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Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity

Our everyday life summons numerous novel sensorimotor experiences, to which our brain needs to adapt in order to function properly. However, tracking plasticity of naturalistic behavior and associated brain modulations is challenging. Here, we tackled this question implementing a prism adaptation-li...

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Autores principales: Wilf, Meytal, Dupuis, Celine, Nardo, Davide, Huber, Diana, Sander, Sibilla, Al-Kaar, Joud, Haroud, Meriem, Perrin, Henri, Fornari, Eleonora, Crottaz-Herbette, Sonia, Serino, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152055/
https://www.ncbi.nlm.nih.gov/pubmed/36288926
http://dx.doi.org/10.1093/cercor/bhac407
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author Wilf, Meytal
Dupuis, Celine
Nardo, Davide
Huber, Diana
Sander, Sibilla
Al-Kaar, Joud
Haroud, Meriem
Perrin, Henri
Fornari, Eleonora
Crottaz-Herbette, Sonia
Serino, Andrea
author_facet Wilf, Meytal
Dupuis, Celine
Nardo, Davide
Huber, Diana
Sander, Sibilla
Al-Kaar, Joud
Haroud, Meriem
Perrin, Henri
Fornari, Eleonora
Crottaz-Herbette, Sonia
Serino, Andrea
author_sort Wilf, Meytal
collection PubMed
description Our everyday life summons numerous novel sensorimotor experiences, to which our brain needs to adapt in order to function properly. However, tracking plasticity of naturalistic behavior and associated brain modulations is challenging. Here, we tackled this question implementing a prism adaptation-like training in virtual reality (VRPA) in combination with functional neuroimaging. Three groups of healthy participants (N = 45) underwent VRPA (with a shift either to the left/right side, or with no shift), and performed functional magnetic resonance imaging (fMRI) sessions before and after training. To capture modulations in free-flowing, task-free brain activity, the fMRI sessions included resting-state and free-viewing of naturalistic videos. We found significant decreases in spontaneous functional connectivity between attentional and default mode (DMN)/fronto-parietal networks, only for the adaptation groups, more pronouncedly in the hemisphere contralateral to the induced shift. In addition, VRPA was found to bias visual responses to naturalistic videos: Following rightward adaptation, we found upregulation of visual response in an area in the parieto-occipital sulcus (POS) only in the right hemisphere. Notably, the extent of POS upregulation correlated with the size of the VRPA-induced after-effect measured in behavioral tests. This study demonstrates that a brief VRPA exposure can change large-scale cortical connectivity and correspondingly bias visual responses to naturalistic sensory inputs.
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spelling pubmed-101520552023-05-03 Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity Wilf, Meytal Dupuis, Celine Nardo, Davide Huber, Diana Sander, Sibilla Al-Kaar, Joud Haroud, Meriem Perrin, Henri Fornari, Eleonora Crottaz-Herbette, Sonia Serino, Andrea Cereb Cortex Original Article Our everyday life summons numerous novel sensorimotor experiences, to which our brain needs to adapt in order to function properly. However, tracking plasticity of naturalistic behavior and associated brain modulations is challenging. Here, we tackled this question implementing a prism adaptation-like training in virtual reality (VRPA) in combination with functional neuroimaging. Three groups of healthy participants (N = 45) underwent VRPA (with a shift either to the left/right side, or with no shift), and performed functional magnetic resonance imaging (fMRI) sessions before and after training. To capture modulations in free-flowing, task-free brain activity, the fMRI sessions included resting-state and free-viewing of naturalistic videos. We found significant decreases in spontaneous functional connectivity between attentional and default mode (DMN)/fronto-parietal networks, only for the adaptation groups, more pronouncedly in the hemisphere contralateral to the induced shift. In addition, VRPA was found to bias visual responses to naturalistic videos: Following rightward adaptation, we found upregulation of visual response in an area in the parieto-occipital sulcus (POS) only in the right hemisphere. Notably, the extent of POS upregulation correlated with the size of the VRPA-induced after-effect measured in behavioral tests. This study demonstrates that a brief VRPA exposure can change large-scale cortical connectivity and correspondingly bias visual responses to naturalistic sensory inputs. Oxford University Press 2022-10-26 /pmc/articles/PMC10152055/ /pubmed/36288926 http://dx.doi.org/10.1093/cercor/bhac407 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Wilf, Meytal
Dupuis, Celine
Nardo, Davide
Huber, Diana
Sander, Sibilla
Al-Kaar, Joud
Haroud, Meriem
Perrin, Henri
Fornari, Eleonora
Crottaz-Herbette, Sonia
Serino, Andrea
Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
title Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
title_full Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
title_fullStr Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
title_full_unstemmed Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
title_short Virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
title_sort virtual reality-based sensorimotor adaptation shapes subsequent spontaneous and naturalistic stimulus-driven brain activity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152055/
https://www.ncbi.nlm.nih.gov/pubmed/36288926
http://dx.doi.org/10.1093/cercor/bhac407
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