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Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes
Sleep is thought to support memory consolidation via reactivation of prior experiences, with particular electrophysiological sleep signatures (slow oscillations (SOs) and sleep spindles) gating the information flow between relevant brain areas. However, empirical evidence for a role of endogenous me...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149676/ https://www.ncbi.nlm.nih.gov/pubmed/34035303 http://dx.doi.org/10.1038/s41467-021-23520-2 |
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author | Schreiner, Thomas Petzka, Marit Staudigl, Tobias Staresina, Bernhard P. |
author_facet | Schreiner, Thomas Petzka, Marit Staudigl, Tobias Staresina, Bernhard P. |
author_sort | Schreiner, Thomas |
collection | PubMed |
description | Sleep is thought to support memory consolidation via reactivation of prior experiences, with particular electrophysiological sleep signatures (slow oscillations (SOs) and sleep spindles) gating the information flow between relevant brain areas. However, empirical evidence for a role of endogenous memory reactivation (i.e., without experimentally delivered memory cues) for consolidation in humans is lacking. Here, we devised a paradigm in which participants acquired associative memories before taking a nap. Multivariate decoding was then used to capture endogenous memory reactivation during non-rapid eye movement (NREM) sleep in surface EEG recordings. Our results reveal reactivation of learning material during SO-spindle complexes, with the precision of SO-spindle coupling predicting reactivation strength. Critically, reactivation strength (i.e. classifier evidence in favor of the previously studied stimulus category) in turn predicts the level of consolidation across participants. These results elucidate the memory function of sleep in humans and emphasize the importance of SOs and spindles in clocking endogenous consolidation processes. |
format | Online Article Text |
id | pubmed-8149676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81496762021-06-01 Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes Schreiner, Thomas Petzka, Marit Staudigl, Tobias Staresina, Bernhard P. Nat Commun Article Sleep is thought to support memory consolidation via reactivation of prior experiences, with particular electrophysiological sleep signatures (slow oscillations (SOs) and sleep spindles) gating the information flow between relevant brain areas. However, empirical evidence for a role of endogenous memory reactivation (i.e., without experimentally delivered memory cues) for consolidation in humans is lacking. Here, we devised a paradigm in which participants acquired associative memories before taking a nap. Multivariate decoding was then used to capture endogenous memory reactivation during non-rapid eye movement (NREM) sleep in surface EEG recordings. Our results reveal reactivation of learning material during SO-spindle complexes, with the precision of SO-spindle coupling predicting reactivation strength. Critically, reactivation strength (i.e. classifier evidence in favor of the previously studied stimulus category) in turn predicts the level of consolidation across participants. These results elucidate the memory function of sleep in humans and emphasize the importance of SOs and spindles in clocking endogenous consolidation processes. Nature Publishing Group UK 2021-05-25 /pmc/articles/PMC8149676/ /pubmed/34035303 http://dx.doi.org/10.1038/s41467-021-23520-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schreiner, Thomas Petzka, Marit Staudigl, Tobias Staresina, Bernhard P. Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
title | Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
title_full | Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
title_fullStr | Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
title_full_unstemmed | Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
title_short | Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
title_sort | endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149676/ https://www.ncbi.nlm.nih.gov/pubmed/34035303 http://dx.doi.org/10.1038/s41467-021-23520-2 |
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