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Curr Biol ; 33(13): 2761-2773.e8, 2023 07 10.
Artigo em Inglês | MEDLINE | ID: mdl-37379841

RESUMO

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.


Assuntos
Claustrum , Transtornos Relacionados ao Uso de Opioides , Camundongos , Humanos , Animais , Claustrum/fisiologia , Analgésicos Opioides/farmacologia , Gânglios da Base/fisiologia , Lobo Frontal , Neurônios/fisiologia , Fentanila/farmacologia
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