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Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall

The waking brain efficiently detects emotional signals to promote survival. However, emotion detection during sleep is poorly understood and may be influenced by individual sleep characteristics or neural reactivity. Notably, dream recall frequency has been associated with stimulus reactivity during...

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Autores principales: Moyne, Maëva, Legendre, Guillaume, Arnal, Luc, Kumar, Samika, Sterpenich, Virginie, Seeck, Margitta, Grandjean, Didier, Schwartz, Sophie, Vuilleumier, Patrik, Domínguez-Borràs, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844542/
https://www.ncbi.nlm.nih.gov/pubmed/35174329
http://dx.doi.org/10.1093/texcom/tgac003
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author Moyne, Maëva
Legendre, Guillaume
Arnal, Luc
Kumar, Samika
Sterpenich, Virginie
Seeck, Margitta
Grandjean, Didier
Schwartz, Sophie
Vuilleumier, Patrik
Domínguez-Borràs, Judith
author_facet Moyne, Maëva
Legendre, Guillaume
Arnal, Luc
Kumar, Samika
Sterpenich, Virginie
Seeck, Margitta
Grandjean, Didier
Schwartz, Sophie
Vuilleumier, Patrik
Domínguez-Borràs, Judith
author_sort Moyne, Maëva
collection PubMed
description The waking brain efficiently detects emotional signals to promote survival. However, emotion detection during sleep is poorly understood and may be influenced by individual sleep characteristics or neural reactivity. Notably, dream recall frequency has been associated with stimulus reactivity during sleep, with enhanced stimulus-driven responses in high vs. low recallers. Using electroencephalography (EEG), we characterized the neural responses of healthy individuals to emotional, neutral voices, and control stimuli, both during wakefulness and NREM sleep. Then, we tested how these responses varied with individual dream recall frequency. Event-related potentials (ERPs) differed for emotional vs. neutral voices, both in wakefulness and NREM. Likewise, EEG arousals (sleep perturbations) increased selectively after the emotional voices, indicating emotion reactivity. Interestingly, sleep ERP amplitude and arousals after emotional voices increased linearly with participants’ dream recall frequency. Similar correlations with dream recall were observed for beta and sigma responses, but not for theta. In contrast, dream recall correlations were absent for neutral or control stimuli. Our results reveal that brain reactivity to affective salience is preserved during NREM and is selectively associated to individual memory for dreams. Our findings also suggest that emotion-specific reactivity during sleep, and not generalized alertness, may contribute to the encoding/retrieval of dreams.
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spelling pubmed-88445422022-02-15 Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall Moyne, Maëva Legendre, Guillaume Arnal, Luc Kumar, Samika Sterpenich, Virginie Seeck, Margitta Grandjean, Didier Schwartz, Sophie Vuilleumier, Patrik Domínguez-Borràs, Judith Cereb Cortex Commun Original Article The waking brain efficiently detects emotional signals to promote survival. However, emotion detection during sleep is poorly understood and may be influenced by individual sleep characteristics or neural reactivity. Notably, dream recall frequency has been associated with stimulus reactivity during sleep, with enhanced stimulus-driven responses in high vs. low recallers. Using electroencephalography (EEG), we characterized the neural responses of healthy individuals to emotional, neutral voices, and control stimuli, both during wakefulness and NREM sleep. Then, we tested how these responses varied with individual dream recall frequency. Event-related potentials (ERPs) differed for emotional vs. neutral voices, both in wakefulness and NREM. Likewise, EEG arousals (sleep perturbations) increased selectively after the emotional voices, indicating emotion reactivity. Interestingly, sleep ERP amplitude and arousals after emotional voices increased linearly with participants’ dream recall frequency. Similar correlations with dream recall were observed for beta and sigma responses, but not for theta. In contrast, dream recall correlations were absent for neutral or control stimuli. Our results reveal that brain reactivity to affective salience is preserved during NREM and is selectively associated to individual memory for dreams. Our findings also suggest that emotion-specific reactivity during sleep, and not generalized alertness, may contribute to the encoding/retrieval of dreams. Oxford University Press 2022-01-27 /pmc/articles/PMC8844542/ /pubmed/35174329 http://dx.doi.org/10.1093/texcom/tgac003 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Moyne, Maëva
Legendre, Guillaume
Arnal, Luc
Kumar, Samika
Sterpenich, Virginie
Seeck, Margitta
Grandjean, Didier
Schwartz, Sophie
Vuilleumier, Patrik
Domínguez-Borràs, Judith
Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall
title Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall
title_full Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall
title_fullStr Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall
title_full_unstemmed Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall
title_short Brain reactivity to emotion persists in NREM sleep and is associated with individual dream recall
title_sort brain reactivity to emotion persists in nrem sleep and is associated with individual dream recall
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844542/
https://www.ncbi.nlm.nih.gov/pubmed/35174329
http://dx.doi.org/10.1093/texcom/tgac003
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