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The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain

The right ventrolateral prefrontal cortex (rVLPFC) is highly engaged in emotion regulation of social pain. However, there is still lack of both inhibition and excitement evidence to prove the causal relationship between this brain region and voluntary emotion regulation. This study used high‐frequen...

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Autores principales: Yu, Wenwen, Li, Yiwei, Cao, Xueying, Mo, Licheng, Chen, Yuming, Zhang, Dandan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400789/
https://www.ncbi.nlm.nih.gov/pubmed/37376719
http://dx.doi.org/10.1002/hbm.26411
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author Yu, Wenwen
Li, Yiwei
Cao, Xueying
Mo, Licheng
Chen, Yuming
Zhang, Dandan
author_facet Yu, Wenwen
Li, Yiwei
Cao, Xueying
Mo, Licheng
Chen, Yuming
Zhang, Dandan
author_sort Yu, Wenwen
collection PubMed
description The right ventrolateral prefrontal cortex (rVLPFC) is highly engaged in emotion regulation of social pain. However, there is still lack of both inhibition and excitement evidence to prove the causal relationship between this brain region and voluntary emotion regulation. This study used high‐frequency (10 Hz) and low‐frequency (1 Hz) repetitive transcranial magnetic stimulation (rTMS) to separately activate or inhibit the rVLPFC in two groups of participants. We recorded participants' emotion ratings as well as their social attitude and prosocial behaviors following emotion regulation. Also, we used eye tracker to record the changes of pupil diameter to measure emotional feelings objectively. A total of 108 healthy participants were randomly assigned to the activated, inhibitory or sham rTMS groups. They were required to accomplish three sequential tasks: the emotion regulation (cognitive reappraisal) task, the favorability rating task, and the donation task. Results show that the rVLPFC‐inhibitory group reported more negative emotions and showed larger pupil diameter while the rVLPFC‐activated group showed less negative emotions and reduced pupil diameter during emotion regulation (both compared with the sham rTMS group). In addition, the activated group gave more positive social evaluation to peers and donated more money to a public welfare activity than the rVLPFC‐inhibitory group, among which the change of social attitude was mediated by regulated emotion. Taken together, these findings reveal that the rVLPFC plays a causal role in voluntary emotion regulation of social pain and can be a potential brain target in treating deficits of emotion regulation in psychiatric disorders.
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spelling pubmed-104007892023-08-05 The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain Yu, Wenwen Li, Yiwei Cao, Xueying Mo, Licheng Chen, Yuming Zhang, Dandan Hum Brain Mapp Research Articles The right ventrolateral prefrontal cortex (rVLPFC) is highly engaged in emotion regulation of social pain. However, there is still lack of both inhibition and excitement evidence to prove the causal relationship between this brain region and voluntary emotion regulation. This study used high‐frequency (10 Hz) and low‐frequency (1 Hz) repetitive transcranial magnetic stimulation (rTMS) to separately activate or inhibit the rVLPFC in two groups of participants. We recorded participants' emotion ratings as well as their social attitude and prosocial behaviors following emotion regulation. Also, we used eye tracker to record the changes of pupil diameter to measure emotional feelings objectively. A total of 108 healthy participants were randomly assigned to the activated, inhibitory or sham rTMS groups. They were required to accomplish three sequential tasks: the emotion regulation (cognitive reappraisal) task, the favorability rating task, and the donation task. Results show that the rVLPFC‐inhibitory group reported more negative emotions and showed larger pupil diameter while the rVLPFC‐activated group showed less negative emotions and reduced pupil diameter during emotion regulation (both compared with the sham rTMS group). In addition, the activated group gave more positive social evaluation to peers and donated more money to a public welfare activity than the rVLPFC‐inhibitory group, among which the change of social attitude was mediated by regulated emotion. Taken together, these findings reveal that the rVLPFC plays a causal role in voluntary emotion regulation of social pain and can be a potential brain target in treating deficits of emotion regulation in psychiatric disorders. John Wiley & Sons, Inc. 2023-06-27 /pmc/articles/PMC10400789/ /pubmed/37376719 http://dx.doi.org/10.1002/hbm.26411 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Yu, Wenwen
Li, Yiwei
Cao, Xueying
Mo, Licheng
Chen, Yuming
Zhang, Dandan
The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
title The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
title_full The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
title_fullStr The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
title_full_unstemmed The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
title_short The role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
title_sort role of ventrolateral prefrontal cortex on voluntary emotion regulation of social pain
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400789/
https://www.ncbi.nlm.nih.gov/pubmed/37376719
http://dx.doi.org/10.1002/hbm.26411
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