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Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice

Brain malformations cause cognitive disability and seizures in both human and animal models. Highly laminated structures such as the neocortex and cerebellum are vulnerable to malformation, affecting lamination and neuronal connectivity as well as causing heterotopia. The objective of the present st...

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Autores principales: Keever, Katherine M., Li, Ying, Womble, Paige D., Sullens, D. Gregory, Otazu, Gonzalo H., Lugo, Joaquin N., Ramos, Raddy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651747/
https://www.ncbi.nlm.nih.gov/pubmed/38027492
http://dx.doi.org/10.3389/fnins.2023.1271744
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author Keever, Katherine M.
Li, Ying
Womble, Paige D.
Sullens, D. Gregory
Otazu, Gonzalo H.
Lugo, Joaquin N.
Ramos, Raddy L.
author_facet Keever, Katherine M.
Li, Ying
Womble, Paige D.
Sullens, D. Gregory
Otazu, Gonzalo H.
Lugo, Joaquin N.
Ramos, Raddy L.
author_sort Keever, Katherine M.
collection PubMed
description Brain malformations cause cognitive disability and seizures in both human and animal models. Highly laminated structures such as the neocortex and cerebellum are vulnerable to malformation, affecting lamination and neuronal connectivity as well as causing heterotopia. The objective of the present study was to determine if sporadic neocortical and/or cerebellar malformations in C57BL/6J mice are correlated with reduced seizure threshold. The inhaled chemi-convulsant flurothyl was used to induce generalized, tonic-clonic seizures in male and female C57BL/6J mice, and the time to seizure onset was recorded as a functional correlate of brain excitability changes. Following seizures, mice were euthanized, and brains were extracted for histology. Cryosections of the neocortex and cerebellar vermis were stained and examined for the presence of molecular layer heterotopia as previously described in C57BL/6J mice. Over 60% of mice had neocortical and/or cerebellar heterotopia. No sex differences were observed in the prevalence of malformations. Significantly reduced seizure onset time was observed dependent on sex and the type of malformation present. These results raise important questions regarding the presence of malformations in C57BL/6J mice used in the study of brain development, epilepsy, and many other diseases of the nervous system.
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spelling pubmed-106517472023-01-01 Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice Keever, Katherine M. Li, Ying Womble, Paige D. Sullens, D. Gregory Otazu, Gonzalo H. Lugo, Joaquin N. Ramos, Raddy L. Front Neurosci Neuroscience Brain malformations cause cognitive disability and seizures in both human and animal models. Highly laminated structures such as the neocortex and cerebellum are vulnerable to malformation, affecting lamination and neuronal connectivity as well as causing heterotopia. The objective of the present study was to determine if sporadic neocortical and/or cerebellar malformations in C57BL/6J mice are correlated with reduced seizure threshold. The inhaled chemi-convulsant flurothyl was used to induce generalized, tonic-clonic seizures in male and female C57BL/6J mice, and the time to seizure onset was recorded as a functional correlate of brain excitability changes. Following seizures, mice were euthanized, and brains were extracted for histology. Cryosections of the neocortex and cerebellar vermis were stained and examined for the presence of molecular layer heterotopia as previously described in C57BL/6J mice. Over 60% of mice had neocortical and/or cerebellar heterotopia. No sex differences were observed in the prevalence of malformations. Significantly reduced seizure onset time was observed dependent on sex and the type of malformation present. These results raise important questions regarding the presence of malformations in C57BL/6J mice used in the study of brain development, epilepsy, and many other diseases of the nervous system. Frontiers Media S.A. 2023-11-02 /pmc/articles/PMC10651747/ /pubmed/38027492 http://dx.doi.org/10.3389/fnins.2023.1271744 Text en Copyright © 2023 Keever, Li, Womble, Sullens, Otazu, Lugo and Ramos. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Keever, Katherine M.
Li, Ying
Womble, Paige D.
Sullens, D. Gregory
Otazu, Gonzalo H.
Lugo, Joaquin N.
Ramos, Raddy L.
Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
title Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
title_full Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
title_fullStr Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
title_full_unstemmed Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
title_short Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
title_sort neocortical and cerebellar malformations affect flurothyl-induced seizures in female c57bl/6j mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651747/
https://www.ncbi.nlm.nih.gov/pubmed/38027492
http://dx.doi.org/10.3389/fnins.2023.1271744
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