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Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling
Growing studies indicate that vigilance states and circadian rhythms can influence seizure occurrence in patients with epilepsy and rodent models of epilepsy. Electrical kindling, referred to brief, repeated stimulations of a limbic structure, is a commonly used model of temporal lobe epilepsy. Kind...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816810/ https://www.ncbi.nlm.nih.gov/pubmed/36620863 http://dx.doi.org/10.3389/fnbeh.2022.1076718 |
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author | Zahra, Anya Sun, Yuqing Aloysius, Nancy Zhang, Liang |
author_facet | Zahra, Anya Sun, Yuqing Aloysius, Nancy Zhang, Liang |
author_sort | Zahra, Anya |
collection | PubMed |
description | Growing studies indicate that vigilance states and circadian rhythms can influence seizure occurrence in patients with epilepsy and rodent models of epilepsy. Electrical kindling, referred to brief, repeated stimulations of a limbic structure, is a commonly used model of temporal lobe epilepsy. Kindling via the classic protocol lasting a few weeks does not generally induce spontaneous recurrent seizures (SRS), but extended kindling that applies over the course of a few months has shown to induce SRS in several animal species. Kindling-induced SRS in monkeys and cats were observed mainly during resting wakefulness or sleep, but the behavioral activities associated with SRS in rodent models of extended kindling remain unknown. We aimed to add information in this area using a mouse model of extended hippocampal kindling. Middle-aged C57 black mice experienced ≥80 hippocampal stimulations (delivered twice daily) and then underwent continuous 24 h electroencephalography (EEG)-video monitoring for SRS detection. SRS were recognized by EEG discharges and associated motor seizures. The five stages of the modified Racine scale for mice were used to score motor seizure severities. Seizure-preceding behaviors were assessed in a 3 min period prior to seizure onset and categorized as active and inactive. Three main observations emerged from the present analysis. (1) SRS were found to predominantly manifest as generalized (stage 3–5) motor seizures in association with tail erection or Straub tail. (2) SRS occurrences were not significantly altered by the light on/off cycle. (3) Generalized (stage 3–5) motor seizures were mainly preceded by inactive behaviors such as immobility, standing still, or apparent sleep without evident volitional movement. Considering deeper subcortical structures implicated in genesis of tail erection in other seizure models, we postulate that genesis of generalized motor seizures in extended kindled mice may involve deeper subcortical structures. Our present data together with previous findings from post-status epilepticus models support the notion that ambient cage behaviors are strong influencing factors of SRS occurrence in rodent models of temporal lobe epilepsy. |
format | Online Article Text |
id | pubmed-9816810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98168102023-01-07 Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling Zahra, Anya Sun, Yuqing Aloysius, Nancy Zhang, Liang Front Behav Neurosci Neuroscience Growing studies indicate that vigilance states and circadian rhythms can influence seizure occurrence in patients with epilepsy and rodent models of epilepsy. Electrical kindling, referred to brief, repeated stimulations of a limbic structure, is a commonly used model of temporal lobe epilepsy. Kindling via the classic protocol lasting a few weeks does not generally induce spontaneous recurrent seizures (SRS), but extended kindling that applies over the course of a few months has shown to induce SRS in several animal species. Kindling-induced SRS in monkeys and cats were observed mainly during resting wakefulness or sleep, but the behavioral activities associated with SRS in rodent models of extended kindling remain unknown. We aimed to add information in this area using a mouse model of extended hippocampal kindling. Middle-aged C57 black mice experienced ≥80 hippocampal stimulations (delivered twice daily) and then underwent continuous 24 h electroencephalography (EEG)-video monitoring for SRS detection. SRS were recognized by EEG discharges and associated motor seizures. The five stages of the modified Racine scale for mice were used to score motor seizure severities. Seizure-preceding behaviors were assessed in a 3 min period prior to seizure onset and categorized as active and inactive. Three main observations emerged from the present analysis. (1) SRS were found to predominantly manifest as generalized (stage 3–5) motor seizures in association with tail erection or Straub tail. (2) SRS occurrences were not significantly altered by the light on/off cycle. (3) Generalized (stage 3–5) motor seizures were mainly preceded by inactive behaviors such as immobility, standing still, or apparent sleep without evident volitional movement. Considering deeper subcortical structures implicated in genesis of tail erection in other seizure models, we postulate that genesis of generalized motor seizures in extended kindled mice may involve deeper subcortical structures. Our present data together with previous findings from post-status epilepticus models support the notion that ambient cage behaviors are strong influencing factors of SRS occurrence in rodent models of temporal lobe epilepsy. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9816810/ /pubmed/36620863 http://dx.doi.org/10.3389/fnbeh.2022.1076718 Text en Copyright © 2022 Zahra, Sun, Aloysius and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Zahra, Anya Sun, Yuqing Aloysius, Nancy Zhang, Liang Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
title | Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
title_full | Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
title_fullStr | Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
title_full_unstemmed | Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
title_short | Convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
title_sort | convulsive behaviors of spontaneous recurrent seizures in a mouse model of extended hippocampal kindling |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816810/ https://www.ncbi.nlm.nih.gov/pubmed/36620863 http://dx.doi.org/10.3389/fnbeh.2022.1076718 |
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