Cargando…
Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding
During times of emotional stress, individuals often engage in emotion regulation to reduce the experiential and physiological impact of negative emotions. Interestingly, emotion regulation strategies also influence memory encoding of the event. Cognitive reappraisal is associated with enhanced memor...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015134/ https://www.ncbi.nlm.nih.gov/pubmed/21212840 http://dx.doi.org/10.3389/fnhum.2010.00230 |
_version_ | 1782195451468972032 |
---|---|
author | Hayes, Jasmeet Pannu Morey, Rajendra A. Petty, Christopher M. Seth, Srishti Smoski, Moria J. McCarthy, Gregory LaBar, Kevin S. |
author_facet | Hayes, Jasmeet Pannu Morey, Rajendra A. Petty, Christopher M. Seth, Srishti Smoski, Moria J. McCarthy, Gregory LaBar, Kevin S. |
author_sort | Hayes, Jasmeet Pannu |
collection | PubMed |
description | During times of emotional stress, individuals often engage in emotion regulation to reduce the experiential and physiological impact of negative emotions. Interestingly, emotion regulation strategies also influence memory encoding of the event. Cognitive reappraisal is associated with enhanced memory while expressive suppression is associated with impaired explicit memory of the emotional event. However, the mechanism by which these emotion regulation strategies affect memory is unclear. We used event-related fMRI to investigate the neural mechanisms that give rise to memory formation during emotion regulation. Twenty-five participants viewed negative pictures while alternately engaging in cognitive reappraisal, expressive suppression, or passive viewing. As part of the subsequent memory design, participants returned to the laboratory two weeks later for a surprise memory test. Behavioral results showed a reduction in negative affect and a retention advantage for reappraised stimuli relative to the other conditions. Imaging results showed that successful encoding during reappraisal was uniquely associated with greater co-activation of the left inferior frontal gyrus, amygdala, and hippocampus, suggesting a possible role for elaborative encoding of negative memories. This study provides neurobehavioral evidence that engaging in cognitive reappraisal is advantageous to both affective and mnemonic processes. |
format | Text |
id | pubmed-3015134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30151342011-01-06 Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding Hayes, Jasmeet Pannu Morey, Rajendra A. Petty, Christopher M. Seth, Srishti Smoski, Moria J. McCarthy, Gregory LaBar, Kevin S. Front Hum Neurosci Neuroscience During times of emotional stress, individuals often engage in emotion regulation to reduce the experiential and physiological impact of negative emotions. Interestingly, emotion regulation strategies also influence memory encoding of the event. Cognitive reappraisal is associated with enhanced memory while expressive suppression is associated with impaired explicit memory of the emotional event. However, the mechanism by which these emotion regulation strategies affect memory is unclear. We used event-related fMRI to investigate the neural mechanisms that give rise to memory formation during emotion regulation. Twenty-five participants viewed negative pictures while alternately engaging in cognitive reappraisal, expressive suppression, or passive viewing. As part of the subsequent memory design, participants returned to the laboratory two weeks later for a surprise memory test. Behavioral results showed a reduction in negative affect and a retention advantage for reappraised stimuli relative to the other conditions. Imaging results showed that successful encoding during reappraisal was uniquely associated with greater co-activation of the left inferior frontal gyrus, amygdala, and hippocampus, suggesting a possible role for elaborative encoding of negative memories. This study provides neurobehavioral evidence that engaging in cognitive reappraisal is advantageous to both affective and mnemonic processes. Frontiers Research Foundation 2010-12-22 /pmc/articles/PMC3015134/ /pubmed/21212840 http://dx.doi.org/10.3389/fnhum.2010.00230 Text en Copyright © 2010 Hayes, Morey, Petty, Seth, Smoski, McCarthy and LaBar. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited. |
spellingShingle | Neuroscience Hayes, Jasmeet Pannu Morey, Rajendra A. Petty, Christopher M. Seth, Srishti Smoski, Moria J. McCarthy, Gregory LaBar, Kevin S. Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding |
title | Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding |
title_full | Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding |
title_fullStr | Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding |
title_full_unstemmed | Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding |
title_short | Staying Cool when Things Get Hot: Emotion Regulation Modulates Neural Mechanisms of Memory Encoding |
title_sort | staying cool when things get hot: emotion regulation modulates neural mechanisms of memory encoding |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015134/ https://www.ncbi.nlm.nih.gov/pubmed/21212840 http://dx.doi.org/10.3389/fnhum.2010.00230 |
work_keys_str_mv | AT hayesjasmeetpannu stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding AT moreyrajendraa stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding AT pettychristopherm stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding AT sethsrishti stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding AT smoskimoriaj stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding AT mccarthygregory stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding AT labarkevins stayingcoolwhenthingsgethotemotionregulationmodulatesneuralmechanismsofmemoryencoding |