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EEG microstates of dreams
Why do people sometimes report that they remember dreams, while at other times they recall no experience? Despite the interest in dreams that may happen during the night, it has remained unclear which brain states determine whether these conscious experiences will occur and what prevents us from wak...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553905/ https://www.ncbi.nlm.nih.gov/pubmed/33051536 http://dx.doi.org/10.1038/s41598-020-74075-z |
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author | Bréchet, Lucie Brunet, Denis Perogamvros, Lampros Tononi, Giulio Michel, Christoph M. |
author_facet | Bréchet, Lucie Brunet, Denis Perogamvros, Lampros Tononi, Giulio Michel, Christoph M. |
author_sort | Bréchet, Lucie |
collection | PubMed |
description | Why do people sometimes report that they remember dreams, while at other times they recall no experience? Despite the interest in dreams that may happen during the night, it has remained unclear which brain states determine whether these conscious experiences will occur and what prevents us from waking up during these episodes. Here we address this issue by comparing the EEG activity preceding awakenings with recalled vs. no recall of dreams using the EEG microstate approach. This approach characterizes transiently stable brain states of sub-second duration that involve neural networks with nearly synchronous dynamics. We found that two microstates (3 and 4) dominated during NREM sleep compared to resting wake. Further, within NREM sleep, microstate 3 was more expressed during periods followed by dream recall, whereas microstate 4 was less expressed. Source localization showed that microstate 3 encompassed the medial frontal lobe, whereas microstate 4 involved the occipital cortex, as well as thalamic and brainstem structures. Since NREM sleep is characterized by low-frequency synchronization, indicative of neuronal bistability, we interpret the increased presence of the “frontal” microstate 3 as a sign of deeper local deactivation, and the reduced presence of the “occipital” microstate 4 as a sign of local activation. The latter may account for the occurrence of dreaming with rich perceptual content, while the former may account for why the dreaming brain may undergo executive disconnection and remain asleep. This study demonstrates that NREM sleep consists of alternating brain states whose temporal dynamics determine whether conscious experience arises. |
format | Online Article Text |
id | pubmed-7553905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75539052020-10-14 EEG microstates of dreams Bréchet, Lucie Brunet, Denis Perogamvros, Lampros Tononi, Giulio Michel, Christoph M. Sci Rep Article Why do people sometimes report that they remember dreams, while at other times they recall no experience? Despite the interest in dreams that may happen during the night, it has remained unclear which brain states determine whether these conscious experiences will occur and what prevents us from waking up during these episodes. Here we address this issue by comparing the EEG activity preceding awakenings with recalled vs. no recall of dreams using the EEG microstate approach. This approach characterizes transiently stable brain states of sub-second duration that involve neural networks with nearly synchronous dynamics. We found that two microstates (3 and 4) dominated during NREM sleep compared to resting wake. Further, within NREM sleep, microstate 3 was more expressed during periods followed by dream recall, whereas microstate 4 was less expressed. Source localization showed that microstate 3 encompassed the medial frontal lobe, whereas microstate 4 involved the occipital cortex, as well as thalamic and brainstem structures. Since NREM sleep is characterized by low-frequency synchronization, indicative of neuronal bistability, we interpret the increased presence of the “frontal” microstate 3 as a sign of deeper local deactivation, and the reduced presence of the “occipital” microstate 4 as a sign of local activation. The latter may account for the occurrence of dreaming with rich perceptual content, while the former may account for why the dreaming brain may undergo executive disconnection and remain asleep. This study demonstrates that NREM sleep consists of alternating brain states whose temporal dynamics determine whether conscious experience arises. Nature Publishing Group UK 2020-10-13 /pmc/articles/PMC7553905/ /pubmed/33051536 http://dx.doi.org/10.1038/s41598-020-74075-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bréchet, Lucie Brunet, Denis Perogamvros, Lampros Tononi, Giulio Michel, Christoph M. EEG microstates of dreams |
title | EEG microstates of dreams |
title_full | EEG microstates of dreams |
title_fullStr | EEG microstates of dreams |
title_full_unstemmed | EEG microstates of dreams |
title_short | EEG microstates of dreams |
title_sort | eeg microstates of dreams |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553905/ https://www.ncbi.nlm.nih.gov/pubmed/33051536 http://dx.doi.org/10.1038/s41598-020-74075-z |
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