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      Sensory Eye Dominance: Relationship Between Eye and Brain

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          Abstract

          Eye dominance refers to the preference to use one eye more than the fellow eye to accomplish a task. However, the dominant eye revealed can be task dependent especially when the tasks are as diverse as instructing the observer to sight a target through a ring, or to report which half-image is perceived more of during binocular rivalry stimulation. Conventionally, the former task is said to reveal motor eye dominance while the latter task reveals sensory eye dominance. While the consensus is that the motor and sensory-dominant eye could be different in some observers, the reason for it is still unclear and has not been much researched. This review mainly focuses on advances made in recent studies of sensory eye dominance. It reviews studies conducted to quantify and relate sensory eye dominance to other visual functions, in particular to stereopsis, as well as studies conducted to explore its plasticity. It is recognized that sensory eye dominance in observers with clinically normal vision shares some similarity with amblyopia at least at the behavioral level, in that both exhibit an imbalance of interocular inhibition. Furthermore, sensory eye dominance is probably manifested at multiple sites along the visual pathway, perhaps including the level of ocular dominance columns. But future studies with high-resolution brain imaging approaches are required to confirm this speculation in the human visual system.

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          Most cited references56

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          SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE.

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            Environmental enrichment in adulthood promotes amblyopia recovery through a reduction of intracortical inhibition.

            Loss of visual acuity caused by abnormal visual experience during development (amblyopia) is an untreatable pathology in adults. We report that environmental enrichment in adult amblyopic rats restored normal visual acuity and ocular dominance. These effects were due to reduced GABAergic inhibition in the visual cortex, accompanied by increased expression of BDNF and reduced density of extracellular-matrix perineuronal nets, and were prevented by enhancement of inhibition through benzodiazepine cortical infusion.
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              Activity changes in early visual cortex reflect monkeys' percepts during binocular rivalry.

              When the two eyes view dissimilar images, we experience binocular rivalry, in which one eye's view dominates for several seconds and is then replaced by that of the other eye. What causes these perceptual changes in the absence of any change in the stimulus? We showed previously that some neurons in monkey cortical area MT show changes in activity during motion rivalry that reflect the perceived direction of motion. To determine whether perception-related modulation of activity occurs in other visual cortical areas, we recorded from individual neurons in V1, V2 and V4 while monkeys reported the perceived orientation of rival gratings of two orthogonal orientations. Many cells, particularly in V4, showed patterns of activity that correlated with the perceptual dominance and suppression of one stimulus. The majority were orientation-selective and could be driven equally well from either eye. It has been previously suggested that binocular rivalry involves reciprocal inhibition between monocular neurons within V1 (for example, see ref. 4), but our results do not support this view; rather, we propose that binocular rivalry arises through interactions between binocular neurons at several levels in the visual pathways, and that similar mechanisms may underlie other multistable perceptual states that occur when viewing ambiguous images.
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                Author and article information

                Journal
                Eye Brain
                Eye Brain
                EB
                eb
                Eye and Brain
                Dove
                1179-2744
                20 January 2020
                2020
                : 12
                : 25-31
                Affiliations
                [1 ]College of Optometry, The Ohio State University , Columbus, OH, USA
                [2 ]Department of Psychological and Brain Sciences, University of Louisville , Louisville, KY, USA
                Author notes
                Correspondence: Teng Leng Ooi College of Optometry, The Ohio State University , 338 West 10th Ave, Columbus, OH43210, USATel +1 614 292 1384Fax +1 614 292 7493 Email ooi.22@osu.edu
                Author information
                http://orcid.org/0000-0001-6313-9016
                Article
                176931
                10.2147/EB.S176931
                6980844
                32021530
                99dddcfb-a94f-4fd0-9c92-00e1b17982d5
                © 2020 Ooi and He.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 01 September 2019
                : 28 December 2019
                Page count
                References: 63, Pages: 7
                Categories
                Review

                binocular rivalry,amblyopia,binocular combination,excitatory-inhibitory balance,plasticity,stereopsis

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