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Involvement of fast-spiking cells in ictal sequences during spontaneous seizures in rats with chronic temporal lobe epilepsy
See Lenck-Santini (doi:10.1093/awx205) for a scientific commentary on this article. Epileptic seizures represent altered neuronal network dynamics, but the temporal evolution and cellular substrates of the neuronal activity patterns associated with spontaneous seizures are not fully understood. We...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248724/ https://www.ncbi.nlm.nih.gov/pubmed/29050390 http://dx.doi.org/10.1093/brain/awx179 |
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author | Neumann, Adam R Raedt, Robrecht Steenland, Hendrik W Sprengers, Mathieu Bzymek, Katarzyna Navratilova, Zaneta Mesina, Lilia Xie, Jeanne Lapointe, Valerie Kloosterman, Fabian Vonck, Kristl Boon, Paul A J M Soltesz, Ivan McNaughton, Bruce L Luczak, Artur |
author_facet | Neumann, Adam R Raedt, Robrecht Steenland, Hendrik W Sprengers, Mathieu Bzymek, Katarzyna Navratilova, Zaneta Mesina, Lilia Xie, Jeanne Lapointe, Valerie Kloosterman, Fabian Vonck, Kristl Boon, Paul A J M Soltesz, Ivan McNaughton, Bruce L Luczak, Artur |
author_sort | Neumann, Adam R |
collection | PubMed |
description | See Lenck-Santini (doi:10.1093/awx205) for a scientific commentary on this article. Epileptic seizures represent altered neuronal network dynamics, but the temporal evolution and cellular substrates of the neuronal activity patterns associated with spontaneous seizures are not fully understood. We used simultaneous recordings from multiple neurons in the hippocampus and neocortex of rats with chronic temporal lobe epilepsy to demonstrate that subsets of cells discharge in a highly stereotypical sequential pattern during ictal events, and that these stereotypical patterns were reproducible across consecutive seizures. In contrast to the canonical view that principal cell discharges dominate ictal events, the ictal sequences were predominantly composed of fast-spiking, putative inhibitory neurons, which displayed unusually strong coupling to local field potential even before seizures. The temporal evolution of activity was characterized by unique dynamics where the most correlated neuronal pairs before seizure onset displayed the largest increases in correlation strength during the seizures. These results demonstrate the selective involvement of fast spiking interneurons in structured temporal sequences during spontaneous ictal events in hippocampal and neocortical circuits in experimental models of chronic temporal lobe epilepsy. |
format | Online Article Text |
id | pubmed-6248724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62487242018-11-28 Involvement of fast-spiking cells in ictal sequences during spontaneous seizures in rats with chronic temporal lobe epilepsy Neumann, Adam R Raedt, Robrecht Steenland, Hendrik W Sprengers, Mathieu Bzymek, Katarzyna Navratilova, Zaneta Mesina, Lilia Xie, Jeanne Lapointe, Valerie Kloosterman, Fabian Vonck, Kristl Boon, Paul A J M Soltesz, Ivan McNaughton, Bruce L Luczak, Artur Brain Original Articles See Lenck-Santini (doi:10.1093/awx205) for a scientific commentary on this article. Epileptic seizures represent altered neuronal network dynamics, but the temporal evolution and cellular substrates of the neuronal activity patterns associated with spontaneous seizures are not fully understood. We used simultaneous recordings from multiple neurons in the hippocampus and neocortex of rats with chronic temporal lobe epilepsy to demonstrate that subsets of cells discharge in a highly stereotypical sequential pattern during ictal events, and that these stereotypical patterns were reproducible across consecutive seizures. In contrast to the canonical view that principal cell discharges dominate ictal events, the ictal sequences were predominantly composed of fast-spiking, putative inhibitory neurons, which displayed unusually strong coupling to local field potential even before seizures. The temporal evolution of activity was characterized by unique dynamics where the most correlated neuronal pairs before seizure onset displayed the largest increases in correlation strength during the seizures. These results demonstrate the selective involvement of fast spiking interneurons in structured temporal sequences during spontaneous ictal events in hippocampal and neocortical circuits in experimental models of chronic temporal lobe epilepsy. Oxford University Press 2017-09 2017-08-04 /pmc/articles/PMC6248724/ /pubmed/29050390 http://dx.doi.org/10.1093/brain/awx179 Text en © The Author (2017). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles Neumann, Adam R Raedt, Robrecht Steenland, Hendrik W Sprengers, Mathieu Bzymek, Katarzyna Navratilova, Zaneta Mesina, Lilia Xie, Jeanne Lapointe, Valerie Kloosterman, Fabian Vonck, Kristl Boon, Paul A J M Soltesz, Ivan McNaughton, Bruce L Luczak, Artur Involvement of fast-spiking cells in ictal sequences during spontaneous seizures in rats with chronic temporal lobe epilepsy |
title | Involvement of fast-spiking cells in ictal sequences during spontaneous
seizures in rats with chronic temporal lobe epilepsy |
title_full | Involvement of fast-spiking cells in ictal sequences during spontaneous
seizures in rats with chronic temporal lobe epilepsy |
title_fullStr | Involvement of fast-spiking cells in ictal sequences during spontaneous
seizures in rats with chronic temporal lobe epilepsy |
title_full_unstemmed | Involvement of fast-spiking cells in ictal sequences during spontaneous
seizures in rats with chronic temporal lobe epilepsy |
title_short | Involvement of fast-spiking cells in ictal sequences during spontaneous
seizures in rats with chronic temporal lobe epilepsy |
title_sort | involvement of fast-spiking cells in ictal sequences during spontaneous
seizures in rats with chronic temporal lobe epilepsy |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248724/ https://www.ncbi.nlm.nih.gov/pubmed/29050390 http://dx.doi.org/10.1093/brain/awx179 |
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