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In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation
Prolonged wakefulness leads to a homeostatic response manifested in increased amplitude and number of electroencephalogram (EEG) slow waves during recovery sleep. Cortical networks show a slow oscillation when the excitatory inputs are reduced (during slow wave sleep, anesthesia), or absent (in vitr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908861/ https://www.ncbi.nlm.nih.gov/pubmed/29674729 http://dx.doi.org/10.1038/s41598-018-24339-6 |
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author | Saberi-Moghadam, Sohrab Simi, Alessandro Setareh, Hesam Mikhail, Cyril Tafti, Mehdi |
author_facet | Saberi-Moghadam, Sohrab Simi, Alessandro Setareh, Hesam Mikhail, Cyril Tafti, Mehdi |
author_sort | Saberi-Moghadam, Sohrab |
collection | PubMed |
description | Prolonged wakefulness leads to a homeostatic response manifested in increased amplitude and number of electroencephalogram (EEG) slow waves during recovery sleep. Cortical networks show a slow oscillation when the excitatory inputs are reduced (during slow wave sleep, anesthesia), or absent (in vitro preparations). It was recently shown that a homeostatic response to electrical stimulation can be induced in cortical cultures. Here we used cortical cultures grown on microelectrode arrays and stimulated them with a cocktail of waking neuromodulators. We found that recovery from stimulation resulted in a dose-dependent homeostatic response. Specifically, the inter-burst intervals decreased, the burst duration increased, the network showed higher cross-correlation and strong phasic synchronized burst activity. Spectral power below <1.75 Hz significantly increased and the increase was related to steeper slopes of bursts. Computer simulation suggested that a small number of clustered neurons could potently drive the behavior of the network both at baseline and during recovery. Thus, this in vitro model appears valuable for dissecting network mechanisms of sleep homeostasis. |
format | Online Article Text |
id | pubmed-5908861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59088612018-04-30 In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation Saberi-Moghadam, Sohrab Simi, Alessandro Setareh, Hesam Mikhail, Cyril Tafti, Mehdi Sci Rep Article Prolonged wakefulness leads to a homeostatic response manifested in increased amplitude and number of electroencephalogram (EEG) slow waves during recovery sleep. Cortical networks show a slow oscillation when the excitatory inputs are reduced (during slow wave sleep, anesthesia), or absent (in vitro preparations). It was recently shown that a homeostatic response to electrical stimulation can be induced in cortical cultures. Here we used cortical cultures grown on microelectrode arrays and stimulated them with a cocktail of waking neuromodulators. We found that recovery from stimulation resulted in a dose-dependent homeostatic response. Specifically, the inter-burst intervals decreased, the burst duration increased, the network showed higher cross-correlation and strong phasic synchronized burst activity. Spectral power below <1.75 Hz significantly increased and the increase was related to steeper slopes of bursts. Computer simulation suggested that a small number of clustered neurons could potently drive the behavior of the network both at baseline and during recovery. Thus, this in vitro model appears valuable for dissecting network mechanisms of sleep homeostasis. Nature Publishing Group UK 2018-04-19 /pmc/articles/PMC5908861/ /pubmed/29674729 http://dx.doi.org/10.1038/s41598-018-24339-6 Text en © The Author(s) 2018 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 Saberi-Moghadam, Sohrab Simi, Alessandro Setareh, Hesam Mikhail, Cyril Tafti, Mehdi In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation |
title | In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation |
title_full | In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation |
title_fullStr | In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation |
title_full_unstemmed | In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation |
title_short | In vitro Cortical Network Firing is Homeostatically Regulated: A Model for Sleep Regulation |
title_sort | in vitro cortical network firing is homeostatically regulated: a model for sleep regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908861/ https://www.ncbi.nlm.nih.gov/pubmed/29674729 http://dx.doi.org/10.1038/s41598-018-24339-6 |
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