Evidence mapPaperPMID 41900940Full record

ArticleLife (Basel, Switzerland)2026

Differences on the Natural Course of Chronic Kidney Disease Progression, Induced by 5/6 Renal Ablation Model in Three Different Rat Stains: Wistar, Lewis, and Fischer 344.

Samuel de Jesus, Paloma Souza Noda, Ana Laura Rubio Francini, Flavio Teles Filho, Mariana Matera Veras, Ane Claudia Fernandes Nunes, Irene de Lourdes Noronha, Camilla Fanelli

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 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

8 authors.

Samuel de JesusLaboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.ORCID 0009-0002-8657-1287
Paloma Souza NodaLaboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.
Ana Laura Rubio FranciniLaboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.ORCID 0000-0002-7724-3890
Flavio Teles FilhoRenal Division, Faculty of Medicine, Federal University of Alagoas, Maceio 57200-000, AL, Brazil.
Mariana Matera VerasLaboratory of Environmental and Experimental Pathology, Department of Pathology, School of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.ORCID 0000-0002-8363-4329
Ane Claudia Fernandes NunesLaboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.ORCID 0000-0002-7838-6463
Irene de Lourdes NoronhaLaboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.
Camilla FanelliLaboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, São Paulo 01246-903, SP, Brazil.ORCID 0000-0003-4425-7708

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/05641-6
6 · The paper itself

Abstract

Almost 10% of the global population suffers from chronic kidney disease (CKD). The inexistence of a therapeutic to restore renal function motivates the scientific community to search for new treatments. The 5/6 nephrectomy (Nx) rat model is widely used to mimic human CKD, but the impact of strain-specific responses on disease progression remains unclear. Here, we aimed to compare CKD development in Wistar, Lewis, and Fischer rats submitted to the Nx model. In summary, even submitted to the same surgical procedure, the three studied rat strains presented distinct patterns of CKD progression: Wistar rats exhibited faster and sustained renal function loss, with exuberant hypertension, proteinuria, and renal inflammation, being considered as excellent models to study rapidly progressive human nephropathy. Lewis animals, in turn, presented mild low-progressive CKD, which make this rat strain especially useful to simulate intermediate degrees of human CKD and to develop long-term tests. Finally, Fischer rats submitted to Nx did not even develop hypertension, proteinuria, or glomerular damage within 30 days. Moreover, compared to Wistar rats, both Lewis and Fischer animals have a relatively higher basal number of nephrons and a lower number of whole blood leukocytes, which may have contributed to the renoprotection exhibited by these rat strains.

Indexed as

5/6 renal ablationchronic kidney diseaseexperimental modelnephron number

Identifiers

PMID41900940
PMCPMC13028075

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.