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Spike ripples in striatum correlate with seizure risk in two mouse models
Epilepsy biomarkers from electroencephalogram recordings are routinely used to assess seizure risk and localization. Two widely adopted biomarkers include: (i) interictal spikes, and (ii) high frequency ripple oscillations. The combination of these two biomarkers, ripples co-occurring with spikes (s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902602/ https://www.ncbi.nlm.nih.gov/pubmed/35274094 http://dx.doi.org/10.1016/j.ebr.2022.100529 |
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author | Shi, Wen Zemel, Dana Sridhar, Sudiksha Mount, Rebecca A. Richardson, R. Mark Eden, Uri T. Han, Xue Kramer, Mark A. Chu, Catherine J. |
author_facet | Shi, Wen Zemel, Dana Sridhar, Sudiksha Mount, Rebecca A. Richardson, R. Mark Eden, Uri T. Han, Xue Kramer, Mark A. Chu, Catherine J. |
author_sort | Shi, Wen |
collection | PubMed |
description | Epilepsy biomarkers from electroencephalogram recordings are routinely used to assess seizure risk and localization. Two widely adopted biomarkers include: (i) interictal spikes, and (ii) high frequency ripple oscillations. The combination of these two biomarkers, ripples co-occurring with spikes (spike ripples), has been proposed as an improved biomarker for the epileptogenic zone and epileptogenicity in humans and rodent models. Whether spike ripples translate to predict seizure risk in rodent seizure models is unknown. Further, recent evidence suggests ictal networks can include deep gray nuclei in humans. Whether pathologic spike ripples and seizures are also observed in the basal ganglia in rodent models has not been explored. We addressed these questions using local field potential recordings from mice with and without striatal seizures after carbachol or 6-hydroxydopamine infusions into the striatum. We found increased spike ripples in the interictal and ictal periods in mice with seizures compared to pre-infusion and post-infusion seizure-free recordings. These data provide evidence of electrographic seizures involving the striatum in mice and support the candidacy of spike ripples as a translational biomarker for seizure risk in mouse models. |
format | Online Article Text |
id | pubmed-8902602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-89026022022-03-09 Spike ripples in striatum correlate with seizure risk in two mouse models Shi, Wen Zemel, Dana Sridhar, Sudiksha Mount, Rebecca A. Richardson, R. Mark Eden, Uri T. Han, Xue Kramer, Mark A. Chu, Catherine J. Epilepsy Behav Rep Article Epilepsy biomarkers from electroencephalogram recordings are routinely used to assess seizure risk and localization. Two widely adopted biomarkers include: (i) interictal spikes, and (ii) high frequency ripple oscillations. The combination of these two biomarkers, ripples co-occurring with spikes (spike ripples), has been proposed as an improved biomarker for the epileptogenic zone and epileptogenicity in humans and rodent models. Whether spike ripples translate to predict seizure risk in rodent seizure models is unknown. Further, recent evidence suggests ictal networks can include deep gray nuclei in humans. Whether pathologic spike ripples and seizures are also observed in the basal ganglia in rodent models has not been explored. We addressed these questions using local field potential recordings from mice with and without striatal seizures after carbachol or 6-hydroxydopamine infusions into the striatum. We found increased spike ripples in the interictal and ictal periods in mice with seizures compared to pre-infusion and post-infusion seizure-free recordings. These data provide evidence of electrographic seizures involving the striatum in mice and support the candidacy of spike ripples as a translational biomarker for seizure risk in mouse models. Elsevier 2022-02-08 /pmc/articles/PMC8902602/ /pubmed/35274094 http://dx.doi.org/10.1016/j.ebr.2022.100529 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Shi, Wen Zemel, Dana Sridhar, Sudiksha Mount, Rebecca A. Richardson, R. Mark Eden, Uri T. Han, Xue Kramer, Mark A. Chu, Catherine J. Spike ripples in striatum correlate with seizure risk in two mouse models |
title | Spike ripples in striatum correlate with seizure risk in two mouse models |
title_full | Spike ripples in striatum correlate with seizure risk in two mouse models |
title_fullStr | Spike ripples in striatum correlate with seizure risk in two mouse models |
title_full_unstemmed | Spike ripples in striatum correlate with seizure risk in two mouse models |
title_short | Spike ripples in striatum correlate with seizure risk in two mouse models |
title_sort | spike ripples in striatum correlate with seizure risk in two mouse models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902602/ https://www.ncbi.nlm.nih.gov/pubmed/35274094 http://dx.doi.org/10.1016/j.ebr.2022.100529 |
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