Evidence map›Paper›PMID 41498917›Full record

ReviewDrugs2026

Biased Kappa-opioid Agonist Strategies in Pain Management: Approaches to Clinical Benefits with Reduced Adverse Effects.

Mellar P Davis, Boris Kiselev

Abstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Mellar P DavisDepartment of Supportive Oncology, Levine Cancer Institute, Morehead Medical Center, 1021 Morehead Medical Dr., Charlotte, NC, 28204, USA. Mellar.Davis@advocatehealth.org.ORCID http://orcid.org/0000-0002-7903-3993
Boris KiselevDepartment of Supportive Oncology, Levine Cancer Institute, Morehead Medical Center, 1021 Morehead Medical Dr., Charlotte, NC, 28204, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mu-opioid receptor (MOR) agonists remain the cornerstone of pain management but are limited by respiratory depression, tolerance, dependence, and mood disturbances. Kappa-opioid receptor (KOR) agonists offer complementary analgesic mechanisms with minimal abuse potential, yet clinical utility is restricted by dysphoria, sedation, and anxiety. This review critically evaluates emerging strategies that leverage both receptor systems through G-protein-biased KOR agonists and bifunctional KOR/MOR ligands. While preclinical evidence suggests that these approaches may provide additive analgesia with reduced adverse effects, significant challenges remain in translating these findings to clinical practice. The controversy surrounding G-protein bias measurement and the limited clinical data available highlight the need for cautious optimism regarding these novel therapeutic approaches.

Indexed as

Analgesics, OpioidPainPain ManagementReceptors, Opioid, kappaAnimalsHumansReceptors, Opioid, muAnalgesics, OpioidReceptors, Opioid, kappaReceptors, Opioid, mu

Identifiers

What OpenQuestion holds

Textmetadata
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.