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Increased neuronal signatures of targeted memory reactivation during slow-wave up states

It is assumed that slow oscillatory up-states represent crucial time windows for memory reactivation and consolidation during sleep. We tested this assumption by utilizing closed-loop targeted memory reactivation: Participants were re-exposed to prior learned foreign vocabulary during up- and down-s...

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Autores principales: Göldi, Maurice, van Poppel, Eva Anna Maria, Rasch, Björn, Schreiner, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389952/
https://www.ncbi.nlm.nih.gov/pubmed/30804371
http://dx.doi.org/10.1038/s41598-019-39178-2
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author Göldi, Maurice
van Poppel, Eva Anna Maria
Rasch, Björn
Schreiner, Thomas
author_facet Göldi, Maurice
van Poppel, Eva Anna Maria
Rasch, Björn
Schreiner, Thomas
author_sort Göldi, Maurice
collection PubMed
description It is assumed that slow oscillatory up-states represent crucial time windows for memory reactivation and consolidation during sleep. We tested this assumption by utilizing closed-loop targeted memory reactivation: Participants were re-exposed to prior learned foreign vocabulary during up- and down-states of slow oscillations. While presenting memory cues during slow oscillatory up-states improved recall performance, down-state cueing did not result in a clear behavioral benefit. Still, no robust behavioral benefit of up- as compared to down-state cueing was observable. At the electrophysiological level however, successful memory reactivation during up-states was associated with a characteristic power increase in the theta and sleep spindle band. No oscillatory changes were observable for down-state cues. Our findings provide experimental support for the assumption that slow oscillatory up-states may represent privileged time windows for memory reactivation, while the interplay of slow oscillations, theta and sleep spindle activity promotes successful memory consolidation during sleep.
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spelling pubmed-63899522019-02-28 Increased neuronal signatures of targeted memory reactivation during slow-wave up states Göldi, Maurice van Poppel, Eva Anna Maria Rasch, Björn Schreiner, Thomas Sci Rep Article It is assumed that slow oscillatory up-states represent crucial time windows for memory reactivation and consolidation during sleep. We tested this assumption by utilizing closed-loop targeted memory reactivation: Participants were re-exposed to prior learned foreign vocabulary during up- and down-states of slow oscillations. While presenting memory cues during slow oscillatory up-states improved recall performance, down-state cueing did not result in a clear behavioral benefit. Still, no robust behavioral benefit of up- as compared to down-state cueing was observable. At the electrophysiological level however, successful memory reactivation during up-states was associated with a characteristic power increase in the theta and sleep spindle band. No oscillatory changes were observable for down-state cues. Our findings provide experimental support for the assumption that slow oscillatory up-states may represent privileged time windows for memory reactivation, while the interplay of slow oscillations, theta and sleep spindle activity promotes successful memory consolidation during sleep. Nature Publishing Group UK 2019-02-25 /pmc/articles/PMC6389952/ /pubmed/30804371 http://dx.doi.org/10.1038/s41598-019-39178-2 Text en © The Author(s) 2019 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/.
spellingShingle Article
Göldi, Maurice
van Poppel, Eva Anna Maria
Rasch, Björn
Schreiner, Thomas
Increased neuronal signatures of targeted memory reactivation during slow-wave up states
title Increased neuronal signatures of targeted memory reactivation during slow-wave up states
title_full Increased neuronal signatures of targeted memory reactivation during slow-wave up states
title_fullStr Increased neuronal signatures of targeted memory reactivation during slow-wave up states
title_full_unstemmed Increased neuronal signatures of targeted memory reactivation during slow-wave up states
title_short Increased neuronal signatures of targeted memory reactivation during slow-wave up states
title_sort increased neuronal signatures of targeted memory reactivation during slow-wave up states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389952/
https://www.ncbi.nlm.nih.gov/pubmed/30804371
http://dx.doi.org/10.1038/s41598-019-39178-2
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