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Neural correlates of visual and tactile path integration and their task related modulation
Self-motion induces sensory signals that allow to determine travel distance (path integration). For veridical path integration, one must distinguish self-generated from externally induced sensory signals. Predictive coding has been suggested to attenuate self-induced sensory responses, while task re...
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/PMC10279659/ https://www.ncbi.nlm.nih.gov/pubmed/37337037 http://dx.doi.org/10.1038/s41598-023-36797-8 |
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author | Rosenblum, Lisa Kreß, Alexander Arikan, B. Ezgi Straube, Benjamin Bremmer, Frank |
author_facet | Rosenblum, Lisa Kreß, Alexander Arikan, B. Ezgi Straube, Benjamin Bremmer, Frank |
author_sort | Rosenblum, Lisa |
collection | PubMed |
description | Self-motion induces sensory signals that allow to determine travel distance (path integration). For veridical path integration, one must distinguish self-generated from externally induced sensory signals. Predictive coding has been suggested to attenuate self-induced sensory responses, while task relevance can reverse the attenuating effect of prediction. But how is self-motion processing affected by prediction and task demands, and do effects generalize across senses? In this fMRI study, we investigated visual and tactile self-motion processing and its modulation by task demands. Visual stimuli simulated forward self-motion across a ground plane. Tactile self-motion stimuli were delivered by airflow across the subjects’ forehead. In one task, subjects replicated a previously observed distance (Reproduction/Active; high behavioral demand) of passive self-displacement (Reproduction/Passive). In a second task, subjects travelled a self-chosen distance (Self/Active; low behavioral demand) which was recorded and played back to them (Self/Passive). For both tasks and sensory modalities, Active as compared to Passive trials showed enhancement in early visual areas and suppression in higher order areas of the inferior parietal lobule (IPL). Contrasting high and low demanding active trials yielded supramodal enhancement in the anterior insula. Suppression in the IPL suggests this area to be a comparator of sensory self-motion signals and predictions thereof. |
format | Online Article Text |
id | pubmed-10279659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102796592023-06-21 Neural correlates of visual and tactile path integration and their task related modulation Rosenblum, Lisa Kreß, Alexander Arikan, B. Ezgi Straube, Benjamin Bremmer, Frank Sci Rep Article Self-motion induces sensory signals that allow to determine travel distance (path integration). For veridical path integration, one must distinguish self-generated from externally induced sensory signals. Predictive coding has been suggested to attenuate self-induced sensory responses, while task relevance can reverse the attenuating effect of prediction. But how is self-motion processing affected by prediction and task demands, and do effects generalize across senses? In this fMRI study, we investigated visual and tactile self-motion processing and its modulation by task demands. Visual stimuli simulated forward self-motion across a ground plane. Tactile self-motion stimuli were delivered by airflow across the subjects’ forehead. In one task, subjects replicated a previously observed distance (Reproduction/Active; high behavioral demand) of passive self-displacement (Reproduction/Passive). In a second task, subjects travelled a self-chosen distance (Self/Active; low behavioral demand) which was recorded and played back to them (Self/Passive). For both tasks and sensory modalities, Active as compared to Passive trials showed enhancement in early visual areas and suppression in higher order areas of the inferior parietal lobule (IPL). Contrasting high and low demanding active trials yielded supramodal enhancement in the anterior insula. Suppression in the IPL suggests this area to be a comparator of sensory self-motion signals and predictions thereof. Nature Publishing Group UK 2023-06-19 /pmc/articles/PMC10279659/ /pubmed/37337037 http://dx.doi.org/10.1038/s41598-023-36797-8 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 Rosenblum, Lisa Kreß, Alexander Arikan, B. Ezgi Straube, Benjamin Bremmer, Frank Neural correlates of visual and tactile path integration and their task related modulation |
title | Neural correlates of visual and tactile path integration and their task related modulation |
title_full | Neural correlates of visual and tactile path integration and their task related modulation |
title_fullStr | Neural correlates of visual and tactile path integration and their task related modulation |
title_full_unstemmed | Neural correlates of visual and tactile path integration and their task related modulation |
title_short | Neural correlates of visual and tactile path integration and their task related modulation |
title_sort | neural correlates of visual and tactile path integration and their task related modulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279659/ https://www.ncbi.nlm.nih.gov/pubmed/37337037 http://dx.doi.org/10.1038/s41598-023-36797-8 |
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