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Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals
BACKGROUND: Due to its severe negative consequences, human violence has been targeted by a vast number of studies. Yet, neurobiological mechanisms underlying violence are still widely unclear and it seems necessary to aim for high ecological validity to learn about mechanisms contributing to violenc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671790/ https://www.ncbi.nlm.nih.gov/pubmed/34758197 http://dx.doi.org/10.1002/brb3.2400 |
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author | Taubner, Svenja Hauschild, Sophie Wisniewski, David Wolter, Silke Roth, Gerhard Fehr, Thorsten |
author_facet | Taubner, Svenja Hauschild, Sophie Wisniewski, David Wolter, Silke Roth, Gerhard Fehr, Thorsten |
author_sort | Taubner, Svenja |
collection | PubMed |
description | BACKGROUND: Due to its severe negative consequences, human violence has been targeted by a vast number of studies. Yet, neurobiological mechanisms underlying violence are still widely unclear and it seems necessary to aim for high ecological validity to learn about mechanisms contributing to violence in real life. METHODS: The present functional magnetic resonance imaging (fMRI) study investigated the neurofunction of individuals with a history of violent offenses compared with that of controls using a laboratory paradigm requesting individuals to empathically engage in videos depicting provocative aggressive and positive social interactions from a first‐person perspective. RESULTS: The contrast of aggressive vs. positive scenarios revealed midbrain activation patterns associated with caudal periaqueductal gray (PAG) in violent offenders; In controls, the rostral PAG was involved. Additionally, only in controls, this contrast revealed an involvement of the amygdaloidal complex. Moreover, in violent offenders the contrast of positive vs. aggressive situations revealed an involvement of areas in the insula, post‐central gyrus and anterior cingulate cortex. CONCLUSIONS: Our results support findings on the differential role of PAG subdivisions in response to threat and point to altered processing of positive social interactions in violent offenders. They further support the notion that changes in PAG recruitment might contribute to violent individuals “taking action” instead of freezing in case of threatening situations. |
format | Online Article Text |
id | pubmed-8671790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86717902021-12-21 Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals Taubner, Svenja Hauschild, Sophie Wisniewski, David Wolter, Silke Roth, Gerhard Fehr, Thorsten Brain Behav Original Research BACKGROUND: Due to its severe negative consequences, human violence has been targeted by a vast number of studies. Yet, neurobiological mechanisms underlying violence are still widely unclear and it seems necessary to aim for high ecological validity to learn about mechanisms contributing to violence in real life. METHODS: The present functional magnetic resonance imaging (fMRI) study investigated the neurofunction of individuals with a history of violent offenses compared with that of controls using a laboratory paradigm requesting individuals to empathically engage in videos depicting provocative aggressive and positive social interactions from a first‐person perspective. RESULTS: The contrast of aggressive vs. positive scenarios revealed midbrain activation patterns associated with caudal periaqueductal gray (PAG) in violent offenders; In controls, the rostral PAG was involved. Additionally, only in controls, this contrast revealed an involvement of the amygdaloidal complex. Moreover, in violent offenders the contrast of positive vs. aggressive situations revealed an involvement of areas in the insula, post‐central gyrus and anterior cingulate cortex. CONCLUSIONS: Our results support findings on the differential role of PAG subdivisions in response to threat and point to altered processing of positive social interactions in violent offenders. They further support the notion that changes in PAG recruitment might contribute to violent individuals “taking action” instead of freezing in case of threatening situations. John Wiley and Sons Inc. 2021-11-10 /pmc/articles/PMC8671790/ /pubmed/34758197 http://dx.doi.org/10.1002/brb3.2400 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Taubner, Svenja Hauschild, Sophie Wisniewski, David Wolter, Silke Roth, Gerhard Fehr, Thorsten Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
title | Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
title_full | Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
title_fullStr | Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
title_full_unstemmed | Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
title_short | Neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
title_sort | neural response to aggressive and positive interactions in violent offenders and nonviolent individuals |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671790/ https://www.ncbi.nlm.nih.gov/pubmed/34758197 http://dx.doi.org/10.1002/brb3.2400 |
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