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Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves
Targeted memory reactivation (TMR) during post-learning sleep is known to enhance motor memory consolidation but the underlying neurophysiological processes remain unclear. Here, we confirm the beneficial effect of auditory TMR on motor performance. At the neural level, TMR enhanced slow wave (SW) c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259015/ https://www.ncbi.nlm.nih.gov/pubmed/35726850 http://dx.doi.org/10.7554/eLife.73930 |
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author | Nicolas, Judith King, Bradley R Levesque, David Lazzouni, Latifa Coffey, Emily Swinnen, Stephan Doyon, Julien Carrier, Julie Albouy, Genevieve |
author_facet | Nicolas, Judith King, Bradley R Levesque, David Lazzouni, Latifa Coffey, Emily Swinnen, Stephan Doyon, Julien Carrier, Julie Albouy, Genevieve |
author_sort | Nicolas, Judith |
collection | PubMed |
description | Targeted memory reactivation (TMR) during post-learning sleep is known to enhance motor memory consolidation but the underlying neurophysiological processes remain unclear. Here, we confirm the beneficial effect of auditory TMR on motor performance. At the neural level, TMR enhanced slow wave (SW) characteristics. Additionally, greater TMR-related phase-amplitude coupling between slow (0.5–2 Hz) and sigma (12–16 Hz) oscillations after the SW peak was related to higher TMR effect on performance. Importantly, sounds that were not associated to learning strengthened SW-sigma coupling at the SW trough. Moreover, the increase in sigma power nested in the trough of the potential evoked by the unassociated sounds was related to the TMR benefit. Altogether, our data suggest that, depending on their precise temporal coordination during post learning sleep, slow and sigma oscillations play a crucial role in either memory reinstatement or protection against irrelevant information; two processes that critically contribute to motor memory consolidation. |
format | Online Article Text |
id | pubmed-9259015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92590152022-07-07 Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves Nicolas, Judith King, Bradley R Levesque, David Lazzouni, Latifa Coffey, Emily Swinnen, Stephan Doyon, Julien Carrier, Julie Albouy, Genevieve eLife Neuroscience Targeted memory reactivation (TMR) during post-learning sleep is known to enhance motor memory consolidation but the underlying neurophysiological processes remain unclear. Here, we confirm the beneficial effect of auditory TMR on motor performance. At the neural level, TMR enhanced slow wave (SW) characteristics. Additionally, greater TMR-related phase-amplitude coupling between slow (0.5–2 Hz) and sigma (12–16 Hz) oscillations after the SW peak was related to higher TMR effect on performance. Importantly, sounds that were not associated to learning strengthened SW-sigma coupling at the SW trough. Moreover, the increase in sigma power nested in the trough of the potential evoked by the unassociated sounds was related to the TMR benefit. Altogether, our data suggest that, depending on their precise temporal coordination during post learning sleep, slow and sigma oscillations play a crucial role in either memory reinstatement or protection against irrelevant information; two processes that critically contribute to motor memory consolidation. eLife Sciences Publications, Ltd 2022-06-21 /pmc/articles/PMC9259015/ /pubmed/35726850 http://dx.doi.org/10.7554/eLife.73930 Text en © 2022, Nicolas et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Nicolas, Judith King, Bradley R Levesque, David Lazzouni, Latifa Coffey, Emily Swinnen, Stephan Doyon, Julien Carrier, Julie Albouy, Genevieve Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
title | Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
title_full | Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
title_fullStr | Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
title_full_unstemmed | Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
title_short | Sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
title_sort | sigma oscillations protect or reinstate motor memory depending on their temporal coordination with slow waves |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9259015/ https://www.ncbi.nlm.nih.gov/pubmed/35726850 http://dx.doi.org/10.7554/eLife.73930 |
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