Literature DB >> 11152723

Influence of contrast on the responses of marmoset lateral geniculate cells to drifting gratings.

J Kremers1, L C Silveira, B E Kilavik.   

Abstract

The responses of lateral geniculate nucleus (LGN) cells in the common marmoset (Callithrix jacchus) to drifting luminance or cone isolating gratings of different spatial frequencies and contrasts were measured. The response noise, defined as the variability of the responses to single sweeps in the complex plane, was independent of stimulus contrast and spatial frequency but increased with increasing overall responsiveness of the cell. The signal-to-noise ratio of parvocellular (PC) cells was smaller than of magnocellular (MC) cells. At each contrast, the response amplitude as a function of spatial frequency could be described with a difference of Gaussians model. With this model, the sizes and the peak sensitivities of the receptive field centers and surrounds were estimated. It was found that receptive field center and surround sizes of LGN cells decrease slightly with increasing contrast. Further, the peak sensitivity decreases with increasing contrast. The two factors are involved in a decrease in responsivity (the response per unit contrast) with increasing contrast which is compatible to response saturation for low spatial frequency stimuli. PC cells did not saturate as much to luminance stimuli although some saturation was found with cone isolating gratings. We found that the response phase lag of both PC and MC cells decreased with increasing contrast, which cannot be explained on the basis of linear response behavior. Apparently the phase of LGN cell responses to drifting gratings is altered in comparison with the retinal inputs by additional nonlinearities.

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Year:  2001        PMID: 11152723     DOI: 10.1152/jn.2001.85.1.235

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  14 in total

1.  Extraclassical receptive field properties of parvocellular, magnocellular, and koniocellular cells in the primate lateral geniculate nucleus.

Authors:  Samuel G Solomon; Andrew J R White; Paul R Martin
Journal:  J Neurosci       Date:  2002-01-01       Impact factor: 6.167

2.  Centre and surround responses of marmoset lateral geniculate neurones at different temporal frequencies.

Authors:  Bjørg Elisabeth Kilavik; Luiz Carlos L Silveira; Jan Kremers
Journal:  J Physiol       Date:  2003-02-01       Impact factor: 5.182

3.  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

4.  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

5.  Interspike interval analysis of retinal ganglion cell receptive fields.

Authors:  Daniel L Rathbun; Henry J Alitto; Theodore G Weyand; W Martin Usrey
Journal:  J Neurophysiol       Date:  2007-05-23       Impact factor: 2.714

6.  Linking lateral interactions in flicker perception to lateral geniculate nucleus cell responses.

Authors:  Vladislav Kozyrev; Luiz Carlos L Silveira; Jan Kremers
Journal:  J Physiol       Date:  2007-04-05       Impact factor: 5.182

7.  Binocular summation for reflexive eye movements.

Authors:  Christian Quaia; Lance M Optican; Bruce G Cumming
Journal:  J Vis       Date:  2018-04-01       Impact factor: 2.240

8.  Transmission of colour and acuity signals by parvocellular cells in marmoset monkeys.

Authors:  Paul R Martin; Esther M Blessing; Péter Buzás; Brett A Szmajda; Jason D Forte
Journal:  J Physiol       Date:  2011-04-11       Impact factor: 5.182

9.  Suppression and Contrast Normalization in Motion Processing.

Authors:  Christian Quaia; Lance M Optican; Bruce G Cumming
Journal:  J Neurosci       Date:  2017-10-10       Impact factor: 6.167

10.  Contrast dependence and differential contributions from somatostatin- and parvalbumin-expressing neurons to spatial integration in mouse V1.

Authors:  Hendrikje Nienborg; Andrea Hasenstaub; Ian Nauhaus; Hiroki Taniguchi; Z Josh Huang; Edward M Callaway
Journal:  J Neurosci       Date:  2013-07-03       Impact factor: 6.167

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