Affiliation:
1. Boehringer Ingelheim Italia S.p.A., Department of Pharmacology, Via Serio 15, 20139 Milano, Italy
Abstract
Abstract
The anti-immobility effect of fluoxetine (40 mg kg−1) in the forced swimming test in mice was antagonized by the 5-HT1c/2 antagonist mesulergine (7·5 mg kg−1) and the dopamine D2 antagonist (±)-sulpiride (12.5 mg kg−1) but not by the 5-HT2/1C antagonist ritanserine (2 mg kg−1), the 5-HT1A/1B antagonist (–)-propranolol (20 mg kg−1) or the 5-HT3 antagonist DAU 6215 (0·1 mg kg−1). All compounds were administered intraperitoneally (i.p.) 6 min before fluoxetine, given i.p. 30 min before testing. The anti-immobility effect of fluoxetine was also prevented by pretreat-ment with p-chlorophenylalanine (300 mg kg−1 twice daily for 3 days) which produced an 80% reduction of 5-HT in brain. The results suggest that fluoxetine reduces immobility time in mice forced to swim, by acting indirectly through a mesulergine-sensitive site, probably the 5-HT1C receptor.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Cited by
39 articles.
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