Evidence map›Paper›PMID 41372020›Full record

ArticleBritish journal of anaesthesia2026

Prostaglandins prevent long-lasting pain in a mouse model of chronic postsurgical pain.

Mohamad Karaky, Lucas V Lima, Anahita Oveisi, Francesca Montagna, Jeffrey S Mogil, Luda Diatchenko

Abstract read
In one paragraph

Article in British journal of anaesthesia, 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

6 authors.

Mohamad KarakyFaculty of Dental Medicine and Oral Health Sciences, Department of Anesthesia, Faculty of Medicine, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada.
Lucas V LimaFaculty of Dental Medicine and Oral Health Sciences, Department of Anesthesia, Faculty of Medicine, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada.
Anahita OveisiFaculty of Dental Medicine and Oral Health Sciences, Department of Anesthesia, Faculty of Medicine, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada.
Francesca MontagnaFaculty of Dental Medicine and Oral Health Sciences, Department of Anesthesia, Faculty of Medicine, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada.
Jeffrey S MogilFaculty of Dental Medicine and Oral Health Sciences, Department of Anesthesia, Faculty of Medicine, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada; Department of Psychology, Faculty of Science, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada.
Luda DiatchenkoFaculty of Dental Medicine and Oral Health Sciences, Department of Anesthesia, Faculty of Medicine, Alan Edwards Centre for Research on Pain, McGill University, Montreal, QC, Canada. Electronic address: luda.diatchenko@mcgill.ca.

Funding

Project-004U54DA049110 · NIDA · JOHNS HOPKINS UNIVERSITY · PI Martin Lindquist, TOR D. WAGER · 2019 to 2026
$14.7M
NIDA NIH HHS U54 DA049110
6 · The paper itself

Abstract

backgroundChronic postsurgical pain (CPSP) affects 5-85% of patients, depending on the surgery type, with minimal treatment options. A previous study showed that immune response inhibition by dexamethasone (DEXA) or NSAIDs in inflammatory pain assays in mice leads to pain prolongation, which can be reversed by injection of neutrophils or neutrophil-released S100A8/A9 proteins. Here we tested whether DEXA or NSAIDs similarly lead to prolonged pain in the mouse paw incisional assay, and if prostaglandin (PG) receptor agonists can prevent and resolve this pain through upregulation of S100A8/A9 in myeloid cells.

methodsCD-1 mice underwent plantar incision and were treated with DEXA, diclofenac, or saline. PG agonists (beraprost, treprostinil, or misoprostol) were administered postsurgery. Mechanical withdrawal thresholds were measured before and at multiple time points after incision injury. Neutrophils were depleted to confirm their involvement. Pathway validation was conducted using STAT3 and S100A8/A9 inhibitors and a STAT3 activator.

resultsSaline-treated mice recovered within 2 weeks, whereas DEXA-treated mice experienced prolonged hyperalgesia for >10 weeks. PG agonists both prevented and reversed the DEXA-induced hyperalgesia. Depletion of neutrophils in DEXA-treated mice impaired the effect of treprostinil. Inhibiting STAT3 or S100A8/A9 delayed recovery, whereas STAT3 activation mimicked treprostinil's effect. Diclofenac produced similar effects on pain duration as DEXA, also in a treprostinil-reversible manner.

conclusionsWe show that prostaglandin agonists can produce a surprising analgesic effect. Prostaglandin receptor agonists show promise in preventing and resolving CPSP by upregulating S100A8/A9 through the PKA-STAT3 pathway in innate immune cells, suggesting a new therapeutic approach for chronic postsurgical pain.

Indexed as

Chronic PainPostoperative PainProstaglandinsAnimalsAnti-Inflammatory Agents, Non-SteroidalCalgranulin ACalgranulin BDexamethasoneDiclofenacDisease Models, AnimalHyperalgesiaMaleMiceAnti-Inflammatory Agents, Non-SteroidalCalgranulin ACalgranulin BDexamethasoneDiclofenacProstaglandinsanti-inflammatory drugschronic postsurgical painneutrophilspain resolutionprostaglandins

Identifiers

PMID41372020
PMCPMC12881684

What Socratic 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 Socratic graph.