Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome

Sebastiano A. Musumeci, Paolo Bosco, Giuseppe Calabrese, Cathy Bakker, Giovanni B. De Sarro, Maurizio Elia, Raffaele Ferri, Ben A. Oostra

Research output: Contribution to journalArticle

Abstract

Purpose: To evaluate their susceptibility to audiogenic seizures, five groups of knockout mice with various forms of fragile X genetic involvement [hemizygous males (n = 46), and homozygous (n = 38) and heterozygous females (n = 45), and their normal male (n = 45) and female (n = 52) littermates] were studied. Methods: All mouse groups were tested at ages 17, 22, 35, and 45 days. Audiogenic seizure susceptibility was scored, and the analysis of variance was used for the evaluation of the effects of age and genetic condition on seizure severity score (SSS). Results: All groups of knockout fragile X mice exhibited SSSs significantly higher than those observed in their wild-type littermates; among knockout mice, hemizygous males and homozygous females showed the highest SSSs. Hemizygous males showed higher SSSs with increasing age, from 17 to 45 days; homozygous females showed a peak at age 22 days, followed by a decrease; finally, heterozygous females had their highest SSSs at age 17 days. Conclusions: This study demonstrates that an increased susceptibility to audiogenic seizures is present in fragile X knockout mice at all the ages tested. These results support the validity of this animal model also for epilepsy and seizures in the human fragile X syndrome.

Original languageEnglish
Pages (from-to)19-23
Number of pages5
JournalEpilepsia
Volume41
Issue number1
Publication statusPublished - 2000

Fingerprint

Fragile X Syndrome
Transgenic Mice
Seizures
Knockout Mice
Reproducibility of Results
Epilepsy
Analysis of Variance
Animal Models

Keywords

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

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

Cite this

Musumeci, S. A., Bosco, P., Calabrese, G., Bakker, C., De Sarro, G. B., Elia, M., ... Oostra, B. A. (2000). Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome. Epilepsia, 41(1), 19-23.

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome. / Musumeci, Sebastiano A.; Bosco, Paolo; Calabrese, Giuseppe; Bakker, Cathy; De Sarro, Giovanni B.; Elia, Maurizio; Ferri, Raffaele; Oostra, Ben A.

In: Epilepsia, Vol. 41, No. 1, 2000, p. 19-23.

Research output: Contribution to journalArticle

Musumeci, SA, Bosco, P, Calabrese, G, Bakker, C, De Sarro, GB, Elia, M, Ferri, R & Oostra, BA 2000, 'Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome', Epilepsia, vol. 41, no. 1, pp. 19-23.
Musumeci SA, Bosco P, Calabrese G, Bakker C, De Sarro GB, Elia M et al. Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome. Epilepsia. 2000;41(1):19-23.
Musumeci, Sebastiano A. ; Bosco, Paolo ; Calabrese, Giuseppe ; Bakker, Cathy ; De Sarro, Giovanni B. ; Elia, Maurizio ; Ferri, Raffaele ; Oostra, Ben A. / Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome. In: Epilepsia. 2000 ; Vol. 41, No. 1. pp. 19-23.
@article{363a8563cefe4c4ea9248972d6503811,
title = "Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome",
abstract = "Purpose: To evaluate their susceptibility to audiogenic seizures, five groups of knockout mice with various forms of fragile X genetic involvement [hemizygous males (n = 46), and homozygous (n = 38) and heterozygous females (n = 45), and their normal male (n = 45) and female (n = 52) littermates] were studied. Methods: All mouse groups were tested at ages 17, 22, 35, and 45 days. Audiogenic seizure susceptibility was scored, and the analysis of variance was used for the evaluation of the effects of age and genetic condition on seizure severity score (SSS). Results: All groups of knockout fragile X mice exhibited SSSs significantly higher than those observed in their wild-type littermates; among knockout mice, hemizygous males and homozygous females showed the highest SSSs. Hemizygous males showed higher SSSs with increasing age, from 17 to 45 days; homozygous females showed a peak at age 22 days, followed by a decrease; finally, heterozygous females had their highest SSSs at age 17 days. Conclusions: This study demonstrates that an increased susceptibility to audiogenic seizures is present in fragile X knockout mice at all the ages tested. These results support the validity of this animal model also for epilepsy and seizures in the human fragile X syndrome.",
keywords = "Audiogenic seizures, Epilepsy, FMR1, Fragile X syndrome, Transgenic mice",
author = "Musumeci, {Sebastiano A.} and Paolo Bosco and Giuseppe Calabrese and Cathy Bakker and {De Sarro}, {Giovanni B.} and Maurizio Elia and Raffaele Ferri and Oostra, {Ben A.}",
year = "2000",
language = "English",
volume = "41",
pages = "19--23",
journal = "Epilepsia",
issn = "0013-9580",
publisher = "Blackwell Publishing Inc.",
number = "1",

}

TY - JOUR

T1 - Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome

AU - Musumeci, Sebastiano A.

AU - Bosco, Paolo

AU - Calabrese, Giuseppe

AU - Bakker, Cathy

AU - De Sarro, Giovanni B.

AU - Elia, Maurizio

AU - Ferri, Raffaele

AU - Oostra, Ben A.

PY - 2000

Y1 - 2000

N2 - Purpose: To evaluate their susceptibility to audiogenic seizures, five groups of knockout mice with various forms of fragile X genetic involvement [hemizygous males (n = 46), and homozygous (n = 38) and heterozygous females (n = 45), and their normal male (n = 45) and female (n = 52) littermates] were studied. Methods: All mouse groups were tested at ages 17, 22, 35, and 45 days. Audiogenic seizure susceptibility was scored, and the analysis of variance was used for the evaluation of the effects of age and genetic condition on seizure severity score (SSS). Results: All groups of knockout fragile X mice exhibited SSSs significantly higher than those observed in their wild-type littermates; among knockout mice, hemizygous males and homozygous females showed the highest SSSs. Hemizygous males showed higher SSSs with increasing age, from 17 to 45 days; homozygous females showed a peak at age 22 days, followed by a decrease; finally, heterozygous females had their highest SSSs at age 17 days. Conclusions: This study demonstrates that an increased susceptibility to audiogenic seizures is present in fragile X knockout mice at all the ages tested. These results support the validity of this animal model also for epilepsy and seizures in the human fragile X syndrome.

AB - Purpose: To evaluate their susceptibility to audiogenic seizures, five groups of knockout mice with various forms of fragile X genetic involvement [hemizygous males (n = 46), and homozygous (n = 38) and heterozygous females (n = 45), and their normal male (n = 45) and female (n = 52) littermates] were studied. Methods: All mouse groups were tested at ages 17, 22, 35, and 45 days. Audiogenic seizure susceptibility was scored, and the analysis of variance was used for the evaluation of the effects of age and genetic condition on seizure severity score (SSS). Results: All groups of knockout fragile X mice exhibited SSSs significantly higher than those observed in their wild-type littermates; among knockout mice, hemizygous males and homozygous females showed the highest SSSs. Hemizygous males showed higher SSSs with increasing age, from 17 to 45 days; homozygous females showed a peak at age 22 days, followed by a decrease; finally, heterozygous females had their highest SSSs at age 17 days. Conclusions: This study demonstrates that an increased susceptibility to audiogenic seizures is present in fragile X knockout mice at all the ages tested. These results support the validity of this animal model also for epilepsy and seizures in the human fragile X syndrome.

KW - Audiogenic seizures

KW - Epilepsy

KW - FMR1

KW - Fragile X syndrome

KW - Transgenic mice

UR - http://www.scopus.com/inward/record.url?scp=0033987591&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033987591&partnerID=8YFLogxK

M3 - Article

C2 - 10643918

AN - SCOPUS:0033987591

VL - 41

SP - 19

EP - 23

JO - Epilepsia

JF - Epilepsia

SN - 0013-9580

IS - 1

ER -