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Human REM sleep recalibrates neural activity in support of memory formation
The proposed mechanisms of sleep-dependent memory consolidation involve the overnight regulation of neural activity at both synaptic and whole-network levels. Now, there is a lack of in vivo data in humans elucidating if, and how, sleep and its varied stages balance neural activity, and if such reca...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456851/ https://www.ncbi.nlm.nih.gov/pubmed/37624898 http://dx.doi.org/10.1126/sciadv.adj1895 |
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author | Lendner, Janna D. Niethard, Niels Mander, Bryce A. van Schalkwijk, Frank J. Schuh-Hofer, Sigrid Schmidt, Hannah Knight, Robert T. Born, Jan Walker, Matthew P. Lin, Jack J. Helfrich, Randolph F. |
author_facet | Lendner, Janna D. Niethard, Niels Mander, Bryce A. van Schalkwijk, Frank J. Schuh-Hofer, Sigrid Schmidt, Hannah Knight, Robert T. Born, Jan Walker, Matthew P. Lin, Jack J. Helfrich, Randolph F. |
author_sort | Lendner, Janna D. |
collection | PubMed |
description | The proposed mechanisms of sleep-dependent memory consolidation involve the overnight regulation of neural activity at both synaptic and whole-network levels. Now, there is a lack of in vivo data in humans elucidating if, and how, sleep and its varied stages balance neural activity, and if such recalibration benefits memory. We combined electrophysiology with in vivo two-photon calcium imaging in rodents as well as intracranial and scalp electroencephalography (EEG) in humans to reveal a key role for non-oscillatory brain activity during rapid eye movement (REM) sleep to mediate sleep-dependent recalibration of neural population dynamics. The extent of this REM sleep recalibration predicted the success of overnight memory consolidation, expressly the modulation of hippocampal—neocortical activity, favoring remembering rather than forgetting. The findings describe a non-oscillatory mechanism how human REM sleep modulates neural population activity to enhance long-term memory. |
format | Online Article Text |
id | pubmed-10456851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-104568512023-08-26 Human REM sleep recalibrates neural activity in support of memory formation Lendner, Janna D. Niethard, Niels Mander, Bryce A. van Schalkwijk, Frank J. Schuh-Hofer, Sigrid Schmidt, Hannah Knight, Robert T. Born, Jan Walker, Matthew P. Lin, Jack J. Helfrich, Randolph F. Sci Adv Neuroscience The proposed mechanisms of sleep-dependent memory consolidation involve the overnight regulation of neural activity at both synaptic and whole-network levels. Now, there is a lack of in vivo data in humans elucidating if, and how, sleep and its varied stages balance neural activity, and if such recalibration benefits memory. We combined electrophysiology with in vivo two-photon calcium imaging in rodents as well as intracranial and scalp electroencephalography (EEG) in humans to reveal a key role for non-oscillatory brain activity during rapid eye movement (REM) sleep to mediate sleep-dependent recalibration of neural population dynamics. The extent of this REM sleep recalibration predicted the success of overnight memory consolidation, expressly the modulation of hippocampal—neocortical activity, favoring remembering rather than forgetting. The findings describe a non-oscillatory mechanism how human REM sleep modulates neural population activity to enhance long-term memory. American Association for the Advancement of Science 2023-08-25 /pmc/articles/PMC10456851/ /pubmed/37624898 http://dx.doi.org/10.1126/sciadv.adj1895 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Lendner, Janna D. Niethard, Niels Mander, Bryce A. van Schalkwijk, Frank J. Schuh-Hofer, Sigrid Schmidt, Hannah Knight, Robert T. Born, Jan Walker, Matthew P. Lin, Jack J. Helfrich, Randolph F. Human REM sleep recalibrates neural activity in support of memory formation |
title | Human REM sleep recalibrates neural activity in support of memory formation |
title_full | Human REM sleep recalibrates neural activity in support of memory formation |
title_fullStr | Human REM sleep recalibrates neural activity in support of memory formation |
title_full_unstemmed | Human REM sleep recalibrates neural activity in support of memory formation |
title_short | Human REM sleep recalibrates neural activity in support of memory formation |
title_sort | human rem sleep recalibrates neural activity in support of memory formation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456851/ https://www.ncbi.nlm.nih.gov/pubmed/37624898 http://dx.doi.org/10.1126/sciadv.adj1895 |
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