Evidence map›Paper›PMID 37973536›Full record

ArticleRMD open2023

New animal model of chronic gout reproduces pathological features of the disease in humans.

Jiwei Wang, Peiqi Hao, Xianrun Sun, Richard Ward, Tao Tang, Xi Chen, Yihong Liu, Guancong Luo, Yang Yang, Cheng Xiang and 2 more

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2023. 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
1.4field-weighted citation impact, top 19% 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.

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, 7 citations in OpenAlex.

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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

12 authors at 2 institutions in 2 countries.

Jiwei WangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Peiqi HaoFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Xianrun SunDepartment of Orthopedic Surgery, Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.
Richard WardCentre for Translational Pharmacology, Institute of Molecular Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Tao TangMedical School, Kunming University of Science and Technology, Kunming, Yunnan, China.
Xi ChenFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Yihong LiuFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Guancong LuoFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Yang YangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Cheng XiangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Su AnFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China tianruixu@kust.edu.cn aslxj@mail.ustc.edu.cn.
Tian-Rui XuFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China tianruixu@kust.edu.cn aslxj@mail.ustc.edu.cn.ORCID 0000-0002-2416-2149
Kunming University of Science and Technology · CNUniversity of Glasgow · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesGout, as the most prevalent form of inflammatory arthritis, necessitates the use of animal models to investigate the molecular mechanisms involved in its development. Therefore, our objective was to develop a novel chronic mouse model of gout that more closely mimics the progression of gout in humans.

methodsA novel chronic mouse model of gout was established by a simple method, which does not require high technical proficiency, predominantly involves daily intraperitoneal injections of potassium oxonate for approximately 4 months, combined with a high fat-diet and injections of acetic acid into the hind paws to facilitate the formation of monosodium urate (MSU). Arthritis scores and paw oedema were assessed, behavioural tests were conducted, and histopathological and imaging evaluations of the arthritic paw joints were performed.

resultsAfter 4 months of induction, mice in the model group exhibited noticeable increases in arthritis severity, joint and cartilage damage, as well as bone erosion. Gomori's methenamine silver stain revealed the presence of MSU crystal deposition or tophi in the paw joints or ankle joints of up to 37.9% of the model mice (11 out of 29 mice). Moreover, treatment with benzbromarone effectively prevented the further development of gout or tophi formation in model mice.

conclusionsOur model more accurately replicates the pathological features of gouty arthritis compared with gout induced by MSU crystal injections. Therefore, it is particularly suitable for further investigations into the pathogenesis of gout and also serves as a valuable platform for screening potential antigout agents.

Indexed as

Arthritis, GoutyGoutAnimalsDisease Models, AnimalGout SuppressantsHumansMiceUric AcidGout SuppressantsUric AcidAntirheumatic AgentsArthritis, ExperimentalGout

Identifiers

PMID37973536
PMCPMC10660916
OpenAlexW4388743557

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.