Anti-platelet effects of bioactive compounds isolated from the bark of Rhus verniciflua Stokes

被引:71
作者
Jeon, Won Kyung
Lee, Ju Hyun
Kim, Ho Kyoung
Lee, A. Yeong
Lee, Sung Ok
Kim, Young Sup
Ryu, Shi Yong
Kim, Soo Young
Lee, Yong Jin
Ko, Byoung Seob [1 ]
机构
[1] Korea Inst Orental Med, Qual Control Herbal Med Dept, Taejon 46124, South Korea
[2] Korea Res Inst Chem Technol, Div Med Sci, Taejon 305606, South Korea
[3] Univ Konkuk, Dept Biol Sci, Seoul, South Korea
[4] Asan Inst Life Sci, Dept Mol Med, Seoul, South Korea
关键词
Rhus verniciflua Stokes (Anacardiaceae); isomaltol; pentagalloyl glucose; GPIlb/IIIa-like expression; P-selectin; calcium mobilization;
D O I
10.1016/j.jep.2005.12.015
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
It has previously been shown that EtOAc extracts of Rhus vemiciflua Stokes (RVS),inhibit the platelet aggregation response. In this report, bioassay-guided fractionation using ADP-, arachidonic acid-, and collagen-induced human platelet aggregation by a whole blood aggregometer yielded the bioactive compounds isomaltol and pentagalloyl glucose from different highly effective fractions. In addition, column chromatography of fractions from RVS yielded another five compounds: butin, fisetin, sulfurefin, butein and 3,4',7,8-tetrahydroxyflavone. We investigated the effects of bioactive compounds from RVS fractions on several markers of platelet activation using receptor expression on platelet membranes, including glycoprotein IIb/IIIa (CD41), GPIIb/IIIa-like expression (PAC-1) and P-selectin (CD62), and intracelluar calcium mobilization responses by flow cytometry in healthy subjects. Dose-dependent inhibition of platelet aggregation and significantly decreased platelet activation were observed for the isomaltol- and pentagalloyl glucose-treated platelets, respectively. These results show that isomaltol and pentagalloyl glucose from the bark of Rhus verniciflua Stokes have potent anti-platelet activity and emphasize the need to further examine the mechanism of these active compounds for platelet modulation. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:62 / 69
页数:8
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