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5-HT2A serotonin receptors in the brain of rats and mice hereditarily predisposed to catalepsy.

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.
AuthorsA V Kulikov, D F Avgustinovich, V G Kolpakov, G B Maslova, N K Popova
JournalPharmacology, biochemistry, and behavior (Pharmacol Biochem Behav) Vol. 50 Issue 3 Pg. 383-7 (Mar 1995) ISSN: 0091-3057 [Print] United States
PMID7617676 (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)

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