Evidence map›Paper›PMID 42250290›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2026

Positive allosteric modulation of the delta opioid receptor attenuates depression-like and pain-like behaviors but does not promote convulsions.

Emily M Jutkiewicz, Benjamin A Palleiko, Isaac J Dripps, Kathryn E Livingston, Bernard P Roques, Benjamin M Clements, John R Traynor

Abstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2026. 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

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

7 authors.

Emily M JutkiewiczDepartment of Pharmacology, Edward F. Domino Research Center, University of Michigan, Ann Arbor, Michigan.
Benjamin A PalleikoDepartment of Pharmacology, Edward F. Domino Research Center, University of Michigan, Ann Arbor, Michigan.
Isaac J DrippsDepartment of Pharmacology, Edward F. Domino Research Center, University of Michigan, Ann Arbor, Michigan.
Kathryn E LivingstonDepartment of Pharmacology, Edward F. Domino Research Center, University of Michigan, Ann Arbor, Michigan.
Bernard P RoquesUnité de Technologies Chimiques et Biologiques pour la Santé, Université Paris Descartes, Paris, France.
Benjamin M ClementsDepartment of Pharmacology, Edward F. Domino Research Center, University of Michigan, Ann Arbor, Michigan.
John R TraynorDepartment of Pharmacology, Edward F. Domino Research Center, University of Michigan, Ann Arbor, Michigan; Department of Medicinal Chemistry, University of Michigan, Ann Arbor, Michigan. Electronic address: jtraynor@umich.edu.

Funding

INTERDEPARTMENTAL TRAINING IN PHARMACOLOGICAL SCIENCEST32GM007767 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ISOM, LORI L. · 1985 to 2019
$10.2M
Allosteric Modulation of the Mu-Opioid ReceptorR37DA039997 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TRAYNOR, JOHN R. · 2015 to 2024
$6.4M
Endogenous enkephalins and reward mechanismsR01DA042092 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JUTKIEWICZ, EMILY M · 2017 to 2021
$1.6M
CTSA Postdoctoral T32 at the University of MichiganT32TR004764 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI VICKI L ELLINGROD, Steven Edward Harte · 2024 to 2026
$1.4M
NCATS NIH HHS T32 TR004764NIDA NIH HHS R01 DA042092NIDA NIH HHS R37 DA039997NIGMS NIH HHS T32 GM007767
6 · The paper itself

Abstract

The delta opioid receptor (DOR) has been a focus of research for the treatment of depression and certain pain disorders. Unfortunately, clinical translation of delta opioid agonists to humans has proved challenging partly because of their propensity to cause convulsions at higher doses. The discovery that the DOR can be allosterically modulated has opened the possibility of developing compounds that may be able to produce some of the positive therapeutic effects, either as standalone treatments to enhance the action of endogenous opioid peptides or as sparing agents allowing the use of lower doses of DOR agonists, which could reduce the chance of inducing convulsions. BMS-986187 is a positive allosteric modulator of DOR. The behavioral effects of BMS-986187 related to depression and pain have not been investigated. In this study, we examined the impact of BMS-986187 on DOR-mediated antidepressant-like effects in the forced swim test, antinociceptive and antiallodynic actions and propensity to cause convulsions. BMS-986187 (1 mg/kg) showed antidepressant-like effects when administered alone, but did not produce convulsions. BMS-986187 (10 mg/kg) also enhanced the antinociceptive and antiallodynic effects of the standard DOR agonist SNC80, with only a very minor effect on SNC80-mediated convulsions. The results suggest the development of positive modulators of DOR for the management of pain and/or depression. SIGNIFICANCE STATEMENT: The delta opioid receptor (DOR) has been suggested as a target to treat depression and pain. However, agonists at this receptor can cause convulsions. This study demonstrates that a positive allosteric modulator of DOR administered alone reduces depression-like behaviors and, in combination with a DOR agonist, shows robust pain-relieving actions, without convulsive effects. This suggests a novel and safe treatment for depression and/or pain.

Indexed as

Behavior, AnimalDepressionPainReceptors, Opioid, deltaSeizuresAllosteric RegulationAnimalsAntidepressive AgentsBenzamidesMaleMiceXanthonesAntidepressive AgentsBenzamidesBMS-986187Receptors, Opioid, deltaXanthonesAllosteric modulationConvulsionsDelta opioid receptorDepressionPain

Identifiers

PMID42250290
PMCPMC13494217

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.