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The role of the entorhinal cortex in epileptiform activities of the hippocampus
BACKGROUND: Temporal lobe epilepsy (TLE) is the commonest type of epilepsy in adults, and the hippocampus is indicated to have a close relationship with TLE. Recent researches also indicate that the entorhinal cortex (EC) is involved in epilepsy. To explore the essential role that the EC may play in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994397/ https://www.ncbi.nlm.nih.gov/pubmed/24656055 http://dx.doi.org/10.1186/1742-4682-11-14 |
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author | Ren, Hui Shi, Ye-Jun Lu, Qin-Chi Liang, Pei-Ji Zhang, Pu-Ming |
author_facet | Ren, Hui Shi, Ye-Jun Lu, Qin-Chi Liang, Pei-Ji Zhang, Pu-Ming |
author_sort | Ren, Hui |
collection | PubMed |
description | BACKGROUND: Temporal lobe epilepsy (TLE) is the commonest type of epilepsy in adults, and the hippocampus is indicated to have a close relationship with TLE. Recent researches also indicate that the entorhinal cortex (EC) is involved in epilepsy. To explore the essential role that the EC may play in epilepsy, a computational model of the hippocampal CA3 region was built, which consisted of pyramidal cells and two types of interneurons. By changing the input signals from the EC, the effects of EC on epileptiform activities of the hippocampus were investigated. Additionally, recent studies have found that the antiepileptic drug valproate (VPA) can block ictal discharges but cannot block interictal discharges in vitro, and the mechanism under this phenomenon is still confusing. In our model, the effects of VPA on epileptiform activities were simulated and some mechanisms were explored. RESULTS: Interictal discharges were induced in the model without the input signals from the EC, whereas the model with the EC input produced ictal discharges when the EC input contained ictal discharges. The GABA-ergic connection strength was enhanced and the NMDA-ergic connection strength was reduced to simulate the effects of VPA, and the simulation results showed that the disappearance of ictal discharges in the model mainly due to the disappearance of ictal discharges in the input signals from the EC. CONCLUSIONS: Simulation results showed that ictal discharges in the EC were necessary for the hippocampus to generate ictal discharges, and VPA might block the ictal discharges in the EC, which led to the disappearance of ictal discharges in the hippocampus. |
format | Online Article Text |
id | pubmed-3994397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39943972014-05-06 The role of the entorhinal cortex in epileptiform activities of the hippocampus Ren, Hui Shi, Ye-Jun Lu, Qin-Chi Liang, Pei-Ji Zhang, Pu-Ming Theor Biol Med Model Research BACKGROUND: Temporal lobe epilepsy (TLE) is the commonest type of epilepsy in adults, and the hippocampus is indicated to have a close relationship with TLE. Recent researches also indicate that the entorhinal cortex (EC) is involved in epilepsy. To explore the essential role that the EC may play in epilepsy, a computational model of the hippocampal CA3 region was built, which consisted of pyramidal cells and two types of interneurons. By changing the input signals from the EC, the effects of EC on epileptiform activities of the hippocampus were investigated. Additionally, recent studies have found that the antiepileptic drug valproate (VPA) can block ictal discharges but cannot block interictal discharges in vitro, and the mechanism under this phenomenon is still confusing. In our model, the effects of VPA on epileptiform activities were simulated and some mechanisms were explored. RESULTS: Interictal discharges were induced in the model without the input signals from the EC, whereas the model with the EC input produced ictal discharges when the EC input contained ictal discharges. The GABA-ergic connection strength was enhanced and the NMDA-ergic connection strength was reduced to simulate the effects of VPA, and the simulation results showed that the disappearance of ictal discharges in the model mainly due to the disappearance of ictal discharges in the input signals from the EC. CONCLUSIONS: Simulation results showed that ictal discharges in the EC were necessary for the hippocampus to generate ictal discharges, and VPA might block the ictal discharges in the EC, which led to the disappearance of ictal discharges in the hippocampus. BioMed Central 2014-03-24 /pmc/articles/PMC3994397/ /pubmed/24656055 http://dx.doi.org/10.1186/1742-4682-11-14 Text en Copyright © 2014 Ren et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ren, Hui Shi, Ye-Jun Lu, Qin-Chi Liang, Pei-Ji Zhang, Pu-Ming The role of the entorhinal cortex in epileptiform activities of the hippocampus |
title | The role of the entorhinal cortex in epileptiform activities of the hippocampus |
title_full | The role of the entorhinal cortex in epileptiform activities of the hippocampus |
title_fullStr | The role of the entorhinal cortex in epileptiform activities of the hippocampus |
title_full_unstemmed | The role of the entorhinal cortex in epileptiform activities of the hippocampus |
title_short | The role of the entorhinal cortex in epileptiform activities of the hippocampus |
title_sort | role of the entorhinal cortex in epileptiform activities of the hippocampus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994397/ https://www.ncbi.nlm.nih.gov/pubmed/24656055 http://dx.doi.org/10.1186/1742-4682-11-14 |
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