Moderate Champagne consumption promotes an acute improvement in acute endothelial-independent vascular function in healthy human volunteers
Moderate Champagne consumption promotes an acute improvement in acute endothelial-independent vascular function in healthy human volunteers
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适量饮用香槟可促进健康志愿者急性内皮依赖性血管功能的急剧改善
DOI:
10.1017/s0007114509992959
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发表时间:
2009
影响因子:
3.6
通讯作者:
J. Spencer
中科院分区:
文献类型:
--
作者:
Dr David Vauzour;Emily J Houseman;T. George;G. Corona;R. Garnotel;K. Jackson;Christelle Sellier;P. Gillery;O. Kennedy;J. Lovegrove;J. Spencer
Epidemiological studies have suggested an inverse correlation between red wine consumption and the incidence of CVD. However, Champagne wine has not been fully investigated for its cardioprotective potential. In order to assess whether acute and moderate Champagne wine consumption is capable of modulating vascular function, we performed a randomised, placebo-controlled, cross-over intervention trial. We show that consumption of Champagne wine, but not a control matched for alcohol, carbohydrate and fruit-derived acid content, induced an acute change in endothelium-independent vasodilatation at 4 and 8 h post-consumption. Although both Champagne wine and the control also induced an increase in endothelium-dependent vascular reactivity at 4 h, there was no significant difference between the vascular effects induced by Champagne or the control at any time point. These effects were accompanied by an acute decrease in the concentration of matrix metalloproteinase (MMP-9), a significant decrease in plasma levels of oxidising species and an increase in urinary excretion of a number of phenolic metabolites. In particular, the mean total excretion of hippuric acid, protocatechuic acid and isoferulic acid were all significantly greater following the Champagne wine intervention compared with the control intervention. Our data suggest that a daily moderate consumption of Champagne wine may improve vascular performance via the delivery of phenolic constituents capable of improving NO bioavailability and reducing matrix metalloproteinase activity.
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影响因子:
15.9
作者:
GALIS, ZS;SUKHOVA, GK;LIBBY, P
通讯作者:
LIBBY, P
影响因子:
6.1
作者:
Dudley, Jocelyn I.;Lekli, Istvan;Das, Dipak K.
通讯作者:
Das, Dipak K.
DOI:
10.1152/ajpheart.01293.2005
发表时间:
2006
期刊:
American journal of physiology. Heart and circulatory physiology
影响因子:
--
作者:
Xu,Shanqin;Ying,Jia;Jiang,Bingbing;Guo,Wei;Adachi,Takeshi;Sharov,Viktor;Lazar,Harold;Menzoian,James;Knyushko,TatyanaV;Bigelow,Diana;Schöneich,Christian;Cohen,RichardA
通讯作者:
Cohen,RichardA
影响因子:
7.1
作者:
Lampe, JW
通讯作者:
Lampe, JW
DOI:
10.1152/ajpheart.01207.2003
发表时间:
2004
期刊:
American journal of physiology. Heart and circulatory physiology
影响因子:
--
作者:
Tawakol,Ahmed;Omland,Torbjørn;Creager,MarkA
通讯作者:
Creager,MarkA