Mj. Eaton et al., COMPARISON OF THE EFFECTS OF THE DOPAMINE-D(2) AGONIST QUINELORANE ONTUBEROINFUNDIBULAR DOPAMINERGIC NEURONAL-ACTIVITY IN MALE AND FEMALE RATS, Brain research, 629(1), 1993, pp. 53-58
The purpose of the present study was to examine the effects of quinelo
rane (LY163502), a potent and selective D2 dopaminergic (DA) receptor
agonist, on the activity of tuberoinfundibular DA neurons in male and
female rats as estimated by determining the concentration of the prima
ry metabolite of dopamine, 3,4-dihydroxyphenylacetic acid (DOPAC), in
terminals of these neurons in the median eminence (ME). In males, quin
elorane produced dose- and time-related increases in the concentration
of DOPAC in the ME which was blocked by the D2 receptor antagonist ra
clopride. The activity of tuberoinfundibular neurons in female rats is
higher than it is in males because circulating levels of prolactin to
nically stimulate these neurons in the female. In female rats, quinelo
rane markedly lowered plasma concentrations of prolactin but failed to
alter DOPAC concentrations in the ME. Pretreatment of female rats wit
h prolactin antiserum induced hypoprolactinemia and reduced DOPAC conc
entrations in the ME; in these animals quinelorane increased ME DOPAC
concentrations. These results indicate that by acting on D2 receptors
quinelorane is able to stimulate tuberoinfundibular DA neurons in both
male and female rats, but in female rats the ability of quinelorane t
o reduce circulating levels of prolactin indirectly reduces the activi
ty of tuberoinfundibular DA neurons and thereby masks the stimulatory
action of this drug on these neurons.