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Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading

Neuroplastic changes induced by sensory learning have been recognized within the cortices of specific modalities as well as within higher ordered multimodal areas. The interplay between these areas is not fully understood, particularly in the case of somatosensory learning. Here we examined function...

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Autores principales: Debowska, Weronika, Wolak, Tomasz, Nowicka, Anna, Kozak, Anna, Szwed, Marcin, Kossut, Malgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061995/
https://www.ncbi.nlm.nih.gov/pubmed/27790087
http://dx.doi.org/10.3389/fnins.2016.00460
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author Debowska, Weronika
Wolak, Tomasz
Nowicka, Anna
Kozak, Anna
Szwed, Marcin
Kossut, Malgorzata
author_facet Debowska, Weronika
Wolak, Tomasz
Nowicka, Anna
Kozak, Anna
Szwed, Marcin
Kossut, Malgorzata
author_sort Debowska, Weronika
collection PubMed
description Neuroplastic changes induced by sensory learning have been recognized within the cortices of specific modalities as well as within higher ordered multimodal areas. The interplay between these areas is not fully understood, particularly in the case of somatosensory learning. Here we examined functional and structural changes induced by short-term tactile training based of Braille reading, a task that requires both significant tactile expertise and mapping of tactile input onto multimodal representations. Subjects with normal vision were trained for 3 weeks to read Braille exclusively by touch and scanned before and after training, while performing a same-different discrimination task on Braille characters and meaningless characters. Functional and diffusion-weighted magnetic resonance imaging sequences were used to assess resulting changes. The strongest training-induced effect was found in the primary somatosensory cortex (SI), where we observed bilateral augmentation in activity accompanied by an increase in fractional anisotropy (FA) within the contralateral SI. Increases of white matter fractional anisotropy were also observed in the secondary somatosensory area (SII) and the thalamus. Outside of somatosensory system, changes in both structure and function were found in i.e., the fusiform gyrus, the medial frontal gyri and the inferior parietal lobule. Our results provide evidence for functional remodeling of the somatosensory pathway and higher ordered multimodal brain areas occurring as a result of short-lasting tactile learning, and add to them a novel picture of extensive white matter plasticity.
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spelling pubmed-50619952016-10-27 Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading Debowska, Weronika Wolak, Tomasz Nowicka, Anna Kozak, Anna Szwed, Marcin Kossut, Malgorzata Front Neurosci Neuroscience Neuroplastic changes induced by sensory learning have been recognized within the cortices of specific modalities as well as within higher ordered multimodal areas. The interplay between these areas is not fully understood, particularly in the case of somatosensory learning. Here we examined functional and structural changes induced by short-term tactile training based of Braille reading, a task that requires both significant tactile expertise and mapping of tactile input onto multimodal representations. Subjects with normal vision were trained for 3 weeks to read Braille exclusively by touch and scanned before and after training, while performing a same-different discrimination task on Braille characters and meaningless characters. Functional and diffusion-weighted magnetic resonance imaging sequences were used to assess resulting changes. The strongest training-induced effect was found in the primary somatosensory cortex (SI), where we observed bilateral augmentation in activity accompanied by an increase in fractional anisotropy (FA) within the contralateral SI. Increases of white matter fractional anisotropy were also observed in the secondary somatosensory area (SII) and the thalamus. Outside of somatosensory system, changes in both structure and function were found in i.e., the fusiform gyrus, the medial frontal gyri and the inferior parietal lobule. Our results provide evidence for functional remodeling of the somatosensory pathway and higher ordered multimodal brain areas occurring as a result of short-lasting tactile learning, and add to them a novel picture of extensive white matter plasticity. Frontiers Media S.A. 2016-10-13 /pmc/articles/PMC5061995/ /pubmed/27790087 http://dx.doi.org/10.3389/fnins.2016.00460 Text en Copyright © 2016 Debowska, Wolak, Nowicka, Kozak, Szwed and Kossut. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Debowska, Weronika
Wolak, Tomasz
Nowicka, Anna
Kozak, Anna
Szwed, Marcin
Kossut, Malgorzata
Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading
title Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading
title_full Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading
title_fullStr Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading
title_full_unstemmed Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading
title_short Functional and Structural Neuroplasticity Induced by Short-Term Tactile Training Based on Braille Reading
title_sort functional and structural neuroplasticity induced by short-term tactile training based on braille reading
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061995/
https://www.ncbi.nlm.nih.gov/pubmed/27790087
http://dx.doi.org/10.3389/fnins.2016.00460
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