Evidence map›Paper›PMID 39617202›Full record

ArticleOsteoarthritis and cartilage2025

Specialized pro-resolving mediator Maresin 1 attenuates pain in a mouse model of osteoarthritis.

Yu-Ru V Shih, Huchen Tao, Anna Gilpin, Yuan-Wen Lee, Sajeeshkumar Madhurakkat Perikamana, Shyni Varghese

Abstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Pro-resolving Annexin A1-derived peptide Ac2-26 reduces nociception and mitigates joint damage in experimental osteoarthritis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  3. Maresins.Biomolecules · 2026
    Review
  4. Review
  5. Article
  6. The research progress and potential applications ofThe British journal of nutrition · 2025
    Review
  7. Article
  8. 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

6 authors.

Yu-Ru V ShihDepartment of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: vernon.shih@duke.edu.
Huchen TaoDepartment of Mechanical Engineering and Materials Science, Duke University, Durham, NC 27710, USA. Electronic address: huchen.tao@duke.edu.
Anna GilpinDepartment of Biomedical Engineering, Duke University, Durham, NC 27710, USA. Electronic address: anna.gilpin@duke.edu.
Yuan-Wen LeeDepartment of Anesthesiology, Taipei Medical University Hospital, Taipei 11031, Taiwan; Department of Anesthesiology, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan. Electronic address: m102093020@tmu.edu.tw.
Sajeeshkumar Madhurakkat PerikamanaDepartment of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27710, USA. Electronic address: mp.sajeesh@duke.edu.
Shyni VargheseDepartment of Orthopaedic Surgery, Duke University School of Medicine, Durham, NC 27710, USA; Department of Mechanical Engineering and Materials Science, Duke University, Durham, NC 27710, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27710, USA. Electronic address: shyni.varghese@duke.edu.

Funding

Modulation of local adenosine signaling to attenuate fracture painR01AR079189 · NIAMS · DUKE UNIVERSITY · PI VARGHESE, SHYNI · 2021 to 2025
$2.8M
Molecular engineering of HA-based lubricants for articular cartilageR01AR082809 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Shyni Varghese, Stefan Zauscher · 2023 to 2026
$2.4M
NIAMS NIH HHS R01 AR079189NIAMS NIH HHS R01 AR082809
6 · The paper itself

Abstract

objectiveWe test whether the specialized pro-resolving molecule Maresin 1 (MaR1) attenuates nociceptive behaviors in mice with osteoarthritis-like pain.

designOsteoarthritis (OA)-like pain behavior was induced by intra-articular injection of monosodium iodoacetate (MIA) and treated with MaR1 (N=6) or vehicle (N=5) by intraperitoneal injection 8 weeks after injury. Mice without MIA injection were used as control (N=6). Nociceptive behaviors were examined by von Frey and dynamic weight bearing measurements. Calcitonin gene-related peptide (CGRP) expression and activated macrophages in the dorsal root ganglion (DRG) were examined by immunofluorescence staining. The inflammatory profile in circulation was assessed by cytokine array. Calcium imaging was performed to assess the in vitro functional response of DRG neurons from animals with OA-like pain behavior to MaR1 with or without RAR Related Orphan Receptor A (RORA) inverse agonist SR3335.

resultsMaR1 attenuated knee pain behavior in treated mice (N=6) compared to non-treated mice (N=5) as shown by increased paw withdrawal threshold with a mean difference of 112.2% (95% CI [49.79, 174.6], p=0.0784) at 4 h and 150.9% (95% CI [104.2, 197.5], p=0.0001) at 4 days post-MaR1 treatment, and increased weight bearing with a mean difference of 20.08% (95% CI [2.798, 37.37], p=0.0277) at 1 day post-MaR1 treatment. CGRP expression and activated macrophages were decreased in the DRG, and inflammatory cytokine levels in the circulation were attenuated. Calcium imaging showed MaR1 reduced the functional response of DRG neurons through RORA.

conclusionsOur results show that MaR1 reduces OA-like pain behavior in mice and could be a potential treatment for OA pain.

Indexed as

Arthritis, ExperimentalDocosahexaenoic AcidsOsteoarthritisOsteoarthritis, KneeAnimalsBehavior, AnimalCalcitonin Gene-Related PeptideDisease Models, AnimalGanglia, SpinalInjections, Intra-ArticularMacrophagesMaleMiceMice, Inbred C57BLPain Measurement7,14-dihydroxydocosa-4,8,10,12,16,19-hexaenoic acidCalcitonin Gene-Related PeptideDocosahexaenoic AcidsDorsal root ganglionInflammationMaresin 1Osteoarthritis painRORASpecialized pro-resolving mediators

Identifiers

PMID39617202
PMCPMC11842212

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Registered trials

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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.