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Distinct µ-opioid ensembles trigger positive and negative fentanyl reinforcement
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Distinct µ-opioid ensembles trigger positive and negative fentanyl reinforcement
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Distinct µ-opioid ensembles trigger positive and negative fentanyl reinforcement
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Journal Article
Distinct µ-opioid ensembles trigger positive and negative fentanyl reinforcement
2024
Overview
Fentanyl is a powerful painkiller that elicits euphoria and positive reinforcement
1
. Fentanyl also leads to dependence, defined by the aversive withdrawal syndrome, which fuels negative reinforcement
2
,
3
(that is, individuals retake the drug to avoid withdrawal). Positive and negative reinforcement maintain opioid consumption, which leads to addiction in one-fourth of users, the largest fraction for all addictive drugs
4
. Among the opioid receptors, µ-opioid receptors have a key role
5
, yet the induction loci of circuit adaptations that eventually lead to addiction remain unknown. Here we injected mice with fentanyl to acutely inhibit γ-aminobutyric acid-expressing neurons in the ventral tegmental area (VTA), causing disinhibition of dopamine neurons, which eventually increased dopamine in the nucleus accumbens. Knockdown of µ-opioid receptors in VTA abolished dopamine transients and positive reinforcement, but withdrawal remained unchanged. We identified neurons expressing µ-opioid receptors in the central amygdala (CeA) whose activity was enhanced during withdrawal. Knockdown of µ-opioid receptors in CeA eliminated aversive symptoms, suggesting that they mediate negative reinforcement. Thus, optogenetic stimulation caused place aversion, and mice readily learned to press a lever to pause optogenetic stimulation of CeA neurons that express µ-opioid receptors. Our study parses the neuronal populations that trigger positive and negative reinforcement in VTA and CeA, respectively. We lay out the circuit organization to develop interventions for reducing fentanyl addiction and facilitating rehabilitation.
Experiments using fentanyl treatment of mice show that µ-opioid receptors mediate positive reinforcement in the ventral tegmental area and negative reinforcement in central amygdala, thereby identifying the circuits that lead to opioid addiction.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 14/34
/ Amygdala
/ Analgesics, Opioid - administration & dosage
/ Analgesics, Opioid - pharmacology
/ Animals
/ Aversion
/ Brain
/ Central Amygdaloid Nucleus - cytology
/ Central Amygdaloid Nucleus - drug effects
/ Central Amygdaloid Nucleus - metabolism
/ Dopamine
/ Dopaminergic Neurons - drug effects
/ Dopaminergic Neurons - metabolism
/ Female
/ Fentanyl
/ Humanities and Social Sciences
/ Male
/ Mice
/ Neurons
/ Nucleus Accumbens - cytology
/ Nucleus Accumbens - drug effects
/ Nucleus Accumbens - metabolism
/ Opioid-Related Disorders - metabolism
/ Opioid-Related Disorders - pathology
/ Receptors, Opioid, mu - metabolism
/ Science
/ Substance Withdrawal Syndrome - metabolism
/ Substance Withdrawal Syndrome - pathology
/ Ventral Tegmental Area - cytology
/ Ventral Tegmental Area - drug effects
