Evidence map›Paper›PMID 41802884›Full record

ArticlePhysiological reports2026

Mas-related G protein-coupled receptor type D deficiency promotes tubulointerstitial injury and fibrosis associated with proteinuria in male mice.

Laura B F Oliveira, Arthur F Iost, Lucas R A Ribeiro, Maria Aparecida R Vieira, Thiago Verano-Braga, Robson A S Santos, Diogo B Peruchetti

Abstract read
In one paragraph

Article in Physiological reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Laura B F OliveiraDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Arthur F IostDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Lucas R A RibeiroDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Maria Aparecida R VieiraDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Thiago Verano-BragaDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Robson A S SantosDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Diogo B PeruchettiDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0002-7572-9731

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) 406792/2022-4Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) INCT-NanobiofarCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Edital PDPG III - Parcerias Estratégicas com os estados IIIFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) AQP-04900-22Fundação de Desenvolvimento da Pesquisa (FUNDEP) 30563*23
6 · The paper itself

Abstract

Kidney diseases are non-communicable, progressive diseases with high morbidity and mortality rates worldwide. A key feature of disease progression is the development of tubulointerstitial injury accompanied by proteinuria, a process mediated in part by dysregulation of the Renin-Angiotensin System (RAS). Recently, a novel protective RAS axis consisting of alamandine (Ala) and its receptor, the Mas-related G protein-coupled receptor type D (MrgD), has been identified. While the Ala/MrgD pathway has been implicated in the cardiovascular regulation, its role in renal physiology remains unknown. In this study, we investigated whether basal MrgD deficiency affects the renal structure and function. Male 8-12-week-old C57Bl6/J wild-type (WT) and MrgD knockout (MrgD-KO) mice were used. MrgD-KO exhibited reduced water intake and urine output, increased tubular reabsorption of Na

Indexed as

ProteinuriaReceptors, G-Protein-CoupledReceptors, PeptideAnimalsFibrosisKidneyMaleMiceMice, Inbred C57BLMice, KnockoutRenin-Angiotensin SystemMrgprd protein, mouseReceptors, G-Protein-CoupledReceptors, Peptidealamandinekidneykidney diseasemas‐related g protein‐coupled receptor type Dproteinuriarenin‐angiotensin systemtubulointerstitial injury

Identifiers

PMID41802884
PMCPMC12971248

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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.