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Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity

Cell culture models are important tools to study epileptogenesis mechanisms. The aim of this work was to characterize the spontaneous and synchronized rhythmic activity developed by cultured hippocampal neurons after transient incubation in zero Mg(2+) to model Status Epilepticus. Cultured hippocamp...

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Autores principales: Mele, Miranda, Vieira, Ricardo, Correia, Bárbara, De Luca, Pasqualino, Duarte, Filipe V., Pinheiro, Paulo S., Duarte, Carlos B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167095/
https://www.ncbi.nlm.nih.gov/pubmed/34059735
http://dx.doi.org/10.1038/s41598-021-90486-y
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author Mele, Miranda
Vieira, Ricardo
Correia, Bárbara
De Luca, Pasqualino
Duarte, Filipe V.
Pinheiro, Paulo S.
Duarte, Carlos B.
author_facet Mele, Miranda
Vieira, Ricardo
Correia, Bárbara
De Luca, Pasqualino
Duarte, Filipe V.
Pinheiro, Paulo S.
Duarte, Carlos B.
author_sort Mele, Miranda
collection PubMed
description Cell culture models are important tools to study epileptogenesis mechanisms. The aim of this work was to characterize the spontaneous and synchronized rhythmic activity developed by cultured hippocampal neurons after transient incubation in zero Mg(2+) to model Status Epilepticus. Cultured hippocampal neurons were transiently incubated with a Mg(2+)-free solution and the activity of neuronal networks was evaluated using single cell calcium imaging and whole-cell current clamp recordings. Here we report the development of synchronized and spontaneous [Ca(2+)](i) transients in cultured hippocampal neurons immediately after transient incubation in a Mg(2+)-free solution. Spontaneous and synchronous [Ca(2+)](i) oscillations were observed when the cells were then incubated in the presence of Mg(2+). Functional studies also showed that transient incubation in Mg(2+)-free medium induces neuronal rhythmic burst activity that was prevented by antagonists of glutamate receptors. In conclusion, we report the development of epileptiform-like activity, characterized by spontaneous and synchronized discharges, in cultured hippocampal neurons transiently incubated in the absence of Mg(2+). This model will allow studying synaptic alterations contributing to the hyperexcitability that underlies the development of seizures and will be useful in pharmacological studies for testing new drugs for the treatment of epilepsy.
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spelling pubmed-81670952021-06-02 Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity Mele, Miranda Vieira, Ricardo Correia, Bárbara De Luca, Pasqualino Duarte, Filipe V. Pinheiro, Paulo S. Duarte, Carlos B. Sci Rep Article Cell culture models are important tools to study epileptogenesis mechanisms. The aim of this work was to characterize the spontaneous and synchronized rhythmic activity developed by cultured hippocampal neurons after transient incubation in zero Mg(2+) to model Status Epilepticus. Cultured hippocampal neurons were transiently incubated with a Mg(2+)-free solution and the activity of neuronal networks was evaluated using single cell calcium imaging and whole-cell current clamp recordings. Here we report the development of synchronized and spontaneous [Ca(2+)](i) transients in cultured hippocampal neurons immediately after transient incubation in a Mg(2+)-free solution. Spontaneous and synchronous [Ca(2+)](i) oscillations were observed when the cells were then incubated in the presence of Mg(2+). Functional studies also showed that transient incubation in Mg(2+)-free medium induces neuronal rhythmic burst activity that was prevented by antagonists of glutamate receptors. In conclusion, we report the development of epileptiform-like activity, characterized by spontaneous and synchronized discharges, in cultured hippocampal neurons transiently incubated in the absence of Mg(2+). This model will allow studying synaptic alterations contributing to the hyperexcitability that underlies the development of seizures and will be useful in pharmacological studies for testing new drugs for the treatment of epilepsy. Nature Publishing Group UK 2021-05-31 /pmc/articles/PMC8167095/ /pubmed/34059735 http://dx.doi.org/10.1038/s41598-021-90486-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mele, Miranda
Vieira, Ricardo
Correia, Bárbara
De Luca, Pasqualino
Duarte, Filipe V.
Pinheiro, Paulo S.
Duarte, Carlos B.
Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
title Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
title_full Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
title_fullStr Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
title_full_unstemmed Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
title_short Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
title_sort transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167095/
https://www.ncbi.nlm.nih.gov/pubmed/34059735
http://dx.doi.org/10.1038/s41598-021-90486-y
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