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Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala
Body perception has been extensively investigated, with one particular focus being the integration of vision and touch within a neuronal body representation. Previous studies have implicated a distributed network comprising the extrastriate body area (EBA), posterior parietal cortex (PPC) and ventra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986852/ https://www.ncbi.nlm.nih.gov/pubmed/35388047 http://dx.doi.org/10.1038/s41598-022-09603-0 |
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author | Fourcade, Antonin Schmidt, Timo Torsten Nierhaus, Till Blankenburg, Felix |
author_facet | Fourcade, Antonin Schmidt, Timo Torsten Nierhaus, Till Blankenburg, Felix |
author_sort | Fourcade, Antonin |
collection | PubMed |
description | Body perception has been extensively investigated, with one particular focus being the integration of vision and touch within a neuronal body representation. Previous studies have implicated a distributed network comprising the extrastriate body area (EBA), posterior parietal cortex (PPC) and ventral premotor cortex (PMv) during illusory self-attribution of a rubber hand. Here, we set up an fMRI paradigm in virtual reality (VR) to study whether and how the self-attribution of (artificial) body parts is altered if these body parts are somehow threatened. Participants (N = 30) saw a spider (aversive stimulus) or a toy-car (neutral stimulus) moving along a 3D-rendered virtual forearm positioned like their real forearm, while tactile stimulation was applied on the real arm in the same (congruent) or opposite (incongruent) direction. We found that the PPC was more activated during congruent stimulation; higher visual areas and the anterior insula (aIns) showed increased activation during aversive stimulus presentation; and the amygdala was more strongly activated for aversive stimuli when there was stronger multisensory integration of body-related information (interaction of aversiveness and congruency). Together, these findings suggest an enhanced processing of aversive stimuli within the amygdala when they represent a bodily threat. |
format | Online Article Text |
id | pubmed-8986852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89868522022-04-08 Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala Fourcade, Antonin Schmidt, Timo Torsten Nierhaus, Till Blankenburg, Felix Sci Rep Article Body perception has been extensively investigated, with one particular focus being the integration of vision and touch within a neuronal body representation. Previous studies have implicated a distributed network comprising the extrastriate body area (EBA), posterior parietal cortex (PPC) and ventral premotor cortex (PMv) during illusory self-attribution of a rubber hand. Here, we set up an fMRI paradigm in virtual reality (VR) to study whether and how the self-attribution of (artificial) body parts is altered if these body parts are somehow threatened. Participants (N = 30) saw a spider (aversive stimulus) or a toy-car (neutral stimulus) moving along a 3D-rendered virtual forearm positioned like their real forearm, while tactile stimulation was applied on the real arm in the same (congruent) or opposite (incongruent) direction. We found that the PPC was more activated during congruent stimulation; higher visual areas and the anterior insula (aIns) showed increased activation during aversive stimulus presentation; and the amygdala was more strongly activated for aversive stimuli when there was stronger multisensory integration of body-related information (interaction of aversiveness and congruency). Together, these findings suggest an enhanced processing of aversive stimuli within the amygdala when they represent a bodily threat. Nature Publishing Group UK 2022-04-06 /pmc/articles/PMC8986852/ /pubmed/35388047 http://dx.doi.org/10.1038/s41598-022-09603-0 Text en © The Author(s) 2022 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 Fourcade, Antonin Schmidt, Timo Torsten Nierhaus, Till Blankenburg, Felix Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
title | Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
title_full | Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
title_fullStr | Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
title_full_unstemmed | Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
title_short | Enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
title_sort | enhanced processing of aversive stimuli on embodied artificial limbs by the human amygdala |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986852/ https://www.ncbi.nlm.nih.gov/pubmed/35388047 http://dx.doi.org/10.1038/s41598-022-09603-0 |
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