Evidence map›Paper›PMID 26792656›Full record

ArticleJournal of physiology and biochemistry2016

Limited beneficial effects of piceatannol supplementation on obesity complications in the obese Zucker rat: gut microbiota, metabolic, endocrine, and cardiac aspects.

E Hijona, L Aguirre, P Pérez-Matute, M J Villanueva-Millán, A Mosqueda-Solis, M Hasnaoui, F Nepveu, J M Senard, L Bujanda, L Aldámiz-Echevarría and 8 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of physiology and biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Stilbenes from Vine Extracts: Therapeutic Potential and Mechanisms.International journal of molecular sciences · 2025
    Review
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  11. Natural Products as Modulators of Sirtuins.Molecules (Basel, Switzerland) · 2020
    Review
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  13. Article
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  15. Article
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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

18 authors at 11 institutions in 2 countries.

E HijonaDepartment of Gastroenterology, Biodonostia Research Institute, University of Basque Country (UPV/EHU), San Sebastián, Spain.
L AguirreNutrition and Obesity Group, Department of Nutrition and Food Science, University of Basque Country (UPV/EHU), Vitoria, Spain. leixuri.aguirre@ehu.eus.
P Pérez-MatuteHIV and Associated Metabolic Alterations Unit, Infectious Diseases Department, Center for Biomedical Research of La Rioja (CIBIR), Logroño, Spain.
M J Villanueva-MillánHIV and Associated Metabolic Alterations Unit, Infectious Diseases Department, Center for Biomedical Research of La Rioja (CIBIR), Logroño, Spain.
A Mosqueda-SolisNutrition and Obesity Group, Department of Nutrition and Food Science, University of Basque Country (UPV/EHU), Vitoria, Spain.
M HasnaouiINSERM U1048, Institute of Metabolic and Cardiovascular Diseases (I2MC), Toulouse, France.
F NepveuUniversity of Toulouse, UPS and IRD, UMR 152 (PHARMA-DEV), F-31062, Toulouse cedex 9, France.
J M SenardINSERM U1048, Institute of Metabolic and Cardiovascular Diseases (I2MC), Toulouse, France.
L BujandaDepartment of Gastroenterology, Biodonostia Research Institute, University of Basque Country (UPV/EHU), San Sebastián, Spain.
L Aldámiz-EchevarríaDivision of Metabolism, Cruces University Hospital and BioCruces Health Research Institute, Plaza de Cruces s/n, 48903, Barakaldo, Spain.
M LlarenaDivision of Metabolism, Cruces University Hospital and BioCruces Health Research Institute, Plaza de Cruces s/n, 48903, Barakaldo, Spain.
F AndradeDivision of Metabolism, Cruces University Hospital and BioCruces Health Research Institute, Plaza de Cruces s/n, 48903, Barakaldo, Spain.
P PerioUniversity of Toulouse, UPS and IRD, UMR 152 (PHARMA-DEV), F-31062, Toulouse cedex 9, France.
F LeboulangerINSERM U1048, Institute of Metabolic and Cardiovascular Diseases (I2MC), Toulouse, France.
L HijonaDepartment of Gastroenterology, Biodonostia Research Institute, University of Basque Country (UPV/EHU), San Sebastián, Spain.
J M Arbones-MainarCIBER Fisiopatología Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Madrid, Spain.
M P PortilloNutrition and Obesity Group, Department of Nutrition and Food Science, University of Basque Country (UPV/EHU), Vitoria, Spain.
C CarpénéINSERM U1048, Institute of Metabolic and Cardiovascular Diseases (I2MC), Toulouse, France.
Instituto de Salud Carlos III · ESUniversity of the Basque Country · ESCenter for Biomedical Research of La Rioja · ESInserm · FRInstitut des Maladies Métaboliques et Cardiovasculaires · FRBioCruces Health research Institute · ESCentre for Biomedical Network Research on Rare Diseases · ESHospital de Cruces · ESInstituto Aragonés de Ciencias de la Salud · ESPharmacochimie et Pharmacologie pour le Développement · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resveratrol is beneficial in obese and diabetic rodents. However, its low bioavailability raises questions about its therapeutic relevance for treating or preventing obesity complications. In this context, many related natural polyphenols are being tested for their putative antidiabetic and anti-obesity effects. This prompted us to study the influence of piceatannol, a polyhydroxylated stilbene, on the prevention of obesity complications in Zucker obese rats. A 6-week supplementation was followed by the determination of various markers in plasma, liver, adipose tissue and heart, together with a large-scale analysis of gut microbiota composition. When given in doses of 15 or 45 mg/kg body weight/day, piceatannol did not reduce either hyperphagia or fat accumulation. It did not modify the profusion of the most abundant phyla in gut, though slight changes were observed in the abundance of several Lactobacillus, Clostridium, and Bacteroides species belonging to Firmicutes and Bacteroidetes. This was accompanied by a tendency to reduce plasma lipopolysaccharides by 30 %, and by a decrease of circulating non-esterified fatty acids, LDL-cholesterol, and lactate. While piceatannol tended to improve lipid handling, it did not mitigate hyperinsulinemia and cardiac hypertrophy. However, it increased cardiac expression of ephrin-B1, a membrane protein that contributes to maintaining cardiomyocyte architecture. Lastly, ascorbyl radical plasma levels and hydrogen peroxide release by adipose tissue were similar in control and treated groups. Thus, piceatannol did not exhibit strong slimming capacities but did limit several obesity complications.

Indexed as

Dietary Supplements3T3-L1 CellsAdipose Tissue, WhiteAdiposityAnimalsAnti-Inflammatory Agents, Non-SteroidalAntioxidantsBiomarkersDysbiosisHeart DiseasesHydrogen PeroxideHyperlipidemiasLiverMaleMiceMyocardium3,3',4,5'-tetrahydroxystilbeneAnti-Inflammatory Agents, Non-SteroidalAntioxidantsBiomarkersHydrogen PeroxideStilbenesAdipokinesAdipose tissueCardiomyocytesGut microbiotaLiverPiceatannolZucker rat

Identifiers

PMID26792656
OpenAlexW2296500637

What OpenQuestion 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 OpenQuestion graph.