Nature Communications · 2024 · 17 citations · 78 references
MedicineNeurobiologyNeuroscienceBehavioral NeurobiologyBehavioral NeuroscienceMolecular NeuroscienceAddictionAddiction NeurobiologyConditioned Place PreferenceDrug DependenceReward PathwaysSynaptic TransmissionMedium Spiny Neuron OrganizationMedium Spiny NeuronsMesolimbic Reward PathwayNeurobiology Of DependenceNeurobiology Of Stimulant AddictionNeurocircuitry Of CravingRelapse NeurobiologyRelapse Triggers
Powerful associations that link drugs of abuse with cues in the drug-paired environment often serve as prepotent relapse triggers. Drug-associated contexts and cues activate ensembles of nucleus accumbens (NAc) neurons, including D1-class medium spiny neurons (MSNs) that typically promote, and D2-class MSNs that typically oppose, drug seeking. We found that in mice, cocaine conditioning upregulated transiently the activity-regulated transcription factor, Neuronal PAS Domain Protein 4 (NPAS4), in a small subset of NAc neurons. The NPAS4+ NAc ensemble was required for cocaine conditioned place preference. We also observed that NPAS4 functions within NAc D2-, but not D1-, MSNs to support cocaine-context associations and cue-induced cocaine, but not sucrose, seeking. Together, our data show that the NPAS4+ ensemble of NAc neurons is essential for cocaine-context associations in mice, and that NPAS4 itself functions in NAc D2-MSNs to support cocaine-context associations by suppressing drug-induced counteradaptations that oppose relapse-related behaviour.
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