Circuits underlying memory and learning, including conditioned-incentive learning, habit learning, and declarative memory (reviewed in Vanderschuren and Everitt11), have been proposed to be involved in drug addiction. The effects of drugs on memory systems suggest ways that neutral stimuli can acquire reinforcing properties and motivational salience, that is, through conditioned-incentive learning. In research on relapse, it has been important to understand why drug-addicted subjects experience an intense desire for the drug when exposed to places where they have taken the drug, to persons with whom previous drug use occurred, and to paraphernalia used to administer the drug. This is clinically relevant because exposure to conditioned cues (stimuli associated with the drug) is a key contributor to relapse. Because DA is involved with prediction of reward (reviewed in Schultz9), we hypothesized that DA might underlie conditioned responses that trigger craving. Studies in laboratory animals support this hypothesis: when neutral stimuli are paired with a drug, they will, with repeated associations, acquire the ability to increase DA in the nucleus accumbens and dorsal striatum, becoming conditioned cues. Furthermore, these neurochemical responses are associated with drug-seeking behavior (reviewed in Vanderschuren and Everitt11). In human beings, PET studies with [11C]raclopride recently confirmed this hypothesis by showing that, in cocaine abusers, drug cues (cocaine-cue video of scenes of subjects taking cocaine) substantially increased DA in the dorsal striatum and that these increases were associated with cocaine craving.12,13 Because the dorsal striatum is implicated in habit learning, this association likely reflects the strengthening of habits as chronicity of addiction progresses. This suggests that a basic neurobiologic disruption in addiction might be a DA-triggered conditioned response that results in habits leading to compulsive drug consumption. It is likely that these conditioned responses reflect adaptations in corticostriatal glutamatergic pathways that regulate DA release (reviewed in Vanderschuren and Everitt11).