Evidence map›Paper›PMID 36496970›Full record

ArticleCells2022

The Therapeutic Effect of Phosphopeptide P140 Attenuates Inflammation Induced by Uric Acid Crystals in Gout Arthritis Mouse Model.

Izabela Galvão, Dylan Mastrippolito, Laura Talamini, Mariana Aganetti, Victor Rocha, Cindy Verdot, Viviani Mendes, Vivian Louise Soares de Oliveira, Amanda Dias Braga, Vinicius Dantas Martins and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. 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

15 authors at 3 institutions in 2 countries.

Izabela GalvãoLaboratory of Microbiota and Immunomodulation, Institute of Biological Sciences, Department of Biochemistry and Immunology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.
Dylan MastrippolitoCNRS UMR7242, Biotechnology and Cell Signaling/Strasbourg Drug Discovery and Development Institute (IMS), University of Strasbourg, 67000 Strasbourg, France.ORCID 0000-0001-5613-7741
Laura TalaminiCNRS UMR7242, Biotechnology and Cell Signaling/Strasbourg Drug Discovery and Development Institute (IMS), University of Strasbourg, 67000 Strasbourg, France.ORCID 0000-0001-6010-2947
Mariana AganettiLaboratory of Microbiota and Immunomodulation, Institute of Biological Sciences, Department of Biochemistry and Immunology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.
Victor RochaLaboratory of Microbiota and Immunomodulation, Institute of Biological Sciences, Department of Biochemistry and Immunology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.
Cindy VerdotCNRS UMR7242, Biotechnology and Cell Signaling/Strasbourg Drug Discovery and Development Institute (IMS), University of Strasbourg, 67000 Strasbourg, France.
Viviani MendesLaboratory of Microbiota and Immunomodulation, Institute of Biological Sciences, Department of Biochemistry and Immunology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.ORCID 0000-0001-6061-8038
Vivian Louise Soares de OliveiraExperimental Rheumatology Laboratory, Immunopharmacology Group, Department of Biochemistry and Immunology, and Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil.ORCID 0000-0002-1798-5171
Amanda Dias BragaExperimental Rheumatology Laboratory, Immunopharmacology Group, Department of Biochemistry and Immunology, and Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil.
Vinicius Dantas MartinsLaboratory of Immunobiology, Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.ORCID 0000-0001-9994-5212
Ana Maria Caetano de FariaLaboratory of Immunobiology, Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.
Flávio A AmaralExperimental Rheumatology Laboratory, Immunopharmacology Group, Department of Biochemistry and Immunology, and Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil.ORCID 0000-0002-1695-0612
Philippe GeorgelImmunoRhumatologie Moléculaire, UMR_S 1109, INSERM, University of Strasbourg, 67000 Strasbourg, France.ORCID 0000-0001-6853-7080
Angélica T VieiraLaboratory of Microbiota and Immunomodulation, Institute of Biological Sciences, Department of Biochemistry and Immunology, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte 31270-901, Brazil.
Sylviane MullerCNRS UMR7242, Biotechnology and Cell Signaling/Strasbourg Drug Discovery and Development Institute (IMS), University of Strasbourg, 67000 Strasbourg, France.ORCID 0000-0002-0481-0620
Universidade Federal de Minas Gerais · BRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) [402530/2020-9] and [420350/2018-7]Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES-PRINT) 001Fundação de Amparo à Pesquisa de Minas Gerais (FAPEMIG) [APQ-03328-18]Instituto Serrapilheira Serra-1912-31552Pro-Reitoria de Pesquisa da Universidade Federal de Minas Gerais -PRPq 2022Region Grand-Est 2020SFRI - STRAT'US project ANR-20-SFRI-0012University of Strasbourg-CNRS-Inserm, IdEx Unistra ANR-10-IDEX-0002
6 · The paper itself

Abstract

Gout is a painful form of inflammatory arthritis characterized by the deposition of monosodium urate (MSU) crystals in the joints. The aim of this study was to investigate the effect of peptide P140 on the inflammatory responses in crystal-induced mouse models of gout and cell models including MSU-treated human cells. Injection of MSU crystals into the knee joint of mice induced neutrophil influx and inflammatory hypernociception. Injection of MSU crystals subcutaneously into the hind paw induced edema and increased pro-inflammatory cytokines levels. Treatment with P140 effectively reduced hypernociception, the neutrophil influx, and pro-inflammatory cytokine levels in these experimental models. Furthermore, P140 modulated neutrophils chemotaxis in vitro and increased apoptosis pathways through augmented caspase 3 activity and reduced NFκB phosphorylation. Moreover, P140 increased the production of the pro-resolving mediator annexin A1 and decreased the expression of the autophagy-related ATG5-ATG12 complex and HSPA8 chaperone protein. Overall, these findings suggest that P140 exerts a significant beneficial effect in a neutrophilic inflammation observed in the model of gout that can be of special interest in the design of new therapeutic strategies.

Indexed as

Arthritis, GoutyGoutAnimalsDisease Models, AnimalHumansInflammationMiceNeutrophilsPhosphopeptidesUric AcidPhosphopeptidesUric AcidautophagyinflammasomeMSU crystal-induced inflammationneutrophilpainpeptide therapy

Identifiers

PMID36496970
PMCPMC9740613
OpenAlexW4309588033

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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.