Abstract
The synthetic opioid fentanyl is a major contributor to the current opioid addiction crisis. We report that claustral neurons projecting to the frontal cortex limit oral fentanyl self-administration in mice. We found that fentanyl transcriptionally activates frontal-projecting claustrum neurons. These neurons also exhibit a unique suppression of Ca2+ activity upon initiation of bouts of fentanyl consumption. Optogenetic stimulation of frontal-projecting claustral neurons, intervening in this suppression, decreased bouts of fentanyl consumption. In contrast, constitutive inhibition of frontal-projecting claustral neurons in the context of a novel, group-housed self-administration procedure increased fentanyl bout consumption. This same manipulation also sensitized conditioned-place preference for fentanyl and enhanced the representation of fentanyl experience in the frontal cortex. Together, our results indicate that claustrum neurons exert inhibitory control over frontal cortical neurons to restrict oral fentanyl intake. Upregulation of activity in the claustro-frontal projection may be a promising strategy for reducing human opioid addiction.
| Original language | English |
|---|---|
| Pages (from-to) | 2761-2773.e8 |
| Journal | Current Biology |
| Volume | 33 |
| Issue number | 13 |
| DOIs | |
| State | Published - 10 Jul 2023 |
Bibliographical note
Publisher Copyright:© 2023 The Author(s)
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This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- anterior cingulate cortex
- claustrum
- conditioned-place preference
- constitutive silencing
- fentanyl
- home-cage behavior
- neuropixels
- opioids
- optogenetics
- orbitofrontal cortex
- photometry
- self-administration
- transcriptomics
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