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Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep

After experiences are encoded, post‐encoding reactivations during sleep have been proposed to mediate long‐term memory consolidation. Spindle–slow oscillation coupling during NREM sleep is a candidate mechanism through which a hippocampal‐cortical dialogue may strengthen a newly formed memory engram...

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Autores principales: Bastian, Lisa, Samanta, Anumita, Ribeiro de Paula, Demetrius, Weber, Frederik D., Schoenfeld, Robby, Dresler, Martin, Genzel, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374888/
https://www.ncbi.nlm.nih.gov/pubmed/35488512
http://dx.doi.org/10.1002/hbm.25893
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author Bastian, Lisa
Samanta, Anumita
Ribeiro de Paula, Demetrius
Weber, Frederik D.
Schoenfeld, Robby
Dresler, Martin
Genzel, Lisa
author_facet Bastian, Lisa
Samanta, Anumita
Ribeiro de Paula, Demetrius
Weber, Frederik D.
Schoenfeld, Robby
Dresler, Martin
Genzel, Lisa
author_sort Bastian, Lisa
collection PubMed
description After experiences are encoded, post‐encoding reactivations during sleep have been proposed to mediate long‐term memory consolidation. Spindle–slow oscillation coupling during NREM sleep is a candidate mechanism through which a hippocampal‐cortical dialogue may strengthen a newly formed memory engram. Here, we investigated the role of fast spindle‐ and slow spindle–slow oscillation coupling in the consolidation of spatial memory in humans with a virtual watermaze task involving allocentric and egocentric learning strategies. Furthermore, we analyzed how resting‐state functional connectivity evolved across learning, consolidation, and retrieval of this task using a data‐driven approach. Our results show task‐related connectivity changes in the executive control network, the default mode network, and the hippocampal network at post‐task rest. The hippocampal network could further be divided into two subnetworks of which only one showed modulation by sleep. Decreased functional connectivity in this subnetwork was associated with higher spindle–slow oscillation coupling power, which was also related to better memory performance at test. Overall, this study contributes to a more holistic understanding of the functional resting‐state networks and the mechanisms during sleep associated to spatial memory consolidation.
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spelling pubmed-93748882022-08-17 Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep Bastian, Lisa Samanta, Anumita Ribeiro de Paula, Demetrius Weber, Frederik D. Schoenfeld, Robby Dresler, Martin Genzel, Lisa Hum Brain Mapp Research Articles After experiences are encoded, post‐encoding reactivations during sleep have been proposed to mediate long‐term memory consolidation. Spindle–slow oscillation coupling during NREM sleep is a candidate mechanism through which a hippocampal‐cortical dialogue may strengthen a newly formed memory engram. Here, we investigated the role of fast spindle‐ and slow spindle–slow oscillation coupling in the consolidation of spatial memory in humans with a virtual watermaze task involving allocentric and egocentric learning strategies. Furthermore, we analyzed how resting‐state functional connectivity evolved across learning, consolidation, and retrieval of this task using a data‐driven approach. Our results show task‐related connectivity changes in the executive control network, the default mode network, and the hippocampal network at post‐task rest. The hippocampal network could further be divided into two subnetworks of which only one showed modulation by sleep. Decreased functional connectivity in this subnetwork was associated with higher spindle–slow oscillation coupling power, which was also related to better memory performance at test. Overall, this study contributes to a more holistic understanding of the functional resting‐state networks and the mechanisms during sleep associated to spatial memory consolidation. John Wiley & Sons, Inc. 2022-04-30 /pmc/articles/PMC9374888/ /pubmed/35488512 http://dx.doi.org/10.1002/hbm.25893 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Bastian, Lisa
Samanta, Anumita
Ribeiro de Paula, Demetrius
Weber, Frederik D.
Schoenfeld, Robby
Dresler, Martin
Genzel, Lisa
Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
title Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
title_full Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
title_fullStr Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
title_full_unstemmed Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
title_short Spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
title_sort spindle–slow oscillation coupling correlates with memory performance and connectivity changes in a hippocampal network after sleep
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374888/
https://www.ncbi.nlm.nih.gov/pubmed/35488512
http://dx.doi.org/10.1002/hbm.25893
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