Evidence map›Paper›PMID 34079544›Full record

ArticleFrontiers in immunology2021

Characteristics of Ang-(1-7)/Mas-Mediated Amelioration of Joint Inflammation and Cardiac Complications in Mice With Collagen-Induced Arthritis.

Zhongjie Wang, Wenhan Huang, Feifeng Ren, Lei Luo, Jun Zhou, Dongmei Huang, Mei Jiang, Huaan Du, Jinqi Fan, Lin Tang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 28 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

10 authors at 3 institutions in 1 country.

Zhongjie WangDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Wenhan HuangDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Feifeng RenDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Lei LuoDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jun ZhouDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Dongmei HuangDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Mei JiangDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Huaan DuDepartment of Cardiovascular, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jinqi FanDepartment of Cardiovascular, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Lin TangDepartment of Rheumatology and Immunology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Chongqing Medical University · CNDalian Medical University · CNSecond Affiliated Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Rheumatoid arthritis (RA) is a disabling disease with a high incidence that is regularly accompanied by cardiovascular complications. Several studies have suggested that renin-angiotensin-aldosterone system (RAAS) is closely associated with RA. The aim of this study was to investigate the mechanisms underlying Angiotensin-(1-7) [Ang-(1-7)] and its Mas receptor agonist (AVE0991) on joint inflammation and cardiac complications in a collagen-induced arthritis (CIA) model. Methods: Collagen type II was injected into DBA/1 mice to construct an arthritis model. CIA mice were treated with Ang-(1-7) (2.0 mg/kg intraperitoneally) and AVE0991 (3.0 mg/kg intraperitoneally). The serum levels of inflammatory cytokines [tumor necrosis factor-alpha (TNF-α), interleukin (IL)-1 β, IL-6, and C-reactive protein (CRP)] were determined by ELISA. The mitogen-activated protein kinase (MAPK) and nuclear factor-kappaB (NF- Results: Ang-(1-7) and AVE0991 reduced the levels of inflammatory cytokines and inhibited the MAPKs and NF- Conclusions: Ang-(1-7) alleviated joint damage caused by inflammation likely through the attenuation of NF-

Indexed as

Angiotensin IAnimalsArthritis, ExperimentalArthritis, RheumatoidBiomarkersBiopsyCytokinesDisease Models, AnimalDisease SusceptibilityFibrosisImmunohistochemistryMaleMicePeptide FragmentsRheumatic Heart DiseaseSignal TransductionAngiotensin Iangiotensin I (1-7)BiomarkersCytokinesPeptide Fragmentsangiotensin-(1–7)arthritiscardiac complicationsMas receptormice

Identifiers

PMID34079544
PMCPMC8165283
OpenAlexW3160074926

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.