PT - JOURNAL ARTICLE AU - Marek, G J AU - Li, A A AU - Seiden, L S TI - Selective 5-hydroxytryptamine2 antagonists have antidepressant-like effects on differential-reinforcement-of-low-rate 72-second schedule. DP - 1989 Jul 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 52--59 VI - 250 IP - 1 4099 - http://jpet.aspetjournals.org/content/250/1/52.short 4100 - http://jpet.aspetjournals.org/content/250/1/52.full SO - J Pharmacol Exp Ther1989 Jul 01; 250 AB - The effects of eleven 5-hydroxytryptamine antagonists with varying selectivity for the 5-hydroxytryptamine2 (5-HT2) relative to the 5-HT1 binding site were assessed in rats responding under a differential-reinforcement-of-low rate 72-sec (DRL 72-s) schedule of reinforcement. Three drugs with a 1000-fold selectivity for the 5-HT2 binding site (ketanserin, ritanserin, pipamperone) increased the reinforcement rate and decreased the response rate similar to antidepressant drugs. The two drugs with roughly the same affinity for both 5-HT1 and 5-HT2 binding sites (methysergide and metergoline) did not increase the reinforcement rate. The maximal increase in the reinforcement rate after 5-HT antagonist administration was positively correlated with the selectivity of the 5-HT antagonists for the 5-HT2 versus the 5-HT1 binding site. The increase in the reinforcement rate after administration of 5-HT antagonists was not correlated with the affinity of the 5-HT antagonists for the alpha-1 adrenergic, alpha-2 adrenergic, histamine-1 or dopamine-2 receptors. The 1000-fold selective 5-HT2 antagonist xylamidine, which does not pass the blood-brain barrier, did not increase the reinforcement rate or decrease the response rate. Thus, selective antagonism of central 5-HT2 relative to 5-HT1 receptors results in antidepressant-like effects on the DRL 72-s schedule. Furthermore, the specificity of the DRL 72-s schedule as a screen for antidepressant drugs was strengthened by the observation that the alpha-1 adrenergic antagonist, prazosin, did not increase the reinforcement rate despite significant decreases in the response rate.