Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Saberi-Moghadam, Sohrab, Simi, Alessandro, Setareh, Hesam, Mikhail, Cyril, Tafti, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783315779495657472
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
work_keys_str_mv AT saberimoghadamsohrab invitrocorticalnetworkfiringishomeostaticallyregulatedamodelforsleepregulation
AT simialessandro invitrocorticalnetworkfiringishomeostaticallyregulatedamodelforsleepregulation
AT setarehhesam invitrocorticalnetworkfiringishomeostaticallyregulatedamodelforsleepregulation
AT mikhailcyril invitrocorticalnetworkfiringishomeostaticallyregulatedamodelforsleepregulation
AT taftimehdi invitrocorticalnetworkfiringishomeostaticallyregulatedamodelforsleepregulation