Inhibitory effect of phenolic compounds from grape seeds (Vitis vinifera L.) on the activity of angiotensin I converting enzyme

被引:22
作者
Afonso, Joana [1 ,2 ]
Passos, Claudia P. [3 ]
Coimbra, Manuel A. [3 ]
Silva, Carlos M. [2 ]
Soares-da-Silva, Patricio [1 ]
机构
[1] Univ Porto, Fac Med, Inst Pharmacol & Therapeut, P-4200319 Porto, Portugal
[2] Univ Aveiro, Dept Chem, CICECO, P-3810193 Aveiro, Portugal
[3] Univ Aveiro, Dept Chem, QOPNA, P-3810193 Aveiro, Portugal
关键词
Angiotensin I converting enzyme; ACE inhibitor; Procyanidins; Grape seeds; Hypertension; PROCYANIDINS; POLYPHENOLS; PLASMA; HEALTH; PROANTHOCYANIDINS; (-)-EPICATECHIN; ANTIOXIDANTS; CONJUGATION; ABSORPTION; EXTRACT;
D O I
10.1016/j.lwt.2013.04.009
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Inhibition of the angiotensin I converting enzyme (ACE) is an important therapeutic approach in the treatment of several cardiovascular disorders. In this study the inhibitory potential of procyanidin-rich fractions of grape seed (Vitis vinifera L.) was evaluated. The inhibitory capacity was assayed by fluorometric determination of the amount of histidyl-leucine released from the substrate utilized in the presence of ACE from rabbit lung. Four purified monomers [(+)-catechin, (-)-epicatechin, (+)-catechin-O-gallate, and (-)-epigallocatechin] were also tested for comparison. Results showed that the natural phenolic extracts exhibit higher inhibitory potential than the monomers, and that fractions with higher average degrees of polymerization (DPn = 8, IC50 = 0.1 mg/L) present lower IC50 than the intermediate ones (DPn = 5, IC50 = 3.5 mg/L). Such findings strengthen the idea that the inhibitor extension, and the number of heterocyclic oxygen and hydroxyl groups in their structures, could define their in vitro action. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:265 / 270
页数:6
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