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Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation
Transcranial direct current stimulation (tDCS) of the occipital lobe may modulate visual cortex neuroplasticity. We assessed the acute effect of visual cortex anodal (a-)tDCS on ocular dominance plasticity induced by short-term monocular deprivation (MD), a well-established technique for inducing ho...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126033/ https://www.ncbi.nlm.nih.gov/pubmed/37095131 http://dx.doi.org/10.1038/s41598-023-33823-7 |
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author | Chen, Xiaoxin Bobier, William Thompson, Benjamin |
author_facet | Chen, Xiaoxin Bobier, William Thompson, Benjamin |
author_sort | Chen, Xiaoxin |
collection | PubMed |
description | Transcranial direct current stimulation (tDCS) of the occipital lobe may modulate visual cortex neuroplasticity. We assessed the acute effect of visual cortex anodal (a-)tDCS on ocular dominance plasticity induced by short-term monocular deprivation (MD), a well-established technique for inducing homeostatic plasticity in the visual system. In Experiment 1, active or sham visual cortex tDCS was applied during the last 20 min of 2-h MD following a within-subjects design (n = 17). Ocular dominance was measured using two computerized tests. The magnitude of ocular dominance plasticity was unaffected by a-tDCS. In Experiment 2 (n = 9), we investigated whether a ceiling effect of MD was masking the effect of active tDCS. We replicated Experiment 1 but used only 30 min of MD. The magnitude of ocular dominance plasticity was decreased with the shorter intervention, but there was still no effect of active a-tDCS. Within the constraints of our experimental design and a-tDCS parameters, visual cortex a-tDCS did not modulate the homeostatic mechanisms that drive ocular dominance plasticity in participants with normal binocular vision. |
format | Online Article Text |
id | pubmed-10126033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101260332023-04-26 Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation Chen, Xiaoxin Bobier, William Thompson, Benjamin Sci Rep Article Transcranial direct current stimulation (tDCS) of the occipital lobe may modulate visual cortex neuroplasticity. We assessed the acute effect of visual cortex anodal (a-)tDCS on ocular dominance plasticity induced by short-term monocular deprivation (MD), a well-established technique for inducing homeostatic plasticity in the visual system. In Experiment 1, active or sham visual cortex tDCS was applied during the last 20 min of 2-h MD following a within-subjects design (n = 17). Ocular dominance was measured using two computerized tests. The magnitude of ocular dominance plasticity was unaffected by a-tDCS. In Experiment 2 (n = 9), we investigated whether a ceiling effect of MD was masking the effect of active tDCS. We replicated Experiment 1 but used only 30 min of MD. The magnitude of ocular dominance plasticity was decreased with the shorter intervention, but there was still no effect of active a-tDCS. Within the constraints of our experimental design and a-tDCS parameters, visual cortex a-tDCS did not modulate the homeostatic mechanisms that drive ocular dominance plasticity in participants with normal binocular vision. Nature Publishing Group UK 2023-04-24 /pmc/articles/PMC10126033/ /pubmed/37095131 http://dx.doi.org/10.1038/s41598-023-33823-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chen, Xiaoxin Bobier, William Thompson, Benjamin Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation |
title | Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation |
title_full | Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation |
title_fullStr | Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation |
title_full_unstemmed | Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation |
title_short | Short-term ocular dominance plasticity is not modulated by visual cortex tDCS but increases with length of monocular deprivation |
title_sort | short-term ocular dominance plasticity is not modulated by visual cortex tdcs but increases with length of monocular deprivation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10126033/ https://www.ncbi.nlm.nih.gov/pubmed/37095131 http://dx.doi.org/10.1038/s41598-023-33823-7 |
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