NPAS4 supports cocaine-conditioned cues in rodents by controlling the cell type-specific activation balance in the nucleus accumbens

Nat Commun. 2024 Aug 8;15(1):5971. doi: 10.1038/s41467-024-50099-1.

Abstract

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.

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors* / genetics
  • Basic Helix-Loop-Helix Transcription Factors* / metabolism
  • Cocaine* / pharmacology
  • Cues*
  • Drug-Seeking Behavior
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons* / drug effects
  • Neurons* / metabolism
  • Nucleus Accumbens* / drug effects
  • Nucleus Accumbens* / metabolism
  • Receptors, Dopamine D2 / metabolism

Substances

  • Cocaine
  • Basic Helix-Loop-Helix Transcription Factors
  • Npas4 protein, mouse
  • Receptors, Dopamine D2