Abstract:
:The Fmr1 knockout (KO) mouse is characterized by an increased audiogenic seizure (AGS) susceptibility and is considered a good animal model for epilepsy and seizures in the human fragile-X (FRAX) syndrome. Here, we tested the hypothesis that the reintroduction of the FMR1 gene is able to revert the AGS susceptibility characterizing Fmr1 KO mice. To this aim, two groups of Fmr1 KO transgenic mice, which have additional copies of the human FMR1 gene (YAC) or FMR1 cDNA (G6) were used. AGS susceptibility of these mice was examined and compared to that of Fmr1 KO, wild type, and wild-type animals in whom the FMR1gene was also introduced (over-expressed). Mice were tested at different ages because AGS susceptibility is age dependent. The intensity of response was scored and the results were analyzed by means of 2-way analysis of variance to evaluate the effects of age and genetic condition. We found that AGS susceptibility rescue is complete in the G6 mice and partial in YAC mice. Our data indicate that the introduction of the human FMR1 gene in Fmr1 KO mice is able to revert the Fmr1 KO epileptic phenotype.
journal_name
Exp Neuroljournal_title
Experimental neurologyauthors
Musumeci SA,Calabrese G,Bonaccorso CM,D'Antoni S,Brouwer JR,Bakker CE,Elia M,Ferri R,Nelson DL,Oostra BA,Catania MVdoi
10.1016/j.expneurol.2006.08.007subject
Has Abstractpub_date
2007-01-01 00:00:00pages
233-40issue
1eissn
0014-4886issn
1090-2430pii
S0014-4886(06)00477-8journal_volume
203pub_type
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