Nucleus Accumbens D2/3 Receptors Predict Trait Impulsivity and Cocaine Reinforcement

Nucleus Accumbens D2/3 Receptors Predict Trait Impulsivity and Cocaine Reinforcement

2007 March 2; 315(5816): 1267–1270 | Jeffrey W. Dalley, Tim D. Fryer, Laurent Brichard, Emma S. J. Robinson, David E. H. Theobald, Kristjan Lääne, Yolanda Peña, Emily R. Murphy, Yasmeene Shah, Katrin Probst, Irina Abakumova, Franklin I. Aigbirhio, Hugh K. Richards, Young Hong, Jean-Claude Baron, Barry J. Everitt, Trevor W. Robbins
The study investigates the relationship between trait impulsivity and cocaine reinforcement in rats, focusing on the role of D2/3 receptors in the nucleus accumbens. Researchers used positron emission tomography (PET) to measure D2/3 receptor availability in the ventral and dorsolateral striatum of cocaine-naïve rats. They found that high-impulsive rats showed significantly reduced D2/3 receptor availability in the ventral striatum compared to non-impulsive rats, with no difference in DA release. This reduction was independent of DA release and was associated with increased rates of intravenous cocaine self-administration. The study also found that prolonged cocaine exposure and subsequent withdrawal in high-impulsive rats led to a selective normalization of premature responding on a sustained visual attention task, suggesting that trait impulsivity is a drug-vulnerable phenotype. These findings highlight the potential involvement of D2-like DA receptors in the development of cocaine addiction and suggest that reduced D2/3 receptor availability may be a predisposing neurobiological trait.The study investigates the relationship between trait impulsivity and cocaine reinforcement in rats, focusing on the role of D2/3 receptors in the nucleus accumbens. Researchers used positron emission tomography (PET) to measure D2/3 receptor availability in the ventral and dorsolateral striatum of cocaine-naïve rats. They found that high-impulsive rats showed significantly reduced D2/3 receptor availability in the ventral striatum compared to non-impulsive rats, with no difference in DA release. This reduction was independent of DA release and was associated with increased rates of intravenous cocaine self-administration. The study also found that prolonged cocaine exposure and subsequent withdrawal in high-impulsive rats led to a selective normalization of premature responding on a sustained visual attention task, suggesting that trait impulsivity is a drug-vulnerable phenotype. These findings highlight the potential involvement of D2-like DA receptors in the development of cocaine addiction and suggest that reduced D2/3 receptor availability may be a predisposing neurobiological trait.
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Understanding Nucleus Accumbens D2%2F3 Receptors Predict Trait Impulsivity and Cocaine Reinforcement