Literature DB >> 4747229

Adaptation and dynamics of cat retinal ganglion cells.

C Enroth-Cugell, R M Shapley.   

Abstract

1. The impulse/quantum (I/Q) ratio was measured as a function of background illumination for rod-dominated, pure central, linear square-wave responses of retinal ganglion cells in the cat.2. The I/Q ratio was constant at low backgrounds (dark adapted state) and inversely proportional to the 0.9 power of the background at high backgrounds (the light adapted state). There was an abrupt transition from the dark-adapted state to the light-adapted state.3. It was possible to define the adaptation level at a particular background as the ratio (I/Q ratio at that background)/(dark adapted I/Q ratio).4. The time course of the square-wave response was correlated with the adaptation level. The response was sustained in the dark-adapted state, partially transient at the transition level, and progressively more transient the lower the impulse/quantum ratio of the ganglion cell became. This was true both for on-centre and off-centre cells.5. The frequency response of the central response mechanism at different adaptation levels was measured. It was a low-pass characteristic in the dark-adapted state and became progressively more of a bandpass characteristic as the cell became more light-adapted.6. The rapidity of onset of adaptation was measured with a time-varying adapting light. The impulse/quantum ratio is reset within 100 msec of the onset of the conditioning light, and is kept at the new value throughout the time the conditioning light is on.7. These results can be explained by a nonlinear feedback model. In the model, it is postulated that the exponential function of the horizontal cell potential controls transmission from rods to bipolars. This model has an abrupt transition from dark- to light-adapted states, and its response dynamics are correlated with adaptation level.

Mesh:

Year:  1973        PMID: 4747229      PMCID: PMC1350567          DOI: 10.1113/jphysiol.1973.sp010308

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


  37 in total

1.  Organization of the primate retina: electron microscopy.

Authors:  J E Dowling; B B Boycott
Journal:  Proc R Soc Lond B Biol Sci       Date:  1966-11-15

2.  Voltage noise in Limulus visual cells.

Authors:  F A Dodge; B W Knight; J Toyoda
Journal:  Science       Date:  1968-04-05       Impact factor: 47.728

3.  Quantitative aspects of sensitivity and summation in the cat retina.

Authors:  B G Cleland; C Enroth-cugell
Journal:  J Physiol       Date:  1968-09       Impact factor: 5.182

4.  Summing properties of the cat's retinal ganglion cell.

Authors:  J Stone; M Fabian
Journal:  Vision Res       Date:  1968-08       Impact factor: 1.886

5.  The cat local electroretinogram to incremental stimuli.

Authors:  R W Rodieck; R W Ford
Journal:  Vision Res       Date:  1969-01       Impact factor: 1.886

6.  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

7.  Cat colour vision: one cone process or several?

Authors:  N W Daw; A L Pearlman
Journal:  J Physiol       Date:  1969-05       Impact factor: 5.182

8.  Optic nerve impulses and Weber's law.

Authors:  H B Barlow
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1965

9.  Spatiotemporal modulation transfer in the human eye.

Authors:  F L van Nes; J J Koenderink; H Nas; M A Bouman
Journal:  J Opt Soc Am       Date:  1967-09

10.  Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording.

Authors:  F S Werblin; J E Dowling
Journal:  J Neurophysiol       Date:  1969-05       Impact factor: 2.714

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  62 in total

1.  Rectification of cGMP-activated channels induced by phosphorylation in dogfish retinal 'on' bipolar cells.

Authors:  R A Shiells; G Falk
Journal:  J Physiol       Date:  2001-09-15       Impact factor: 5.182

2.  A dopamine- and protein kinase A-dependent mechanism for network adaptation in retinal ganglion cells.

Authors:  C F Vaquero; A Pignatelli; G J Partida; A T Ishida
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

3.  Short-term adaptation and incremental responses of single auditory-nerve fibers.

Authors:  R L Smith; J J Zwislocki
Journal:  Biol Cybern       Date:  1975       Impact factor: 2.086

4.  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

5.  Retinal intrinsic optical signals in a cat model of primary congenital glaucoma.

Authors:  Jesse B Schallek; Gillian J McLellan; Suresh Viswanathan; Daniel Y Ts'o
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-04-18       Impact factor: 4.799

6.  Non-linear spatial summation in cat retinal ganglion cells at different background levels.

Authors:  R A Linsenmeier; H G Jakiela
Journal:  Exp Brain Res       Date:  1979-07-02       Impact factor: 1.972

7.  Retinal ganglion cell adaptation to small luminance fluctuations.

Authors:  Daniel K Freeman; Gilberto Graña; Christopher L Passaglia
Journal:  J Neurophysiol       Date:  2010-06-10       Impact factor: 2.714

8.  Visual stimulation switches the polarity of excitatory input to starburst amacrine cells.

Authors:  Anna L Vlasits; Rémi Bos; Ryan D Morrie; Cécile Fortuny; John G Flannery; Marla B Feller; Michal Rivlin-Etzion
Journal:  Neuron       Date:  2014-08-21       Impact factor: 17.173

9.  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

10.  Neuronal plasticity in the afferent visual system. I. Effect of flicker stimulation on responses of retinal and geniculate units in the cat.

Authors:  C S Adorjani; R von der Heydt; G Baumgartner
Journal:  Psychol Res       Date:  1975-12-18
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