Literature DB >> 2881303

End-stopped cells and binocular depth discrimination in the striate cortex of cats.

R Maske, S Yamane, P O Bishop.   

Abstract

Proposals concerning neural mechanisms for binocular depth discrimination have been criticized on the grounds that only striate cells with a preferred stimulus orientation not too far from the vertical can make significant horizontal disparity discriminations. We investigated this claim by preparing a two-dimensional array of position-disparity response profiles to moving light and dark bars from each of 18 cells in the simple family. From these arrays, it was possible to reconstruct disparity response profiles along any axis across the receptive field, irrespective of the cell's optimal stimulus orientation. This analysis showed that cells with a predominantly excitatory binocular response (N = 10) can make precise horizontal disparity discriminations, independent of their optimal stimulus orientation, provided that they are sufficiently end stopped. End-free cells, on the other hand, are effective for horizontal disparity discriminations only if their preferred orientation are near the vertical. Nearly all striate cells we examined were end-stopped to some degree and nearly half had an end inhibition sufficient to reduce the monocular response from the dominant eye to half its maximal amplitude. Cells having a predominantly inhibitory disparity response profile of the symmetric type (N = 8) have an inhibitory profile along every axis across the receptive field. An outline is given of a neural mechanism for the determination of absolute viewing distance based on the sensitivities of striate cells to vertical retinal-image disparities.

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Year:  1986        PMID: 2881303     DOI: 10.1098/rspb.1986.0085

Source DB:  PubMed          Journal:  Proc R Soc Lond B Biol Sci        ISSN: 0950-1193


  13 in total

1.  Asymmetric suppression outside the classical receptive field of the visual cortex.

Authors:  G A Walker; I Ohzawa; R D Freeman
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Image features selected by neurons of the cat primary visual cortex.

Authors:  I A Shevelev
Journal:  Neurosci Behav Physiol       Date:  2000 Sep-Oct

3.  The disinhibitory zone of the striate neuron receptive field and its sensitivity to cross-like figures.

Authors:  N A Lazareva; I A Shevelev; R V Novikova; A S Tikhomirov; G A Sharaev; D Yu Tsutskiridze
Journal:  Neurosci Behav Physiol       Date:  2002 Nov-Dec

4.  Depth-related visually evoked potentials by dynamic random-dot stereograms in humans: negative correlation between the peaks elicited by convergent and divergent disparities.

Authors:  Babür Sahinoğlu
Journal:  Eur J Appl Physiol       Date:  2003-12-24       Impact factor: 3.078

5.  Binocular interaction and disparity coding at the 17-18 border: contribution of the corpus callosum.

Authors:  F Lepore; A Samson; M C Paradis; M Ptito; J P Guillemot
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

Review 6.  Early computational processing in binocular vision and depth perception.

Authors:  Jenny Read
Journal:  Prog Biophys Mol Biol       Date:  2005-01       Impact factor: 3.667

7.  The time course of disinhibition of visual cortex neurons and sensitivity to cross-shaped figures.

Authors:  I A Shevelev; N A Lazareva; K A Saltykov; R V Novikova; A S Tikhomirov; G A Sharaev; D Yu Tsutskiridze
Journal:  Neurosci Behav Physiol       Date:  2006-01

8.  Binocular interactions and disparity coding in area 21a of cat extrastriate visual cortex.

Authors:  C Wang; B Dreher
Journal:  Exp Brain Res       Date:  1996-03       Impact factor: 1.972

9.  Binocular phase interactions in area 21a of the cat.

Authors:  R M Vickery; J W Morley
Journal:  J Physiol       Date:  1999-01-15       Impact factor: 5.182

10.  Understanding the cortical specialization for horizontal disparity.

Authors:  Jenny C A Read; Bruce G Cumming
Journal:  Neural Comput       Date:  2004-10       Impact factor: 2.026

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