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Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders

Scale-free analysis of brain activity reveals a complexity of synchronous neuronal firing which is different from that assessed using classic rhythmic quantifications such as spectral analysis of the electroencephalogram (EEG). In humans, scale-free activity of the EEG depends on the behavioral stat...

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Autores principales: Lina, Jean-Marc, O’Callaghan, Emma Kate, Mongrain, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509677/
https://www.ncbi.nlm.nih.gov/pubmed/33089154
http://dx.doi.org/10.3390/clockssleep1010006
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author Lina, Jean-Marc
O’Callaghan, Emma Kate
Mongrain, Valérie
author_facet Lina, Jean-Marc
O’Callaghan, Emma Kate
Mongrain, Valérie
author_sort Lina, Jean-Marc
collection PubMed
description Scale-free analysis of brain activity reveals a complexity of synchronous neuronal firing which is different from that assessed using classic rhythmic quantifications such as spectral analysis of the electroencephalogram (EEG). In humans, scale-free activity of the EEG depends on the behavioral state and reflects cognitive processes. We aimed to verify if fractal patterns of the mouse EEG also show variations with behavioral states and topography, and to identify molecular determinants of brain scale-free activity using the ‘multifractal formalism’ (Wavelet-Leaders). We found that scale-free activity was more anti-persistent (i.e., more different between time scales) during wakefulness, less anti-persistent (i.e., less different between time scales) during non-rapid eye movement sleep, and generally intermediate during rapid eye movement sleep. The scale-invariance of the frontal/motor cerebral cortex was generally more anti-persistent than that of the posterior cortex, and scale-invariance during wakefulness was strongly modulated by time of day and the absence of the synaptic protein Neuroligin-1. Our results expose that the complexity of the scale-free pattern of organized neuronal firing depends on behavioral state in mice, and that patterns expressed during wakefulness are modulated by one synaptic component.
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spelling pubmed-75096772020-10-20 Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders Lina, Jean-Marc O’Callaghan, Emma Kate Mongrain, Valérie Clocks Sleep Article Scale-free analysis of brain activity reveals a complexity of synchronous neuronal firing which is different from that assessed using classic rhythmic quantifications such as spectral analysis of the electroencephalogram (EEG). In humans, scale-free activity of the EEG depends on the behavioral state and reflects cognitive processes. We aimed to verify if fractal patterns of the mouse EEG also show variations with behavioral states and topography, and to identify molecular determinants of brain scale-free activity using the ‘multifractal formalism’ (Wavelet-Leaders). We found that scale-free activity was more anti-persistent (i.e., more different between time scales) during wakefulness, less anti-persistent (i.e., less different between time scales) during non-rapid eye movement sleep, and generally intermediate during rapid eye movement sleep. The scale-invariance of the frontal/motor cerebral cortex was generally more anti-persistent than that of the posterior cortex, and scale-invariance during wakefulness was strongly modulated by time of day and the absence of the synaptic protein Neuroligin-1. Our results expose that the complexity of the scale-free pattern of organized neuronal firing depends on behavioral state in mice, and that patterns expressed during wakefulness are modulated by one synaptic component. MDPI 2018-10-20 /pmc/articles/PMC7509677/ /pubmed/33089154 http://dx.doi.org/10.3390/clockssleep1010006 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lina, Jean-Marc
O’Callaghan, Emma Kate
Mongrain, Valérie
Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders
title Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders
title_full Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders
title_fullStr Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders
title_full_unstemmed Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders
title_short Scale-Free Dynamics of the Mouse Wakefulness and Sleep Electroencephalogram Quantified Using Wavelet-Leaders
title_sort scale-free dynamics of the mouse wakefulness and sleep electroencephalogram quantified using wavelet-leaders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509677/
https://www.ncbi.nlm.nih.gov/pubmed/33089154
http://dx.doi.org/10.3390/clockssleep1010006
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