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Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally

To what extent oculomotor and attention systems are linked remains strongly debated. Previous studies suggested that saccadic adaptation, a well-studied model of oculomotor plasticity, and orienting of attention rely on overlapping networks in the parietal cortex and can functionally interact. Using...

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Autores principales: Nicolas, Judith, Bidet-Caulet, Aurélie, Pélisson, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882914/
https://www.ncbi.nlm.nih.gov/pubmed/31780727
http://dx.doi.org/10.1038/s41598-019-54256-1
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author Nicolas, Judith
Bidet-Caulet, Aurélie
Pélisson, Denis
author_facet Nicolas, Judith
Bidet-Caulet, Aurélie
Pélisson, Denis
author_sort Nicolas, Judith
collection PubMed
description To what extent oculomotor and attention systems are linked remains strongly debated. Previous studies suggested that saccadic adaptation, a well-studied model of oculomotor plasticity, and orienting of attention rely on overlapping networks in the parietal cortex and can functionally interact. Using a Posner-like paradigm in healthy human subjects, we demonstrate for the first time that saccadic adaptation boosts endogenous attention orienting. Indeed, the discrimination of perifoveal targets benefits more from central cues after backward adaptation of leftward voluntary saccades than after a control saccade task. We propose that the overlap of underlying neural networks actually consists of neuronal populations co-activated by oculomotor plasticity and endogenous attention deployed perifoveally. The functional coupling demonstrated here plaids for conceptual models not belonging to the framework of the premotor theory of attention as the latter has been rejected precisely for this voluntary/endogenous modality. These results also open new perspective for rehabilitation of visuo-attentional deficits.
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spelling pubmed-68829142019-12-31 Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally Nicolas, Judith Bidet-Caulet, Aurélie Pélisson, Denis Sci Rep Article To what extent oculomotor and attention systems are linked remains strongly debated. Previous studies suggested that saccadic adaptation, a well-studied model of oculomotor plasticity, and orienting of attention rely on overlapping networks in the parietal cortex and can functionally interact. Using a Posner-like paradigm in healthy human subjects, we demonstrate for the first time that saccadic adaptation boosts endogenous attention orienting. Indeed, the discrimination of perifoveal targets benefits more from central cues after backward adaptation of leftward voluntary saccades than after a control saccade task. We propose that the overlap of underlying neural networks actually consists of neuronal populations co-activated by oculomotor plasticity and endogenous attention deployed perifoveally. The functional coupling demonstrated here plaids for conceptual models not belonging to the framework of the premotor theory of attention as the latter has been rejected precisely for this voluntary/endogenous modality. These results also open new perspective for rehabilitation of visuo-attentional deficits. Nature Publishing Group UK 2019-11-28 /pmc/articles/PMC6882914/ /pubmed/31780727 http://dx.doi.org/10.1038/s41598-019-54256-1 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nicolas, Judith
Bidet-Caulet, Aurélie
Pélisson, Denis
Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
title Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
title_full Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
title_fullStr Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
title_full_unstemmed Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
title_short Inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
title_sort inducing oculomotor plasticity to disclose the functional link between voluntary saccades and endogenous attention deployed perifoveally
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882914/
https://www.ncbi.nlm.nih.gov/pubmed/31780727
http://dx.doi.org/10.1038/s41598-019-54256-1
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