The effect of serotonin(1A) receptor agonism on antipsychotic drug-induceddopamine release in rat striatum and nucleus accumbens

Serotonin (5-HT)(1A) receptor agonism may be of interest in regard to both the antipsychotic action and extrapyramidal symptoms (EPS) of antipsychotic drugs (APD) based, in part, on the effect of 5-HT1A receptor stimulation o n the release of dopamine (DA) in the nucleus accumbens (NAC) and striatum (STR), respectively. We investigated the effect of R(+)-8-hydroxy-2-(di-n-p ropylamino)-tetralin (R(+)-8-OH-DPAT) and n-[2-[4-(2-methoxyphenyl)-1-piper aziny]ethyl]-n-(2-pyridinyl)cyclohexanecarboxamide trihydrochloride (WAY100 635), a selective 5-HT1A receptor agonist and antagonist, respectively, on basal and APD-induced DA release. In both STR and NAC, R(+)-8-OH-DPAT (0.2 mg/kg) decreased basal DA release; R(+)-8-OH-DPAT (0.05 mg/kg) inhibited DA release produced by the 5-HT2A/D-2 receptor antagonists clozapine (20 mg/k g), low dose risperidone (0.01 and 0.03 mg/kg) and amperozide (10 mg/kg), b ut not that produced by high dose risperidone (0.1 and 1.0 mg/kg) or halope ridol (0.01-1.0 mg/kg), potent D-2 receptor antagonists. This R(+)-8-OH-DPA T-induced inhibition of the effects of clozapine, risperidone and amperozid e was antagonized by WAY100635 (0.05 mg/kg). WAY100635 (0.1-0.5 mg/kg) alon e increased DA release in the STR but not NAC. The selective 5-HT2A recepto r antagonist M100907 (1 mg/kg) did not alter the effect of R(+)-8-OH-DPAT o r WAY100635 alone on basal DA release in either region. These results sugge st that 5-HT1A receptor stimulation inhibits basal and some APD-induced DA release in the STR and NAC, and that this effect is unlikely to be mediated by an interaction with 5-HT2A receptors. The significance of these results for EPS and antipsychotic action is discussed. (C) 2000 Elsevier Science B .V. All rights reserved.