INHIBITION OF PLATELET ACTIVATION AND ENDOTHELIAL-CELL INJURY BY FLAVAN-3-OL AND SAIKOSAPONIN COMPOUNDS

被引：26

作者：

CHANG, WC ^{[1
]}

HSU, FL ^{[1
]}

机构：

[1] TAIPEI MED COLL,SCH PHARM,TAIPEI,TAIWAN

来源：

PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 1991年 / 44卷 / 01期

关键词：

D O I：

10.1016/0952-3278(91)90144-T

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

The effects of flavan-3-ol and saikosaponin compounds on platelet aggregation, platelet thromboxane biosynthesis and H2O2-induced endothelial cell injury were studied. Seven flavan-3-ol compounds isolated from Camellia sinensis L. var sinensis O. Kuntze (Theaceae) and three saikosaponin compounds isolated from Bupleurum falcatum L. (Umbelliferae) were used. Among the 10 compounds tested, only epigallocatechin and saikosaponin a significantly inhibited human platelet aggregation induced by ADP, and the potency of inhibition was comparable with aspirin. Both of epigallocatechin and saikosaponin a dose-dependently inhibited the platelet thromboxane formation from exogenous and endogenous arachidonic acid. In the prevention of H2O2-induced endothelial cell injury in culture, only gallocatechin-3-0-gallate and epicatechin-3-0-gallate were effective. The inhibitory effect of epigallocatechin and saikosaponin a on platelet activation and the cytoprotective effect of gallocatechin-3-0-gallate and epicatechin-3-0-gallate on H2O2-induced endothelial cell injury could give evidence of explaining the possible role of flavan-3-ol and saikosaponin compounds in maintaining vascular homeostasis.

引用

页码：51 / 56

页数：6

共 15 条

[1] A NEW INVITRO METHOD USING FURA-2 FOR THE QUANTIFICATION OF ENDOTHELIAL-CELL INJURY [J].