Abstract |
Mutations in the GABA(A) receptor gamma2 subunit are associated with childhood absence epilepsy and febrile seizures. To understand better the molecular basis of absence epilepsy in man, we developed a mouse model harboring a gamma2 subunit point mutation (R43Q) found in a large Australian family. Mice heterozygous for the mutation demonstrated behavioral arrest associated with 6-to 7-Hz spike-and-wave discharges, which are blocked by ethosuximide, a first-line treatment for absence epilepsy in man. Seizures in the mouse showed an abrupt onset at around age 20 days corresponding to the childhood nature of this disease. Reduced cell surface expression of gamma2(R43Q) was seen in heterozygous mice in the absence of any change in alpha1 subunit surface expression, ruling out a dominant-negative effect. GABA(A)-mediated synaptic currents recorded from cortical pyramidal neurons revealed a small but significant reduction that was not seen in the reticular or ventrobasal thalamic nuclei. We hypothesize that a subtle reduction in cortical inhibition underlies childhood absence epilepsy seen in humans harboring the R43Q mutation.
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Authors | Heneu O Tan, Christopher A Reid, Frank N Single, Philip J Davies, Cindy Chiu, Susan Murphy, Alison L Clarke, Leanne Dibbens, Heinz Krestel, John C Mulley, Mathew V Jones, Peter H Seeburg, Bert Sakmann, Samuel F Berkovic, Rolf Sprengel, Steven Petrou |
Journal | Proceedings of the National Academy of Sciences of the United States of America
(Proc Natl Acad Sci U S A)
Vol. 104
Issue 44
Pg. 17536-41
(Oct 30 2007)
ISSN: 0027-8424 [Print] United States |
PMID | 17947380
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Protein Subunits
- Receptors, GABA-A
- Ethosuximide
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Topics |
- Animals
- Disease Models, Animal
- Epilepsy, Absence
(drug therapy, genetics, metabolism, physiopathology)
- Ethosuximide
(pharmacology)
- Genetic Predisposition to Disease
- Mice
- Phenotype
- Protein Subunits
(genetics, metabolism)
- Receptors, GABA-A
(genetics, metabolism)
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