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Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex
Animal studies support the hypothesis that in slow-wave sleep, replay of waking neocortical activity under hippocampal guidance leads to memory consolidation. However, no intracranial electrophysiological evidence for replay exists in humans. We identified consistent sequences of population firing p...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727134/ https://www.ncbi.nlm.nih.gov/pubmed/29234075 http://dx.doi.org/10.1038/s41598-017-17469-w |
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author | Jiang, Xi Shamie, Isaac K. Doyle, Werner Friedman, Daniel Dugan, Patricia Devinsky, Orrin Eskandar, Emad Cash, Sydney S. Thesen, Thomas Halgren, Eric |
author_facet | Jiang, Xi Shamie, Isaac K. Doyle, Werner Friedman, Daniel Dugan, Patricia Devinsky, Orrin Eskandar, Emad Cash, Sydney S. Thesen, Thomas Halgren, Eric |
author_sort | Jiang, Xi |
collection | PubMed |
description | Animal studies support the hypothesis that in slow-wave sleep, replay of waking neocortical activity under hippocampal guidance leads to memory consolidation. However, no intracranial electrophysiological evidence for replay exists in humans. We identified consistent sequences of population firing peaks across widespread cortical regions during complete waking periods. The occurrence of these “Motifs” were compared between sleeps preceding the waking period (“Sleep-Pre”) when the Motifs were identified, and those following (“Sleep-Post”). In all subjects, the majority of waking Motifs (most of which were novel) had more matches in Sleep-Post than in Sleep-Pre. In rodents, hippocampal replay occurs during local sharp-wave ripples, and the associated neocortical replay tends to occur during local sleep spindles and down-to-up transitions. These waves may facilitate consolidation by sequencing cell-firing and encouraging plasticity. Similarly, we found that Motifs were coupled to neocortical spindles, down-to-up transitions, theta bursts, and hippocampal sharp-wave ripples. While Motifs occurring during cognitive task performance were more likely to have more matches in subsequent sleep, our studies provide no direct demonstration that the replay of Motifs contributes to consolidation. Nonetheless, these results confirm a core prediction of the dominant neurobiological theory of human memory consolidation. |
format | Online Article Text |
id | pubmed-5727134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57271342017-12-13 Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex Jiang, Xi Shamie, Isaac K. Doyle, Werner Friedman, Daniel Dugan, Patricia Devinsky, Orrin Eskandar, Emad Cash, Sydney S. Thesen, Thomas Halgren, Eric Sci Rep Article Animal studies support the hypothesis that in slow-wave sleep, replay of waking neocortical activity under hippocampal guidance leads to memory consolidation. However, no intracranial electrophysiological evidence for replay exists in humans. We identified consistent sequences of population firing peaks across widespread cortical regions during complete waking periods. The occurrence of these “Motifs” were compared between sleeps preceding the waking period (“Sleep-Pre”) when the Motifs were identified, and those following (“Sleep-Post”). In all subjects, the majority of waking Motifs (most of which were novel) had more matches in Sleep-Post than in Sleep-Pre. In rodents, hippocampal replay occurs during local sharp-wave ripples, and the associated neocortical replay tends to occur during local sleep spindles and down-to-up transitions. These waves may facilitate consolidation by sequencing cell-firing and encouraging plasticity. Similarly, we found that Motifs were coupled to neocortical spindles, down-to-up transitions, theta bursts, and hippocampal sharp-wave ripples. While Motifs occurring during cognitive task performance were more likely to have more matches in subsequent sleep, our studies provide no direct demonstration that the replay of Motifs contributes to consolidation. Nonetheless, these results confirm a core prediction of the dominant neurobiological theory of human memory consolidation. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727134/ /pubmed/29234075 http://dx.doi.org/10.1038/s41598-017-17469-w Text en © The Author(s) 2017 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 Jiang, Xi Shamie, Isaac K. Doyle, Werner Friedman, Daniel Dugan, Patricia Devinsky, Orrin Eskandar, Emad Cash, Sydney S. Thesen, Thomas Halgren, Eric Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex |
title | Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex |
title_full | Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex |
title_fullStr | Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex |
title_full_unstemmed | Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex |
title_short | Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex |
title_sort | replay of large-scale spatio-temporal patterns from waking during subsequent nrem sleep in human cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727134/ https://www.ncbi.nlm.nih.gov/pubmed/29234075 http://dx.doi.org/10.1038/s41598-017-17469-w |
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