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Generalized cue reactivity in rat dopamine neurons after opioids

Author

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  • Collin M. Lehmann

    (University of Pittsburgh)

  • Nora E. Miller

    (University of Pittsburgh)

  • Varun S. Nair

    (University of Pittsburgh)

  • Kauê M. Costa

    (University of Alabama at Birmingham)

  • Geoffrey Schoenbaum

    (National Institutes of Health)

  • Khaled Moussawi

    (University of Pittsburgh
    University of California San Francisco)

Abstract

Cue reactivity is the maladaptive neurobiological and behavioral response upon exposure to drug cues and is a major driver of relapse. A widely accepted assumption is that drugs of abuse result in disparate dopamine responses to cues that predict drug vs. natural rewards. The leading hypothesis is that drug-induced dopamine release represents a persistently positive reward prediction error that causes runaway enhancement of dopamine responses to drug cues, leading to their pathological overvaluation. However, this hypothesis has not been directly tested. Here, we develop Pavlovian and operant procedures in male rats to measure firing responses within the same dopamine neurons to drug versus natural reward cues, which we find to be similarly enhanced compared to cues predicting natural rewards in drug-naive controls. This enhancement is associated with increased behavioral reactivity to the drug cue, suggesting that dopamine neuronal activity may still be relevant to cue reactivity, albeit not as previously hypothesized. These results challenge the prevailing hypothesis of cue reactivity, warranting revised models of dopaminergic function in opioid addiction, and provide insights into the neurobiology of cue reactivity with potential implications for relapse prevention.

Suggested Citation

  • Collin M. Lehmann & Nora E. Miller & Varun S. Nair & Kauê M. Costa & Geoffrey Schoenbaum & Khaled Moussawi, 2025. "Generalized cue reactivity in rat dopamine neurons after opioids," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55504-3
    DOI: 10.1038/s41467-024-55504-3
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