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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...

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Detalles Bibliográficos
Autores principales: Petzka, Marit, Chatburn, Alex, Charest, Ian, Balanos, George M., Staresina, Bernhard P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2022
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.
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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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