Evidence map›Paper›PMID 31035535›Full record

ArticleMolecules (Basel, Switzerland)2019

Polyphenols-Rich Fruit (

Aline Boveto Santamarina, Giovana Jamar, Laís Vales Mennitti, Daniel Araki Ribeiro, Caroline Margonato Cardoso, Veridiana Vera de Rosso, Lila Missae Oyama, Luciana Pellegrini Pisani

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 24 citations in OpenAlex.

  1. Effects of Juçara (Nutrients · 2023
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Use ofBiomolecules · 2020
    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 at 2 institutions in 1 country.

Aline Boveto SantamarinaPrograma de Pós-Graduação Interdisciplinar em Ciências da Saúde, Universidade Federal de São Paulo, Santos 11015-020, Brazil. alinesantamarina@gmail.com.
Giovana JamarPrograma de Pós-Graduação Interdisciplinar em Ciências da Saúde, Universidade Federal de São Paulo, Santos 11015-020, Brazil. gi.jamar@gmail.com.
Laís Vales MennittiPrograma de Pós-Graduação Interdisciplinar em Ciências da Saúde, Universidade Federal de São Paulo, Santos 11015-020, Brazil. laisvmennitti@hotmail.com.
Daniel Araki RibeiroDepartamento de Biociências, Universidade Federal de São Paulo, Santos 11015-020, Brazil. daribeiro@unifesp.br.
Caroline Margonato CardosoPrograma de Pós-Graduação Interdisciplinar em Ciências da Saúde, Universidade Federal de São Paulo, Santos 11015-020, Brazil. camargonato@gmail.com.
Veridiana Vera de RossoDepartamento de Biociências, Universidade Federal de São Paulo, Santos 11015-020, Brazil. veriderosso@yahoo.com.ORCID 0000-0001-7327-7471
Lila Missae OyamaDepartamento de Fisiologia, Universidade Federal de São Paulo, São Paulo 04023-062, Brazil. lmoyama@gmail.com.
Luciana Pellegrini PisaniDepartamento de Biociências, Universidade Federal de São Paulo, Santos 11015-020, Brazil. lucianapisani@gmail.com.ORCID 0000-0001-6579-6167
Universidade Federal de São Paulo · BRInstituto de Saúde · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico felowshipFundação de Amparo à Pesquisa do Estado de São Paulo 2016/14133-0 and 2015/13875-0
6 · The paper itself

Abstract

Juçara berry is a potential inflammatory modulator, rich in dietary fiber, fatty acids, and anthocyanins. Considering this, we evaluated the high-fat diet (HFD) intake supplemented with different doses of freeze-dried juçara pulp on the TLR4 pathway. Twenty-seven male Wistar rats with ad libitum access to food and water were divided into four experimental groups: control standard chow group (C); high-fat diet control group (HFC); high-fat diet juçara 0.25% group (HFJ0.25%); and high-fat diet juçara 0.5% group (HFJ0.5%). The inflammatory parameters were analyzed by ELISA and Western blotting in liver and retroperitoneal adipose tissue (RET). The HFJ0.25% group had the energy intake, aspartate transaminase (AST) levels, and liver triacylglycerol accumulation reduced; also, the tumor necrosis factor α (TNF-α) and TNF receptor-associated factor 6 (TRAF6) expression in RET were reduced. However, there were no changes in other protein expressions in liver and adipose tissue. Adiposity and pNFκBp50 had a positive correlation in HFC and HFJ0.5%, but not in the C group and HFJ0.25%. The necrosis hepatic score did not change with treatment; however, the serum (AST) levels and the hepatic triacylglycerol were increased in HFC and HFJ0.5%. These results demonstrated that one week of HFD intake triggered pro-inflammatory mechanisms and liver injury. Additionally, 0.25% juçara prevented inflammatory pathway activation, body weight gain, and liver damage.

Indexed as

Adipose TissueAnimalsAnti-Inflammatory AgentsBiomarkersBody WeightCytokinesDiet, High-FatEuterpeFruitInflammationInflammation MediatorsLipid MetabolismLiverMaleNF-kappa BPolyphenolsAnti-Inflammatory AgentsBiomarkersCytokinesInflammation MediatorsNF-kappa BPolyphenolsadipose tissueinflammationjuçaralivernutraceutical foodshort-term high-fat diet

Identifiers

PMID31035535
PMCPMC6539628
OpenAlexW2942429573

What OpenQuestion 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 OpenQuestion graph.