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Glia-neuron interactions underlie state transitions to generalized seizures

Brain activity and connectivity alter drastically during epileptic seizures. The brain networks shift from a balanced resting state to a hyperactive and hypersynchronous state. It is, however, less clear which mechanisms underlie the state transitions. By studying neural and glial activity in zebraf...

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Autores principales: Diaz Verdugo, Carmen, Myren-Svelstad, Sverre, Aydin, Ecem, Van Hoeymissen, Evelien, Deneubourg, Celine, Vanderhaeghe, Silke, Vancraeynest, Julie, Pelgrims, Robbrecht, Cosacak, Mehmet Ilyas, Muto, Akira, Kizil, Caghan, Kawakami, Koichi, Jurisch-Yaksi, Nathalie, Yaksi, Emre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707163/
https://www.ncbi.nlm.nih.gov/pubmed/31444362
http://dx.doi.org/10.1038/s41467-019-11739-z
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author Diaz Verdugo, Carmen
Myren-Svelstad, Sverre
Aydin, Ecem
Van Hoeymissen, Evelien
Deneubourg, Celine
Vanderhaeghe, Silke
Vancraeynest, Julie
Pelgrims, Robbrecht
Cosacak, Mehmet Ilyas
Muto, Akira
Kizil, Caghan
Kawakami, Koichi
Jurisch-Yaksi, Nathalie
Yaksi, Emre
author_facet Diaz Verdugo, Carmen
Myren-Svelstad, Sverre
Aydin, Ecem
Van Hoeymissen, Evelien
Deneubourg, Celine
Vanderhaeghe, Silke
Vancraeynest, Julie
Pelgrims, Robbrecht
Cosacak, Mehmet Ilyas
Muto, Akira
Kizil, Caghan
Kawakami, Koichi
Jurisch-Yaksi, Nathalie
Yaksi, Emre
author_sort Diaz Verdugo, Carmen
collection PubMed
description Brain activity and connectivity alter drastically during epileptic seizures. The brain networks shift from a balanced resting state to a hyperactive and hypersynchronous state. It is, however, less clear which mechanisms underlie the state transitions. By studying neural and glial activity in zebrafish models of epileptic seizures, we observe striking differences between these networks. During the preictal period, neurons display a small increase in synchronous activity only locally, while the gap-junction-coupled glial network was highly active and strongly synchronized across large distances. The transition from a preictal state to a generalized seizure leads to an abrupt increase in neural activity and connectivity, which is accompanied by a strong alteration in glia-neuron interactions and a massive increase in extracellular glutamate. Optogenetic activation of glia excites nearby neurons through the action of glutamate and gap junctions, emphasizing a potential role for glia-glia and glia-neuron connections in the generation of epileptic seizures.
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spelling pubmed-67071632019-08-26 Glia-neuron interactions underlie state transitions to generalized seizures Diaz Verdugo, Carmen Myren-Svelstad, Sverre Aydin, Ecem Van Hoeymissen, Evelien Deneubourg, Celine Vanderhaeghe, Silke Vancraeynest, Julie Pelgrims, Robbrecht Cosacak, Mehmet Ilyas Muto, Akira Kizil, Caghan Kawakami, Koichi Jurisch-Yaksi, Nathalie Yaksi, Emre Nat Commun Article Brain activity and connectivity alter drastically during epileptic seizures. The brain networks shift from a balanced resting state to a hyperactive and hypersynchronous state. It is, however, less clear which mechanisms underlie the state transitions. By studying neural and glial activity in zebrafish models of epileptic seizures, we observe striking differences between these networks. During the preictal period, neurons display a small increase in synchronous activity only locally, while the gap-junction-coupled glial network was highly active and strongly synchronized across large distances. The transition from a preictal state to a generalized seizure leads to an abrupt increase in neural activity and connectivity, which is accompanied by a strong alteration in glia-neuron interactions and a massive increase in extracellular glutamate. Optogenetic activation of glia excites nearby neurons through the action of glutamate and gap junctions, emphasizing a potential role for glia-glia and glia-neuron connections in the generation of epileptic seizures. Nature Publishing Group UK 2019-08-23 /pmc/articles/PMC6707163/ /pubmed/31444362 http://dx.doi.org/10.1038/s41467-019-11739-z Text en © The Author(s) 2019 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
Diaz Verdugo, Carmen
Myren-Svelstad, Sverre
Aydin, Ecem
Van Hoeymissen, Evelien
Deneubourg, Celine
Vanderhaeghe, Silke
Vancraeynest, Julie
Pelgrims, Robbrecht
Cosacak, Mehmet Ilyas
Muto, Akira
Kizil, Caghan
Kawakami, Koichi
Jurisch-Yaksi, Nathalie
Yaksi, Emre
Glia-neuron interactions underlie state transitions to generalized seizures
title Glia-neuron interactions underlie state transitions to generalized seizures
title_full Glia-neuron interactions underlie state transitions to generalized seizures
title_fullStr Glia-neuron interactions underlie state transitions to generalized seizures
title_full_unstemmed Glia-neuron interactions underlie state transitions to generalized seizures
title_short Glia-neuron interactions underlie state transitions to generalized seizures
title_sort glia-neuron interactions underlie state transitions to generalized seizures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707163/
https://www.ncbi.nlm.nih.gov/pubmed/31444362
http://dx.doi.org/10.1038/s41467-019-11739-z
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