Evidence map›Paper›PMID 41129844›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2025

Effects of δ opioid receptor stimulation via SNC80 on conditioned reinforcing properties of a remifentanil-associated stimulus.

Stephen H Robertson, Gwendolyn E Burgess, Emily M Jutkiewicz, Kenner C Rice

Abstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Stephen H RobertsonPsychology Department, Susquehanna University, Selinsgrove, Pennsylvania; Department of Pharmacology, University of Michigan, Ann Arbor, Michigan. Electronic address: robertsons@susqu.edu.
Gwendolyn E BurgessDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan.
Emily M JutkiewiczDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan.
Kenner C RiceMolecular Targets and Medications Discovery Branch, Drug Design and Synthesis Section, National Institute on Drug Abuse, Bethesda, Maryland.

Funding

POSTDOCTORAL TRAINING IN THE BIOLOGY OF DRUG ABUSET32DA007268 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TRAYNOR, JOHN R. · 1991 to 2021
$6.7M
NIDA Training Program in Neuroscience-Administrative SupplementT32DA007281 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Shelly Beth Flagel · 1995 to 2026
$5.7M
Endogenous enkephalins and reward mechanismsR01DA042092 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JUTKIEWICZ, EMILY M · 2017 to 2021
$1.6M
Opioidergic mechanisms underlying cocaine conditioned reinforcementF31DA053697 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RYSZTAK, LAUREN GRACE · 2021 to 2023
$97k
NIDA NIH HHS F31 DA053697NIDA NIH HHS R01 DA042092NIDA NIH HHS T32 DA007268NIDA NIH HHS T32 DA007281
6 · The paper itself

Abstract

Substance use disorder is associated with a high rate of relapse driven by the rewarding and motivational properties of drug-associated stimuli. We examined the extent to which the δ opioid receptor (DOR) mediated the conditioned reinforcing properties of drug-associated stimuli across 4 experiments and 2 operant procedures in Sprague-Dawley rats. In experiment 1, we assessed the extent to which SNC80 (DOR agonist) altered responding during extinction in a remifentanil self-administration procedure. In experiment 2, we assessed the extent to which SNC80 altered responding for a remifentanil-associated stimulus in the new response acquisition procedure. In experiment 3, we assessed the extent to which the effects of SNC80 were altered in standard versus enhanced stimulus control conditions in the new response acquisition procedure. In experiment 4, we assessed the extent to which naltrindole (DOR antagonist) was able to block SNC80-induced alterations in responding for a remifentanil-associated stimulus in the new response acquisition procedure. In experiment 5, we assessed the extent to which pretreatments of SNC80 altered Pavlovian conditioning in the new response acquisition procedure. These experiments support the role of the DOR system in mediating the rewarding properties of drug-associated stimuli, such that SNC80 dose-dependently enhanced responding for a remifentanil-associated stimulus across self-administration and new response acquisition procedures. These effects were blocked by naltrindole, demonstrating that these are DOR-mediated effects. DORs may represent a promising target to address relapse. SIGNIFICANCE STATEMENT: Conditioned reinforcing effects of an opioid-associated cue were enhanced following stimulation of δ opioid receptors (DORs), and this effect was blocked via DOR antagonism, which suggests the role of DORs in mediating drug-associated conditioned reinforcement.

Indexed as

BenzamidesPiperazinesReceptors, Opioid, deltaReinforcement, PsychologyRemifentanilAnalgesics, OpioidAnimalsConditioning, ClassicalConditioning, OperantMaleNaltrexoneNarcotic AntagonistsRatsRats, Sprague-DawleySelf Administration4-(alpha-(4-allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl)-N,N-diethylbenzamideAnalgesics, OpioidBenzamidesNaltrexonenaltrindoleNarcotic AntagonistsPiperazinesReceptors, Opioid, deltaRemifentanilConditioned reinforcementNew response acquisitionRemifentanilSelf-administrationSNC80δ opioid receptor

Identifiers

PMID41129844
PMCPMC12799568

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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.