R(+)-8-OH-DPAT, a selective 5-HT1A receptor agonist, attenuated amphetamine-induced dopamine synthesis in rat striatum, but not nucleus accumbens or medial prefrontal cortex
T. Kuroki et al., R(+)-8-OH-DPAT, a selective 5-HT1A receptor agonist, attenuated amphetamine-induced dopamine synthesis in rat striatum, but not nucleus accumbens or medial prefrontal cortex, BRAIN RES, 872(1-2), 2000, pp. 204-207
R(+)-8-OH-DPAT (0.05, but not 0.025, 0.1, 1 mg/kg), a 5-HT1A receptor agoni
st, decreased l-3,4-dihydroxyphenylalanine (DOPA) accumulation in rat stria
tum following NSD-1015, an l-aromatic amino acid decarboxylase inhibitor. A
mphetamine (1 mg/kg) increased striatal DOPA accumulation, an effect attenu
ated by R(+)-8-OH-DPAT (0.05 mg/kg). However, both amphetamine (1 mg/kg) an
d R(+)-8-OH-DPAT (0.05 mg/kg) decreased cortical DOPA accumulation; there w
ere no additional decreases from their combination. Neither amphetamine (1
mg/kg), R(+)-8-OH-DPAT (0.05 mg/kg), or the combination, significantly affe
cted DOPA accumulation in the nucleus accumbens. The significance of and po
ssible mechanisms for these findings are discussed. (C) 2000 Elsevier Scien
ce B.V. All rights reserved.