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

被引:2
作者
Agouni, Abdelali [1 ,2 ]
Mostefai, Hadj Ahmed [1 ]
Lagrue, Anne-Helene [1 ]
Sladkova, Martina [1 ,3 ]
Rouet, Philippe [4 ]
Desmoulin, Franck [5 ]
Pechanova, Olga [3 ]
Martinez, Maria Carmen [1 ,6 ]
Andriantsitohaina, Ramaroson [1 ,6 ]
机构
[1] Univ Bretagne Loire, Univ Angers, INSERM U1063, Stress Oxydant & Pathol Matab, Angers, France
[2] Qatar Univ, Pharmaceut Sci Sect, Coll Pharm, Doha, Qatar
[3] Slovak Acad Sci, Inst Normal & Pathol Physiol, Bratislava, Slovakia
[4] UMR UT3 CNRS 5288, Team Evolutionary Med Obes & Heart Failure Mol &, Ave Jean Poulhes, Toulouse, France
[5] Univ Toulouse, INSERM, UPS, ToNIC,Toulouse NeuroImaging Ctr, Toulouse, France
[6] CHU Angers, Angers, France
关键词
OXIDATIVE STRESS; CIRCULATING MICROPARTICLES; CARDIOVASCULAR ALTERATIONS; ENDOPLASMIC-RETICULUM; ENDOTHELIAL FUNCTION; VASCULAR REACTIVITY; TEA POLYPHENOLS; OBESITY; EXPRESSION; DISEASE;
D O I
10.1155/2017/8536910
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:12
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