F. Chaperon et Mh. Thiebot, EFFECTS OF DOPAMINERGIC D3-RECEPTOR-PREFERRING LIGANDS ON THE ACQUISITION OF PLACE CONDITIONING IN RATS, Behavioural pharmacology, 7(1), 1996, pp. 105-109
The involvement of a D3 receptor-mediated control of dopamine (DA) fun
ction in motivational processes was investigated in rats by examining
the ability of two D3 receptor-preferring ligands (7-OH-DPAT and l-naf
adotride) to establish incentive learning and/or to modulate the reinf
orcing properties of food. This was done using a place conditioning pr
ocedure which consisted of repeated pairings of a drug (or food + drug
) with a single environmental cue, the door texture of an open field.
(+/-)7-OH-DPAT, a partially selective D3 receptor agonist, produced a
biphasic effect: the time spent on the drug-paired texture was reduced
by 4 and 8 mu g/kg and lengthened by 4.0 mg/kg, suggesting intrinsic
aversive and appetitive potentials, depending on the dose. The D3 rece
ptor preferring antagonist, l-nafadotride, did not establish place con
ditioning and seemed therefore devoid of intrinsic reinforcing propert
ies. However, when food was provided during the conditioning sessions
preceded by drug administration, a low dose of l-nafadotride (0.12 mg/
kg) but not higher doses, lengthened the time spent on the food-paired
texture. Although the preferential affinity ratio of the two ligands
in favour of the D3 vs. D2 subtype is low, these results suggest that
DA function in the structures involved in incentive learning could be
controlled through inhibitory D3 (or 'D2-like') receptor-mediated proc
esses. Conditioned place aversion would indicate an impaired DA transm
ission due to a selective stimulation of these receptors, whereas thei
r selective blockade would induce the inverse effect, providing that D
A release was sufficient (as during eating) in the pathways involved i
n reward-related processes. The reversal of the effects of the two com
pounds at larger doses would likely result from an interaction with ot
her subtypes of 'D2-like' receptors.