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The optimal calibration hypothesis: how life history modulates the brain's social pain network

A growing body of work demonstrates that the brain responds similarly to physical and social injury. Both experiences are associated with activity in the dorsal anterior cingulate cortex (dACC) and anterior insula. This dual functionality of the dACC and anterior insula underscores the evolutionary...

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Autores principales: Chester, David S., Pond, Richard S., Richman, Stephanie B., DeWall, C. Nathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389670/
https://www.ncbi.nlm.nih.gov/pubmed/22783189
http://dx.doi.org/10.3389/fnevo.2012.00010
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author Chester, David S.
Pond, Richard S.
Richman, Stephanie B.
DeWall, C. Nathan
author_facet Chester, David S.
Pond, Richard S.
Richman, Stephanie B.
DeWall, C. Nathan
author_sort Chester, David S.
collection PubMed
description A growing body of work demonstrates that the brain responds similarly to physical and social injury. Both experiences are associated with activity in the dorsal anterior cingulate cortex (dACC) and anterior insula. This dual functionality of the dACC and anterior insula underscores the evolutionary importance of maintaining interpersonal bonds. Despite the weight that evolution has placed on social injury, the pain response to social rejection varies substantially across individuals. For example, work from our lab demonstrated that the brain's social pain response is moderated by attachment style: anxious-attachment was associated with greater intensity and avoidant-attachment was associated with less intensity in dACC and insula activation. In an attempt to explain these divergent responses in the social pain network, we propose the optimal calibration hypothesis, which posits variation in social rejection in early life history stages shifts the threshold of an individual's social pain network such that the resulting pain sensitivity will be increased by volatile social rejection and reduced by chronic social rejection. Furthermore, the social pain response may be exacerbated when individuals are rejected by others of particular importance to a given life history stage (e.g., potential mates during young adulthood, parents during infancy and childhood).
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spelling pubmed-33896702012-07-10 The optimal calibration hypothesis: how life history modulates the brain's social pain network Chester, David S. Pond, Richard S. Richman, Stephanie B. DeWall, C. Nathan Front Evol Neurosci Neuroscience A growing body of work demonstrates that the brain responds similarly to physical and social injury. Both experiences are associated with activity in the dorsal anterior cingulate cortex (dACC) and anterior insula. This dual functionality of the dACC and anterior insula underscores the evolutionary importance of maintaining interpersonal bonds. Despite the weight that evolution has placed on social injury, the pain response to social rejection varies substantially across individuals. For example, work from our lab demonstrated that the brain's social pain response is moderated by attachment style: anxious-attachment was associated with greater intensity and avoidant-attachment was associated with less intensity in dACC and insula activation. In an attempt to explain these divergent responses in the social pain network, we propose the optimal calibration hypothesis, which posits variation in social rejection in early life history stages shifts the threshold of an individual's social pain network such that the resulting pain sensitivity will be increased by volatile social rejection and reduced by chronic social rejection. Furthermore, the social pain response may be exacerbated when individuals are rejected by others of particular importance to a given life history stage (e.g., potential mates during young adulthood, parents during infancy and childhood). Frontiers Media S.A. 2012-07-05 /pmc/articles/PMC3389670/ /pubmed/22783189 http://dx.doi.org/10.3389/fnevo.2012.00010 Text en Copyright © 2012 Chester, Pond, Richman and DeWall. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Chester, David S.
Pond, Richard S.
Richman, Stephanie B.
DeWall, C. Nathan
The optimal calibration hypothesis: how life history modulates the brain's social pain network
title The optimal calibration hypothesis: how life history modulates the brain's social pain network
title_full The optimal calibration hypothesis: how life history modulates the brain's social pain network
title_fullStr The optimal calibration hypothesis: how life history modulates the brain's social pain network
title_full_unstemmed The optimal calibration hypothesis: how life history modulates the brain's social pain network
title_short The optimal calibration hypothesis: how life history modulates the brain's social pain network
title_sort optimal calibration hypothesis: how life history modulates the brain's social pain network
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389670/
https://www.ncbi.nlm.nih.gov/pubmed/22783189
http://dx.doi.org/10.3389/fnevo.2012.00010
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