Evidence map›Paper›PMID 40022640›Full record

ArticleWound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society

Buprenorphine blunts inflammatory response and wound progression after skin exposure to nitrogen mustard.

Jingbo Pang, Emma Santoro, Rita E Roberts, Jeanette Purcell, Jeffrey D Fortman, Timothy J Koh

Abstract read
In one paragraph

Article in Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Buprenorphine blunts inflammatory response and wound progression after skin exposure to nitrogen mustard.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

6 authors.

Jingbo PangCenter for Wound Healing and Tissue Regeneration, Department of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, Illinois, USA.ORCID 0000-0001-8325-8434
Emma SantoroBiologic Resources Laboratory, University of Illinois at Chicago, Chicago, Illinois, USA.
Rita E RobertsCenter for Wound Healing and Tissue Regeneration, Department of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, Illinois, USA.
Jeanette PurcellBiologic Resources Laboratory, University of Illinois at Chicago, Chicago, Illinois, USA.
Jeffrey D FortmanBiologic Resources Laboratory, University of Illinois at Chicago, Chicago, Illinois, USA.
Timothy J KohCenter for Wound Healing and Tissue Regeneration, Department of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, Illinois, USA.ORCID 0000-0001-6549-7060

Funding

Macrophage Phenotypes and Tissue RepairR35GM136228 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI TIMOTHY J KOH · 2020 to 2026
$3.7M
The Role of Macrophages in Vesicant Skin Injury and RepairR34AR081456 · NIAMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KOH, TIMOTHY J · 2023 to 2025
$711k
NIAMS NIH HHS R34 AR081456NIAMS NIH HHS R34GM136228NIGMS NIH HHS R35 GM136228
6 · The paper itself

Abstract

Opioid analgesics are often used to alleviate pain in rodent models of skin wound injury and repair. However, previous studies have demonstrated that opioids can alter the inflammatory response to injury and subsequent wound healing. The purpose of this study was to determine the impact of different formulations of buprenorphine on mouse behaviour, inflammatory response and wound progression following skin exposure to nitrogen mustard (NM). Administration of either short-acting or long-acting formulations of buprenorphine in conjunction with skin NM exposure resulted in body weight loss, reduced activity and behavioural changes. Both short-acting and long-acting formulations also dampened aspects of the inflammatory response to NM exposure, including reduced levels of the chemokines CCL3 and CXCL2 and reduced accumulation of pro-inflammatory macrophages. The diminished inflammatory response was associated with reduced skin injury assessed both externally and histologically. These results have important implications for the use of opioid analgesics in studies involving vesicant exposure as well as the potential for the use of opioids as a countermeasure after NM exposure.

Indexed as

Analgesics, OpioidBuprenorphineInflammationMechlorethamineSkinWound HealingAnimalsChemical Warfare AgentsDisease Models, AnimalMaleMiceMice, Inbred C57BLAnalgesics, OpioidBuprenorphineChemical Warfare AgentsMechlorethamineinflammationmouse modelopioid analgesicvesicant injury

Identifiers

PMID40022640
PMCPMC11871815

What OpenQuestion holds

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LicenceCC BY-NC
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.