Evidence map›Paper›PMID 38853878›Full record

ArticlebioRxiv : the preprint server for biology2024

Generalized cue reactivity in dopamine neurons after opioids.

Collin M Lehmann, Nora E Miller, Varun S Nair, Kauê M Costa, Geoffrey Schoenbaum, Khaled Moussawi

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Collin M LehmannDepartment of Psychiatry, University of Pittsburgh; Pittsburgh, 15219, USA.
Nora E MillerDepartment of Psychiatry, University of Pittsburgh; Pittsburgh, 15219, USA.
Varun S NairDepartment of Psychiatry, University of Pittsburgh; Pittsburgh, 15219, USA.
Kauê M CostaDepartment of Psychology, University of Alabama at Birmingham; Birmingham, 35233, USA.
Geoffrey SchoenbaumNational Institute on Drug Abuse, National Institutes of Health; Baltimore, 21224, USA.
Khaled MoussawiDepartment of Psychiatry, University of Pittsburgh; Pittsburgh, 15219, USA.

Funding

Associative learning, decision-making, and addictionZIADA000587 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI SCHOENBAUM, GEOFFREY · 2012 to 2025
$47.7M
Limbic Pallidum DBS for the treatment of severe alcohol use disorderUG3AA030505 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI COFFMAN, BRIAN A, GONZALEZ-MARTINEZ, JORGE ALVARO · 2022 to 2023
$1.4M
TMS effects on circuit plasticity and drug seeking in mice - Diversity SupplementR00DA048085 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MOUSSAWI, KHALED · 2021 to 2023
$930k
Information encoding by spatiotemporal patterns of dopamine releaseR00DA055641 · NIDA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kauê Machado Costa · 2024 to 2026
$747k
NIAAA NIH HHS UG3 AA030505NIDA NIH HHS R00 DA048085NIDA NIH HHS R00 DA055641
6 · The paper itself

Abstract

Cue reactivity is the maladaptive neurobiological and behavioral response upon exposure to drug cues and is a major driver of relapse. The leading hypothesis is that dopamine release by addictive drugs represents a persistently positive reward prediction error that causes runaway enhancement of dopamine responses to drug cues, leading to their pathological overvaluation compared to non-drug reward alternatives. However, this hypothesis has not been directly tested. Here we developed Pavlovian and operant procedures to measure firing responses, within the same dopamine neurons, to drug versus natural reward cues, which we found to be similarly enhanced compared to cues predicting natural rewards in drug-naïve controls. This enhancement was associated with increased behavioral reactivity to the drug cue, suggesting that dopamine release is still critical to cue reactivity, albeit not as previously hypothesized. These results challenge the prevailing hypothesis of cue reactivity, warranting new models of dopaminergic function in drug addiction, and provide critical insights into the neurobiology of cue reactivity with potential implications for relapse prevention.

Identifiers

PMID38853878
PMCPMC11160774

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.