Evidence map›Paper›PMID 38831961›Full record

ArticleJournal of obesity2024

Beneficial Effects of Capybara Oil Supplementation on Steatosis and Liver Apoptosis in Obese Mice.

Luciana Lontro Alves, Priscila Gomes Pereira, Bianca Torres Ciambarella, Miguel Porto Campos, Kíssila Rabelo, Ana Lúcia Rosa Nascimento, Raíssa Leal de Carvalho Dos Santos Cunha, Cherley Borba Vieira Andrade, Alan Cesar Nunes Moraes, Andressa Bernardi and 3 more

Abstract read
In one paragraph

Article in Journal of obesity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Polyphenol-RichMolecules (Basel, Switzerland) · 2026
    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

13 authors.

Luciana Lontro AlvesUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0002-2869-2788
Priscila Gomes PereiraUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0002-0480-2604
Bianca Torres CiambarellaUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0003-1718-5059
Miguel Porto CamposUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Kíssila RabeloUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0001-7579-7788
Ana Lúcia Rosa NascimentoUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Raíssa Leal de Carvalho Dos Santos CunhaUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.
Cherley Borba Vieira AndradeUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0002-4320-4252
Alan Cesar Nunes MoraesUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0002-6594-1050
Andressa BernardiInflammation Laboratory, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Fernanda Verdini GuimarãesInflammation Laboratory, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Jemima Fuentes Ribeiro da SilvaUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0001-7867-3131
Jorge José de CarvalhoUltrastructure and Tissue Biology Laboratory, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.ORCID 0000-0002-9426-6381

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is a complex chronic disease characterized by excess body fat (adipose) that is harmful to health and has been a major global health problem. It may be associated with several diseases, such as nonalcoholic fatty liver disease (NAFLD). Polyunsaturated fatty acids (PUFA) are lipid mediators that have anti-inflammatory characteristics and can be found in animals and plants, with capybara oil (CO) being a promising source. So, we intend to evaluate the hepatic pathophysiological alterations in C57Bl/6 mice with NAFLD, caused by obesity, and the possible beneficial effects of OC in the treatment of this disease. Eighteen 3-month-old male C57Bl/6 mice received a control or high-fat diet for 18 weeks. From the 15th to the 18th week, the animals received treatment-through orogastric gavage-with placebo or free capybara oil (5 g/kg). Parameters inherent to body mass, glucose tolerance, evaluation of liver enzymes, percentage of hepatic steatosis, oxidative stress, the process of cell death with the apoptotic biomarkers (Bax, Bcl2, and Cytochrome C), and the ultrastructure of hepatocytes were analyzed. Even though the treatment with CO was not able to disassemble the effects on the physiological parameters, it proved to be beneficial in reversing the morphological and ultrastructural damage present in the hepatocytes. Thus, demonstrating that CO has beneficial effects in reducing steatosis and the apoptotic pathway, it is a promising treatment for NAFLD.

Indexed as

ApoptosisLiverNon-alcoholic Fatty Liver DiseaseOilsAnimalsEnzyme ActivationHepatocytesMaleMiceMice, Inbred C57BLObesityOxidative StressOxidoreductasesRodentiaOilsOxidoreductases

Identifiers

PMID38831961
PMCPMC11147678

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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.