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

Abstract 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 Mg2+ to model Status Epilepticus. Cultured hi...

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Autores principales: Miranda Mele, Ricardo Vieira, Bárbara Correia, Pasqualino De Luca, Filipe V. Duarte, Paulo S. Pinheiro, Carlos B. Duarte
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3e6dc83da6f64a38871222111d585ee4
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spelling oai:doaj.org-article:3e6dc83da6f64a38871222111d585ee42021-12-02T18:25:02ZTransient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity10.1038/s41598-021-90486-y2045-2322https://doaj.org/article/3e6dc83da6f64a38871222111d585ee42021-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-90486-yhttps://doaj.org/toc/2045-2322Abstract 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 Mg2+ to model Status Epilepticus. Cultured hippocampal neurons were transiently incubated with a Mg2+-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 [Ca2+]i transients in cultured hippocampal neurons immediately after transient incubation in a Mg2+-free solution. Spontaneous and synchronous [Ca2+]i oscillations were observed when the cells were then incubated in the presence of Mg2+. Functional studies also showed that transient incubation in Mg2+-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 Mg2+. 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.Miranda MeleRicardo VieiraBárbara CorreiaPasqualino De LucaFilipe V. DuartePaulo S. PinheiroCarlos B. DuarteNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Miranda Mele
Ricardo Vieira
Bárbara Correia
Pasqualino De Luca
Filipe V. Duarte
Paulo S. Pinheiro
Carlos B. Duarte
Transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
description Abstract 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 Mg2+ to model Status Epilepticus. Cultured hippocampal neurons were transiently incubated with a Mg2+-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 [Ca2+]i transients in cultured hippocampal neurons immediately after transient incubation in a Mg2+-free solution. Spontaneous and synchronous [Ca2+]i oscillations were observed when the cells were then incubated in the presence of Mg2+. Functional studies also showed that transient incubation in Mg2+-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 Mg2+. 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.
format article
author Miranda Mele
Ricardo Vieira
Bárbara Correia
Pasqualino De Luca
Filipe V. Duarte
Paulo S. Pinheiro
Carlos B. Duarte
author_facet Miranda Mele
Ricardo Vieira
Bárbara Correia
Pasqualino De Luca
Filipe V. Duarte
Paulo S. Pinheiro
Carlos B. Duarte
author_sort Miranda Mele
title 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_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_sort transient incubation of cultured hippocampal neurons in the absence of magnesium induces rhythmic and synchronized epileptiform-like activity
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3e6dc83da6f64a38871222111d585ee4
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AT ricardovieira transientincubationofculturedhippocampalneuronsintheabsenceofmagnesiuminducesrhythmicandsynchronizedepileptiformlikeactivity
AT barbaracorreia transientincubationofculturedhippocampalneuronsintheabsenceofmagnesiuminducesrhythmicandsynchronizedepileptiformlikeactivity
AT pasqualinodeluca transientincubationofculturedhippocampalneuronsintheabsenceofmagnesiuminducesrhythmicandsynchronizedepileptiformlikeactivity
AT filipevduarte transientincubationofculturedhippocampalneuronsintheabsenceofmagnesiuminducesrhythmicandsynchronizedepileptiformlikeactivity
AT paulospinheiro transientincubationofculturedhippocampalneuronsintheabsenceofmagnesiuminducesrhythmicandsynchronizedepileptiformlikeactivity
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