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Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays

Hippocampal seizures are a defining feature of mesial temporal lobe epilepsy (MTLE). Area CA1 of the hippocampus is commonly implicated in the generation of seizures, which may occur because of the activity of endogenous cell populations or of inputs from other regions within the hippocampal formati...

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Autores principales: Mulcahey, Patrick J., Chen, Yuzhang, Driscoll, Nicolette, Murphy, Brendan B., Dickens, Olivia O., Johnson, A. T. Charlie, Vitale, Flavia, Takano, Hajime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087744/
https://www.ncbi.nlm.nih.gov/pubmed/35470227
http://dx.doi.org/10.1523/ENEURO.0386-21.2022
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author Mulcahey, Patrick J.
Chen, Yuzhang
Driscoll, Nicolette
Murphy, Brendan B.
Dickens, Olivia O.
Johnson, A. T. Charlie
Vitale, Flavia
Takano, Hajime
author_facet Mulcahey, Patrick J.
Chen, Yuzhang
Driscoll, Nicolette
Murphy, Brendan B.
Dickens, Olivia O.
Johnson, A. T. Charlie
Vitale, Flavia
Takano, Hajime
author_sort Mulcahey, Patrick J.
collection PubMed
description Hippocampal seizures are a defining feature of mesial temporal lobe epilepsy (MTLE). Area CA1 of the hippocampus is commonly implicated in the generation of seizures, which may occur because of the activity of endogenous cell populations or of inputs from other regions within the hippocampal formation. Simultaneously observing activity at the cellular and network scales in vivo remains challenging. Here, we present a novel technology for simultaneous electrophysiology and multicellular calcium imaging of CA1 pyramidal cells (PCs) in mice enabled by a transparent graphene-based microelectrode array (Gr MEA). We examine PC firing at seizure onset, oscillatory coupling, and the dynamics of the seizure traveling wave as seizures evolve. Finally, we couple features derived from both modalities to predict the speed of the traveling wave using bootstrap aggregated regression trees. Analysis of the most important features in the regression trees suggests a transition among states in the evolution of hippocampal seizures.
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spelling pubmed-90877442022-05-10 Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays Mulcahey, Patrick J. Chen, Yuzhang Driscoll, Nicolette Murphy, Brendan B. Dickens, Olivia O. Johnson, A. T. Charlie Vitale, Flavia Takano, Hajime eNeuro Research Article: New Research Hippocampal seizures are a defining feature of mesial temporal lobe epilepsy (MTLE). Area CA1 of the hippocampus is commonly implicated in the generation of seizures, which may occur because of the activity of endogenous cell populations or of inputs from other regions within the hippocampal formation. Simultaneously observing activity at the cellular and network scales in vivo remains challenging. Here, we present a novel technology for simultaneous electrophysiology and multicellular calcium imaging of CA1 pyramidal cells (PCs) in mice enabled by a transparent graphene-based microelectrode array (Gr MEA). We examine PC firing at seizure onset, oscillatory coupling, and the dynamics of the seizure traveling wave as seizures evolve. Finally, we couple features derived from both modalities to predict the speed of the traveling wave using bootstrap aggregated regression trees. Analysis of the most important features in the regression trees suggests a transition among states in the evolution of hippocampal seizures. Society for Neuroscience 2022-05-09 /pmc/articles/PMC9087744/ /pubmed/35470227 http://dx.doi.org/10.1523/ENEURO.0386-21.2022 Text en Copyright © 2022 Mulcahey et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Mulcahey, Patrick J.
Chen, Yuzhang
Driscoll, Nicolette
Murphy, Brendan B.
Dickens, Olivia O.
Johnson, A. T. Charlie
Vitale, Flavia
Takano, Hajime
Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays
title Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays
title_full Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays
title_fullStr Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays
title_full_unstemmed Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays
title_short Multimodal, Multiscale Insights into Hippocampal Seizures Enabled by Transparent, Graphene-Based Microelectrode Arrays
title_sort multimodal, multiscale insights into hippocampal seizures enabled by transparent, graphene-based microelectrode arrays
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087744/
https://www.ncbi.nlm.nih.gov/pubmed/35470227
http://dx.doi.org/10.1523/ENEURO.0386-21.2022
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