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A probabilistic model for the ultradian timing of REM sleep in mice
A salient feature of mammalian sleep is the alternation between rapid eye movement (REM) and non-REM (NREM) sleep. However, how these two sleep stages influence each other and thereby regulate the timing of REM sleep episodes is still largely unresolved. Here, we developed a statistical model that s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423363/ https://www.ncbi.nlm.nih.gov/pubmed/34432801 http://dx.doi.org/10.1371/journal.pcbi.1009316 |
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author | Park, Sung-Ho Baik, Justin Hong, Jiso Antila, Hanna Kurland, Benjamin Chung, Shinjae Weber, Franz |
author_facet | Park, Sung-Ho Baik, Justin Hong, Jiso Antila, Hanna Kurland, Benjamin Chung, Shinjae Weber, Franz |
author_sort | Park, Sung-Ho |
collection | PubMed |
description | A salient feature of mammalian sleep is the alternation between rapid eye movement (REM) and non-REM (NREM) sleep. However, how these two sleep stages influence each other and thereby regulate the timing of REM sleep episodes is still largely unresolved. Here, we developed a statistical model that specifies the relationship between REM and subsequent NREM sleep to quantify how REM sleep affects the following NREM sleep duration and its electrophysiological features in mice. We show that a lognormal mixture model well describes how the preceding REM sleep duration influences the amount of NREM sleep till the next REM sleep episode. The model supports the existence of two different types of sleep cycles: Short cycles form closely interspaced sequences of REM sleep episodes, whereas during long cycles, REM sleep is first followed by an interval of NREM sleep during which transitions to REM sleep are extremely unlikely. This refractory period is characterized by low power in the theta and sigma range of the electroencephalogram (EEG), low spindle rate and frequent microarousals, and its duration proportionally increases with the preceding REM sleep duration. Using our model, we estimated the propensity for REM sleep at the transition from NREM to REM sleep and found that entering REM sleep with higher propensity resulted in longer REM sleep episodes with reduced EEG power. Compared with the light phase, the buildup of REM sleep propensity was slower during the dark phase. Our data-driven modeling approach uncovered basic principles underlying the timing and duration of REM sleep episodes in mice and provides a flexible framework to describe the ultradian regulation of REM sleep in health and disease. |
format | Online Article Text |
id | pubmed-8423363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84233632021-09-08 A probabilistic model for the ultradian timing of REM sleep in mice Park, Sung-Ho Baik, Justin Hong, Jiso Antila, Hanna Kurland, Benjamin Chung, Shinjae Weber, Franz PLoS Comput Biol Research Article A salient feature of mammalian sleep is the alternation between rapid eye movement (REM) and non-REM (NREM) sleep. However, how these two sleep stages influence each other and thereby regulate the timing of REM sleep episodes is still largely unresolved. Here, we developed a statistical model that specifies the relationship between REM and subsequent NREM sleep to quantify how REM sleep affects the following NREM sleep duration and its electrophysiological features in mice. We show that a lognormal mixture model well describes how the preceding REM sleep duration influences the amount of NREM sleep till the next REM sleep episode. The model supports the existence of two different types of sleep cycles: Short cycles form closely interspaced sequences of REM sleep episodes, whereas during long cycles, REM sleep is first followed by an interval of NREM sleep during which transitions to REM sleep are extremely unlikely. This refractory period is characterized by low power in the theta and sigma range of the electroencephalogram (EEG), low spindle rate and frequent microarousals, and its duration proportionally increases with the preceding REM sleep duration. Using our model, we estimated the propensity for REM sleep at the transition from NREM to REM sleep and found that entering REM sleep with higher propensity resulted in longer REM sleep episodes with reduced EEG power. Compared with the light phase, the buildup of REM sleep propensity was slower during the dark phase. Our data-driven modeling approach uncovered basic principles underlying the timing and duration of REM sleep episodes in mice and provides a flexible framework to describe the ultradian regulation of REM sleep in health and disease. Public Library of Science 2021-08-25 /pmc/articles/PMC8423363/ /pubmed/34432801 http://dx.doi.org/10.1371/journal.pcbi.1009316 Text en © 2021 Park et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Park, Sung-Ho Baik, Justin Hong, Jiso Antila, Hanna Kurland, Benjamin Chung, Shinjae Weber, Franz A probabilistic model for the ultradian timing of REM sleep in mice |
title | A probabilistic model for the ultradian timing of REM sleep in mice |
title_full | A probabilistic model for the ultradian timing of REM sleep in mice |
title_fullStr | A probabilistic model for the ultradian timing of REM sleep in mice |
title_full_unstemmed | A probabilistic model for the ultradian timing of REM sleep in mice |
title_short | A probabilistic model for the ultradian timing of REM sleep in mice |
title_sort | probabilistic model for the ultradian timing of rem sleep in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423363/ https://www.ncbi.nlm.nih.gov/pubmed/34432801 http://dx.doi.org/10.1371/journal.pcbi.1009316 |
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