Evidence map›Paper›PMID 39370677›Full record

ArticleThe American journal of sports medicine2024

Mast Cells Mediate Acute Inflammatory Responses After Glenoid Labral Tears and Can Be Inhibited With Cromolyn in a Rat Model.

Cynthia M Co, Bhavya Vaish, Le Q Hoang, Tam Nguyen, Joseph Borrelli, Peter J Millett, Liping Tang

Abstract read
In one paragraph

Article in The American journal of sports medicine, 2024. 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

7 authors.

Cynthia M CoDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, USA.
Bhavya VaishDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, USA.
Le Q HoangDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, USA.ORCID 0000-0002-8072-8477
Tam NguyenDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, USA.
Joseph BorrelliDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, USA.
Peter J MillettDepartment of Orthopedic Surgery, The Steadman Clinic, Vail, Colorado, USA.ORCID 0000-0002-8298-3746
Liping TangDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, USA.ORCID 0000-0002-3393-7073

Funding

Biomolecule releasing adhesive for cell-mediated labral repairR01AR081979 · NIAMS · UNIVERSITY OF TEXAS ARLINGTON · PI Liping Tang · 2023 to 2026
$1.6M
NIAMS NIH HHS R01 AR081979
6 · The paper itself

Abstract

backgroundInjuries to the glenoid labrum have been recognized as a source of joint pain and discomfort, which may be associated with the inflammatory responses that lead to the deterioration of labral tissue. However, it is unclear whether the torn labrum prompts mast cell (MC) activation, resulting in synovial inflammatory responses that lead to labral tissue degeneration. PURPOSE: To determine the potential influence of activated MC on synovial inflammatory responses and subsequent labral tissue degeneration and shoulder function deterioration in a rat model by monitoring MC behavior and sequential inflammatory responses within the synovial tissue and labral tissue after injury, suture repair, and MC stabilizer administration. STUDY

designControlled laboratory study.

methodsAnteroinferior glenoid labral tears were generated in the right shoulder of rats (n = 20) and repaired using a tunneled suture technique. Synovial tissue inflammatory responses were modulated in some rats with intraperitoneal administration of an MC stabilizer-cromolyn (n = 10). At weeks 1 and 3, MC activation, synovial inflammatory responses, and labral degeneration were histologically evaluated. Simultaneously, gait analysis was performed before and after surgical repair to assess the worsening of the shoulder function after the injury and treatment.

resultsResident MC degranulation after labral injury (50.48% ± 8.23% activated at week 1) contributed to the initiation of synovial tissue inflammatory cell recruitment, inflammatory product release, matrix metalloproteinase-13, and subsequent labral tissue extracellular matrix degeneration. The administration of cromolyn, an MC stabilizer, was found to significantly diminish injury-mediated inflammatory responses (inflammatory cell infiltration and subsequent proinflammatory product secretion) and improve shoulder functional recovery.

conclusionMC activation is responsible for labral tear-associated synovial inflammation and labral degeneration. The administration of cromolyn can significantly diminish the cascade of inflammatory reactions after labral injury. CLINICAL RELEVANCE: Our findings support the concept that MC stabilizers may be used as a complementary therapeutic option in the treatment and repair of labral tears.

Indexed as

Cromolyn SodiumDisease Models, AnimalMast CellsRats, Sprague-DawleyShoulder InjuriesAnimalsInflammationMaleRatsShoulder JointCromolyn Sodiumcromolynglenoidlabrummast cellssynovium

Identifiers

PMID39370677
PMCPMC11542330

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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.