Examining the role of dopamine D2 and D3 receptors in Pavlovian conditioned approach behaviors

•Sign-trackers attribute greater incentive salience to a lever-cue than goal-trackers.•Agonism or antagonism of both D2/D3 receptors disrupts sign- and goal-tracking.•Selective antagonism of D3 receptors does not affect sign- or goal-tracking.•D2 receptor signaling is critical for the expression of...

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Published in:Behavioural brain research Vol. 305; pp. 87 - 99
Main Authors: Fraser, Kurt M., Haight, Joshua L., Gardner, Eliot L., Flagel, Shelly B.
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 15-05-2016
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Summary:•Sign-trackers attribute greater incentive salience to a lever-cue than goal-trackers.•Agonism or antagonism of both D2/D3 receptors disrupts sign- and goal-tracking.•Selective antagonism of D3 receptors does not affect sign- or goal-tracking.•D2 receptor signaling is critical for the expression of sign- and goal-tracking. Elucidating the neurobiological mechanisms underlying individual differences in the extent to which reward cues acquire the ability to act as incentive stimuli may contribute to the development of successful treatments for addiction and related disorders. We used the sign-tracker/goal-tracker animal model to examine the role of dopamine D2 and D3 receptors in the propensity to attribute incentive salience to reward cues. Following Pavlovian training, wherein a discrete lever-cue was paired with food reward, rats were classified as sign- or goal-trackers based on the resultant conditioned response. We examined the effects of D2/D3 agonists, 7-OH-DPAT (0.01–0.32mg/kg) or pramipexole (0.032–0.32mg/kg), the D2/D3 antagonist raclopride (0.1mg/kg), and the selective D3 antagonist, SB-277011A (6 or 24mg/kg), on the expression of sign- and goal-tracking conditioned responses. The lever-cue acquired predictive value and elicited a conditioned response for sign- and goal-trackers, but only for sign-trackers did it also acquire incentive value. Following administration of either 7-OH-DPAT, pramipexole, or raclopride, the performance of the previously acquired conditioned response was attenuated for both sign- and goal-trackers. For sign-trackers, the D2/D3 agonist, 7-OH-DPAT, also attenuated the conditioned reinforcing properties of the lever-cue. The selective D3 antagonist did not affect either conditioned response. Alterations in D2/D3 receptor signaling, but not D3 signaling alone, transiently attenuate a previously acquired Pavlovian conditioned response, regardless of whether the response is a result of incentive motivational processes. These findings suggest activity at the dopamine D2 receptor is critical for a reward cue to maintain either its incentive or predictive qualities.
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ISSN:0166-4328
1872-7549
DOI:10.1016/j.bbr.2016.02.022