Abstract |
Specific binding of [3H] ketanserin to 5-HT2A serotonin receptor sites in the corpus striatum and frontal cortex and the effect of 5-HT2A antagonists in rats and mice hereditarily predisposed to catalepsy has been studied. Cyproheptadine inhibited the expression of inherited catalepsy in rats and mice, whereas more selective 5-HT2A antagonists, ritanserin and ketanserin, failed to affect the catalepsy. A decrease in [3H] ketanserin-specific binding site density in the striatum of cataleptic animals compared to their noncataleptic counterparts was found. It was suggested that the decrease in the density of 5-HT2A receptor binding sites in the striatum represents a result of their downregulation due to increased serotonergic neurotransmission in the striatum of cataleptic animals.
|
Authors | A V Kulikov, D F Avgustinovich, V G Kolpakov, G B Maslova, N K Popova |
Journal | Pharmacology, biochemistry, and behavior
(Pharmacol Biochem Behav)
Vol. 50
Issue 3
Pg. 383-7
(Mar 1995)
ISSN: 0091-3057 [Print] United States |
PMID | 7617676
(Publication Type: Journal Article)
|
Chemical References |
- Receptors, Serotonin
- Serotonin Antagonists
|
Topics |
- Animals
- Catalepsy
(genetics, metabolism)
- Corpus Striatum
(metabolism)
- Disease Susceptibility
- Evaluation Studies as Topic
- Frontal Lobe
(metabolism)
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Inbred CBA
- Radioligand Assay
- Rats
- Rats, Wistar
- Receptors, Serotonin
(drug effects, metabolism)
- Serotonin Antagonists
(pharmacology)
|