Cocoa inhibits platelet activation and function

被引:0
作者
Rein, D
Paglieroni, TG
Wun, T
Pearson, DA
Schmitz, HH
Gosselin, R
Keen, CL
机构
[1] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
[2] Sacramento Med Fdn, Ctr Blood Res, Sacramento, CA USA
[3] Univ Calif Davis, Med Ctr, Dept Hematol & Oncol, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Med Ctr, Dept Pathol, Sacramento, CA 95817 USA
[5] Mars Inc, Hackettstown, NJ USA
关键词
cocoa beverage; chocolate; platelet activation; platelet glycoprotein; glycoprotein IIb-IIIa complex; P-selectin; CD62P; whole-blood flow cytometry; platelet function tests; blood coagulation; hemostasis; cardiovascular disease; dietary polyphenols;
D O I
暂无
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Epidemiologic studies have shown inverse associations between dietary polyphenols and mortality from coronary heart disease. However, the basis for this protective association is uncertain. Food polyphenols reportedly have antioxidant properties and decrease platelet function in vitro. Objective: This study sought to evaluate whether consumption of a polyphenol-rich cocoa beverage modulates human platelet activation and primary hemostasis. Design: Peripheral blood was obtained from 30 healthy subjects before and 2 and 6 h after ingestion of a cocoa beverage (n = 10), a caffeine-containing control beverage (12 = 10). or water (n = 10). Platelet activation was measured in terms of expression of activation-dependent platelet antigens and platelet microparticle formation by using fluorescent-labeled monoclonal antibodies and flow cytometry. Primary platelet-related hemostasis was measured with a platelet function analyzer. Results: Ex vivo epinephrine- or ADP-stimulated expression of the fibrinogen-binding conformation of glycoprotein IIb-IIIa was lower 2 and 6 h after consumption of cocoa than before consumption. Cocoa consumption also decreased ADP-stimulated P-selectin expression. In contrast, epinephrine-induced platelet glycoprotein IIb-IIIa expression increased after consumption of the caffeine-containing beverage but not after water consumption. Platelet microparticle formation decreased 2 and 6 h after cocoa consumption but increased after caffeine and water consumption. Primary hemostasis in response to epinephrine in vitro was inhibited 6 h after cocoa consumption. The caffeine-containing beverage inhibited ADP-induced primary hemostasis 2 and 6 h after consumption. Conclusions: Cocoa consumption suppressed ADP- or epinephrine-stimulated platelet activation and platelet microparticle formation. Cocoa consumption had an aspirin-like effect on primary hemostasis.
引用
收藏
页码:30 / 35
页数:6
相关论文
共 56 条
[1]   A simple, whole blood method for assessment of platelet function: Application to dietary intervention [J].
Allman-Farinelli, MA ;
Bendall, L ;
Troy, J ;
Versluis, C ;
Hall, D ;
Favaloro, EJ ;
Berndt, MC .
THROMBOSIS RESEARCH, 1998, 90 (04) :163-169
[2]   COLLABORATIVE OVERVIEW OF RANDOMIZED TRIALS OF ANTIPLATELET THERAPY .1. PREVENTION OF DEATH, MYOCARDIAL-INFARCTION, AND STROKE BY PROLONGED ANTIPLATELET THERAPY IN VARIOUS CATEGORIES OF PATIENTS [J].
ALTMAN, R ;
CARRERAS, L ;
DIAZ, R ;
FIGUEROA, E ;
PAOLASSO, E ;
PARODI, JC ;
CADE, JF ;
DONNAN, G ;
EADIE, MJ ;
GAVAGHAN, TP ;
OSULLIVAN, EF ;
PARKIN, D ;
RENNY, JTG ;
SILAGY, C ;
VINAZZER, H ;
ZEKERT, F ;
ADRIAENSEN, H ;
BERTRANDHARDY, JM ;
BRAN, M ;
DAVID, JL ;
DRICOT, J ;
LAVENNEPARDONGE, E ;
LIMET, R ;
LOWENTHAL, A ;
MORIAU, M ;
SCHAPIRA, S ;
SMETS, P ;
SYMOENS, J ;
VERHAEGHE, R ;
VERSTRAETE, M ;
ATALLAH, A ;
BARNETT, H ;
BATISTA, R ;
BLAKELY, J ;
CAIRNS, JA ;
COTE, R ;
CROUCH, J ;
EVANS, G ;
FINDLAY, JM ;
GENT, M ;
LANGLOIS, Y ;
LECLERC, J ;
NORRIS, J ;
PINEO, GF ;
POWERS, PJ ;
ROBERTS, R ;
SCHWARTZ, L ;
SICURELLA, J ;
TAYLOR, W ;
THEROUX, P .
BMJ-BRITISH MEDICAL JOURNAL, 1994, 308 (6921) :81-100
[3]  
ARDLIE NG, 1967, THROMB DIATH HAEMOST, V18, P670
[4]  
BAK AAA, 1990, NETH J MED, V37, P242
[5]   Transcellular activation of platelets and endothelial cells by bioactive lipids in platelet microparticles [J].
Barry, OP ;
Pratico, D ;
Lawson, JA ;
FitzGerald, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (09) :2118-2127
[6]   INHIBITION OF AGGREGATION AND SECRETION OF HUMAN-PLATELETS BY QUERCETIN AND OTHER FLAVONOIDS - STRUCTURE ACTIVITY RELATIONSHIPS [J].
BERETZ, A ;
CAZENAVE, JP ;
ANTON, R .
AGENTS AND ACTIONS, 1982, 12 (03) :382-387
[7]  
BIAGGIONI I, 1991, J PHARMACOL EXP THER, V258, P588
[8]  
BIRKETT DJ, 1985, DRUG METAB DISPOS, V13, P725
[9]   USE OF A MONOCLONAL-ANTIBODY DIRECTED AGAINST THE PLATELET GLYCOPROTEIN IIB/IIIA RECEPTOR IN HIGH-RISK CORONARY ANGIOPLASTY [J].
CALIFF, RM ;
SHADOFF, N ;
VALETT, N ;
BATES, E ;
GALEANA, A ;
KNOPF, W ;
SHAFTEL, J ;
BENDER, MJ ;
AVERSANO, T ;
RAQUENO, J ;
GURBEL, P ;
COWFER, J ;
COHEN, M ;
CROSS, P ;
BITTL, J ;
EDDINGS, K ;
TAYLOR, M ;
DEROSA, K ;
HATTEL, L ;
COOPER, L ;
ESHELMAN, B ;
FINTEL, D ;
NIEMYSKI, P ;
KLEIN, L ;
KENNEDY, H ;
THORNTON, T ;
KEREIAKES, D ;
MARTIN, L ;
ANDERSON, L ;
HIGBY, N ;
ELLIS, S ;
BREZINA, K ;
GEORGE, B ;
CHAPEKIS, A ;
SMITH, D ;
ANWAR, A ;
GERBER, TL ;
PRITCHARD, GL ;
MYLER, R ;
SHAW, R ;
MURPHY, M ;
WARD, K ;
MADIGAN, NP ;
BLANKENSHIP, J ;
HALBERT, M ;
FLANAGAN, C ;
TANNENBAUM, M ;
POLICH, M ;
STEVENSON, C ;
TCHENG, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (14) :956-961
[10]  
COE SD, 1996, TRUE HIST CHOCOLATE, P280