Abstract

The obtained results revealed that joint administration of desipramine or reboxetine and metyrapone (a glucocorticoid synthesis inhibitor) had more potent antidepressant-like activity in the forced swimming test (FST) in rats compared to treatment with either drug alone. WAY 100636 (a 5-HT1A antagonist), and prazosin (an α1-adrenergic antagonist), used in doses ineffective in the FST, inhibited the antidepressant-like effect induced by co-administration of desipramine (10mg/kg) or reboxetine (10mg/kg) and metyrapone (50mg/kg). The above-mentioned findings suggest that, among other mechanisms, the 5-HT1A and α1-adrenergic receptors may play a role in this effect. Furthermore, they may be of particular importance to the pharmacotherapy of drug-resistant depression.

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