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Dynamic pupillary exchange engages brain regions encoding social salience

Covert exchange of autonomic responses may shape social affective behavior, as observed in mirroring of pupillary responses during sadness processing. We examined how, independent of facial emotional expression, dynamic coherence between one's own and another's pupil size modulates regiona...

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Detalles Bibliográficos
Autores principales: Harrison, Neil A., Gray, Marcus A., Critchley, Hugo D.
Formato: Texto
Lenguaje:English
Publicado: Taylor & Francis 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913324/
https://www.ncbi.nlm.nih.gov/pubmed/19048432
http://dx.doi.org/10.1080/17470910802553508
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author Harrison, Neil A.
Gray, Marcus A.
Critchley, Hugo D.
author_facet Harrison, Neil A.
Gray, Marcus A.
Critchley, Hugo D.
author_sort Harrison, Neil A.
collection PubMed
description Covert exchange of autonomic responses may shape social affective behavior, as observed in mirroring of pupillary responses during sadness processing. We examined how, independent of facial emotional expression, dynamic coherence between one's own and another's pupil size modulates regional brain activity. Fourteen subjects viewed pairs of eye stimuli while undergoing fMRI. Using continuous pupillometry biofeedback, the size of the observed pupils was varied, correlating positively or negatively with changes in participants’ own pupils. Viewing both static and dynamic stimuli activated right fusiform gyrus. Observing dynamically changing pupils activated STS and amygdala, regions engaged by non-static and salient facial features. Discordance between observed and observer's pupillary changes enhanced activity within bilateral anterior insula, left amygdala and anterior cingulate. In contrast, processing positively correlated pupils enhanced activity within left frontal operculum. Our findings suggest pupillary signals are monitored continuously during social interactions and that incongruent changes activate brain regions involved in tracking motivational salience and attentionally meaningful information. Naturalistically, dynamic coherence in pupillary change follows fluctuations in ambient light. Correspondingly, in social contexts discordant pupil response is likely to reflect divergence of dispositional state. Our data provide empirical evidence for an autonomically mediated extension of forward models of motor control into social interaction.
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spelling pubmed-29133242010-08-05 Dynamic pupillary exchange engages brain regions encoding social salience Harrison, Neil A. Gray, Marcus A. Critchley, Hugo D. Soc Neurosci Article Covert exchange of autonomic responses may shape social affective behavior, as observed in mirroring of pupillary responses during sadness processing. We examined how, independent of facial emotional expression, dynamic coherence between one's own and another's pupil size modulates regional brain activity. Fourteen subjects viewed pairs of eye stimuli while undergoing fMRI. Using continuous pupillometry biofeedback, the size of the observed pupils was varied, correlating positively or negatively with changes in participants’ own pupils. Viewing both static and dynamic stimuli activated right fusiform gyrus. Observing dynamically changing pupils activated STS and amygdala, regions engaged by non-static and salient facial features. Discordance between observed and observer's pupillary changes enhanced activity within bilateral anterior insula, left amygdala and anterior cingulate. In contrast, processing positively correlated pupils enhanced activity within left frontal operculum. Our findings suggest pupillary signals are monitored continuously during social interactions and that incongruent changes activate brain regions involved in tracking motivational salience and attentionally meaningful information. Naturalistically, dynamic coherence in pupillary change follows fluctuations in ambient light. Correspondingly, in social contexts discordant pupil response is likely to reflect divergence of dispositional state. Our data provide empirical evidence for an autonomically mediated extension of forward models of motor control into social interaction. Taylor & Francis 2008-12-01 2009-06 /pmc/articles/PMC2913324/ /pubmed/19048432 http://dx.doi.org/10.1080/17470910802553508 Text en © 2008 Psychology Press http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Taylor & Francis journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Harrison, Neil A.
Gray, Marcus A.
Critchley, Hugo D.
Dynamic pupillary exchange engages brain regions encoding social salience
title Dynamic pupillary exchange engages brain regions encoding social salience
title_full Dynamic pupillary exchange engages brain regions encoding social salience
title_fullStr Dynamic pupillary exchange engages brain regions encoding social salience
title_full_unstemmed Dynamic pupillary exchange engages brain regions encoding social salience
title_short Dynamic pupillary exchange engages brain regions encoding social salience
title_sort dynamic pupillary exchange engages brain regions encoding social salience
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913324/
https://www.ncbi.nlm.nih.gov/pubmed/19048432
http://dx.doi.org/10.1080/17470910802553508
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