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Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations

Short-term monocular deprivation alters visual perception in adult humans, increasing the dominance of the deprived eye, for example, as measured with binocular rivalry. This form of plasticity may depend upon the inhibition/excitation balance in the visual cortex. Recent work suggests that cortical...

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Autores principales: Binda, Paola, Lunghi, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253512/
https://www.ncbi.nlm.nih.gov/pubmed/28163935
http://dx.doi.org/10.1155/2017/6724631
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author Binda, Paola
Lunghi, Claudia
author_facet Binda, Paola
Lunghi, Claudia
author_sort Binda, Paola
collection PubMed
description Short-term monocular deprivation alters visual perception in adult humans, increasing the dominance of the deprived eye, for example, as measured with binocular rivalry. This form of plasticity may depend upon the inhibition/excitation balance in the visual cortex. Recent work suggests that cortical excitability is reliably tracked by dilations and constrictions of the pupils of the eyes. Here, we ask whether monocular deprivation produces a systematic change of pupil behavior, as measured at rest, that is independent of the change of visual perception. During periods of minimal sensory stimulation (in the dark) and task requirements (minimizing body and gaze movements), slow pupil oscillations, “hippus,” spontaneously appear. We find that hippus amplitude increases after monocular deprivation, with larger hippus changes in participants showing larger ocular dominance changes (measured by binocular rivalry). This tight correlation suggests that a single latent variable explains both the change of ocular dominance and hippus. We speculate that the neurotransmitter norepinephrine may be implicated in this phenomenon, given its important role in both plasticity and pupil control. On the practical side, our results indicate that measuring the pupil hippus (a simple and short procedure) provides a sensitive index of the change of ocular dominance induced by short-term monocular deprivation, hence a proxy for plasticity.
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spelling pubmed-52535122017-02-05 Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations Binda, Paola Lunghi, Claudia Neural Plast Research Article Short-term monocular deprivation alters visual perception in adult humans, increasing the dominance of the deprived eye, for example, as measured with binocular rivalry. This form of plasticity may depend upon the inhibition/excitation balance in the visual cortex. Recent work suggests that cortical excitability is reliably tracked by dilations and constrictions of the pupils of the eyes. Here, we ask whether monocular deprivation produces a systematic change of pupil behavior, as measured at rest, that is independent of the change of visual perception. During periods of minimal sensory stimulation (in the dark) and task requirements (minimizing body and gaze movements), slow pupil oscillations, “hippus,” spontaneously appear. We find that hippus amplitude increases after monocular deprivation, with larger hippus changes in participants showing larger ocular dominance changes (measured by binocular rivalry). This tight correlation suggests that a single latent variable explains both the change of ocular dominance and hippus. We speculate that the neurotransmitter norepinephrine may be implicated in this phenomenon, given its important role in both plasticity and pupil control. On the practical side, our results indicate that measuring the pupil hippus (a simple and short procedure) provides a sensitive index of the change of ocular dominance induced by short-term monocular deprivation, hence a proxy for plasticity. Hindawi Publishing Corporation 2017 2017-01-09 /pmc/articles/PMC5253512/ /pubmed/28163935 http://dx.doi.org/10.1155/2017/6724631 Text en Copyright © 2017 P. Binda and C. Lunghi. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Binda, Paola
Lunghi, Claudia
Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations
title Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations
title_full Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations
title_fullStr Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations
title_full_unstemmed Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations
title_short Short-Term Monocular Deprivation Enhances Physiological Pupillary Oscillations
title_sort short-term monocular deprivation enhances physiological pupillary oscillations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253512/
https://www.ncbi.nlm.nih.gov/pubmed/28163935
http://dx.doi.org/10.1155/2017/6724631
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