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Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks
OBJECTIVE: The switch between nonseizure and seizure states involves profound alterations in network excitability and synchrony. In this study, we aimed to identify and compare features of neural excitability and dynamics across multiple zebrafish seizure and epilepsy models. METHODS: Inspired by vi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804334/ https://www.ncbi.nlm.nih.gov/pubmed/36222083 http://dx.doi.org/10.1111/epi.17380 |
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author | Myren‐Svelstad, Sverre Jamali, Ahmed Ophus, Sunniva S. D'gama, Percival P. Ostenrath, Anna M. Mutlu, Aytac Kadir Hoffshagen, Helene Homme Hotz, Adriana L. Neuhauss, Stephan C. F. Jurisch‐Yaksi, Nathalie Yaksi, Emre |
author_facet | Myren‐Svelstad, Sverre Jamali, Ahmed Ophus, Sunniva S. D'gama, Percival P. Ostenrath, Anna M. Mutlu, Aytac Kadir Hoffshagen, Helene Homme Hotz, Adriana L. Neuhauss, Stephan C. F. Jurisch‐Yaksi, Nathalie Yaksi, Emre |
author_sort | Myren‐Svelstad, Sverre |
collection | PubMed |
description | OBJECTIVE: The switch between nonseizure and seizure states involves profound alterations in network excitability and synchrony. In this study, we aimed to identify and compare features of neural excitability and dynamics across multiple zebrafish seizure and epilepsy models. METHODS: Inspired by video‐electroencephalographic recordings in patients, we developed a framework to study spontaneous and photically evoked neural and locomotor activity in zebrafish larvae, by combining high‐throughput behavioral tracking and whole‐brain in vivo two‐photon calcium imaging. RESULTS: Our setup allowed us to dissect behavioral and physiological features that are divergent or convergent across multiple models. We observed that spontaneous locomotor and neural activity exhibit great diversity across models. Nonetheless, during photic stimulation, hyperexcitability and rapid response dynamics were well conserved across multiple models, highlighting the reliability of photically evoked activity for high‐throughput assays. Intriguingly, in several models, we observed that the initial elevated photic response is often followed by rapid decay of neural activity and a prominent depressed state. Elevated photic response and following depressed state in seizure‐prone networks are significantly reduced by the antiseizure medication valproic acid. Finally, rapid decay and depression of neural activity following photic stimulation temporally overlap with slow recruitment of astroglial calcium signals that are enhanced in seizure‐prone networks. SIGNIFICANCE: We argue that fast decay of neural activity and depressed states following photic response are likely due to homeostatic mechanisms triggered by excessive neural activity. An improved understanding of the interplay between elevated and depressed excitability states might suggest tailored epilepsy therapies. |
format | Online Article Text |
id | pubmed-9804334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98043342023-01-03 Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks Myren‐Svelstad, Sverre Jamali, Ahmed Ophus, Sunniva S. D'gama, Percival P. Ostenrath, Anna M. Mutlu, Aytac Kadir Hoffshagen, Helene Homme Hotz, Adriana L. Neuhauss, Stephan C. F. Jurisch‐Yaksi, Nathalie Yaksi, Emre Epilepsia Research Article OBJECTIVE: The switch between nonseizure and seizure states involves profound alterations in network excitability and synchrony. In this study, we aimed to identify and compare features of neural excitability and dynamics across multiple zebrafish seizure and epilepsy models. METHODS: Inspired by video‐electroencephalographic recordings in patients, we developed a framework to study spontaneous and photically evoked neural and locomotor activity in zebrafish larvae, by combining high‐throughput behavioral tracking and whole‐brain in vivo two‐photon calcium imaging. RESULTS: Our setup allowed us to dissect behavioral and physiological features that are divergent or convergent across multiple models. We observed that spontaneous locomotor and neural activity exhibit great diversity across models. Nonetheless, during photic stimulation, hyperexcitability and rapid response dynamics were well conserved across multiple models, highlighting the reliability of photically evoked activity for high‐throughput assays. Intriguingly, in several models, we observed that the initial elevated photic response is often followed by rapid decay of neural activity and a prominent depressed state. Elevated photic response and following depressed state in seizure‐prone networks are significantly reduced by the antiseizure medication valproic acid. Finally, rapid decay and depression of neural activity following photic stimulation temporally overlap with slow recruitment of astroglial calcium signals that are enhanced in seizure‐prone networks. SIGNIFICANCE: We argue that fast decay of neural activity and depressed states following photic response are likely due to homeostatic mechanisms triggered by excessive neural activity. An improved understanding of the interplay between elevated and depressed excitability states might suggest tailored epilepsy therapies. John Wiley and Sons Inc. 2022-08-12 2022-10 /pmc/articles/PMC9804334/ /pubmed/36222083 http://dx.doi.org/10.1111/epi.17380 Text en © 2022 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Article Myren‐Svelstad, Sverre Jamali, Ahmed Ophus, Sunniva S. D'gama, Percival P. Ostenrath, Anna M. Mutlu, Aytac Kadir Hoffshagen, Helene Homme Hotz, Adriana L. Neuhauss, Stephan C. F. Jurisch‐Yaksi, Nathalie Yaksi, Emre Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
title | Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
title_full | Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
title_fullStr | Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
title_full_unstemmed | Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
title_short | Elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
title_sort | elevated photic response is followed by a rapid decay and depressed state in ictogenic networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804334/ https://www.ncbi.nlm.nih.gov/pubmed/36222083 http://dx.doi.org/10.1111/epi.17380 |
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