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Neural mass modeling of slow-fast dynamics of seizure initiation and abortion

Epilepsy is a dynamic and complex neurological disease affecting about 1% of the worldwide population, among which 30% of the patients are drug-resistant. Epilepsy is characterized by recurrent episodes of paroxysmal neural discharges (the so-called seizures), which manifest themselves through a lar...

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Autores principales: Köksal Ersöz, Elif, Modolo, Julien, Bartolomei, Fabrice, Wendling, Fabrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676664/
https://www.ncbi.nlm.nih.gov/pubmed/33166277
http://dx.doi.org/10.1371/journal.pcbi.1008430
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author Köksal Ersöz, Elif
Modolo, Julien
Bartolomei, Fabrice
Wendling, Fabrice
author_facet Köksal Ersöz, Elif
Modolo, Julien
Bartolomei, Fabrice
Wendling, Fabrice
author_sort Köksal Ersöz, Elif
collection PubMed
description Epilepsy is a dynamic and complex neurological disease affecting about 1% of the worldwide population, among which 30% of the patients are drug-resistant. Epilepsy is characterized by recurrent episodes of paroxysmal neural discharges (the so-called seizures), which manifest themselves through a large-amplitude rhythmic activity observed in depth-EEG recordings, in particular in local field potentials (LFPs). The signature characterizing the transition to seizures involves complex oscillatory patterns, which could serve as a marker to prevent seizure initiation by triggering appropriate therapeutic neurostimulation methods. To investigate such protocols, neurophysiological lumped-parameter models at the mesoscopic scale, namely neural mass models, are powerful tools that not only mimic the LFP signals but also give insights on the neural mechanisms related to different stages of seizures. Here, we analyze the multiple time-scale dynamics of a neural mass model and explain the underlying structure of the complex oscillations observed before seizure initiation. We investigate population-specific effects of the stimulation and the dependence of stimulation parameters on synaptic timescales. In particular, we show that intermediate stimulation frequencies (>20 Hz) can abort seizures if the timescale difference is pronounced. Those results have the potential in the design of therapeutic brain stimulation protocols based on the neurophysiological properties of tissue.
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spelling pubmed-76766642020-12-02 Neural mass modeling of slow-fast dynamics of seizure initiation and abortion Köksal Ersöz, Elif Modolo, Julien Bartolomei, Fabrice Wendling, Fabrice PLoS Comput Biol Research Article Epilepsy is a dynamic and complex neurological disease affecting about 1% of the worldwide population, among which 30% of the patients are drug-resistant. Epilepsy is characterized by recurrent episodes of paroxysmal neural discharges (the so-called seizures), which manifest themselves through a large-amplitude rhythmic activity observed in depth-EEG recordings, in particular in local field potentials (LFPs). The signature characterizing the transition to seizures involves complex oscillatory patterns, which could serve as a marker to prevent seizure initiation by triggering appropriate therapeutic neurostimulation methods. To investigate such protocols, neurophysiological lumped-parameter models at the mesoscopic scale, namely neural mass models, are powerful tools that not only mimic the LFP signals but also give insights on the neural mechanisms related to different stages of seizures. Here, we analyze the multiple time-scale dynamics of a neural mass model and explain the underlying structure of the complex oscillations observed before seizure initiation. We investigate population-specific effects of the stimulation and the dependence of stimulation parameters on synaptic timescales. In particular, we show that intermediate stimulation frequencies (>20 Hz) can abort seizures if the timescale difference is pronounced. Those results have the potential in the design of therapeutic brain stimulation protocols based on the neurophysiological properties of tissue. Public Library of Science 2020-11-09 /pmc/articles/PMC7676664/ /pubmed/33166277 http://dx.doi.org/10.1371/journal.pcbi.1008430 Text en © 2020 Ersöz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Köksal Ersöz, Elif
Modolo, Julien
Bartolomei, Fabrice
Wendling, Fabrice
Neural mass modeling of slow-fast dynamics of seizure initiation and abortion
title Neural mass modeling of slow-fast dynamics of seizure initiation and abortion
title_full Neural mass modeling of slow-fast dynamics of seizure initiation and abortion
title_fullStr Neural mass modeling of slow-fast dynamics of seizure initiation and abortion
title_full_unstemmed Neural mass modeling of slow-fast dynamics of seizure initiation and abortion
title_short Neural mass modeling of slow-fast dynamics of seizure initiation and abortion
title_sort neural mass modeling of slow-fast dynamics of seizure initiation and abortion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676664/
https://www.ncbi.nlm.nih.gov/pubmed/33166277
http://dx.doi.org/10.1371/journal.pcbi.1008430
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