Cargando…
Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123
High-gamma (HG; 80-150 Hz) activity in macroscopic clinical records is considered a marker for critical brain regions involved in seizure initiation; it is correlated with pathological multiunit firing during neocortical seizures in the seizure core, an area identified by correlated multiunit spikin...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876490/ https://www.ncbi.nlm.nih.gov/pubmed/27257623 http://dx.doi.org/10.1523/ENEURO.0141-15.2016 |
_version_ | 1782433249185759232 |
---|---|
author | Eissa, Tahra L. Tryba, Andrew K. Marcuccilli, Charles J. Ben-Mabrouk, Faiza Smith, Elliot H. Lew, Sean M. Goodman, Robert R. McKhann, Guy M. Frim, David M. Pesce, Lorenzo L. Kohrman, Michael H. Emerson, Ronald G. Schevon, Catherine A. van Drongelen, Wim |
author_facet | Eissa, Tahra L. Tryba, Andrew K. Marcuccilli, Charles J. Ben-Mabrouk, Faiza Smith, Elliot H. Lew, Sean M. Goodman, Robert R. McKhann, Guy M. Frim, David M. Pesce, Lorenzo L. Kohrman, Michael H. Emerson, Ronald G. Schevon, Catherine A. van Drongelen, Wim |
author_sort | Eissa, Tahra L. |
collection | PubMed |
description | High-gamma (HG; 80-150 Hz) activity in macroscopic clinical records is considered a marker for critical brain regions involved in seizure initiation; it is correlated with pathological multiunit firing during neocortical seizures in the seizure core, an area identified by correlated multiunit spiking and low frequency seizure activity. However, the effects of the spatiotemporal dynamics of seizure on HG power generation are not well understood. Here, we studied HG generation and propagation, using a three-step, multiscale signal analysis and modeling approach. First, we analyzed concurrent neuronal and microscopic network HG activity in neocortical slices from seven intractable epilepsy patients. We found HG activity in these networks, especially when neurons displayed paroxysmal depolarization shifts and network activity was highly synchronized. Second, we examined HG activity acquired with microelectrode arrays recorded during human seizures (n = 8). We confirmed the presence of synchronized HG power across microelectrode records and the macroscale, both specifically associated with the core region of the seizure. Third, we used volume conduction-based modeling to relate HG activity and network synchrony at different network scales. We showed that local HG oscillations require high levels of synchrony to cross scales, and that this requirement is met at the microscopic scale, but not within macroscopic networks. Instead, we present evidence that HG power at the macroscale may result from harmonics of ongoing seizure activity. Ictal HG power marks the seizure core, but the generating mechanism can differ across spatial scales. |
format | Online Article Text |
id | pubmed-4876490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-48764902016-06-02 Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 Eissa, Tahra L. Tryba, Andrew K. Marcuccilli, Charles J. Ben-Mabrouk, Faiza Smith, Elliot H. Lew, Sean M. Goodman, Robert R. McKhann, Guy M. Frim, David M. Pesce, Lorenzo L. Kohrman, Michael H. Emerson, Ronald G. Schevon, Catherine A. van Drongelen, Wim eNeuro New Research High-gamma (HG; 80-150 Hz) activity in macroscopic clinical records is considered a marker for critical brain regions involved in seizure initiation; it is correlated with pathological multiunit firing during neocortical seizures in the seizure core, an area identified by correlated multiunit spiking and low frequency seizure activity. However, the effects of the spatiotemporal dynamics of seizure on HG power generation are not well understood. Here, we studied HG generation and propagation, using a three-step, multiscale signal analysis and modeling approach. First, we analyzed concurrent neuronal and microscopic network HG activity in neocortical slices from seven intractable epilepsy patients. We found HG activity in these networks, especially when neurons displayed paroxysmal depolarization shifts and network activity was highly synchronized. Second, we examined HG activity acquired with microelectrode arrays recorded during human seizures (n = 8). We confirmed the presence of synchronized HG power across microelectrode records and the macroscale, both specifically associated with the core region of the seizure. Third, we used volume conduction-based modeling to relate HG activity and network synchrony at different network scales. We showed that local HG oscillations require high levels of synchrony to cross scales, and that this requirement is met at the microscopic scale, but not within macroscopic networks. Instead, we present evidence that HG power at the macroscale may result from harmonics of ongoing seizure activity. Ictal HG power marks the seizure core, but the generating mechanism can differ across spatial scales. Society for Neuroscience 2016-05-23 /pmc/articles/PMC4876490/ /pubmed/27257623 http://dx.doi.org/10.1523/ENEURO.0141-15.2016 Text en Copyright © 2016 Eissa et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://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 | New Research Eissa, Tahra L. Tryba, Andrew K. Marcuccilli, Charles J. Ben-Mabrouk, Faiza Smith, Elliot H. Lew, Sean M. Goodman, Robert R. McKhann, Guy M. Frim, David M. Pesce, Lorenzo L. Kohrman, Michael H. Emerson, Ronald G. Schevon, Catherine A. van Drongelen, Wim Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 |
title | Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 |
title_full | Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 |
title_fullStr | Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 |
title_full_unstemmed | Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 |
title_short | Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex123 |
title_sort | multiscale aspects of generation of high-gamma activity during seizures in human neocortex123 |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876490/ https://www.ncbi.nlm.nih.gov/pubmed/27257623 http://dx.doi.org/10.1523/ENEURO.0141-15.2016 |
work_keys_str_mv | AT eissatahral multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT trybaandrewk multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT marcuccillicharlesj multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT benmabroukfaiza multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT smithellioth multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT lewseanm multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT goodmanrobertr multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT mckhannguym multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT frimdavidm multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT pescelorenzol multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT kohrmanmichaelh multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT emersonronaldg multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT schevoncatherinea multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 AT vandrongelenwim multiscaleaspectsofgenerationofhighgammaactivityduringseizuresinhumanneocortex123 |