Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome

被引:211
作者
Musumeci, SA
Bosco, P
Calabrese, G
Bakker, C
De Sarro, GB
Elia, M
Ferri, R
Oostra, BA
机构
[1] Oasi Inst Res Mental Retardat Brain Aging, Dept Neurol, I-94018 Troina, EN, Italy
[2] Oasi Inst Res Mental Retardat Brain Aging, Lab Genet Diag, Troina, Italy
[3] Univ Reggio Calabria, Sch Med, Dept Expt & Clin Med, Chair Pharmacol, I-89100 Reggio Calabria, Italy
[4] Erasmus Univ, Dept Clin Genet, Rotterdam, Netherlands
[5] Erasmus Univ, Ctr Biomed Genet, Rotterdam, Netherlands
关键词
fragile X syndrome; FMR1; transgenic mice; audiogenic seizures; epilepsy;
D O I
10.1111/j.1528-1157.2000.tb01499.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 sus ceptibility 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.
引用
收藏
页码:19 / 23
页数:5
相关论文
共 34 条
[1]   NUCLEUS BASALIS MAGNOCELLULARIS AND HIPPOCAMPUS ARE THE MAJOR SITES OF FMR-1 EXPRESSION IN THE HUMAN FETAL BRAIN [J].
ABITBOL, M ;
MENINI, C ;
DELEZOIDE, AL ;
RHYNER, T ;
VEKEMANS, M ;
MALLET, J .
NATURE GENETICS, 1993, 4 (02) :147-153
[2]   HUMAN AND MURINE FMR-1 - ALTERNATIVE SPLICING AND TRANSLATIONAL INITIATION DOWNSTREAM OF THE CGG-REPEAT [J].
ASHLEY, CT ;
SUTCLIFFE, JS ;
KUNST, CB ;
LEINER, HA ;
EICHLER, EE ;
NELSON, DL ;
WARREN, ST .
NATURE GENETICS, 1993, 4 (03) :244-251
[3]  
BAKKER CE, 1994, CELL, V78, P23
[4]   Sound-induced seizures in serotonin 5-HT2C receptor mutant mice [J].
Brennan, TJ ;
Seeley, WW ;
Kilgard, M ;
Schreiner, CE ;
Tecott, LH .
NATURE GENETICS, 1997, 16 (04) :387-390
[5]   Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits [J].
Comery, TA ;
Harris, JB ;
Willems, PJ ;
Oostra, BA ;
Irwin, SA ;
Weiler, IJ ;
Greenough, WT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5401-5404
[6]   CONSERVATION OF CGG REGION IN FMR1 GENE IN MAMMALS [J].
DEELEN, W ;
BAKKER, C ;
HALLEY, DJJ ;
OOSTRA, BA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (04) :513-516
[7]   AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME [J].
DESAI, HB ;
DONAT, J ;
SHOKEIR, MHK ;
MUNOZ, DG .
NEUROLOGY, 1990, 40 (02) :378-380
[8]   THE FMR-1 PROTEIN IS CYTOPLASMIC, MOST ABUNDANT IN NEURONS AND APPEARS NORMAL IN CARRIERS OF A FRAGILE X PREMUTATION [J].
DEVYS, D ;
LUTZ, Y ;
ROUYER, N ;
BELLOCQ, JP ;
MANDEL, JL .
NATURE GENETICS, 1993, 4 (04) :335-340
[9]   The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals [J].
Eberhart, DE ;
Malter, HE ;
Feng, Y ;
Warren, ST .
HUMAN MOLECULAR GENETICS, 1996, 5 (08) :1083-1091
[10]   SEIZURE SUSCEPTIBILITY IN DBA AND C57 MICE - THE EFFECTS OF VARIOUS CONVULSANTS [J].
ENGSTROM, FL ;
WOODBURY, DM .
EPILEPSIA, 1988, 29 (04) :389-395