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Iprindole is a tricyclic antidepressant.1,2 It binds to the serotonin (5-HT) receptor subtypes 5-HT2A and 5-HT2C in radioligand binding assays (Kis = 0.217 and 0.206 µM, respectively) but only weakly inhibits norepinephrine (NE) and 5-HT uptake in mouse brain slices (IC50s = 9 and 50 µM, respectively).1,3 Iprindole reduces immobility in the forced swim test in rats when administered at a dose of 10 mg/kg once per day for 21 days.2
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1. A comparison of the inhibitory activities of iprindole and imipramine on the uptake of 5-
2. Chronic treatment with iprindole reduces immobility of rats in the behavioural “despair” test by activating dopaminergic mechanisms in the brain. J. Pharm. Pharmacol. 38(4), 313-315 (1986).
3. Interactions of selective serotonin reuptake inhibitors with the serotonin 5-