INHIBITION OF PLATELET ACTIVATION AND ENDOTHELIAL-CELL INJURY BY POLYPHENOLIC COMPOUNDS ISOLATED FROM LONICERA-JAPONICA THUNB

被引:71
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 | 1992年 / 45卷 / 04期
关键词
D O I
10.1016/0952-3278(92)90088-Z
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
Effects of the polyphenolic compounds isolated from Lonicera japonica Thunb on platelet aggregation, platelet thromboxane biosynthesis and hydrogen peroxide-induced endothelial cell injury were studied. With regard to the inhibitory effect on human platelet aggregation, methyl caffeate, 3,4-di-O-caffeoylquinic acid and methyl 3,4-di-O-caffeoylquinate had a strong effect. They significantly inhibited the second wave of platelet aggregation induced by ADP. Concerning thromboxane biosynthesis triggered by calcium ionophore A23187 in platelets, methyl caffeate and methyl 3,4-di-O-caffeoylquinate had the most potent inhibitory effect. Methyl 3,4-di-O-caffeoylquinate directly inhibited the conversion of arachidonic acid to thromboxane by platelet microsomes, while methyl caffeate did not have any significant effect on thromboxane biosynthesis in platelet microsomes. In the prevention of hydrogen peroxide-induced endothelial cell injury in culture, protocatechuic acid, methyl caffeate, methyl chlorogenic acid and luteolin were significantly effective. The inhibitory effect on platelet activation and the cytoprotective effect on hydrogen peroxide-induced cell injury may explain the possible role of polyphenolic compounds isolated from Lonicera japonica Thunb in maintaining vascular homeostasis.
引用
收藏
页码:307 / 312
页数:6
相关论文
共 13 条
[1]   A NEW INVITRO METHOD USING FURA-2 FOR THE QUANTIFICATION OF ENDOTHELIAL-CELL INJURY [J].
ABE, M ;
MORITA, I ;
MUROTA, S .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1988, 34 (01) :69-74
[2]   THE RESPIRATORY BURST OF PHAGOCYTES [J].
BABIOR, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (03) :599-601
[3]  
CHANG MH, 1986, PHARM APPLICATIONS C, P822
[4]   INHIBITION OF PLATELET-AGGREGATION AND ARACHIDONATE METABOLISM IN PLATELETS BY PROCYANIDINS [J].
CHANG, WC ;
HSU, FL .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1989, 38 (03) :181-188
[5]   THROMBOXANES - NEW GROUP OF BIOLOGICALLY-ACTIVE COMPOUNDS DERIVED FROM PROSTAGLANDIN ENDOPEROXIDES [J].
HAMBERG, M ;
SVENSSON, J ;
SAMUELSSON, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (08) :2994-2998
[6]   TISSUE-INJURY IN INFLAMMATION - OXIDANTS, PROTEINASES, AND CATIONIC PROTEINS [J].
HENSON, PM ;
JOHNSTON, RB .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (03) :669-674
[7]  
KIMURA Y, 1985, CHEM PHARM BULL, V33, P2028
[8]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[9]   HUMAN ARTERIAL-WALL CELLS SECRETE FACTORS THAT ARE CHEMOTACTIC FOR MONOCYTES [J].
MAZZONE, T ;
JENSEN, M ;
CHAIT, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (16) :5094-5097
[10]   OXYGEN RADICALS MEDIATE ENDOTHELIAL CELL DAMAGE BY COMPLEMENT-STIMULATED GRANULOCYTES - INVITRO MODEL OF IMMUNE VASCULAR DAMAGE [J].
SACKS, T ;
MOLDOW, CF ;
CRADDOCK, PR ;
BOWERS, TK ;
JACOB, HS .
JOURNAL OF CLINICAL INVESTIGATION, 1978, 61 (05) :1161-1167