Literature DB >> 11131514

Spatial summation in lateral geniculate nucleus and visual cortex.

H E Jones1, I M Andolina, N M Oakely, P C Murphy, A M Sillito.   

Abstract

We have compared the spatial summation characteristics of cells in the primary visual cortex with those of cells in the dorsal lateral geniculate nucleus (LGN) that provide the input to the cortex. We explored the influence of varying the diameter of a patch of grating centred over the receptive field and quantitatively determined the optimal summation diameter and the degree of surround suppression for cells at both levels of the visual system using the same stimulus parameters. The mean optimal summation size for LGN cells (0.90 degrees) was much smaller than that of cortical cells (3.58 degrees). Virtually all LGN cells exhibited strong surround suppression with a mean value of 74%+/-1.61% SEM for the population as a whole. This potent surround suppression in the cells providing the input to the cortex suggests that cortical cells must integrate their much larger summation fields from the low firing rates associated with the suppression plateau of the LGN cell responses. Our data suggest that the strongest input to cortical cells will arise from geniculate cells representing areas of visual space located at the borders of a visual stimulus. We suggest that analysis of response properties by patterns centred over the receptive fields of cells may give a misleading impression of the process of the representation. Analysis of pattern terminations or salient borders over the receptive field may provide much more insight into the processing algorithms involved in stimulus representation.

Mesh:

Year:  2000        PMID: 11131514     DOI: 10.1007/s002210000574

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  39 in total

1.  Contrast's effect on spatial summation by macaque V1 neurons.

Authors:  M P Sceniak; D L Ringach; M J Hawken; R Shapley
Journal:  Nat Neurosci       Date:  1999-08       Impact factor: 24.884

2.  Synaptic interactions between thalamic inputs to simple cells in cat visual cortex.

Authors:  W M Usrey; J M Alonso; R C Reid
Journal:  J Neurosci       Date:  2000-07-15       Impact factor: 6.167

3.  Suppression outside the classical cortical receptive field.

Authors:  G A Walker; I Ohzawa; R D Freeman
Journal:  Vis Neurosci       Date:  2000 May-Jun       Impact factor: 3.241

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Journal:  Vision Res       Date:  1992-05       Impact factor: 1.886

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Authors:  C D Gilbert
Journal:  J Physiol       Date:  1977-06       Impact factor: 5.182

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Authors:  D Y Ts'o; C D Gilbert
Journal:  J Neurosci       Date:  1988-05       Impact factor: 6.167

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Authors:  S M Sherman; C Koch
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

8.  Relationships between horizontal interactions and functional architecture in cat striate cortex as revealed by cross-correlation analysis.

Authors:  D Y Ts'o; C D Gilbert; T N Wiesel
Journal:  J Neurosci       Date:  1986-04       Impact factor: 6.167

9.  Polyneuronal innervation of spiny stellate neurons in cat visual cortex.

Authors:  B Ahmed; J C Anderson; R J Douglas; K A Martin; J C Nelson
Journal:  J Comp Neurol       Date:  1994-03-01       Impact factor: 3.215

10.  The spatial extent of excitatory and inhibitory zones in the receptive field of superficial layer hypercomplex cells.

Authors:  A M Sillito
Journal:  J Physiol       Date:  1977-12       Impact factor: 5.182

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  33 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

Review 2.  Corticothalamic interactions in the transfer of visual information.

Authors:  Adam M Sillito; Helen E Jones
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

Review 3.  Corticogeniculate feedback and visual processing in the primate.

Authors:  Farran Briggs; W Martin Usrey
Journal:  J Physiol       Date:  2010-08-19       Impact factor: 5.182

4.  Suppressive surrounds and contrast gain in magnocellular-pathway retinal ganglion cells of macaque.

Authors:  Samuel G Solomon; Barry B Lee; Hao Sun
Journal:  J Neurosci       Date:  2006-08-23       Impact factor: 6.167

5.  Cue-invariant detection of centre-surround discontinuity by V1 neurons in awake macaque monkey.

Authors:  Zhi-Ming Shen; Wei-Feng Xu; Chao-Yi Li
Journal:  J Physiol       Date:  2007-06-28       Impact factor: 5.182

6.  Origin and dynamics of extraclassical suppression in the lateral geniculate nucleus of the macaque monkey.

Authors:  Henry J Alitto; W Martin Usrey
Journal:  Neuron       Date:  2008-01-10       Impact factor: 17.173

Review 7.  Emerging views of corticothalamic function.

Authors:  Farran Briggs; W Martin Usrey
Journal:  Curr Opin Neurobiol       Date:  2008-10-06       Impact factor: 6.627

8.  Neurometabolic coupling differs for suppression within and beyond the classical receptive field in visual cortex.

Authors:  Baowang Li; Ralph D Freeman
Journal:  J Physiol       Date:  2011-05-09       Impact factor: 5.182

9.  A cross-species comparison of corticogeniculate structure and function.

Authors:  J Michael Hasse; Farran Briggs
Journal:  Vis Neurosci       Date:  2017-11-16       Impact factor: 3.241

10.  Morphological bases of suppressive and facilitative spatial summation in the striate cortex of the cat.

Authors:  Xue-Mei Song; Ye Wang; Zhao Zhu; Chao-Yi Li
Journal:  PLoS One       Date:  2010-11-29       Impact factor: 3.240

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