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

Citation
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
Citations number
22
Categorie Soggetti
Neurosciences & Behavoir
Journal title
BRAIN RESEARCH
ISSN journal
00068993 → ACNP
Volume
872
Issue
1-2
Year of publication
2000
Pages
204 - 207
Database
ISI
SICI code
0006-8993(20000728)872:1-2<204:RAS5RA>2.0.ZU;2-9
Abstract
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.