Evidence map›Paper›PMID 27209322›Full record

ArticleArthritis research & therapy2016

Monosodium urate crystals induce oxidative stress in human synoviocytes.

Yessica Zamudio-Cuevas, Karina Martínez-Flores, Javier Fernández-Torres, Yahir A Loissell-Baltazar, Daniel Medina-Luna, Ambar López-Macay, Javier Camacho-Galindo, Cristina Hernández-Díaz, Mónica G Santamaría-Olmedo, Edgar Oliver López-Villegas and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04012294 (Effects of Allopurinol on Inflammatory Markers and Morphostructural Changes Evidenced by Musculoskeletal Ultrasound in Individuals With Asymptomatic Hyperuricemia. A Proof of Concept), which is not on this map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.4field-weighted citation impact, top 8% 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.

NCT04012294 phase3unknown statusnot on this mapstarted 2019, after this paper: background citation

Effects of Allopurinol on Inflammatory Markers and Morphostructural Changes Evidenced by Musculoskeletal Ultrasound in Individuals With Asymptomatic Hyperuricemia. A Proof of Concept

TypeinterventionalSponsorInstituto Nacional de Cardiologia Ignacio ChavezRan2019 to 2021Enrolled200ConditionsMusculoskeletal Degeneration, Inflammation, HyperuricemiaArmsAllopurinol Pill
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Prooxidant effect of uric acid on human leukocytic DNA: An in vitro and ex vivo study.Turkish journal of biology = Turk biyoloji dergisi · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. A review on benefits of quercetin in hyperuricemia and gouty arthritis.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Review
  20. 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

16 authors at 3 institutions in 2 countries.

Yessica Zamudio-CuevasLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Karina Martínez-FloresLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Javier Fernández-TorresLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Yahir A Loissell-BaltazarLaboratorio de Microbiología Molecular, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas (ENCB), Instituto Politécnico Nacional (IPN), Prolongación de Carpio y Plan de Ayala S/N Col. Casco de Santo Tomas, Miguel Hidalgo, 11340, Mexico City, Mexico.
Daniel Medina-LunaLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Ambar López-MacayLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Javier Camacho-GalindoLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Cristina Hernández-DíazLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Mónica G Santamaría-OlmedoLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Edgar Oliver López-VillegasLaboratorio Central de Microscopía, Departamento de Investigación, ENCB, IPN, Prolongación de Carpio y Plan de Ayala S/N Col. Santo Tomás, Miguel Hidalgo, 11340, Mexico City, Mexico.
Francesca OlivieroRheumatology Unit, Department of Medicine-DIMED, University of Padova, Via Giustiniani, 2, Padova, 35128, Italy.
Anna ScanuRheumatology Unit, Department of Medicine-DIMED, University of Padova, Via Giustiniani, 2, Padova, 35128, Italy.
Jorge Francisco Cerna-CortésLaboratorio de Microbiología Molecular, Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas (ENCB), Instituto Politécnico Nacional (IPN), Prolongación de Carpio y Plan de Ayala S/N Col. Casco de Santo Tomas, Miguel Hidalgo, 11340, Mexico City, Mexico.
Marwin GutierrezLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Carlos PinedaLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico.
Alberto López-ReyesLaboratorio de Líquido Sinovial, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra", Calzada México-Xochimilco 289, Tlalpan, 14389, Mexico City, Mexico. allorey@yahoo.com.
Instituto Nacional de Rehabilitación · MXInstituto Politécnico Nacional · MXUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGout is the most common inflammatory arthropathy of metabolic origin and it is characterized by intense inflammation, the underlying mechanisms of which are unknown. The aim of this study was to evaluate the oxidative stress in human fibroblast-like synoviocytes (FLS) exposed to monosodium urate (MSU) crystals, which trigger an inflammatory process.

methodsHuman FLS isolated from synovial tissue explants were stimulated with MSU crystals (75 μg/mL) for 24 h. Cellular viability was evaluated by crystal violet staining, apoptosis was assessed using Annexin V, and the cellular content of reactive oxygen species (ROS) and nitrogen species (RNS) (O2 (-), H2O2, NO) was assessed with image-based cytometry and fluorometric methods. In order to determine protein oxidation levels, protein carbonyls were detected through oxyblot analysis, and cell ultrastructural changes were assessed by transmission electron microscopy.

resultsThe viability of FLS exposed to MSU crystals decreased by 30 % (P < 0.05), while apoptosis increased by 42 % (P = 0.01). FLS stimulated with MSU crystals exhibited a 2.1-fold increase in H2O2 content and a 1.5-fold increase in O2 (-) and NO levels. Oxyblots revealed that the spots obtained from FLS protein lysates exposed to MSU crystals exhibited protein carbonyl immunoreactivity, which reflects the presence of oxidatively modified proteins. Concomitantly, MSU crystals triggered the induction of changes in the morphostructure of FLS, such as the thickening and discontinuity of the endoplasmic reticulum, and the formation of vacuoles and misfolded glycoproteins.

conclusionsOur results prove that MSU crystals induce the release of ROS and RNS in FLS, subsequently oxidizing proteins and altering the cellular oxidative state of the endoplasmic reticulum, which results in FLS apoptosis.

Indexed as

ApoptosisBlotting, WesternCells, CulturedCell SurvivalFibroblastsFlow CytometryFluorescent Antibody TechniqueGoutHumansMicroscopy, Electron, TransmissionOxidative StressReactive Nitrogen SpeciesReactive Oxygen SpeciesReal-Time Polymerase Chain ReactionSynoviocytesUric AcidReactive Nitrogen SpeciesReactive Oxygen SpeciesUric AcidGoutMonosodium urate crystalsOxidative stressSynoviocytes

Identifiers

PMID27209322
PMCPMC4875700
OpenAlexW2399646749

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.