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Focal impaired awareness seizures in a rodent model: A functional anatomy

OBJECTIVE: Patients with temporal lobe epilepsy (TLE) frequently report debilitating comorbidities such as memory impairments, anxiety, and depression. An extensive neuronal network generates epileptic seizures and associated comorbidities, but a detailed description of this network is unavailable,...

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Detalles Bibliográficos
Autores principales: Adotevi, Nadia, Kapur, Jaideep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886100/
https://www.ncbi.nlm.nih.gov/pubmed/34822222
http://dx.doi.org/10.1002/epi4.12563
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author Adotevi, Nadia
Kapur, Jaideep
author_facet Adotevi, Nadia
Kapur, Jaideep
author_sort Adotevi, Nadia
collection PubMed
description OBJECTIVE: Patients with temporal lobe epilepsy (TLE) frequently report debilitating comorbidities such as memory impairments, anxiety, and depression. An extensive neuronal network generates epileptic seizures and associated comorbidities, but a detailed description of this network is unavailable, which requires the generation of neuronal activation maps in experimental animals. METHODS: We recorded electrographic seizures from the hippocampi during a kindling‐evoked focal impaired awareness seizure with observed freezing, facial twitching, and involuntary head bobbing. We mapped seizure circuits activated during these seizures by permanently tagging neurons through activity‐induced immediate early genes, combined with immunohistochemical approaches. RESULTS: There was bilateral activation of circuits necessary for memory consolidation, including the hippocampal complex, entorhinal cortex, cingulate gyrus, retrosplenial cortex, piriform cortex, and septohippocampal complex in kindled animals compared with unstimulated awake behaving mice. Neuronal circuits in the ventral hippocampus, amygdala, and anterior cingulate cortex, which regulate the stress response of hypothalamic‐pituitary‐adrenal axis, were also markedly activated during a focal impaired awareness seizure. SIGNIFICANCE: This study highlights neuronal circuits preferentially activated during a focal awareness impaired seizure in a rodent model. Many of the seizure‐activated neuronal circuits are critical modulators of memory consolidation and long‐term stress/depression response. The hijack of these memory and depression regulatory systems by a focal seizure could account for the frequent reports of comorbidities such as memory impairment and depression in many TLE patients.
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spelling pubmed-88861002022-03-04 Focal impaired awareness seizures in a rodent model: A functional anatomy Adotevi, Nadia Kapur, Jaideep Epilepsia Open Original Articles OBJECTIVE: Patients with temporal lobe epilepsy (TLE) frequently report debilitating comorbidities such as memory impairments, anxiety, and depression. An extensive neuronal network generates epileptic seizures and associated comorbidities, but a detailed description of this network is unavailable, which requires the generation of neuronal activation maps in experimental animals. METHODS: We recorded electrographic seizures from the hippocampi during a kindling‐evoked focal impaired awareness seizure with observed freezing, facial twitching, and involuntary head bobbing. We mapped seizure circuits activated during these seizures by permanently tagging neurons through activity‐induced immediate early genes, combined with immunohistochemical approaches. RESULTS: There was bilateral activation of circuits necessary for memory consolidation, including the hippocampal complex, entorhinal cortex, cingulate gyrus, retrosplenial cortex, piriform cortex, and septohippocampal complex in kindled animals compared with unstimulated awake behaving mice. Neuronal circuits in the ventral hippocampus, amygdala, and anterior cingulate cortex, which regulate the stress response of hypothalamic‐pituitary‐adrenal axis, were also markedly activated during a focal impaired awareness seizure. SIGNIFICANCE: This study highlights neuronal circuits preferentially activated during a focal awareness impaired seizure in a rodent model. Many of the seizure‐activated neuronal circuits are critical modulators of memory consolidation and long‐term stress/depression response. The hijack of these memory and depression regulatory systems by a focal seizure could account for the frequent reports of comorbidities such as memory impairment and depression in many TLE patients. John Wiley and Sons Inc. 2021-12-17 /pmc/articles/PMC8886100/ /pubmed/34822222 http://dx.doi.org/10.1002/epi4.12563 Text en © 2021 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Adotevi, Nadia
Kapur, Jaideep
Focal impaired awareness seizures in a rodent model: A functional anatomy
title Focal impaired awareness seizures in a rodent model: A functional anatomy
title_full Focal impaired awareness seizures in a rodent model: A functional anatomy
title_fullStr Focal impaired awareness seizures in a rodent model: A functional anatomy
title_full_unstemmed Focal impaired awareness seizures in a rodent model: A functional anatomy
title_short Focal impaired awareness seizures in a rodent model: A functional anatomy
title_sort focal impaired awareness seizures in a rodent model: a functional anatomy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886100/
https://www.ncbi.nlm.nih.gov/pubmed/34822222
http://dx.doi.org/10.1002/epi4.12563
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