ANTIPLATELET CONSTITUENTS OF GARLIC AND ONION

被引:78
作者
MAKHEJA, AN
BAILEY, JM
机构
[1] Department of Biochemistry and Molecular Biology, George Washington University School of Medicine, Washington, DC
来源
AGENTS AND ACTIONS | 1990年 / 29卷 / 3-4期
关键词
D O I
10.1007/BF01966468
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have identified three main antiplatelet constituents, namely adenosine, allicin and paraffinic polysulfides in both garlic and onion. Adenosine and allicin both inhibited platelet aggregation without affecting cyclooxygenase and lipoxygenase metabolites of arachidonic acid. The trisulfides inhibited platelet aggregation as well as thromboxane synthesis along with induction of new lipoxygenase metabolites. The data indicate that the observed in vivo antiplatelet effects of ingesting onion and garlic are attributable more to the adenosine than to the allicin and paraffinic polysulfide constituents. © 1990 Birkhäuser Verlag.
引用
收藏
页码:360 / 363
页数:4
相关论文
共 27 条
[1]   SELECTIVE SUPPRESSION OF PLATELET THROMBOXANE FORMATION WITH SPARING OF VASCULAR PROSTACYCLIN SYNTHESIS BY AQUEOUS EXTRACT OF GARLIC IN RABBITS [J].
ALI, M ;
MOHAMMED, SY .
PROSTAGLANDINS LEUKOTRIENES AND MEDICINE, 1986, 25 (2-3) :139-146
[2]  
ARIGA T, 1981, LANCET, V1, P150
[3]  
BAGHURST KI, 1977, LANCET, V1, P101
[4]  
BAILEY JM, 1979, ATHEROSCLEROSIS, V32, P195
[5]  
BAYER T, 1988, LANCET, V2, P906
[6]   (E,Z)-AJOENE - A POTENT ANTITHROMBOTIC AGENT FROM GARLIC [J].
BLOCK, E ;
AHMAD, S ;
JAIN, MK ;
CRECELY, RW ;
APITZCASTRO, R ;
CRUZ, MR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (26) :8295-8296
[7]   EFFECT OF GARLIC ON HUMAN PLATELET-AGGREGATION INVITRO [J].
BORDIA, A .
ATHEROSCLEROSIS, 1978, 30 (04) :355-360
[8]  
BOULLIN DJ, 1981, LANCET, V1, P766
[9]  
CASTRO RA, 1983, THROMB RES, V32, P155
[10]   ANTI-ASTHMATIC EFFECTS OF ONIONS - ALK(EN)YLSULFINOTHIOIC ACID ALK(EN)YL-ESTERS INHIBIT HISTAMINE-RELEASE, LEUKOTRIENE AND THROMBOXANE BIOSYNTHESIS INVITRO AND COUNTERACT PAF AND ALLERGEN-INDUCED BRONCHIAL OBSTRUCTION INVIVO [J].
DORSCH, W ;
WAGNER, H ;
BAYER, T ;
FESSLER, B ;
HEIN, G ;
RING, J ;
SCHEFTNER, P ;
SIEBER, W ;
STRASSER, T ;
WEISS, E .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (23) :4479-4486