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Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice

Modulation of brain activity is one of the main mechanisms capable of demonstrating the synchronization dynamics of neural oscillations. In epilepsy, modulation is a key concept since seizures essentially result from neural hypersynchronization and hyperexcitability. In this study, we have introduce...

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Autores principales: Pinheiro, Daniel J. L. L., Oliveira, Leandro F., Souza, Isis N. O., Brogin, João A. Ferres, Bueno, Douglas D., Miranda, Iranaia Assunção, Da Poian, Andrea T., Ferreira, Sergio T., Figueiredo, Claudia P., Clarke, Julia R., Cavalheiro, Esper A., Faber, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174408/
https://www.ncbi.nlm.nih.gov/pubmed/32317689
http://dx.doi.org/10.1038/s41598-020-63685-2
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author Pinheiro, Daniel J. L. L.
Oliveira, Leandro F.
Souza, Isis N. O.
Brogin, João A. Ferres
Bueno, Douglas D.
Miranda, Iranaia Assunção
Da Poian, Andrea T.
Ferreira, Sergio T.
Figueiredo, Claudia P.
Clarke, Julia R.
Cavalheiro, Esper A.
Faber, Jean
author_facet Pinheiro, Daniel J. L. L.
Oliveira, Leandro F.
Souza, Isis N. O.
Brogin, João A. Ferres
Bueno, Douglas D.
Miranda, Iranaia Assunção
Da Poian, Andrea T.
Ferreira, Sergio T.
Figueiredo, Claudia P.
Clarke, Julia R.
Cavalheiro, Esper A.
Faber, Jean
author_sort Pinheiro, Daniel J. L. L.
collection PubMed
description Modulation of brain activity is one of the main mechanisms capable of demonstrating the synchronization dynamics of neural oscillations. In epilepsy, modulation is a key concept since seizures essentially result from neural hypersynchronization and hyperexcitability. In this study, we have introduced a time-dependent index based on the Kullback-Leibler divergence to quantify the effects of phase and frequency modulations of neural oscillations in neonatal mice exhibiting epileptiform activity induced by Zika virus (ZIKV) infection. Through this index, we demonstrate that fast oscillations (gamma and beta 2) are the more susceptible modulated rhythms in terms of phase, during seizures, whereas slow waves (delta and theta) mainly undergo changes in frequency. The index also allowed detection of specific patterns associated with the interdependent modulation of phase and frequency in neural activity. Furthermore, by comparing ZIKV modulations with the general computational model Epileptors, we verify different signatures related to the brain rhythms modulation in phase and frequency. These findings instigate new studies on the effects of ZIKV infection on neuronal networks from electrophysiological activities, and how different mechanisms can trigger epilepsy.
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spelling pubmed-71744082020-04-24 Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice Pinheiro, Daniel J. L. L. Oliveira, Leandro F. Souza, Isis N. O. Brogin, João A. Ferres Bueno, Douglas D. Miranda, Iranaia Assunção Da Poian, Andrea T. Ferreira, Sergio T. Figueiredo, Claudia P. Clarke, Julia R. Cavalheiro, Esper A. Faber, Jean Sci Rep Article Modulation of brain activity is one of the main mechanisms capable of demonstrating the synchronization dynamics of neural oscillations. In epilepsy, modulation is a key concept since seizures essentially result from neural hypersynchronization and hyperexcitability. In this study, we have introduced a time-dependent index based on the Kullback-Leibler divergence to quantify the effects of phase and frequency modulations of neural oscillations in neonatal mice exhibiting epileptiform activity induced by Zika virus (ZIKV) infection. Through this index, we demonstrate that fast oscillations (gamma and beta 2) are the more susceptible modulated rhythms in terms of phase, during seizures, whereas slow waves (delta and theta) mainly undergo changes in frequency. The index also allowed detection of specific patterns associated with the interdependent modulation of phase and frequency in neural activity. Furthermore, by comparing ZIKV modulations with the general computational model Epileptors, we verify different signatures related to the brain rhythms modulation in phase and frequency. These findings instigate new studies on the effects of ZIKV infection on neuronal networks from electrophysiological activities, and how different mechanisms can trigger epilepsy. Nature Publishing Group UK 2020-04-21 /pmc/articles/PMC7174408/ /pubmed/32317689 http://dx.doi.org/10.1038/s41598-020-63685-2 Text en © The Author(s) 2020 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
Pinheiro, Daniel J. L. L.
Oliveira, Leandro F.
Souza, Isis N. O.
Brogin, João A. Ferres
Bueno, Douglas D.
Miranda, Iranaia Assunção
Da Poian, Andrea T.
Ferreira, Sergio T.
Figueiredo, Claudia P.
Clarke, Julia R.
Cavalheiro, Esper A.
Faber, Jean
Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice
title Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice
title_full Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice
title_fullStr Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice
title_full_unstemmed Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice
title_short Modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal Zika virus infection in mice
title_sort modulation in phase and frequency of neural oscillations during epileptiform activity induced by neonatal zika virus infection in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174408/
https://www.ncbi.nlm.nih.gov/pubmed/32317689
http://dx.doi.org/10.1038/s41598-020-63685-2
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