Evidence map›Paper›PMID 34502521›Full record

ArticleInternational journal of molecular sciences2021

Methotrexate Ameliorates Systemic Inflammation and Septic Associated-Lung Damage in a Cecal Ligation and Puncture Septic Rat Model.

Josep Bringué, Raquel Guillamat-Prats, Maria Luisa Martinez, Eva Torrents, Marta Camprubí-Rimblas, Lluís Blanch, Antonio Artigas

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 16 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

7 authors at 4 institutions in 1 country.

Josep BringuéInstitut d' Investigació i Innovació Parc Taulí (I3PT), 08201 Sabadell, Spain.ORCID 0000-0002-9873-3354
Raquel Guillamat-PratsInstitut d' Investigació i Innovació Parc Taulí (I3PT), 08201 Sabadell, Spain.ORCID 0000-0001-6960-0985
Maria Luisa MartinezCritical Care Center-Hospital Universitario General de Catalunya, 08190 Sant Cugat del Valles, Spain.ORCID 0000-0002-7691-3397
Eva TorrentsCritical Care Center-Corporació Sanitària i Universitària Parc Taulí, 08201 Sabadell, Spain.
Marta Camprubí-RimblasInstitut d' Investigació i Innovació Parc Taulí (I3PT), 08201 Sabadell, Spain.ORCID 0000-0002-4085-5324
Lluís BlanchInstitut d' Investigació i Innovació Parc Taulí (I3PT), 08201 Sabadell, Spain.
Antonio ArtigasInstitut d' Investigació i Innovació Parc Taulí (I3PT), 08201 Sabadell, Spain.ORCID 0000-0002-8029-1017
Universitat Autònoma de Barcelona · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESCorporació Sanitària Parc Taulí · ESHospital General de Catalunya · ES

Funding

CIBER de Enfermedades Respiratorias (CIBERES) Ayudas de Iniciación a la Investigación CIBERES 2015Cofinanciado por el Fondo Europeo de Desarrollo Regional (FEDER) PI15/02204Fundació Parc Taulí CIR2015/009 and CIR2016/068Instituto de Salud Carlos III PI15/02204
6 · The paper itself

Abstract

backgroundSepsis is a serious, heterogeneous clinical entity produced by a severe and systemic host inflammatory response to infection. Methotrexate (MTX) is a folate-antagonist that induces the generation of adenosine and also inhibits JAK/STAT pathway; MTX it is widely used as an anti-inflammatory drug to control the immune system.

objectiveThe aim of this study was to assess the beneficial effects of a single and low dose of MTX in the systemic response and acute lung injury (ALI) induced by sepsis. As in the clinics, we treated our animals with antibiotics and fluids and performed the source control to mimic the current clinic treatment. METHODS AND MAIN

resultsSepsis was induced in rats by a cecal ligation puncture (CLP) procedure. Six hours after induction of sepsis, we proceeded to the source control; fluids and antibiotics were administered at 6 h and 24 h after CLP. MTX (2.5 mg/Kg) was administered 6 h after the first surgery in one CLP experimental group and to one Sham group. A protective effect of MTX was observed through a significant reduction of pro-inflammatory cytokines and a decrease infiltration of inflammatory cells in the lung. In addition, we found a regulation in adenosine receptor A2aR and the metalloproteinases by MTX.

conclusionA single, low dose of MTX attenuates sepsis lung-associated damage by decreasing pro-inflammatory response, infiltration of pro-inflammatory cells and avoiding defective tissue lung remodeling.

Indexed as

Acute Lung InjuryAnimalsAnti-Inflammatory AgentsCecumDisease Models, AnimalInflammationLigationLungMaleMethotrexatePuncturesRatsRats, Sprague-DawleySepsisAnti-Inflammatory AgentsMethotrexateacute lung injuryacute respiratory distress syndromemethotrexatesepsissystemic inflammation

Identifiers

PMID34502521
PMCPMC8431751
OpenAlexW3196840004

What OpenQuestion holds

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LicenceCC BY
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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.