Evidence map›Paper›PMID 42831236›Full record

ArticleCell biochemistry and function2026

Capybara Oil-Based Nanoemulsion Attenuates Obesity-Induced Renal Injury Through Modulation of Inflammation, Oxidative Stress, and Fibrosis in Mice.

Priscila G Pereira, Luciana L Alves, Bianca T Ciambarella, Stela R Ferrarini, Ana Lúcia R Nascimento, Cherley B V Andrade, Alan Cesar N Moraes, Andressa Bernardi, Fernanda V Guimarães, Miguel P Campos and 5 more

Abstract read
In one paragraph

Article in Cell biochemistry and function, 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. Article
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

15 authors.

Priscila G PereiraUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.
Luciana L AlvesUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-2869-2788
Bianca T CiambarellaUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0003-1718-5059
Stela R FerrariniPharmaceutical Nanotechnology Laboratory, Federal University of Mato Grosso (UFMT), Sinop, Brazil.
Ana Lúcia R NascimentoUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.
Cherley B V AndradeUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-4320-4252
Alan Cesar N MoraesUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-6594-1050
Andressa BernardiLaboratory of Inflammation, Oswaldo Cruz Institute (IOC), Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-5079-5866
Fernanda V GuimarãesLaboratory of Inflammation, Oswaldo Cruz Institute (IOC), Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro, Brazil.
Miguel P CamposUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0009-0004-8023-7039
Denia M S ValladãoQuality Control Laboratory, Federal University of Mato Grosso (UFMT), Sinop, Brazil.ORCID https://orcid.org/0000-0002-2643-1963
Letícia CruzPharmaceutical Technology Laboratory, Department of Industrial Pharmacy, Federal University of Santa Maria (UFSM), Santa Maria, Brazil.
Jemima F R da SilvaUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-7867-3131
Kíssila RabeloUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-7579-7788
Jorge J de CarvalhoUltrastructure and Tissue Biology Laboratory, Department of Histology and Embryology, Institute of Biology Roberto Alcantara Gomes (IBRAG), Rio de Janeiro State University (UERJ), Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0002-9426-6381

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 316464/2021-0Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/202.995/2018Universidade do Estado do Rio de Janeiro
6 · The paper itself

Abstract

Obesity is a multifactorial disorder associated with systemic metabolic alterations and increased risk of renal injury, largely driven by chronic inflammation and oxidative stress. Bioactive lipids, particularly polyunsaturated fatty acids, have been shown to exert protective effects; however, their instability and susceptibility to oxidation may limit their therapeutic potential. In this study, we investigated the effects of a capybara oil-based nanoemulsion (NE-CO) on renal dysfunction in a mouse model of obesity. Male mice were subjected to diet-induced obesity and treated with NE-CO (100 mg/kg/day) for 4 weeks. Metabolic parameters, systolic blood pressure, urinary biomarkers, and renal morphology were evaluated. In addition, markers of inflammation, oxidative stress, and fibrosis were assessed to elucidate potential mechanisms. NE-CO treatment significantly reduced body mass and systolic blood pressure, while improving renal function, as evidenced by decreased proteinuria and normalization of urinary creatinine levels. Histological and ultrastructural analyzes revealed marked improvements in renal cortical organization. These effects were accompanied by reduced expression of pro-inflammatory markers, enhanced antioxidant defenses, and attenuation of fibrotic remodeling. Collectively, these findings demonstrate that NE-CO mitigates obesity-induced renal injury, at least in part, through modulation of inflammatory, oxidative, and fibrotic pathways. This study highlights the therapeutic potential of bioactive lipid delivery systems in the context of metabolic and renal disorders.

Indexed as

InflammationKidney DiseasesObesityOxidative StressAnimalsEmulsionsFibrosisKidneyMaleMiceMice, Inbred C57BLEmulsionscapybara oilkidney injurynanoemulsionobesityomega‐3

Identifiers

PMID42831236
PMCPMC13635768

What Socratic holds

Textmetadata
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.