Stimulation of serotonin[sub 1B] receptors induces conditioned place aversion and facilitates cocaine place conditioning in rats.

Rationale: Changes in serotonin[sub 1B] (5-HT[sub 1B]) receptor function appear to modify the reinforcing properties of cocaine, but the direction of this effect is not completely clear. Pharmacological stimulation of 5HT[sub 1B] enhanced the rewarding properties of self-administered cocaine while attenuating the threshold-reducing effect of cocaine in the intracerebral brain stimulation procedure. Objective: The present study investigates how pharmacological modification of 5-HT[sub 1B] receptor-mediated neurotransmission influence cocaine motivational properties in the conditioned place preference paradigm in rats. Methods: In separate groups of rats the motivational properties of CP 94,253, a selective 5-HT[sub 1B] agonist, or GR 127935, a 5-HT[sub 1B/D] receptor partial agonist, given alone or in combination, were determined. To evaluate their influence on cocaine-induced place conditioning, CP 94,253, that was found to be aversive, was given every day before each conditioning session, while GR 127935, which given alone had no effect, was administered only before cocaine conditioning sessions. Results: CP 94,253, injected IP at 2.5 and 10 (but not 0.5) mg/kg produced place aversion in the place conditioning paradigm. The aversive effect of 2.5 mg/kg CP 94,253 was completely reversed by 10 mg/kg SC GR 127935. Given before every conditioning session, CP 94,253 did not modify place conditioning by four injections of 10 mg/kg cocaine but at 2.5 mg/kg it potentiated a sub-threshold dose of cocaine. The place preference caused by these two drugs was completely reversed by 10 mg/kg GR 127935. The antagonism by GR 127935 of CP 94,253's effects was shown not to be due to the induction of state-dependent effects. Conclusion: The results suggest that stimulation of 5-HT[sub 1B] receptors causes place aversion, and enhances the effect of low doses of cocaine in the conditioned place preference paradigm. [ABSTRACT FROM AUTHOR]