Cargando…
Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm
Adult homeostatic visual plasticity can be induced by short-term patching, heralded by a shift in ocular dominance in favor of the deprived eye after monocular occlusion. The potential to boost visual neuroplasticity with environmental enrichment such as exercise has also been explored; however, the...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543434/ https://www.ncbi.nlm.nih.gov/pubmed/34668930 http://dx.doi.org/10.1167/jov.21.11.12 |
_version_ | 1784589635242950656 |
---|---|
author | Virathone, Lucas Nguyen, Bao N. Dobson, Fiona Carter, Olivia L. McKendrick, Allison M. |
author_facet | Virathone, Lucas Nguyen, Bao N. Dobson, Fiona Carter, Olivia L. McKendrick, Allison M. |
author_sort | Virathone, Lucas |
collection | PubMed |
description | Adult homeostatic visual plasticity can be induced by short-term patching, heralded by a shift in ocular dominance in favor of the deprived eye after monocular occlusion. The potential to boost visual neuroplasticity with environmental enrichment such as exercise has also been explored; however, the results are inconsistent, with some studies finding no additive effect of exercise. Studies to date have only considered the effect of patching alone or in combination with exercise. Whether exercise alone affects typical outcome measures of experimental estimates of short-term visual neuroplasticity is unknown. We therefore measured binocular rivalry in 20 healthy young adults (20–34 years old) at baseline and after three 2-hour interventions: patching (of the dominant eye) only, patching with exercise, and exercise only. Consistent with previous work, the patching interventions produced a shift in ocular dominance toward the deprived (dominant) eye. Mild- to moderate-intensity exercise in the absence of patching had several effects on binocular rivalry metrics, including a reduction in the dominant eye percept. The proportion of mixed percept and the time to first switch (onset rivalry) did not change from baseline across all interventions. Thus, we demonstrate that exercise alone can impact binocular rivalry outcomes measures. We did not observe a synergistic effect between patching and exercise in our data. |
format | Online Article Text |
id | pubmed-8543434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85434342021-10-29 Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm Virathone, Lucas Nguyen, Bao N. Dobson, Fiona Carter, Olivia L. McKendrick, Allison M. J Vis Article Adult homeostatic visual plasticity can be induced by short-term patching, heralded by a shift in ocular dominance in favor of the deprived eye after monocular occlusion. The potential to boost visual neuroplasticity with environmental enrichment such as exercise has also been explored; however, the results are inconsistent, with some studies finding no additive effect of exercise. Studies to date have only considered the effect of patching alone or in combination with exercise. Whether exercise alone affects typical outcome measures of experimental estimates of short-term visual neuroplasticity is unknown. We therefore measured binocular rivalry in 20 healthy young adults (20–34 years old) at baseline and after three 2-hour interventions: patching (of the dominant eye) only, patching with exercise, and exercise only. Consistent with previous work, the patching interventions produced a shift in ocular dominance toward the deprived (dominant) eye. Mild- to moderate-intensity exercise in the absence of patching had several effects on binocular rivalry metrics, including a reduction in the dominant eye percept. The proportion of mixed percept and the time to first switch (onset rivalry) did not change from baseline across all interventions. Thus, we demonstrate that exercise alone can impact binocular rivalry outcomes measures. We did not observe a synergistic effect between patching and exercise in our data. The Association for Research in Vision and Ophthalmology 2021-10-20 /pmc/articles/PMC8543434/ /pubmed/34668930 http://dx.doi.org/10.1167/jov.21.11.12 Text en Copyright 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Article Virathone, Lucas Nguyen, Bao N. Dobson, Fiona Carter, Olivia L. McKendrick, Allison M. Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
title | Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
title_full | Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
title_fullStr | Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
title_full_unstemmed | Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
title_short | Exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
title_sort | exercise alone impacts short-term adult visual neuroplasticity in a monocular deprivation paradigm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543434/ https://www.ncbi.nlm.nih.gov/pubmed/34668930 http://dx.doi.org/10.1167/jov.21.11.12 |
work_keys_str_mv | AT virathonelucas exercisealoneimpactsshorttermadultvisualneuroplasticityinamonoculardeprivationparadigm AT nguyenbaon exercisealoneimpactsshorttermadultvisualneuroplasticityinamonoculardeprivationparadigm AT dobsonfiona exercisealoneimpactsshorttermadultvisualneuroplasticityinamonoculardeprivationparadigm AT carterolivial exercisealoneimpactsshorttermadultvisualneuroplasticityinamonoculardeprivationparadigm AT mckendrickallisonm exercisealoneimpactsshorttermadultvisualneuroplasticityinamonoculardeprivationparadigm |