Evidence map›Paper›PMID 28660008›Full record

ArticleOxidative medicine and cellular longevity2017

Paradoxical Effect of Nonalcoholic Red Wine Polyphenol Extract, Provinols™, in the Regulation of Cyclooxygenases in Vessels from Zucker Fatty Rats (

Abdelali Agouni, Hadj Ahmed Mostefai, Anne-Hélène Lagrue, Martina Sladkova, Philippe Rouet, Franck Desmoulin, Olga Pechanova, Maria Carmen Martínez, Ramaroson Andriantsitohaina

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2017. 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
0.1field-weighted citation impact, top 63% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Effect of Bioactive Compound ofOxidative medicine and cellular longevity · 2017
    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

9 authors at 4 institutions in 3 countries.

Abdelali AgouniINSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d'Angers, Université Bretagne Loire, Angers, France.ORCID 0000-0002-8363-1582
Hadj Ahmed MostefaiINSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d'Angers, Université Bretagne Loire, Angers, France.
Anne-Hélène LagrueINSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d'Angers, Université Bretagne Loire, Angers, France.
Martina SladkovaINSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d'Angers, Université Bretagne Loire, Angers, France.
Philippe RouetUMR UT3 CNRS 5288, Team Evolutionary Medicine, Obesity and Heart Failure: Molecular and Clinical Investigations, Avenue Jean Poulhes, Toulouse, France.
Franck DesmoulinToNIC, Toulouse NeuroImaging Center, Université de Toulouse, Inserm, UPS, Toulouse, France.
Olga PechanovaInstitute of Normal and Pathological Physiology, Slovak Academy of Sciences, Bratislava, Slovakia.ORCID 0000-0001-5476-2949
Maria Carmen MartínezINSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d'Angers, Université Bretagne Loire, Angers, France.ORCID 0000-0003-3897-7397
Ramaroson AndriantsitohainaINSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d'Angers, Université Bretagne Loire, Angers, France.ORCID 0000-0002-4770-3585
Inserm · FRCentre National de la Recherche Scientifique · FRSlovak Academy of Sciences · SKUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this work was to study the vascular effects of dietary supplementation of a nonalcoholic red wine polyphenol extract, Provinols, in Zucker fatty (ZF) obese rats. ZF or lean rats received diet supplemented or not with Provinols for 8 weeks. Vasoconstriction in response to phenylephrine (Phe) was then assessed in small mesenteric arteries (SMA) and the aorta with emphasis on the contribution of cyclooxygenases (COX). Although no difference in vasoconstriction was observed between ZF and lean rats both in SMA and the aorta, Provinols affected the contribution of COX-derived vasoconstrictor agents. The nonselective COX inhibitor, indomethacin, reduced vasoconstriction in vessels from both groups; however, lower efficacy was observed in Provinols-treated rats. This was associated with a reduction in thromboxane-A2 and 8-isoprostane release. The selective COX-2 inhibitor, NS398, reduced to the same extent vasoconstriction in aortas from ZF and Provinols-treated ZF rats. However, NS398 reduced response to Phe only in SMA from ZF rats. This was associated with a reduction in 8-isoprostane and prostaglandin-E release. Paradoxically, Provinols decreased COX-2 expression in the aorta, while it increased its expression in SMA. We provide here evidence of a subtle and paradoxical regulation of COX pathway by Provinols vessels from obese rats to maintain vascular tone within a physiological range.

Indexed as

WineAnimalsCyclooxygenase 2 InhibitorsHumansObesityPhenylephrinePolyphenolsRatsRats, ZuckerCyclooxygenase 2 InhibitorsPhenylephrinePolyphenols

Identifiers

PMID28660008
PMCPMC5474272
OpenAlexW2620562597

What OpenQuestion holds

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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.