Cargando…
Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy
Large-scale brain networks are increasingly recognized as important for the generation of seizures in epilepsy. However, how a network evolves from a healthy state through the process of epileptogenesis remains unclear. To address this question, here, we study longitudinal epicranial background EEG...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709215/ https://www.ncbi.nlm.nih.gov/pubmed/31346002 http://dx.doi.org/10.1523/ENEURO.0059-19.2019 |
_version_ | 1783446158514847744 |
---|---|
author | Słowiński, Piotr Sheybani, Laurent Michel, Christoph M. Richardson, Mark P. Quairiaux, Charles Terry, John R. Goodfellow, Marc |
author_facet | Słowiński, Piotr Sheybani, Laurent Michel, Christoph M. Richardson, Mark P. Quairiaux, Charles Terry, John R. Goodfellow, Marc |
author_sort | Słowiński, Piotr |
collection | PubMed |
description | Large-scale brain networks are increasingly recognized as important for the generation of seizures in epilepsy. However, how a network evolves from a healthy state through the process of epileptogenesis remains unclear. To address this question, here, we study longitudinal epicranial background EEG recordings (30 electrodes, EEG free from epileptiform activity) of a mouse model of mesial temporal lobe epilepsy. We analyze functional connectivity networks and observe that over the time course of epileptogenesis the networks become increasingly asymmetric. Furthermore, computational modelling reveals that a set of nodes, located outside of the region of initial insult, emerges as particularly important for the network dynamics. These findings are consistent with experimental observations, thus demonstrating that ictogenic mechanisms can be revealed on the EEG, that computational models can be used to monitor unfolding epileptogenesis and that both the primary focus and epileptic network play a role in epileptogenesis. |
format | Online Article Text |
id | pubmed-6709215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-67092152019-08-26 Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy Słowiński, Piotr Sheybani, Laurent Michel, Christoph M. Richardson, Mark P. Quairiaux, Charles Terry, John R. Goodfellow, Marc eNeuro New Research Large-scale brain networks are increasingly recognized as important for the generation of seizures in epilepsy. However, how a network evolves from a healthy state through the process of epileptogenesis remains unclear. To address this question, here, we study longitudinal epicranial background EEG recordings (30 electrodes, EEG free from epileptiform activity) of a mouse model of mesial temporal lobe epilepsy. We analyze functional connectivity networks and observe that over the time course of epileptogenesis the networks become increasingly asymmetric. Furthermore, computational modelling reveals that a set of nodes, located outside of the region of initial insult, emerges as particularly important for the network dynamics. These findings are consistent with experimental observations, thus demonstrating that ictogenic mechanisms can be revealed on the EEG, that computational models can be used to monitor unfolding epileptogenesis and that both the primary focus and epileptic network play a role in epileptogenesis. Society for Neuroscience 2019-08-12 /pmc/articles/PMC6709215/ /pubmed/31346002 http://dx.doi.org/10.1523/ENEURO.0059-19.2019 Text en Copyright © 2019 Słowiński et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Słowiński, Piotr Sheybani, Laurent Michel, Christoph M. Richardson, Mark P. Quairiaux, Charles Terry, John R. Goodfellow, Marc Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy |
title | Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy |
title_full | Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy |
title_fullStr | Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy |
title_full_unstemmed | Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy |
title_short | Background EEG Connectivity Captures the Time-Course of Epileptogenesis in a Mouse Model of Epilepsy |
title_sort | background eeg connectivity captures the time-course of epileptogenesis in a mouse model of epilepsy |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709215/ https://www.ncbi.nlm.nih.gov/pubmed/31346002 http://dx.doi.org/10.1523/ENEURO.0059-19.2019 |
work_keys_str_mv | AT słowinskipiotr backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy AT sheybanilaurent backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy AT michelchristophm backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy AT richardsonmarkp backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy AT quairiauxcharles backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy AT terryjohnr backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy AT goodfellowmarc backgroundeegconnectivitycapturesthetimecourseofepileptogenesisinamousemodelofepilepsy |