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An opioid-gated thalamoaccumbal circuit for the suppression of reward seeking in mice

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Listed:
  • Kelsey M. Vollmer

    (Medical University of South Carolina)

  • Lisa M. Green

    (Medical University of South Carolina)

  • Roger I. Grant

    (Medical University of South Carolina)

  • Kion T. Winston

    (Medical University of South Carolina)

  • Elizabeth M. Doncheck

    (Medical University of South Carolina)

  • Christopher W. Bowen

    (Medical University of South Carolina)

  • Jacqueline E. Paniccia

    (Medical University of South Carolina
    Medical University of South Carolina)

  • Rachel E. Clarke

    (Medical University of South Carolina
    Medical University of South Carolina)

  • Annika Tiller

    (Medical University of South Carolina)

  • Preston N. Siegler

    (Medical University of South Carolina)

  • Bogdan Bordieanu

    (Medical University of South Carolina)

  • Benjamin M. Siemsen

    (Medical University of South Carolina)

  • Adam R. Denton

    (Medical University of South Carolina
    Medical University of South Carolina)

  • Annaka M. Westphal

    (Medical University of South Carolina)

  • Thomas C. Jhou

    (Medical University of South Carolina)

  • Jennifer A. Rinker

    (Medical University of South Carolina)

  • Jacqueline F. McGinty

    (Medical University of South Carolina)

  • Michael D. Scofield

    (Medical University of South Carolina)

  • James M. Otis

    (Medical University of South Carolina
    Medical University of South Carolina)

Abstract

Suppression of dangerous or inappropriate reward-motivated behaviors is critical for survival, whereas therapeutic or recreational opioid use can unleash detrimental behavioral actions and addiction. Nevertheless, the neuronal systems that suppress maladaptive motivated behaviors remain unclear, and whether opioids disengage those systems is unknown. In a mouse model using two-photon calcium imaging in vivo, we identify paraventricular thalamostriatal neuronal ensembles that are inhibited upon sucrose self-administration and seeking, yet these neurons are tonically active when behavior is suppressed by a fear-provoking predator odor, a pharmacological stressor, or inhibitory learning. Electrophysiological, optogenetic, and chemogenetic experiments reveal that thalamostriatal neurons innervate accumbal parvalbumin interneurons through synapses enriched with calcium permeable AMPA receptors, and activity within this circuit is necessary and sufficient for the suppression of sucrose seeking regardless of the behavioral suppressor administered. Furthermore, systemic or intra-accumbal opioid injections rapidly dysregulate thalamostriatal ensemble dynamics, weaken thalamostriatal synaptic innervation of downstream neurons, and unleash reward-seeking behaviors in a manner that is reversed by genetic deletion of thalamic µ-opioid receptors. Overall, our findings reveal a thalamostriatal to parvalbumin interneuron circuit that is both required for the suppression of reward seeking and rapidly disengaged by opioids.

Suggested Citation

  • Kelsey M. Vollmer & Lisa M. Green & Roger I. Grant & Kion T. Winston & Elizabeth M. Doncheck & Christopher W. Bowen & Jacqueline E. Paniccia & Rachel E. Clarke & Annika Tiller & Preston N. Siegler & B, 2022. "An opioid-gated thalamoaccumbal circuit for the suppression of reward seeking in mice," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-34517-w
    DOI: 10.1038/s41467-022-34517-w
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    2. Masashi Hasegawa & Ziyan Huang & Ricardo Paricio-Montesinos & Jan Gründemann, 2024. "Network state changes in sensory thalamus represent learned outcomes," Nature Communications, Nature, vol. 15(1), pages 1-14, December.

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