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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,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8886100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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