Nature Communications (Aug 2024)

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

  • Brandon W. Hughes,
  • Jessica L. Huebschman,
  • Evgeny Tsvetkov,
  • Benjamin M. Siemsen,
  • Kirsten K. Snyder,
  • Rose Marie Akiki,
  • Daniel J. Wood,
  • Rachel D. Penrod,
  • Michael D. Scofield,
  • Stefano Berto,
  • Makoto Taniguchi,
  • Christopher W. Cowan

DOI
https://doi.org/10.1038/s41467-024-50099-1
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 18

Abstract

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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.