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Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load
Sleep is generally considered to be a state of large-scale synchrony across thalamus and neocortex; however, recent work has challenged this idea by reporting isolated sleep rhythms such as slow oscillations and spindles. What is the spatial scale of sleep rhythms? To answer this question, we adapte...
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/PMC9242645/ https://www.ncbi.nlm.nih.gov/pubmed/35766286 http://dx.doi.org/10.7554/eLife.75769 |
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author | Mofrad, Maryam H Gilmore, Greydon Koller, Dominik Mirsattari, Seyed M Burneo, Jorge G Steven, David A Khan, Ali R Suller Marti, Ana Muller, Lyle |
author_facet | Mofrad, Maryam H Gilmore, Greydon Koller, Dominik Mirsattari, Seyed M Burneo, Jorge G Steven, David A Khan, Ali R Suller Marti, Ana Muller, Lyle |
author_sort | Mofrad, Maryam H |
collection | PubMed |
description | Sleep is generally considered to be a state of large-scale synchrony across thalamus and neocortex; however, recent work has challenged this idea by reporting isolated sleep rhythms such as slow oscillations and spindles. What is the spatial scale of sleep rhythms? To answer this question, we adapted deep learning algorithms initially developed for detecting earthquakes and gravitational waves in high-noise settings for analysis of neural recordings in sleep. We then studied sleep spindles in non-human primate electrocorticography (ECoG), human electroencephalogram (EEG), and clinical intracranial electroencephalogram (iEEG) recordings in the human. Within each recording type, we find widespread spindles occur much more frequently than previously reported. We then analyzed the spatiotemporal patterns of these large-scale, multi-area spindles and, in the EEG recordings, how spindle patterns change following a visual memory task. Our results reveal a potential role for widespread, multi-area spindles in consolidation of memories in networks widely distributed across primate cortex. |
format | Online Article Text |
id | pubmed-9242645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92426452022-06-30 Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load Mofrad, Maryam H Gilmore, Greydon Koller, Dominik Mirsattari, Seyed M Burneo, Jorge G Steven, David A Khan, Ali R Suller Marti, Ana Muller, Lyle eLife Computational and Systems Biology Sleep is generally considered to be a state of large-scale synchrony across thalamus and neocortex; however, recent work has challenged this idea by reporting isolated sleep rhythms such as slow oscillations and spindles. What is the spatial scale of sleep rhythms? To answer this question, we adapted deep learning algorithms initially developed for detecting earthquakes and gravitational waves in high-noise settings for analysis of neural recordings in sleep. We then studied sleep spindles in non-human primate electrocorticography (ECoG), human electroencephalogram (EEG), and clinical intracranial electroencephalogram (iEEG) recordings in the human. Within each recording type, we find widespread spindles occur much more frequently than previously reported. We then analyzed the spatiotemporal patterns of these large-scale, multi-area spindles and, in the EEG recordings, how spindle patterns change following a visual memory task. Our results reveal a potential role for widespread, multi-area spindles in consolidation of memories in networks widely distributed across primate cortex. eLife Sciences Publications, Ltd 2022-06-29 /pmc/articles/PMC9242645/ /pubmed/35766286 http://dx.doi.org/10.7554/eLife.75769 Text en © 2022, Mofrad 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 | Computational and Systems Biology Mofrad, Maryam H Gilmore, Greydon Koller, Dominik Mirsattari, Seyed M Burneo, Jorge G Steven, David A Khan, Ali R Suller Marti, Ana Muller, Lyle Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
title | Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
title_full | Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
title_fullStr | Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
title_full_unstemmed | Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
title_short | Waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
title_sort | waveform detection by deep learning reveals multi-area spindles that are selectively modulated by memory load |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242645/ https://www.ncbi.nlm.nih.gov/pubmed/35766286 http://dx.doi.org/10.7554/eLife.75769 |
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