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A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network
Social signals such as eye contact and motor actions are essential elements of social interactions. However, our knowledge about the interplay of gaze signals and the control of actions remains limited. In a group of 30 healthy participants, we investigated the effect of gaze (direct gaze vs averted...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917026/ https://www.ncbi.nlm.nih.gov/pubmed/31593216 http://dx.doi.org/10.1093/scan/nsz071 |
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author | Zillekens, Imme Christina Schliephake, Lena Maria Brandi, Marie-Luise Schilbach, Leonhard |
author_facet | Zillekens, Imme Christina Schliephake, Lena Maria Brandi, Marie-Luise Schilbach, Leonhard |
author_sort | Zillekens, Imme Christina |
collection | PubMed |
description | Social signals such as eye contact and motor actions are essential elements of social interactions. However, our knowledge about the interplay of gaze signals and the control of actions remains limited. In a group of 30 healthy participants, we investigated the effect of gaze (direct gaze vs averted) on behavioral and neural measures of action control as assessed by a spatial congruency task (spatially congruent vs incongruent button presses in response to gaze shifts). Behavioral results demonstrate that inter-individual differences in condition-specific incongruency costs were associated with autistic traits. While there was no interaction effect of gaze and action control on brain activation, in a context of incongruent responses to direct gaze shifts, a psychophysiological interaction analysis showed increased functional coupling between the right temporoparietal junction, a key region in gaze processing, and the inferior frontal gyri, which have been related to both social cognition and motor inhibition. Conversely, incongruency costs to averted gaze were reflected in increased connectivity with action control areas implicated in top-down attentional processes. Our findings indicate that direct gaze perception inter-individually modulates motor actions and enforces the functional integration of gaze-related social cognition and action control processes, thereby connecting functional elements of social interactions. |
format | Online Article Text |
id | pubmed-6917026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69170262019-12-20 A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network Zillekens, Imme Christina Schliephake, Lena Maria Brandi, Marie-Luise Schilbach, Leonhard Soc Cogn Affect Neurosci Original Article Social signals such as eye contact and motor actions are essential elements of social interactions. However, our knowledge about the interplay of gaze signals and the control of actions remains limited. In a group of 30 healthy participants, we investigated the effect of gaze (direct gaze vs averted) on behavioral and neural measures of action control as assessed by a spatial congruency task (spatially congruent vs incongruent button presses in response to gaze shifts). Behavioral results demonstrate that inter-individual differences in condition-specific incongruency costs were associated with autistic traits. While there was no interaction effect of gaze and action control on brain activation, in a context of incongruent responses to direct gaze shifts, a psychophysiological interaction analysis showed increased functional coupling between the right temporoparietal junction, a key region in gaze processing, and the inferior frontal gyri, which have been related to both social cognition and motor inhibition. Conversely, incongruency costs to averted gaze were reflected in increased connectivity with action control areas implicated in top-down attentional processes. Our findings indicate that direct gaze perception inter-individually modulates motor actions and enforces the functional integration of gaze-related social cognition and action control processes, thereby connecting functional elements of social interactions. Oxford University Press 2019-10-08 /pmc/articles/PMC6917026/ /pubmed/31593216 http://dx.doi.org/10.1093/scan/nsz071 Text en © The Author(s) 2019. Published by Oxford University Press. http://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 (http://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 Zillekens, Imme Christina Schliephake, Lena Maria Brandi, Marie-Luise Schilbach, Leonhard A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network |
title | A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network |
title_full | A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network |
title_fullStr | A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network |
title_full_unstemmed | A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network |
title_short | A look at actions: direct gaze modulates functional connectivity of the right TPJ with an action control network |
title_sort | look at actions: direct gaze modulates functional connectivity of the right tpj with an action control network |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917026/ https://www.ncbi.nlm.nih.gov/pubmed/31593216 http://dx.doi.org/10.1093/scan/nsz071 |
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