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Effects of inhibitors of α1-ARs or serotonin receptors (5-HTRs), or activators of α2-ARs on cAMP levels in 661W cells. Studies were performed as described in the legend for Fig. 2. In some cases, drugs were combined for the full 4 days of study. Fo (forskolin) activates adenylyl cyclase and thus increases intracellular levels of cAMP. RO (RO 04-6790) is a 5-HT6R antagonist. n = 3 for all groups, except n = 2 for RO and Fo groups.
