Abstract
Genetically epilepsy-prone rats (GEPR-9s) were derived from Sprague-Dawley rats (SD). The number of kainate-induced wet dog shake behavior (WDS) responses was found to decrease significantly in GEPR-9s compared to SD. WDS responses were potentiated by 5-hydroxytryptophan or 2,5-dimethoxy-4-iodoamphetamine and antagonized by ritanserin. The antagonizing effect of ritanserin on WDS latency was more evident in GEPR-9s than in SD, and hippocampal expression of activity-regulated cytoskeleton-associated protein paralleled the severity of WDS. The results suggest that downstream serotonergic synaptic activation is less pronounced in GEPR-9s than in SD and that the serotonergic agent may directly activate postsynaptic 5-HT2A receptors in both strains.
Original language | English |
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Pages (from-to) | 401-404 |
Number of pages | 4 |
Journal | Journal of Pharmacological Sciences |
Volume | 110 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2009 |
Keywords
- Genetically epilepsy-prone rat
- Kainic acid
- Wet dog shake
ASJC Scopus subject areas
- Molecular Medicine
- Pharmacology