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Sleep spindles track cortical learning patterns for memory consolidation
Memory consolidation—the transformation of labile memory traces into stable long-term representations—is facilitated by post-learning sleep. Computational and biophysical models suggest that sleep spindles may play a key mechanistic role for consolidation, igniting structural changes at cortical sit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616732/ https://www.ncbi.nlm.nih.gov/pubmed/35561681 http://dx.doi.org/10.1016/j.cub.2022.04.045 |
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author | Petzka, Marit Chatburn, Alex Charest, Ian Balanos, George M. Staresina, Bernhard P. |
author_facet | Petzka, Marit Chatburn, Alex Charest, Ian Balanos, George M. Staresina, Bernhard P. |
author_sort | Petzka, Marit |
collection | PubMed |
description | Memory consolidation—the transformation of labile memory traces into stable long-term representations—is facilitated by post-learning sleep. Computational and biophysical models suggest that sleep spindles may play a key mechanistic role for consolidation, igniting structural changes at cortical sites involved in prior learning. Here, we tested the resulting prediction that spindles are most pronounced over learning-related cortical areas and that the extent of this learning-spindle overlap predicts behavioral measures of memory consolidation. Using high-density scalp electroencephalography (EEG) and polysomnography (PSG) in healthy volunteers, we first identified cortical areas engaged during a temporospatial associative memory task (power decreases in the alpha/beta frequency range, 6–20 Hz). Critically, we found that participant-specific topographies (i.e., spatial distributions) of post-learning sleep spindle amplitude correlated with participant-specific learning topographies. Importantly, the extent to which spindles tracked learning patterns further predicted memory consolidation across participants. Our results provide empirical evidence for a role of post-learning sleep spindles in tracking learning networks, thereby facilitating memory consolidation. |
format | Online Article Text |
id | pubmed-9616732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96167322022-10-31 Sleep spindles track cortical learning patterns for memory consolidation Petzka, Marit Chatburn, Alex Charest, Ian Balanos, George M. Staresina, Bernhard P. Curr Biol Article Memory consolidation—the transformation of labile memory traces into stable long-term representations—is facilitated by post-learning sleep. Computational and biophysical models suggest that sleep spindles may play a key mechanistic role for consolidation, igniting structural changes at cortical sites involved in prior learning. Here, we tested the resulting prediction that spindles are most pronounced over learning-related cortical areas and that the extent of this learning-spindle overlap predicts behavioral measures of memory consolidation. Using high-density scalp electroencephalography (EEG) and polysomnography (PSG) in healthy volunteers, we first identified cortical areas engaged during a temporospatial associative memory task (power decreases in the alpha/beta frequency range, 6–20 Hz). Critically, we found that participant-specific topographies (i.e., spatial distributions) of post-learning sleep spindle amplitude correlated with participant-specific learning topographies. Importantly, the extent to which spindles tracked learning patterns further predicted memory consolidation across participants. Our results provide empirical evidence for a role of post-learning sleep spindles in tracking learning networks, thereby facilitating memory consolidation. Cell Press 2022-06-06 /pmc/articles/PMC9616732/ /pubmed/35561681 http://dx.doi.org/10.1016/j.cub.2022.04.045 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Petzka, Marit Chatburn, Alex Charest, Ian Balanos, George M. Staresina, Bernhard P. Sleep spindles track cortical learning patterns for memory consolidation |
title | Sleep spindles track cortical learning patterns for memory consolidation |
title_full | Sleep spindles track cortical learning patterns for memory consolidation |
title_fullStr | Sleep spindles track cortical learning patterns for memory consolidation |
title_full_unstemmed | Sleep spindles track cortical learning patterns for memory consolidation |
title_short | Sleep spindles track cortical learning patterns for memory consolidation |
title_sort | sleep spindles track cortical learning patterns for memory consolidation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616732/ https://www.ncbi.nlm.nih.gov/pubmed/35561681 http://dx.doi.org/10.1016/j.cub.2022.04.045 |
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