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In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish

STXBP1 mutations are associated with encephalopathy, developmental delay, intellectual disability, and epilepsy. While neural networks are known to operate at a critical state in the healthy brain, network behavior during pathological epileptic states remains unclear. Examining activity during perio...

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Detalles Bibliográficos
Autores principales: Liu, Jing, Salvati, Kathryn A., Baraban, Scott C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184515/
https://www.ncbi.nlm.nih.gov/pubmed/34142057
http://dx.doi.org/10.1016/j.isci.2021.102558
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author Liu, Jing
Salvati, Kathryn A.
Baraban, Scott C.
author_facet Liu, Jing
Salvati, Kathryn A.
Baraban, Scott C.
author_sort Liu, Jing
collection PubMed
description STXBP1 mutations are associated with encephalopathy, developmental delay, intellectual disability, and epilepsy. While neural networks are known to operate at a critical state in the healthy brain, network behavior during pathological epileptic states remains unclear. Examining activity during periods between well-characterized ictal-like events (i.e., interictal period) could provide a valuable step toward understanding epileptic networks. To study these networks in the context of STXBP1 mutations, we combine a larval zebrafish model with in vivo fast confocal calcium imaging and extracellular local field potential recordings. Stxbp1b mutants display transient periods of elevated activity among local clusters of interacting neurons. These network “cascade” events were significantly larger in size and duration in mutants. At mesoscale resolution, cascades exhibit neurodevelopmental abnormalities. At single-cell scale, we describe spontaneous hyper-synchronized neuronal ensembles. That calcium imaging reveals uniquely disordered brain states during periods between pathological ictal-like seizure events is striking and represents a potential interictal biomarker.
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spelling pubmed-81845152021-06-16 In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish Liu, Jing Salvati, Kathryn A. Baraban, Scott C. iScience Article STXBP1 mutations are associated with encephalopathy, developmental delay, intellectual disability, and epilepsy. While neural networks are known to operate at a critical state in the healthy brain, network behavior during pathological epileptic states remains unclear. Examining activity during periods between well-characterized ictal-like events (i.e., interictal period) could provide a valuable step toward understanding epileptic networks. To study these networks in the context of STXBP1 mutations, we combine a larval zebrafish model with in vivo fast confocal calcium imaging and extracellular local field potential recordings. Stxbp1b mutants display transient periods of elevated activity among local clusters of interacting neurons. These network “cascade” events were significantly larger in size and duration in mutants. At mesoscale resolution, cascades exhibit neurodevelopmental abnormalities. At single-cell scale, we describe spontaneous hyper-synchronized neuronal ensembles. That calcium imaging reveals uniquely disordered brain states during periods between pathological ictal-like seizure events is striking and represents a potential interictal biomarker. Elsevier 2021-05-19 /pmc/articles/PMC8184515/ /pubmed/34142057 http://dx.doi.org/10.1016/j.isci.2021.102558 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Jing
Salvati, Kathryn A.
Baraban, Scott C.
In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
title In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
title_full In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
title_fullStr In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
title_full_unstemmed In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
title_short In vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
title_sort in vivo calcium imaging reveals disordered interictal network dynamics in epileptic stxbp1b zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184515/
https://www.ncbi.nlm.nih.gov/pubmed/34142057
http://dx.doi.org/10.1016/j.isci.2021.102558
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