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Reorganization of thalamocortical connections in congenitally blind humans

Cross‐modal plasticity in blind individuals has been reported over the past decades showing that nonvisual information is carried and processed by “visual” brain structures. However, despite multiple efforts, the structural underpinnings of cross‐modal plasticity in congenitally blind individuals re...

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Autores principales: Marins, Theo F., Russo, Maite, Rodrigues, Erika C., Monteiro, Marina, Moll, Jorge, Felix, Daniel, Bouzas, Julia, Arcanjo, Helena, Vargas, Claudia D., Tovar‐Moll, Fernanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980890/
https://www.ncbi.nlm.nih.gov/pubmed/36661404
http://dx.doi.org/10.1002/hbm.26192
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author Marins, Theo F.
Russo, Maite
Rodrigues, Erika C.
Monteiro, Marina
Moll, Jorge
Felix, Daniel
Bouzas, Julia
Arcanjo, Helena
Vargas, Claudia D.
Tovar‐Moll, Fernanda
author_facet Marins, Theo F.
Russo, Maite
Rodrigues, Erika C.
Monteiro, Marina
Moll, Jorge
Felix, Daniel
Bouzas, Julia
Arcanjo, Helena
Vargas, Claudia D.
Tovar‐Moll, Fernanda
author_sort Marins, Theo F.
collection PubMed
description Cross‐modal plasticity in blind individuals has been reported over the past decades showing that nonvisual information is carried and processed by “visual” brain structures. However, despite multiple efforts, the structural underpinnings of cross‐modal plasticity in congenitally blind individuals remain unclear. We mapped thalamocortical connectivity and assessed the integrity of white matter of 10 congenitally blind individuals and 10 sighted controls. We hypothesized an aberrant thalamocortical pattern of connectivity taking place in the absence of visual stimuli from birth as a potential mechanism of cross‐modal plasticity. In addition to the impaired microstructure of visual white matter bundles, we observed structural connectivity changes between the thalamus and occipital and temporal cortices. Specifically, the thalamic territory dedicated to connections with the occipital cortex was smaller and displayed weaker connectivity in congenitally blind individuals, whereas those connecting with the temporal cortex showed greater volume and increased connectivity. The abnormal pattern of thalamocortical connectivity included the lateral and medial geniculate nuclei and the pulvinar nucleus. For the first time in humans, a remapping of structural thalamocortical connections involving both unimodal and multimodal thalamic nuclei has been demonstrated, shedding light on the possible mechanisms of cross‐modal plasticity in humans. The present findings may help understand the functional adaptations commonly observed in congenitally blind individuals.
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spelling pubmed-99808902023-03-03 Reorganization of thalamocortical connections in congenitally blind humans Marins, Theo F. Russo, Maite Rodrigues, Erika C. Monteiro, Marina Moll, Jorge Felix, Daniel Bouzas, Julia Arcanjo, Helena Vargas, Claudia D. Tovar‐Moll, Fernanda Hum Brain Mapp Research Articles Cross‐modal plasticity in blind individuals has been reported over the past decades showing that nonvisual information is carried and processed by “visual” brain structures. However, despite multiple efforts, the structural underpinnings of cross‐modal plasticity in congenitally blind individuals remain unclear. We mapped thalamocortical connectivity and assessed the integrity of white matter of 10 congenitally blind individuals and 10 sighted controls. We hypothesized an aberrant thalamocortical pattern of connectivity taking place in the absence of visual stimuli from birth as a potential mechanism of cross‐modal plasticity. In addition to the impaired microstructure of visual white matter bundles, we observed structural connectivity changes between the thalamus and occipital and temporal cortices. Specifically, the thalamic territory dedicated to connections with the occipital cortex was smaller and displayed weaker connectivity in congenitally blind individuals, whereas those connecting with the temporal cortex showed greater volume and increased connectivity. The abnormal pattern of thalamocortical connectivity included the lateral and medial geniculate nuclei and the pulvinar nucleus. For the first time in humans, a remapping of structural thalamocortical connections involving both unimodal and multimodal thalamic nuclei has been demonstrated, shedding light on the possible mechanisms of cross‐modal plasticity in humans. The present findings may help understand the functional adaptations commonly observed in congenitally blind individuals. John Wiley & Sons, Inc. 2023-01-20 /pmc/articles/PMC9980890/ /pubmed/36661404 http://dx.doi.org/10.1002/hbm.26192 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Marins, Theo F.
Russo, Maite
Rodrigues, Erika C.
Monteiro, Marina
Moll, Jorge
Felix, Daniel
Bouzas, Julia
Arcanjo, Helena
Vargas, Claudia D.
Tovar‐Moll, Fernanda
Reorganization of thalamocortical connections in congenitally blind humans
title Reorganization of thalamocortical connections in congenitally blind humans
title_full Reorganization of thalamocortical connections in congenitally blind humans
title_fullStr Reorganization of thalamocortical connections in congenitally blind humans
title_full_unstemmed Reorganization of thalamocortical connections in congenitally blind humans
title_short Reorganization of thalamocortical connections in congenitally blind humans
title_sort reorganization of thalamocortical connections in congenitally blind humans
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980890/
https://www.ncbi.nlm.nih.gov/pubmed/36661404
http://dx.doi.org/10.1002/hbm.26192
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