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A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep
In this paper, we show that neuronal assemblies plated on Micro Electrode Arrays present synchronized, low frequency firing patterns similar to in vivo slow wave oscillations, which are a key parameter of sleep-like state. Although neuronal cultures lack the characteristic high-frequency waves of wa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935686/ https://www.ncbi.nlm.nih.gov/pubmed/27458335 http://dx.doi.org/10.3389/fnins.2016.00315 |
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author | Colombi, Ilaria Tinarelli, Federico Pasquale, Valentina Tucci, Valter Chiappalone, Michela |
author_facet | Colombi, Ilaria Tinarelli, Federico Pasquale, Valentina Tucci, Valter Chiappalone, Michela |
author_sort | Colombi, Ilaria |
collection | PubMed |
description | In this paper, we show that neuronal assemblies plated on Micro Electrode Arrays present synchronized, low frequency firing patterns similar to in vivo slow wave oscillations, which are a key parameter of sleep-like state. Although neuronal cultures lack the characteristic high-frequency waves of wakefulness, it is possible to modulate their spontaneous firing pattern through the administration of specific neurotransmitters such as acetylcholine. We thus stimulated the cortical cultures with an agonist of acetylcholine receptor, Carbachol, which caused a desynchronization of the spontaneous firing of the cultures. We recorded and monitored the cultures for a period of over 31 h. We analyzed the electrophysiological signals by exploiting novel methodological approaches, taking into account the different temporal scales of the recorded signals, and considering both spikes and local field potentials. Supporting the electrophysiological analysis results, gene expressions of targeted genes showed the activation of specific markers involved in sleep-wake rhythms. Our results demonstrate that the Carbachol treatment induces desynchronization of neuronal activity, altering sleep-like properties in an in vitro model. |
format | Online Article Text |
id | pubmed-4935686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49356862016-07-25 A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep Colombi, Ilaria Tinarelli, Federico Pasquale, Valentina Tucci, Valter Chiappalone, Michela Front Neurosci Neuroscience In this paper, we show that neuronal assemblies plated on Micro Electrode Arrays present synchronized, low frequency firing patterns similar to in vivo slow wave oscillations, which are a key parameter of sleep-like state. Although neuronal cultures lack the characteristic high-frequency waves of wakefulness, it is possible to modulate their spontaneous firing pattern through the administration of specific neurotransmitters such as acetylcholine. We thus stimulated the cortical cultures with an agonist of acetylcholine receptor, Carbachol, which caused a desynchronization of the spontaneous firing of the cultures. We recorded and monitored the cultures for a period of over 31 h. We analyzed the electrophysiological signals by exploiting novel methodological approaches, taking into account the different temporal scales of the recorded signals, and considering both spikes and local field potentials. Supporting the electrophysiological analysis results, gene expressions of targeted genes showed the activation of specific markers involved in sleep-wake rhythms. Our results demonstrate that the Carbachol treatment induces desynchronization of neuronal activity, altering sleep-like properties in an in vitro model. Frontiers Media S.A. 2016-07-07 /pmc/articles/PMC4935686/ /pubmed/27458335 http://dx.doi.org/10.3389/fnins.2016.00315 Text en Copyright © 2016 Colombi, Tinarelli, Pasquale, Tucci and Chiappalone. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Colombi, Ilaria Tinarelli, Federico Pasquale, Valentina Tucci, Valter Chiappalone, Michela A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep |
title | A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep |
title_full | A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep |
title_fullStr | A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep |
title_full_unstemmed | A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep |
title_short | A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep |
title_sort | simplified in vitro experimental model encompasses the essential features of sleep |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935686/ https://www.ncbi.nlm.nih.gov/pubmed/27458335 http://dx.doi.org/10.3389/fnins.2016.00315 |
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