Evidence map›Paper›PMID 35914624›Full record

ReviewNeuroscience and biobehavioral reviews2022

The opioid system in depression.

Luke A Jelen, James M Stone, Allan H Young, Mitul A Mehta

Open access · hybridAbstract readReview
In one paragraph

Review in Neuroscience and biobehavioral reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 5 pooled it
7.7field-weighted citation impact, top 1% of its field
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

54 citing papers in PubMed, 5 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Is the antidepressant efficacy of ketamine and esketamine mediated via opioid mechanisms?European psychiatry : the journal of the Association of European Psychiatrists · 2026
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  9. Structural basis of opioid receptor activation by PCP and ketamine.Nature structural & molecular biology · 2026
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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 at 3 institutions in 1 country.

Luke A JelenInstitute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; South London and Maudsley NHS Foundation Trust, London, United Kingdom. Electronic address: luke.jelen@kcl.ac.uk.
James M StoneDepartment of Neuroscience and Imaging, University of Sussex, United Kingdom.
Allan H YoungInstitute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; South London and Maudsley NHS Foundation Trust, London, United Kingdom.
Mitul A MehtaInstitute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
King's College London · GBSouth London and Maudsley NHS Foundation Trust · GBUniversity of Sussex · GB

Funding

CIHRDepartment of Health CRF-2016-10023Medical Research Council MR/R005885/1Medical Research Council MR/R005931/1Medical Research Council MR/S003444/1Medical Research Council MR/T028084/1Wellcome Trust 200102/Z/15/ZWellcome Trust 212952/Z/18/Z
6 · The paper itself

Abstract

Opioid receptors are widely distributed throughout the brain and play an essential role in modulating aspects of human mood, reward, and well-being. Accumulating evidence indicates the endogenous opioid system is dysregulated in depression and that pharmacological modulators of mu, delta, and kappa opioid receptors hold potential for the treatment of depression. Here we review animal and clinical data, highlighting evidence to support: dysregulation of the opioid system in depression, evidence for opioidergic modulation of behavioural processes and brain regions associated with depression, and evidence for opioidergic modulation in antidepressant responses. We evaluate clinical trials that have examined the safety and efficacy of opioidergic agents in depression and consider how the opioid system may be involved in the effects of other treatments, including ketamine, that are currently understood to exert antidepressant effects through non-opioidergic actions. Finally, we explore key neurochemical and molecular mechanisms underlying the potential therapeutic effects of opioid system engagement, that together provides a rationale for further investigation into this relevant target in the treatment of depression.

Indexed as

Analgesics, OpioidDepressionAnimalsAntidepressive AgentsHumansReceptors, OpioidReceptors, Opioid, kappaReceptors, Opioid, muAnalgesics, OpioidAntidepressive AgentsReceptors, OpioidReceptors, Opioid, kappaReceptors, Opioid, muDelta opioid receptor (DOR)DepressionKappa opioid receptor (KOR)Mu opioid receptor (MOR)Nociceptin opioid receptor (NOP)Opioid system

Identifiers

PMID35914624
PMCPMC10166717
OpenAlexW4288760145

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.