Wz. Yu et al., Pharmacology of flavor preference conditioning in sham-feeding rats: Effects of dopamine receptor antagonists, PHARM BIO B, 65(4), 2000, pp. 635-647
Opioid and dopamine systems are both implicated in the response to sweet so
lutions. Our laboratory previously reported that the opioid antagonist, nal
trexone, reduced the intake of sweet solutions, yet had little or no effect
on sucrose-conditioned flavor preferences in sham-feeding rats. The presen
t study examined the role of dopamine D-1 and D-2 receptors in the expressi
on of flavor preferences conditioned by the sweet taste of sucrose. All ses
sions were conducted under sham-feeding conditions to minimize postingestiv
e influences. Training was accomplished by adding a novel flavor (CS+) to a
16% sucrose solution, a different flavor (CS-) to a less-preferred 0.2% sa
ccharin solution in alternating, one-bottle sessions. Preferences were asse
ssed in two-bottle tests with the CS+ and CS- flavors presented in mixed su
crose (8%)-saccharin (0.1%) solutions following systemic doses of 0, 50, 20
0, 400, or 800 nmol/kg of the D-2 antagonist, raclopride (Experiment 1) or
the D-1 antagonist, SCH23390 (Experiment 2) under either food-restricted or
unrestricted conditions. Rats significantly preferred the CS+ solutions in
vehicle tests, and displayed equipotent and dose-dependent reductions in t
otal intake and CS+ preference following either D-1 or D-2 receptor antagon
ism. Similar results were obtained with SCH23390 and raclopride in Experime
nt 3 conducted with water restricted rats. These data indicate that dopamin
ergic D-1 and D-2 receptors play pivotal and functionally equivalent roles
in the expression of flavor preferences conditioned by the sweet taste of s
ucrose. (C) 2000 Elsevier Science Inc.