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Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice
Epilepsy is characterized by spontaneous non-provoked seizures, yet the mechanisms that trigger a seizure and allow its evolution remain underexplored. To dissect out phases of ictogenesis, we evoked hypersynchronous activity with optogenetic stimulation. Focal optogenetic activation of putative exc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522592/ https://www.ncbi.nlm.nih.gov/pubmed/37752179 http://dx.doi.org/10.1038/s41467-023-41711-x |
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author | Mueller, John-Sebastian Tescarollo, Fabio C. Huynh, Trong Brenner, Daniel A. Valdivia, Daniel J. Olagbegi, Kanyin Sangappa, Sahana Chen, Spencer C. Sun, Hai |
author_facet | Mueller, John-Sebastian Tescarollo, Fabio C. Huynh, Trong Brenner, Daniel A. Valdivia, Daniel J. Olagbegi, Kanyin Sangappa, Sahana Chen, Spencer C. Sun, Hai |
author_sort | Mueller, John-Sebastian |
collection | PubMed |
description | Epilepsy is characterized by spontaneous non-provoked seizures, yet the mechanisms that trigger a seizure and allow its evolution remain underexplored. To dissect out phases of ictogenesis, we evoked hypersynchronous activity with optogenetic stimulation. Focal optogenetic activation of putative excitatory neurons in the mouse hippocampal CA1 reliably evoked convulsive seizures in awake mice. A time-vs-time pulsogram plot characterized the evolution of the EEG pulse response from a light evoked response to induced seizure activity. Our results depict ictogenesis as a stepwise process comprised of three distinctive phases demarcated by two transition points. The induction phase undergoes the first transition to reverberant phase activity, followed by the second transition into the paroxysmal phase or a seizure. Non-seizure responses are confined to either induction or reverberant phases. The pulsogram was then constructed in seizures recorded from a murine model of temporal lobe epilepsy and it depicted a similar reverberance preceding spontaneous seizures. The discovery of these distinct phases of ictogenesis may offer means to abort a seizure before it develops. |
format | Online Article Text |
id | pubmed-10522592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105225922023-09-28 Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice Mueller, John-Sebastian Tescarollo, Fabio C. Huynh, Trong Brenner, Daniel A. Valdivia, Daniel J. Olagbegi, Kanyin Sangappa, Sahana Chen, Spencer C. Sun, Hai Nat Commun Article Epilepsy is characterized by spontaneous non-provoked seizures, yet the mechanisms that trigger a seizure and allow its evolution remain underexplored. To dissect out phases of ictogenesis, we evoked hypersynchronous activity with optogenetic stimulation. Focal optogenetic activation of putative excitatory neurons in the mouse hippocampal CA1 reliably evoked convulsive seizures in awake mice. A time-vs-time pulsogram plot characterized the evolution of the EEG pulse response from a light evoked response to induced seizure activity. Our results depict ictogenesis as a stepwise process comprised of three distinctive phases demarcated by two transition points. The induction phase undergoes the first transition to reverberant phase activity, followed by the second transition into the paroxysmal phase or a seizure. Non-seizure responses are confined to either induction or reverberant phases. The pulsogram was then constructed in seizures recorded from a murine model of temporal lobe epilepsy and it depicted a similar reverberance preceding spontaneous seizures. The discovery of these distinct phases of ictogenesis may offer means to abort a seizure before it develops. Nature Publishing Group UK 2023-09-26 /pmc/articles/PMC10522592/ /pubmed/37752179 http://dx.doi.org/10.1038/s41467-023-41711-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mueller, John-Sebastian Tescarollo, Fabio C. Huynh, Trong Brenner, Daniel A. Valdivia, Daniel J. Olagbegi, Kanyin Sangappa, Sahana Chen, Spencer C. Sun, Hai Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice |
title | Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice |
title_full | Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice |
title_fullStr | Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice |
title_full_unstemmed | Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice |
title_short | Ictogenesis proceeds through discrete phases in hippocampal CA1 seizures in mice |
title_sort | ictogenesis proceeds through discrete phases in hippocampal ca1 seizures in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522592/ https://www.ncbi.nlm.nih.gov/pubmed/37752179 http://dx.doi.org/10.1038/s41467-023-41711-x |
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