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

Author:

Agouni Abdelali12ORCID,Mostefai Hadj Ahmed1,Lagrue Anne-Hélène1,Sladkova Martina13,Rouet Philippe4,Desmoulin Franck5,Pechanova Olga3ORCID,Martínez Maria Carmen16ORCID,Andriantsitohaina Ramaroson16ORCID

Affiliation:

1. INSERM U1063, Stress Oxydant et Pathologies métaboliques, Université d’Angers, Université Bretagne Loire, Angers, France

2. Pharmaceutical Science Section, College of Pharmacy, Qatar University, Doha, Qatar

3. Institute of Normal and Pathological Physiology, Slovak Academy of Sciences, Bratislava, Slovakia

4. UMR UT3 CNRS 5288, Team Evolutionary Medicine, Obesity and Heart Failure: Molecular and Clinical Investigations, Avenue Jean Poulhes, Toulouse, France

5. ToNIC, Toulouse NeuroImaging Center, Université de Toulouse, Inserm, UPS, Toulouse, France

6. CHU, Angers, France

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.

Funder

Institut national de la santé et de la recherche médicale

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

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