Literature DB >> 8367474

Response variability in retinal ganglion cells of primates.

L J Croner1, K Purpura, E Kaplan.   

Abstract

The signal encoded by a sensory neuron is usually characterized as the cell's average response to repeated presentations of a stimulus. However, each stimulus presentation elicits a slightly different response. This response variability may obscure the signal represented by neural activity, but it might also be an important aspect of a neuron's message and in some instances may even serve useful function. Here we present evidence that response variability (noise) in primate retinal ganglion cells at photopic light levels is (i) independent of the amplitude of either the stimulus or the response and is therefore additive, (ii) independent of receptive field size and retinal eccentricity, and (iii) similar for all primate ganglion cells. Our results show that the primate retina maintains a uniform noise level across the entire visual field and suggest that the noise originates within the ganglion cells themselves.

Mesh:

Year:  1993        PMID: 8367474      PMCID: PMC47301          DOI: 10.1073/pnas.90.17.8128

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  18 in total

1.  The contrast sensitivity of retinal ganglion cells of the cat.

Authors:  C Enroth-Cugell; J G Robson
Journal:  J Physiol       Date:  1966-12       Impact factor: 5.182

2.  Dissection of the neuron network in the catfish inner retina. IV. Bidirectional interactions between amacrine and ganglion cells.

Authors:  H M Sakai; K I Naka
Journal:  J Neurophysiol       Date:  1990-01       Impact factor: 2.714

3.  Parasol and midget ganglion cells of the primate retina.

Authors:  M Watanabe; R W Rodieck
Journal:  J Comp Neurol       Date:  1989-11-15       Impact factor: 3.215

4.  Dissection of the neuron network in the catfish inner retina. II. Interactions between ganglion cells.

Authors:  H M Sakai; K Naka
Journal:  J Neurophysiol       Date:  1988-11       Impact factor: 2.714

5.  Dissection of the neuron network in the catfish inner retina. I. Transmission to ganglion cells.

Authors:  H M Sakai; K Naka
Journal:  J Neurophysiol       Date:  1988-11       Impact factor: 2.714

6.  Interactions between ganglion cells in cat retina.

Authors:  D N Mastronarde
Journal:  J Neurophysiol       Date:  1983-02       Impact factor: 2.714

7.  Statistics of the maintained discharge of cat retinal ganglion cells.

Authors:  L J Frishman; M W Levine
Journal:  J Physiol       Date:  1983-06       Impact factor: 5.182

8.  The dependence of response amplitude and variance of cat visual cortical neurones on stimulus contrast.

Authors:  D J Tolhurst; J A Movshon; I D Thompson
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

9.  Receptive field properties of x and y cells in the cat retina derived from contrast sensitivity measurements.

Authors:  R A Linsenmeier; L J Frishman; H G Jakiela; C Enroth-Cugell
Journal:  Vision Res       Date:  1982       Impact factor: 1.886

10.  Quantitative analysis of cat retinal ganglion cell response to visual stimuli.

Authors:  R W Rodieck
Journal:  Vision Res       Date:  1965-12       Impact factor: 1.886

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  34 in total

1.  Reliability of a fly motion-sensitive neuron depends on stimulus parameters.

Authors:  A K Warzecha; J Kretzberg; M Egelhaaf
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

2.  Decorrelation and efficient coding by retinal ganglion cells.

Authors:  Xaq Pitkow; Markus Meister
Journal:  Nat Neurosci       Date:  2012-03-11       Impact factor: 24.884

3.  Impact of noise on retinal coding of visual signals.

Authors:  Christopher L Passaglia; John B Troy
Journal:  J Neurophysiol       Date:  2004-04-07       Impact factor: 2.714

4.  Segregation of chromatic and luminance signals using a novel grating stimulus.

Authors:  Barry B Lee; Hao Sun; Arne Valberg
Journal:  J Physiol       Date:  2010-10-11       Impact factor: 5.182

5.  A method for estimating intrinsic noise in electroretinographic (ERG) signals.

Authors:  Andrew J Zele; Beatrix Feigl; Pradeep K Kambhampati; Amithavikram R Hathibelagal; Jan Kremers
Journal:  Doc Ophthalmol       Date:  2015-08-19       Impact factor: 2.379

6.  Origin of information-limiting noise correlations.

Authors:  Ingmar Kanitscheider; Ruben Coen-Cagli; Alexandre Pouget
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-30       Impact factor: 11.205

7.  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

8.  Response variability of marmoset parvocellular neurons.

Authors:  J D Victor; E M Blessing; J D Forte; P Buzás; P R Martin
Journal:  J Physiol       Date:  2006-11-23       Impact factor: 5.182

9.  Hue maps in primate striate cortex.

Authors:  Youping Xiao; Alexander Casti; Jun Xiao; Ehud Kaplan
Journal:  Neuroimage       Date:  2006-12-22       Impact factor: 6.556

10.  The perception of a familiar face is no more than the sum of its parts.

Authors:  Jason M Gold; Jarrett D Barker; Shawn Barr; Jennifer L Bittner; Alexander Bratch; W Drew Bromfield; Roy A Goode; Mary Jones; Doori Lee; Aparna Srinath
Journal:  Psychon Bull Rev       Date:  2014-12
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