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Asynchronous suppression of visual cortex during absence seizures in stargazer mice

Absence epilepsy is a common childhood disorder featuring frequent cortical spike-wave seizures with a loss of awareness and behavior. Using the calcium indicator GCaMP6 with in vivo 2-photon cellular microscopy and simultaneous electrocorticography, we examined the collective activity profiles of i...

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Autores principales: Meyer, Jochen, Maheshwari, Atul, Noebels, Jeffrey, Smirnakis, Stelios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955878/
https://www.ncbi.nlm.nih.gov/pubmed/29769525
http://dx.doi.org/10.1038/s41467-018-04349-8
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author Meyer, Jochen
Maheshwari, Atul
Noebels, Jeffrey
Smirnakis, Stelios
author_facet Meyer, Jochen
Maheshwari, Atul
Noebels, Jeffrey
Smirnakis, Stelios
author_sort Meyer, Jochen
collection PubMed
description Absence epilepsy is a common childhood disorder featuring frequent cortical spike-wave seizures with a loss of awareness and behavior. Using the calcium indicator GCaMP6 with in vivo 2-photon cellular microscopy and simultaneous electrocorticography, we examined the collective activity profiles of individual neurons and surrounding neuropil across all layers in V1 during spike-wave seizure activity over prolonged periods in stargazer mice. We show that most (~80%) neurons in all cortical layers reduce their activity during seizures, whereas a smaller pool activates or remains neutral. Unexpectedly, ictal participation of identified single-unit activity is not fixed, but fluctuates on a flexible time scale from seizure to seizure. Pairwise correlation analysis of calcium activity reveals a surprising lack of synchrony among neurons and neuropil patches in all layers during seizures. Our results demonstrate asynchronous suppression of visual cortex during absence seizures, with potential implications for understanding cortical network function during EEG states of reduced awareness.
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spelling pubmed-59558782018-05-21 Asynchronous suppression of visual cortex during absence seizures in stargazer mice Meyer, Jochen Maheshwari, Atul Noebels, Jeffrey Smirnakis, Stelios Nat Commun Article Absence epilepsy is a common childhood disorder featuring frequent cortical spike-wave seizures with a loss of awareness and behavior. Using the calcium indicator GCaMP6 with in vivo 2-photon cellular microscopy and simultaneous electrocorticography, we examined the collective activity profiles of individual neurons and surrounding neuropil across all layers in V1 during spike-wave seizure activity over prolonged periods in stargazer mice. We show that most (~80%) neurons in all cortical layers reduce their activity during seizures, whereas a smaller pool activates or remains neutral. Unexpectedly, ictal participation of identified single-unit activity is not fixed, but fluctuates on a flexible time scale from seizure to seizure. Pairwise correlation analysis of calcium activity reveals a surprising lack of synchrony among neurons and neuropil patches in all layers during seizures. Our results demonstrate asynchronous suppression of visual cortex during absence seizures, with potential implications for understanding cortical network function during EEG states of reduced awareness. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955878/ /pubmed/29769525 http://dx.doi.org/10.1038/s41467-018-04349-8 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
Meyer, Jochen
Maheshwari, Atul
Noebels, Jeffrey
Smirnakis, Stelios
Asynchronous suppression of visual cortex during absence seizures in stargazer mice
title Asynchronous suppression of visual cortex during absence seizures in stargazer mice
title_full Asynchronous suppression of visual cortex during absence seizures in stargazer mice
title_fullStr Asynchronous suppression of visual cortex during absence seizures in stargazer mice
title_full_unstemmed Asynchronous suppression of visual cortex during absence seizures in stargazer mice
title_short Asynchronous suppression of visual cortex during absence seizures in stargazer mice
title_sort asynchronous suppression of visual cortex during absence seizures in stargazer mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955878/
https://www.ncbi.nlm.nih.gov/pubmed/29769525
http://dx.doi.org/10.1038/s41467-018-04349-8
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