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Seizure development in the acute intrahippocampal epileptic focus

Currently, an epileptic seizure is considered to involve a temporary network that exists for a finite period of time. Formation of this network evolves through spread of epileptiform activity from a seizure onset zone (SOZ). Propagation of seizures evoked by kainic acid injection in hippocampus to d...

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Autores principales: Li, Lin, Kriukova, Kseniia, Engel, Jerome, Bragin, Anatol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780458/
https://www.ncbi.nlm.nih.gov/pubmed/29362494
http://dx.doi.org/10.1038/s41598-018-19675-6
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author Li, Lin
Kriukova, Kseniia
Engel, Jerome
Bragin, Anatol
author_facet Li, Lin
Kriukova, Kseniia
Engel, Jerome
Bragin, Anatol
author_sort Li, Lin
collection PubMed
description Currently, an epileptic seizure is considered to involve a temporary network that exists for a finite period of time. Formation of this network evolves through spread of epileptiform activity from a seizure onset zone (SOZ). Propagation of seizures evoked by kainic acid injection in hippocampus to different brain areas was analyzed at macro- and micro-intervals. The mean latency of seizure occurrence in different brain areas varied between 0.5 sec and 85 sec (mean 14.9 ± 14.5 (SD)), and it increased after each consecutive seizure in areas located contralateral to the area of injection, but not in the ipsilateral sites. We have shown that only 41% of epileptic individual events in target brain areas were driven by epileptic events generated in the SOZ once the seizure began. Fifty-nine percent of epileptiform events in target areas occurred one millisecond before or after events in the SOZ. These data illustrate that during seizure maintenance, only some individual epileptiform events in areas outside of SOZ could be consistently triggered by the SOZ; and the majority must be triggered by a driver located outside the SOZ or brain areas involved in ictal activity could be coupled to each other via an unknown mechanism such as stochastic resonance.
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spelling pubmed-57804582018-02-06 Seizure development in the acute intrahippocampal epileptic focus Li, Lin Kriukova, Kseniia Engel, Jerome Bragin, Anatol Sci Rep Article Currently, an epileptic seizure is considered to involve a temporary network that exists for a finite period of time. Formation of this network evolves through spread of epileptiform activity from a seizure onset zone (SOZ). Propagation of seizures evoked by kainic acid injection in hippocampus to different brain areas was analyzed at macro- and micro-intervals. The mean latency of seizure occurrence in different brain areas varied between 0.5 sec and 85 sec (mean 14.9 ± 14.5 (SD)), and it increased after each consecutive seizure in areas located contralateral to the area of injection, but not in the ipsilateral sites. We have shown that only 41% of epileptic individual events in target brain areas were driven by epileptic events generated in the SOZ once the seizure began. Fifty-nine percent of epileptiform events in target areas occurred one millisecond before or after events in the SOZ. These data illustrate that during seizure maintenance, only some individual epileptiform events in areas outside of SOZ could be consistently triggered by the SOZ; and the majority must be triggered by a driver located outside the SOZ or brain areas involved in ictal activity could be coupled to each other via an unknown mechanism such as stochastic resonance. Nature Publishing Group UK 2018-01-23 /pmc/articles/PMC5780458/ /pubmed/29362494 http://dx.doi.org/10.1038/s41598-018-19675-6 Text en © The Author(s) 2018 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
Li, Lin
Kriukova, Kseniia
Engel, Jerome
Bragin, Anatol
Seizure development in the acute intrahippocampal epileptic focus
title Seizure development in the acute intrahippocampal epileptic focus
title_full Seizure development in the acute intrahippocampal epileptic focus
title_fullStr Seizure development in the acute intrahippocampal epileptic focus
title_full_unstemmed Seizure development in the acute intrahippocampal epileptic focus
title_short Seizure development in the acute intrahippocampal epileptic focus
title_sort seizure development in the acute intrahippocampal epileptic focus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780458/
https://www.ncbi.nlm.nih.gov/pubmed/29362494
http://dx.doi.org/10.1038/s41598-018-19675-6
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