Publication | Open Access
Involvement of the Dorsal Striatum in Cue-Controlled Cocaine Seeking
389
Citations
69
References
2005
Year
Neutral Environmental StimuliBehavioral AddictionPersistent DrugCocaineSocial SciencesBehavioral SciencesDorsal StriatumPsychoactive DrugPsychiatryBehavioral NeuroscienceNeuropharmacologyReward SystemNervous SystemGlutamate TransmissionDopamineSubstance AbuseAddictionNeuroscienceMedicine
Neutral environmental cues can acquire motivational power and drive drug craving, but while nucleus accumbens dopamine does not mediate this conditioned reinforcement, dorsal striatal dopamine activity rises during cue‑driven cocaine seeking. The study aimed to assess the contribution of dorsal striatal dopamine and glutamate transmission to cue‑controlled cocaine seeking. Blocking dorsal striatal dopamine or AMPA/KA receptors markedly reduced cue‑controlled cocaine seeking, whereas NMDA blockade had no effect, indicating that dorsal striatal DA and AMPA/KA signaling are essential for this behavior and likely underlie its habitual component.
Through association with the interoceptive effects of drugs of abuse, neutral environmental stimuli can gain motivational properties themselves, becoming conditioned reinforcers that can evoke craving and relapse to drug seeking. Nucleus accumbens dopamine (DA) neurotransmission plays an important role in the reinforcing effect of cocaine itself, but, unlike nucleus accumbens glutamate, it seems not to mediate the conditioned reinforcing properties of cocaine-paired stimuli. Dorsal striatal DA transmission, in contrast, has been shown to be enhanced during cocaine seeking under a second-order schedule of reinforcement, which depends on the conditioned reinforcing properties of cocaine-associated stimuli. Therefore, the aim of the present study was to evaluate the role of DA and glutamate transmission in the dorsal striatum in cue-controlled cocaine seeking. Infusion of the DA receptor antagonist alpha-flupenthixol into the dorsal striatum decreased cocaine seeking under a second-order schedule of reinforcement. In addition, intradorsal striatal infusion of the AMPA/kainate (KA) receptor antagonist LY293558 (3SR, 4aRS, 6RS, 8aRS-6-[2-(iH-tetrazol-5-yl)ethyl]-1,2,3,4,4a,5,6,7,8,8a-decahydroiso-quinoline-3-carboxylic acid), but not the NMDA receptor antagonist AP-5, also decreased cue-controlled cocaine seeking. These data show that stimulation of DA and AMPA/KA receptors in the dorsal striatum is critical for well established drug seeking that depends on the reinforcing effects of cocaine-associated stimuli. In addition, given the importance of the dorsal striatum in stimulus-response habit learning, these data suggest that the habitual or compulsive quality of persistent drug seeking depends on dorsal striatal mechanisms.
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