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红葡萄中的多酚对人cGMP特异性磷酸二酯酶5的体外抑制作用。

In vitro inhibition of human cGMP-specific phosphodiesterase-5 by polyphenols from red grapes.

作者信息

Dell'Agli Mario, Galli Germana V, Vrhovsek Urska, Mattivi Fulvio, Bosisio Enrica

机构信息

Department of Pharmacological Sciences, Faculty of Pharmacy, University of Milan, via Balzaretti 9, 20133 Milan, Italy.

出版信息

J Agric Food Chem. 2005 Mar 23;53(6):1960-5. doi: 10.1021/jf048497+.

Abstract

A moderate consumption of red wine may reduce the risk of cardiovascular diseases via wine-derived phenolic compounds. A variety of biological mechanisms have been proposed for wine-derived phenolic compounds including nitric oxide-mediated vasorelaxation. This study examined whether the vasodilating effect of wine-derived phenolic compounds was associated with the inhibition of phosphodiesterases (PDEs) and, in particular, PDE5. For this purpose, human recombinant PDE5A1 isoform was prepared by expression of the full-length cDNA of PDE5A1 into COS-7 cells. Red wine and the extracts from grape skin inhibited PDE5A1 activity, whereas the seed extracts had a negligible effect. The mixture of anthocyanins inhibited the enzyme activity (IC50 = 11.6 microM), with malvidin-3-O-beta-glucoside (IC50 = 35.4 microM) and malvidin (IC50 = 24.9 microM) the most potent among the monoglucosides and aglycons, respectively. trans-Resveratrol and trans-piceid exhibited negligible effects, whereas hydroxycinnamates were completely inactive. These results indicate that polyphenols-induced vasorelaxation may also be sustained by smooth muscle PDE inhibition by anthocyanins present in red wines and grapes.

摘要

适量饮用红酒可能通过红酒中的酚类化合物降低心血管疾病风险。关于红酒中的酚类化合物,人们提出了多种生物学机制,包括一氧化氮介导的血管舒张。本研究检测了红酒中酚类化合物的血管舒张作用是否与磷酸二酯酶(PDEs)的抑制作用相关,尤其是与PDE5的抑制作用相关。为此,通过将PDE5A1的全长cDNA表达至COS-7细胞中制备人重组PDE5A1亚型。红酒和葡萄皮提取物抑制PDE5A1活性,而葡萄籽提取物的作用可忽略不计。花青素混合物抑制该酶活性(IC50 = 11.6 microM),其中在单糖苷和苷元中,矢车菊素-3-O-β-葡萄糖苷(IC50 = 35.4 microM)和矢车菊素(IC50 = 24.9 microM)的抑制作用最强。反式白藜芦醇和反式白藜芦醇苷的作用可忽略不计,而羟基肉桂酸完全无活性。这些结果表明,红酒和葡萄中存在的花青素对平滑肌PDE的抑制作用也可能维持多酚诱导的血管舒张。

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