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Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures

Fast and slow neural waves have been observed to propagate in the human brain during seizures. Yet the nature of these waves is difficult to study in a surgical setting. Here, we report an observation of two different traveling waves propagating in the in-vitro epileptic hippocampus at speeds simila...

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Autores principales: Chiang, Chia-Chu, Wei, Xile, Ananthakrishnan, Arvind Keshav, Shivacharan, Rajat S., Gonzalez-Reyes, Luis E., Zhang, Mingming, Durand, Dominique M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784157/
https://www.ncbi.nlm.nih.gov/pubmed/29367722
http://dx.doi.org/10.1038/s41598-018-19925-7
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author Chiang, Chia-Chu
Wei, Xile
Ananthakrishnan, Arvind Keshav
Shivacharan, Rajat S.
Gonzalez-Reyes, Luis E.
Zhang, Mingming
Durand, Dominique M.
author_facet Chiang, Chia-Chu
Wei, Xile
Ananthakrishnan, Arvind Keshav
Shivacharan, Rajat S.
Gonzalez-Reyes, Luis E.
Zhang, Mingming
Durand, Dominique M.
author_sort Chiang, Chia-Chu
collection PubMed
description Fast and slow neural waves have been observed to propagate in the human brain during seizures. Yet the nature of these waves is difficult to study in a surgical setting. Here, we report an observation of two different traveling waves propagating in the in-vitro epileptic hippocampus at speeds similar to those in the human brain. A fast traveling spike and a slow moving wave were recorded simultaneously with a genetically encoded voltage sensitive fluorescent protein (VSFP Butterfly 1.2) and a high speed camera. The results of this study indicate that the fast traveling spike is NMDA-sensitive but the slow moving wave is not. Image analysis and model simulation demonstrate that the slow moving wave is moving slowly, generating the fast traveling spike and is, therefore, a moving source of the epileptiform activity. This slow moving wave is associated with a propagating neural calcium wave detected with calcium dye (OGB-1) but is independent of NMDA receptors, not related to ATP release, and much faster than those previously recorded potassium waves. Computer modeling suggests that the slow moving wave can propagate by the ephaptic effect like epileptiform activity. These findings provide an alternative explanation for slow propagation seizure wavefronts associated with fast propagating spikes.
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spelling pubmed-57841572018-02-07 Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures Chiang, Chia-Chu Wei, Xile Ananthakrishnan, Arvind Keshav Shivacharan, Rajat S. Gonzalez-Reyes, Luis E. Zhang, Mingming Durand, Dominique M. Sci Rep Article Fast and slow neural waves have been observed to propagate in the human brain during seizures. Yet the nature of these waves is difficult to study in a surgical setting. Here, we report an observation of two different traveling waves propagating in the in-vitro epileptic hippocampus at speeds similar to those in the human brain. A fast traveling spike and a slow moving wave were recorded simultaneously with a genetically encoded voltage sensitive fluorescent protein (VSFP Butterfly 1.2) and a high speed camera. The results of this study indicate that the fast traveling spike is NMDA-sensitive but the slow moving wave is not. Image analysis and model simulation demonstrate that the slow moving wave is moving slowly, generating the fast traveling spike and is, therefore, a moving source of the epileptiform activity. This slow moving wave is associated with a propagating neural calcium wave detected with calcium dye (OGB-1) but is independent of NMDA receptors, not related to ATP release, and much faster than those previously recorded potassium waves. Computer modeling suggests that the slow moving wave can propagate by the ephaptic effect like epileptiform activity. These findings provide an alternative explanation for slow propagation seizure wavefronts associated with fast propagating spikes. Nature Publishing Group UK 2018-01-24 /pmc/articles/PMC5784157/ /pubmed/29367722 http://dx.doi.org/10.1038/s41598-018-19925-7 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
Chiang, Chia-Chu
Wei, Xile
Ananthakrishnan, Arvind Keshav
Shivacharan, Rajat S.
Gonzalez-Reyes, Luis E.
Zhang, Mingming
Durand, Dominique M.
Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
title Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
title_full Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
title_fullStr Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
title_full_unstemmed Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
title_short Slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
title_sort slow moving neural source in the epileptic hippocampus can mimic progression of human seizures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784157/
https://www.ncbi.nlm.nih.gov/pubmed/29367722
http://dx.doi.org/10.1038/s41598-018-19925-7
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