Oxygen free radicals and platelet activation

被引:199
作者
Iuliano, L
Colavita, AR
Leo, R
Pratico, D
Violi, F
机构
[1] UNIV ROMA LA SAPIENZA, INST CLIN MED 1, I-00185 ROME, ITALY
[2] UNIV PENN, SCH MED, CTR EXPT THERAPEUT, PHILADELPHIA, PA 19104 USA
关键词
free radicals; platelets; atherosclerosis; antioxidants;
D O I
10.1016/S0891-5849(96)00488-1
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
This article reviews our current understanding of the role of oxygen free radicals in platelet activation. Several studies have indicated that platelets, in analogy to other circulating blood cells, are able to produce oxygen free radicals, which are likely to play an important role in the mechanism of platelet activation and aggregation. Platelet activation has been obtained with very low, physiologically relevant concentrations of radicals generated chemically, by leukocytes, and by hemoglobin derived from membrane leakage of erythrocytes. Knowledge of the role of reactive species in platelet physiology is relevant because platelets are brought into close contact with other cells capable of producing free radicals, such as neutrophils, macrophages, and endothelial cells, during the formation of thrombus. The physiopatological importance of these findings is high because it is now emerging that free radicals may have a role in the mechanism of atherosclerosis and its thrombotic complications. where the causative role of platelets is well documented. This background suggests therapeutic interventions with antioxidants as antiplatelet agents to improve the pharmacological effect of classical antiplatelet drug such as aspirin. Copyright (C) 1997 Elsevier Science Inc.
引用
收藏
页码:999 / 1006
页数:8
相关论文
共 76 条
[61]   REVERSIBLE BINDING OF NITRIC-OXIDE BY A SALIVARY HEME PROTEIN FROM A BLOODSUCKING INSECT [J].
RIBEIRO, JMC ;
HAZZARD, JMH ;
NUSSENZVEIG, RH ;
CHAMPAGNE, DE ;
WALKER, FA .
SCIENCE, 1993, 260 (5107) :539-541
[62]   DIPHENYLENE IODONIUM, AN INHIBITOR OF FREE-RADICAL FORMATION, INHIBITS PLATELET-AGGREGATION [J].
SALVEMINI, D ;
RADZISZEWSKI, W ;
MOLLACE, V ;
MOORE, A ;
WILLOUGHBY, D ;
VANE, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 199 (01) :15-18
[63]   SUPEROXIDE ANIONS ENHANCE PLATELET-ADHESION AND AGGREGATION [J].
SALVEMINI, D ;
DENUCCI, G ;
SNEDDON, JM ;
VANE, JR .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (04) :1145-1150
[64]   SHORT-TERM VITAMIN-E SUPPLEMENTATION HAS NO EFFECT ON PLATELET-FUNCTION, PLASMA PHOSPHOLIPASE-A2 AND LYSO-PAF IN MALE-VOLUNTEERS [J].
SILBERT, PL ;
LEONG, LLL ;
STURM, MJ ;
STROPHAIR, J ;
TAYLOR, RR .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1990, 17 (09) :645-651
[65]   BIOCHEMISTRY OF NITRIC-OXIDE AND ITS REDOX-ACTIVATED FORMS [J].
STAMLER, JS ;
SINGEL, DJ ;
LOSCALZO, J .
SCIENCE, 1992, 258 (5090) :1898-1902
[66]   VITAMIN-E - INHIBITOR OF PLATELET-RELEASE REACTION [J].
STEINER, M ;
ANASTASI, J .
JOURNAL OF CLINICAL INVESTIGATION, 1976, 57 (03) :732-737
[67]  
TAYLOR L, 1983, J BIOL CHEM, V258, P6855
[68]  
TEST ST, 1984, J BIOL CHEM, V259, P399
[69]   VITAMIN-E CONCENTRATIONS IN HUMAN-BLOOD PLASMA AND PLATELETS [J].
VATASSERY, GT ;
KREZOWSKI, AM ;
ECKFELDT, JH .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1983, 37 (06) :1020-1024
[70]   INHIBITION OF CYCLOOXYGENASE-INDEPENDENT PLATELET-AGGREGATION BY SODIUM-SALICYLATE [J].
VIOLI, F ;
ALESSANDRI, C ;
PRATICO, D ;
GUZZO, A ;
GHISELLI, A ;
BALSANO, F .
THROMBOSIS RESEARCH, 1989, 54 (06) :583-593