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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...

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Autores principales: Colombi, Ilaria, Tinarelli, Federico, Pasquale, Valentina, Tucci, Valter, Chiappalone, Michela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
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.
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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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