Literature DB >> 1586654

Binocular interactions in the cat's dorsal lateral geniculate nucleus, II: Effects on dominant-eye spatial-frequency and contrast processing.

L Tong1, W Guido, N Tumosa, P D Spear, S Heidenreich.   

Abstract

The present study tested the hypothesis that nondominant-eye influences on lateral geniculate nucleus (LGN) neurons affect the processing of spatial and contrast information from the dominant eye. To do this, we determined the effects of stimulating the nondominant eye at its optimal spatial frequency on the responses of LGN cells to sine-wave gratings of different spatial frequency and contrast presented to the dominant eye. Detailed testing was carried out on 49 cells that had statistically significant responses to stimulation of the nondominant eye alone. Spatial-frequency response functions to nondominant-eye stimulation indicated that the responses were spatially tuned, as reported previously (Guido et al., 1989). Optimal spatial frequencies through the nondominant eye were significantly correlated with the optimal spatial frequencies through the dominant eye (r = 0.54; P less than 0.0001), and the optimal spatial frequencies were fairly similar for the two eyes. Nondominant-eye stimulation changed the maximal amplitude of the fundamental (F1) response to dominant-eye stimulation for only about 45% (22 of 49) of the cells that responded to nondominant-eye stimulation alone. The response vs. contrast function through the dominant eye was altered for 73% of the cells (51% independent of spatial frequency). Three types of effects were observed: a change in the initial slope of the response vs. contrast function (contrast gain), a change in the response amplitude at which saturation occurred, or an overall change in response at all contrasts. The incidence of these changes was similar for X and Y cells in LGN layers A, A1, and C (only four W cells were tested). Nondominant-eye stimulation had little or no effect on the sizes or sensitivities of the receptive-field centers or surrounds for the dominant eye. In addition, nondominant-eye stimulation had little or no effect on optimal spatial frequency, spatial resolution, or the bandwidth of spatial-frequency contrast sensitivity curves for the dominant eye. Possible functions of binocular interactions in the LGN are considered. The present results suggest a role in interocular contrast-gain control. Interocular contrast differences can occur before the acquisition of binocular fusion, when the two eyes are viewing different aspects of a visual stimulus. Psychophysical and physiological studies suggest that an interocular mechanism exists to maintain relatively constant binocular interactions despite differences in interocular contrast. The present results suggest that at least part of this mechanism occurs in the LGN.

Mesh:

Year:  1992        PMID: 1586654     DOI: 10.1017/s0952523800005654

Source DB:  PubMed          Journal:  Vis Neurosci        ISSN: 0952-5238            Impact factor:   3.241


  9 in total

1.  Binocular processing in the cat's dorsal lateral geniculate nucleus. III. Spatial frequency, orientation, and direction sensitivity of nondominant-eye influences.

Authors:  R J Moore; P D Spear; C B Kim; J T Xue
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

2.  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

3.  Correlation-based development of ocularly matched orientation and ocular dominance maps: determination of required input activities.

Authors:  E Erwin; K D Miller
Journal:  J Neurosci       Date:  1998-12-01       Impact factor: 6.167

4.  Non-dominant suppression in the dorsal lateral geniculate nucleus of the cat: laminar differences and class specificity.

Authors:  C Wang; B Dreher; W Burke
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

5.  Binocular combination of luminance profiles.

Authors:  Jian Ding; Dennis M Levi
Journal:  J Vis       Date:  2017-11-01       Impact factor: 2.240

6.  Synaptic organization of thalamocortical axon collaterals in the perigeniculate nucleus and dorsal lateral geniculate nucleus.

Authors:  Martha E Bickford; Haiyang Wei; Michael A Eisenback; Ranida D Chomsung; Arkadiusz S Slusarczyk; Aygul B Dankowsi
Journal:  J Comp Neurol       Date:  2008-05-10       Impact factor: 3.215

Review 7.  Binocular response modulation in the lateral geniculate nucleus.

Authors:  Kacie Dougherty; Michael C Schmid; Alexander Maier
Journal:  J Comp Neurol       Date:  2018-03-09       Impact factor: 3.215

8.  Binocular Suppression in the Macaque Lateral Geniculate Nucleus Reveals Early Competitive Interactions between the Eyes.

Authors:  Kacie Dougherty; Brock M Carlson; Michele A Cox; Jacob A Westerberg; Wolf Zinke; Michael C Schmid; Paul R Martin; Alexander Maier
Journal:  eNeuro       Date:  2021-04-08

9.  Contextual Modulation of Feedforward Inputs to Primary Visual Cortex.

Authors:  Benjamin S Lankow; W Martin Usrey
Journal:  Front Syst Neurosci       Date:  2022-02-01
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.