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The role of eye-specific attention in ocular dominance plasticity
It is well known how selective attention biases information processing in real time, but few work investigates the aftereffects of prolonged attention, let alone the underlying neural mechanisms. To examine perceptual aftereffect after prolonged attention to a monocular pathway, movie images played...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930618/ https://www.ncbi.nlm.nih.gov/pubmed/35332915 http://dx.doi.org/10.1093/cercor/bhac116 |
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author | Song, Fangxing Lyu, Lili Zhao, Jiaxu Bao, Min |
author_facet | Song, Fangxing Lyu, Lili Zhao, Jiaxu Bao, Min |
author_sort | Song, Fangxing |
collection | PubMed |
description | It is well known how selective attention biases information processing in real time, but few work investigates the aftereffects of prolonged attention, let alone the underlying neural mechanisms. To examine perceptual aftereffect after prolonged attention to a monocular pathway, movie images played normally were presented to normal adult’s one eye (attended eye), while movie images of the same episode but played backwards were presented to the opposite eye (unattended eye). One hour of watching this dichoptic movie caused a shift of perceptual ocular dominance towards the unattended eye. Interestingly, the aftereffect positively correlated with the advantage of neural activity for the attended-eye over unattended-eye signals at the frontal electrodes measured with steady-state visual evoked potentials. Moreover, the aftereffect disappeared when interocular competition was minimized during adaptation. These results suggest that top-down eye-specific attention can induce ocular dominance plasticity through binocular rivalry mechanisms. The present study opens the route to explain at least part of short-term ocular dominance plasticity with the ocular-opponency-neuron model, which may be an interesting complement to the homeostatic compensation theory. |
format | Online Article Text |
id | pubmed-9930618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99306182023-02-16 The role of eye-specific attention in ocular dominance plasticity Song, Fangxing Lyu, Lili Zhao, Jiaxu Bao, Min Cereb Cortex Original Article It is well known how selective attention biases information processing in real time, but few work investigates the aftereffects of prolonged attention, let alone the underlying neural mechanisms. To examine perceptual aftereffect after prolonged attention to a monocular pathway, movie images played normally were presented to normal adult’s one eye (attended eye), while movie images of the same episode but played backwards were presented to the opposite eye (unattended eye). One hour of watching this dichoptic movie caused a shift of perceptual ocular dominance towards the unattended eye. Interestingly, the aftereffect positively correlated with the advantage of neural activity for the attended-eye over unattended-eye signals at the frontal electrodes measured with steady-state visual evoked potentials. Moreover, the aftereffect disappeared when interocular competition was minimized during adaptation. These results suggest that top-down eye-specific attention can induce ocular dominance plasticity through binocular rivalry mechanisms. The present study opens the route to explain at least part of short-term ocular dominance plasticity with the ocular-opponency-neuron model, which may be an interesting complement to the homeostatic compensation theory. Oxford University Press 2022-03-24 /pmc/articles/PMC9930618/ /pubmed/35332915 http://dx.doi.org/10.1093/cercor/bhac116 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Song, Fangxing Lyu, Lili Zhao, Jiaxu Bao, Min The role of eye-specific attention in ocular dominance plasticity |
title | The role of eye-specific attention in ocular dominance plasticity |
title_full | The role of eye-specific attention in ocular dominance plasticity |
title_fullStr | The role of eye-specific attention in ocular dominance plasticity |
title_full_unstemmed | The role of eye-specific attention in ocular dominance plasticity |
title_short | The role of eye-specific attention in ocular dominance plasticity |
title_sort | role of eye-specific attention in ocular dominance plasticity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930618/ https://www.ncbi.nlm.nih.gov/pubmed/35332915 http://dx.doi.org/10.1093/cercor/bhac116 |
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