Evidence map›Paper›PMID 26730742›Full record

ArticlePloS one2016

Aldosterone Induces Renal Fibrosis and Inflammatory M1-Macrophage Subtype via Mineralocorticoid Receptor in Rats.

Beatriz Martín-Fernández, Alfonso Rubio-Navarro, Isabel Cortegano, Sandra Ballesteros, Mario Alía, Pablo Cannata-Ortiz, Elena Olivares-Álvaro, Jesús Egido, Belén de Andrés, María Luisa Gaspar and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 108 citations in OpenAlex.

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  5. Diabetic kidney disease, biomarkers, and finerenone.Diabetes, obesity & metabolism · 2026
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7 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 1 country.

Beatriz Martín-FernándezDepartment of Physiology, Faculty of Medicine, Complutense University, 28040, Madrid, Spain.
Alfonso Rubio-NavarroRenal, Vascular and Diabetes Research Lab, IIS-Fundación Jiménez Díaz, Autonoma University (UAM), 28040, Madrid, Spain.
Isabel CorteganoDepartment of Immunology, Centro Nacional de Microbiología, Instituto de Salud Carlos III (ISCIII), Majadahonda, 28220, Madrid, Spain.
Sandra BallesterosDepartment of Physiology, Faculty of Medicine, Complutense University, 28040, Madrid, Spain.
Mario AlíaDepartment of Immunology, Centro Nacional de Microbiología, Instituto de Salud Carlos III (ISCIII), Majadahonda, 28220, Madrid, Spain.
Pablo Cannata-OrtizDepartment of Pathology, IIS-Fundación Jiménez Díaz, Autonoma University (UAM), 28040, Madrid, Spain.
Elena Olivares-ÁlvaroDepartment of Physiology, Faculty of Medicine, Complutense University, 28040, Madrid, Spain.
Jesús EgidoRenal, Vascular and Diabetes Research Lab, IIS-Fundación Jiménez Díaz, Autonoma University (UAM), 28040, Madrid, Spain.
Belén de AndrésDepartment of Immunology, Centro Nacional de Microbiología, Instituto de Salud Carlos III (ISCIII), Majadahonda, 28220, Madrid, Spain.
María Luisa GasparDepartment of Immunology, Centro Nacional de Microbiología, Instituto de Salud Carlos III (ISCIII), Majadahonda, 28220, Madrid, Spain.
Natalia de Las HerasDepartment of Physiology, Faculty of Medicine, Complutense University, 28040, Madrid, Spain.
Vicente LaheraDepartment of Physiology, Faculty of Medicine, Complutense University, 28040, Madrid, Spain.
Juan Antonio MorenoRenal, Vascular and Diabetes Research Lab, IIS-Fundación Jiménez Díaz, Autonoma University (UAM), 28040, Madrid, Spain.
Universidad Complutense de Madrid · ESUniversidad Autónoma de Madrid · ESInstituto de Salud Carlos III · ESCentro Nacional de Microbiologia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to evaluate macrophages heterogeneity and structural, functional and inflammatory alterations in rat kidney by aldosterone + salt administration. The effects of treatment with spironolactone on above parameters were also analyzed. Male Wistar rats received aldosterone (1 mgkg-1d-1) + 1% NaCl for 3 weeks. Half of the animals were treated with spironolactone (200 mg kg-1d-1). Systolic and diastolic blood pressures were elevated (p<0.05) in aldosterone + salt-treated rats. Relative kidney weight, collagen content, fibronectin, macrophage infiltrate, CTGF, Col I, MMP2, TNF-α, CD68, Arg2, and SGK-1 were increased (p<0.05) in aldosterone + salt-treated rats, being reduced by spironolactone (p<0.05). Increased iNOS and IFN-γ mRNA gene expression (M1 macrophage markers) was observed in aldosterone + salt rats, whereas no significant differences were observed in IL-10 and gene ArgI mRNA expression or ED2 protein content (M2 macrophage markers). All the observed changes were blocked with spironolactone treatment. Macrophage depletion with liposomal clodronate reduced macrophage influx and inflammatory M1 markers (INF-γ or iNOS), whereas interstitial fibrosis was only partially reduced after this intervention, in aldosterone plus salt-treated rats. In conclusion, aldosterone + salt administration mediates inflammatory M1 macrophage phenotype and increased fibrosis throughout mineralocorticoid receptors activation.

Indexed as

AldosteroneAnimalsFibrosisInflammationKidneyKidney DiseasesMacrophagesMaleMineralocorticoid Receptor AntagonistsRatsRats, WistarReceptors, MineralocorticoidSodium ChlorideSpironolactoneAldosteroneMineralocorticoid Receptor AntagonistsReceptors, MineralocorticoidSodium ChlorideSpironolactone

Identifiers

PMID26730742
PMCPMC4701403
OpenAlexW2222589555

What OpenQuestion holds

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LicenceCC BY
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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.