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1.
Genes Brain Behav ; 8(2): 248-55, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19077119

ABSTRACT

Febrile seizures (FS) are the most common seizure type in children and recurrent FS are a risk factor for developing temporal lobe epilepsy. Although the mechanisms underlying FS are largely unknown, recent family, twin and animal studies indicate that genetics are important in FS susceptibility. Here, a forward genetic strategy was used employing mouse chromosome substitution strains (CSS) to identify novel FS susceptibility quantitative trait loci (QTLs). FS were induced by exposure to warm air at postnatal day 14. Video electroencephalogram monitoring identified tonic-clonic convulsion onset, defined as febrile seizure latency (FSL), as a reliable phenotypic parameter to determine FS susceptibility. FSL was determined in both sexes of the host strain (C57BL/6J), the donor strain (A/J) and CSS. C57BL/6J mice were more susceptible to FS than A/J mice. Phenotypic screening of the CSS panel identified six strains(CSS1, -2, -6 -10, -13 and -X) carrying QTLs for FS susceptibility. CSS1, -10 and -13 were less susceptible (protective QTLs), whereas CSS2, -6 and -X were more susceptible (susceptibility QTLs) to FS than the C57BL/6J strain. Our data show that mouse FS susceptibility is determined by complex genetics, which is distinct from that for chemically induced seizures. This is the first dataset using CSS to screen for a seizure trait in mouse pups. It provides evidence for common FS susceptibility QTLs that serve as starting points to fine map FS susceptibility QTLs and to identify FS susceptibility genes. This will increase our understanding of human FS, working toward the identification of new therapeutic targets.


Subject(s)
Chromosomes, Mammalian/genetics , Quantitative Trait Loci/genetics , Seizures, Febrile/genetics , Animals , Behavior, Animal/physiology , Body Temperature/genetics , Body Temperature/physiology , Data Interpretation, Statistical , Electroencephalography , Female , Genetic Linkage/genetics , Male , Mice , Mice, Inbred A , Mice, Inbred C57BL , Phenotype , Seizures, Febrile/psychology
2.
Genes Brain Behav ; 7(5): 578-86, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18363854

ABSTRACT

Febrile seizures (FS) are the most prevalent seizures in children. Although FS are largely benign, complex FS increase the risk to develop temporal lobe epilepsy (TLE). Studies in rat models for FS have provided information about functional changes in the hippocampus after complex FS. However, our knowledge about the genes and pathways involved in the causes and consequences of FS is still limited. To enable molecular, genetic and knockout studies, we developed and characterized an FS model in mice and used it as a phenotypic screen to analyze FS susceptibility. Hyperthermia was induced by warm air in 10- to 14-day-old mice and induced FS in all animals. Under the conditions used, seizure-induced behavior in mice and rats was similar. In adulthood, treated mice showed increased hippocampal Ih current and seizure susceptibility, characteristics also seen after FS in rats. Of the seven genetically diverse mouse strains screened for FS susceptibility, C57BL/6J mice were among the most susceptible, whereas A/J mice were among the most resistant. Strains genetically similar to C57BL/6J also showed a susceptible phenotype. Our phenotypic data suggest that complex genetics underlie FS susceptibility and show that the C57BL/6J strain is highly susceptible to FS. As this strain has been described as resistant to convulsants, our data indicate that susceptibility genes for FS and convulsants are distinct. Insight into the mechanisms underlying seizure susceptibility and FS may help to identify markers for the early diagnosis of children at risk for complex FS and TLE and may provide new leads for treatment.


Subject(s)
Genetic Predisposition to Disease/genetics , Mice, Inbred C57BL/genetics , Seizures, Febrile/genetics , Seizures, Febrile/physiopathology , Animals , Behavior, Animal , Convulsants/pharmacology , Electrophysiology , Fever/genetics , Fever/physiopathology , Hippocampus/physiopathology , Male , Mice , Mice, Inbred AKR , Mice, Inbred BALB C , Mice, Inbred C3H , Mice, Inbred DBA , Pentylenetetrazole/pharmacology , Phenotype , Rats , Rats, Sprague-Dawley , Seizures, Febrile/chemically induced , Species Specificity
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