Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenes

Sebastiano A. Musumeci, Giuseppe Calabrese, Carmela M. Bonaccorso, Simona D'Antoni, Judith R. Brouwer, Cathy E. Bakker, Maurizio Elia, Raffaele Ferri, David L. Nelson, Ben A. Oostra, Maria Vincenza Catania

Research output: Contribution to journalArticlepeer-review


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.

Original languageEnglish
Pages (from-to)233-240
Number of pages8
JournalExperimental Neurology
Issue number1
Publication statusPublished - Jan 2007


  • Audiogenic seizures
  • Epilepsy
  • FMR1
  • FMRP
  • Fragile X syndrome
  • Transgenic mice

ASJC Scopus subject areas

  • Neurology
  • Neuroscience(all)


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