Evidence map›Paper›PMID 31568781›Full record

ArticleEuropean journal of pharmacology2019

Nalbuphine, a kappa opioid receptor agonist and mu opioid receptor antagonist attenuates pruritus, decreases IL-31, and increases IL-10 in mice with contact dermatitis.

Saadet Inan, Alvaro Torres-Huerta, Liselotte E Jensen, Nae J Dun, Alan Cowan

Open access · greenAbstract read
In one paragraph

Article in European journal of pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 56 citations in OpenAlex.

  1. Trial
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  7. Article
  8. Opioid-Induced Pruritus: A Case Series on Novel Uses of Nalbuphine in the Emergency Department.Journal of the American College of Emergency Physicians open · 2025
    Article
  9. Review
  10. Review
  11. Article
  12. Article
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  17. International journal of molecular sciences · 2023
    Article
  18. Observational
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  20. Review
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

5 authors at 1 institution in 1 country.

Saadet InanCenter for Substance Abuse Research, Lewis Katz Medical School at Temple University, Philadelphia, PA, USA. Electronic address: sinan@temple.edu.
Alvaro Torres-HuertaDepartment of Microbiology and Immunology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Liselotte E JensenDepartment of Microbiology and Immunology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Nae J DunDepartment of Pharmacology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Alan CowanCenter for Substance Abuse Research, Lewis Katz Medical School at Temple University, Philadelphia, PA, USA; Department of Pharmacology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Temple University · US

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Anjali M Rajadhyaksha · 2000 to 2026
$34.6M
Interleukin-36 cytokines in antiviral immune responsesR01AI125111 · NIAID · TEMPLE UNIV OF THE COMMONWEALTH · PI JENSEN, LISELOTTE E · 2016 to 2020
$2.0M
NIAID NIH HHS R01 AI125111NIDA NIH HHS P30 DA013429
6 · The paper itself

Abstract

Chronic itch is one of the disturbing symptoms of inflammatory skin diseases. Kappa opioid receptor agonists are effective in suppressing scratching in mice against different pruritogens. Nalbuphine, a nonscheduled kappa opioid receptor agonist and mu opioid receptor antagonist, has been in clinical use for post-operative pain management since the 1980s and recently has been in clinical trials for chronic itch of prurigo nodularis (https://www.trevitherapeutics.com/nalbuphine). We studied whether nalbuphine is effective against chronic scratching induced by rostral neck application of 1-fluoro-2,4-dinitrobenzene (DNFB), an accepted mouse model of contact dermatitis to study pruritoceptive itch. Mice were treated once a week with either saline or nalbuphine 20 min before the third, fifth, seventh, and ninth sensitizations with DNFB and the number of scratching bouts was counted for 30 min. Skin samples from the neck of mice at week 4 were used to measure protein levels and mRNA expressions of chemokines and cytokines. Different sets of mice were used to study sedation and anhedonic-like behavior of nalbuphine. We found that: nalbuphine (a) antagonized scratching in a dose- and time-dependent manner without affecting locomotion, b) decreased IL-31, and increased anti-inflammatory IL-10, and c) induced more elevations in the levels of CCL2, CCL3, CCL12, CXCL1, CXCL2, CXCL9, CXCL10, IL-1β, IL-16, TIMP-1, M-CSF, TREM-1 and M1-type macrophages compared to saline. Increases in chemokines and cytokines and M1 macrophages by nalbuphine suggest an inflammatory phase of healing in damaged skin due to scratching. Our data indicate that nalbuphine is an effective antipruritic in murine model of pruritoceptive itch.

Indexed as

AnimalsChemokinesDermatitis, ContactInterleukin-10InterleukinsMacrophagesMaleMiceMonocytesNalbuphinePruritusReceptors, Opioid, kappaReceptors, Opioid, muChemokinesInterleukin-10interleukin-31, mouseInterleukinsNalbuphineReceptors, Opioid, kappaReceptors, Opioid, muChemokinesContact dermatitisCytokinesDNFBNalbuphinePruritus

Identifiers

PMID31568781
PMCPMC6913640
OpenAlexW2975335306

What OpenQuestion holds

Textmetadata
LicenceTDM
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.