) cells remains constant. Brisk-sustained (X) cells respond faster than do brisk-transient (Y) cells to stimuli smaller than the receptive field centre.4. No systematic difference exists between brisk-sustained (X) and brisk-transient (Y) cells in regard to the temporal variability of the response. The standard deviation of the latency for stimuli of optimal size decreases from 2.0-8.0 msec at medium stimulus contrast to 0.6-2.0 msec at high stimulus contrast.5. The response of OFF-centre cells to the disappearance of a light spot is always slower than that of an ON-centre cell of the same class to the onset of this stimulus. However, when OFF-centre cells are stimulated with dark spots, their response latency does not differ from that of ON-centre cells of the same class.6. No simple relationship exists between the response latency and the response amplitude. At medium and high discharge rates, most brisk-transient (Y) cells respond faster than an adjacent brisk-sustained (X) cell with equal response. At the same response amplitude, the latencies become shorter as the background illumination is raised. The same discharge rate can be obtained with stimuli of sub-optimal and supra-optimal size, but the latency for the larger stimulus is shorter than that for the smaller one. Latency, therefore, is an additional parameter characterizing the light-evoked response.

Mesh:

Year:  1982        PMID: 7131312      PMCID: PMC1225652          DOI: 10.1113/jphysiol.1982.sp014258

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


  48 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.  Contrasts in spatial organization of receptive fields at geniculate and retinal levels: centre, surround and outer surround.

Authors:  P Hammond
Journal:  J Physiol       Date:  1973-01       Impact factor: 5.182

3.  Receptive field organization of 'sustained' and 'transient' retinal ganglion cells which subserve different function roles.

Authors:  H Ikeda; M J Wright
Journal:  J Physiol       Date:  1972-12       Impact factor: 5.182

4.  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

5.  Conduction velocity as a parameter in the organisation of the afferent relay in the cat's lateral geniculate nucleus.

Authors:  J Stone; K P Hoffman
Journal:  Brain Res       Date:  1971-09-24       Impact factor: 3.252

6.  Transient and steady state stimulus-response relations for cat retinal ganglion cells.

Authors:  R W Winters; J W Walters
Journal:  Vision Res       Date:  1970-06       Impact factor: 1.886

7.  Responses of cat retinal ganglion cells to brief flashes of light.

Authors:  W R Levick; J L Zacks
Journal:  J Physiol       Date:  1970-03       Impact factor: 5.182

8.  Quantitative aspects of gain and latency in the cat retina.

Authors:  B G Cleland; C Enroth-Cugell
Journal:  J Physiol       Date:  1970-01       Impact factor: 5.182

9.  Receptive field organization of cat optic nerve fibers with special reference to conduction velocity.

Authors:  Y Fukada
Journal:  Vision Res       Date:  1971-03       Impact factor: 1.886

10.  Another tungsten microelectrode.

Authors:  W R Levick
Journal:  Med Biol Eng       Date:  1972-07
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2.  Pretectal jerk neuron activity during saccadic eye movements and visual stimulations in the cat.

Authors:  G Schweigart; K P Hoffmann
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

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5.  Modeling of region-specific fMRI BOLD neurovascular response functions in rat brain reveals residual differences that correlate with the differences in regional evoked potentials.

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6.  Spatial and temporal features of synaptic to discharge receptive field transformation in cat area 17.

Authors:  Lionel G Nowak; Maria V Sanchez-Vives; David A McCormick
Journal:  J Neurophysiol       Date:  2009-11-11       Impact factor: 2.714

7.  The structure and precision of retinal spike trains.

Authors:  M J Berry; D K Warland; M Meister
Journal:  Proc Natl Acad Sci U S A       Date:  1997-05-13       Impact factor: 11.205

8.  Selectivity of direct and network-mediated stimulation of the retinal ganglion cells with epi-, sub- and intraretinal electrodes.

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Journal:  J Neural Eng       Date:  2014-03-10       Impact factor: 5.379

9.  Correlation of activity in neighbouring goldfish ganglion cells: relationship between latency and lag.

Authors:  J A Johnsen; M W Levine
Journal:  J Physiol       Date:  1983-12       Impact factor: 5.182

10.  Action and localization of gamma-aminobutyric acid in the cat retina.

Authors:  J Bolz; T Frumkes; T Voigt; H Wässle
Journal:  J Physiol       Date:  1985-05       Impact factor: 5.182

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