| Literature DB >> 23201443 |
Lisa A Gabel1, Monica Manglani, Natalia Ibanez, Jessica Roberts, Raddy L Ramos, Glenn D Rosen.
Abstract
Malformations of cortical development (MCD) are linked to epilepsy in humans. MCD encompass a broad spectrum of malformations, which occur as the principal pathology or a secondary disruption. Recently, Rosen et al. (2012) reported that BXD29-Trl4(lps-2J)/J mice have subcortical nodular heterotopias with partial agenesis of the corpus callosum (p-ACC). Additionally Ramos et al. (2008) demonstrated that C57BL/10J mice exhibit cortical heterotopias with no additional cortical abnormalities. We examined the seizure susceptibility of these mice to determine if the presence (BXD29-Trl4(lps-2J)/J) or absence (C57BL/10J) of p-ACC, in strains with MCD, confers a differential response to chemi-convulsive treatment. Our results indicate that C57BL/10J mice with layer I heterotopia are more susceptible, whereas BXD29-Trl4(lps-2J)/J mice with more severe subcortical nodular heterotopia and p-ACC are more resistant to seizure behavior induced by pentylenetetrazole. These data suggest that p-ACC may confer seizure resistance in models of MCD.Entities:
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Year: 2012 PMID: 23201443 PMCID: PMC3743552 DOI: 10.1016/j.brainres.2012.11.040
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252