Evidence map›Paper›PMID 26495970›Full record

ArticlePloS one2015

Renal Effects and Underlying Molecular Mechanisms of Long-Term Salt Content Diets in Spontaneously Hypertensive Rats.

Rebeca Caldeira Machado Berger, Paula Frizera Vassallo, Renato de Oliveira Crajoinas, Marilene Luzia Oliveira, Flávia Letícia Martins, Breno Valentim Nogueira, Daisy Motta-Santos, Isabella Binotti Araújo, Ludimila Forechi, Adriana Castello Costa Girardi and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  7. Cardiorenal Disease in COVID-19 Patients.Journal of the renin-angiotensin-aldosterone system : JRAAS · 2022
    Review
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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

12 authors at 3 institutions in 1 country.

Rebeca Caldeira Machado BergerDepartment of Physiological Science-Federal University of Espirito Santo, Vitória, ES, Brazil.
Paula Frizera VassalloDepartment of Physiological Science-Federal University of Espirito Santo, Vitória, ES, Brazil.
Renato de Oliveira CrajoinasHeart Institute (InCor) University of São Paulo Medical School, São Paulo, SP, Brazil.
Marilene Luzia OliveiraDepartment of Physiology and Biophysics -Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Flávia Letícia MartinsHeart Institute (InCor) University of São Paulo Medical School, São Paulo, SP, Brazil.
Breno Valentim NogueiraDepartment of Morphology-Federal University of Espirito Santo, Vitória, ES, Brazil.
Daisy Motta-SantosHeart Institute (InCor) University of São Paulo Medical School, São Paulo, SP, Brazil.
Isabella Binotti AraújoDepartment of Morphology-Federal University of Espirito Santo, Vitória, ES, Brazil.
Ludimila ForechiDepartment of Physiological Science-Federal University of Espirito Santo, Vitória, ES, Brazil.
Adriana Castello Costa GirardiHeart Institute (InCor) University of São Paulo Medical School, São Paulo, SP, Brazil.
Robson Augusto Souza SantosDepartment of Physiology and Biophysics -Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
José Geraldo MillDepartment of Physiological Science-Federal University of Espirito Santo, Vitória, ES, Brazil.
Universidade Federal do Espírito Santo · BRUniversidade de São Paulo · BRUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several evidences have shown that salt excess is an important determinant of cardiovascular and renal derangement in hypertension. The present study aimed to investigate the renal effects of chronic high or low salt intake in the context of hypertension and to elucidate the molecular mechanisms underlying such effects. To this end, newly weaned male SHR were fed with diets only differing in NaCl content: normal salt (NS: 0.3%), low salt (LS: 0.03%), and high salt diet (HS: 3%) until 7 months of age. Analysis of renal function, morphology, and evaluation of the expression of the main molecular components involved in the renal handling of albumin, including podocyte slit-diaphragm proteins and proximal tubule endocytic receptors were performed. The relationship between diets and the balance of the renal angiotensin-converting enzyme (ACE) and ACE2 enzymes was also examined. HS produced glomerular hypertrophy and decreased ACE2 and nephrin expressions, loss of morphological integrity of the podocyte processes, and increased proteinuria, characterized by loss of albumin and high molecular weight proteins. Conversely, severe hypertension was attenuated and renal dysfunction was prevented by LS since proteinuria was much lower than in the NS SHRs. This was associated with a decrease in kidney ACE/ACE2 protein and activity ratio and increased cubilin renal expression. Taken together, these results suggest that LS attenuates hypertension progression in SHRs and preserves renal function. The mechanisms partially explaining these findings include modulation of the intrarenal ACE/ACE2 balance and the increased cubilin expression. Importantly, HS worsens hypertensive kidney injury and decreases the expression nephrin, a key component of the slit diaphragm.

Indexed as

Angiotensin-Converting Enzyme 2AnimalsDiet, Sodium-RestrictedGlomerular Filtration BarrierHypertensionIntracellular Signaling Peptides and ProteinsKidneyMaleMembrane ProteinsPeptidyl-Dipeptidase ARats, Inbred SHRRenin-Angiotensin SystemSodium Chloride, DietaryAce2 protein, ratAngiotensin-Converting Enzyme 2Intracellular Signaling Peptides and ProteinsMembrane ProteinsnephrinNPHS2 proteinPeptidyl-Dipeptidase ASodium Chloride, Dietary

Identifiers

PMID26495970
PMCPMC4619858
OpenAlexW2165144951

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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.