Abstract
Expression of preproenkephalin, dynorphin and D2 dopamine receptor mRNAs was examined in selected regions of the forebrain of homozygous and heterozygous tottering mice, using in situ hybridization histochemistry. Homozygous tottering mice carry an autosomal recessive mutation causing them to exhibit petit mal-like epilepsy. Preproenkephalin mRNA levels were significantly higher in the lateral caudate and the core of the nucleus accumbens of homozygous tottering mice compared to wild-type controls. No differences were observed in the expression of dynorphin and D2 receptor mRNA distribution in brain regions examined in the mutant mice as compared to wild-type controls.
Original language | English (US) |
---|---|
Pages (from-to) | 321-324 |
Number of pages | 4 |
Journal | Molecular Brain Research |
Volume | 46 |
Issue number | 1-2 |
DOIs | |
State | Published - Jun 1997 |
Externally published | Yes |
Keywords
- D dopamine receptor
- Dynorphin
- Enkephalin
- Epilepsy
- Hybridization histochemistry, in situ
- mRNA
- Striatum
ASJC Scopus subject areas
- Molecular Biology
- Cellular and Molecular Neuroscience