Abstract:
:The effects of the selective 5-HT1A agonists 8-OH-DPAT and flesinoxan and the selective 5-HT2 antagonists ritanserin and ketanserin on immobility time in rats bred for predisposition to catalepsy have been studied. Treatment with 8-OH-DPAT as well as flesinoxan caused a marked dose-dependent decrease in immobility time. Ritanserin and ketanserin did not affect immobility time at any dose tested. It was suggested that 5HT1A rather than 5-HT2 serotonin receptors are involved in the catalepsy and that an hereditary predisposition to catalepsy may be the result of an inherited alteration in 5-HT1A receptors.
journal_name
Psychopharmacology (Berl)journal_title
Psychopharmacologyauthors
Kulikov AV,Kolpakov VG,Maslova GB,Kozintsev I,Popova NKdoi
10.1007/BF02245460subject
Has Abstractpub_date
1994-02-01 00:00:00pages
172-4issue
1eissn
0033-3158issn
1432-2072journal_volume
114pub_type
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