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
[51]  
MILLER CC, 1994, J BIOL CHEM, V269, P3529
[52]   CYTOSKELETAL ALTERATIONS IN HUMAN-PLATELETS EXPOSED TO OXIDATIVE STRESS ARE MEDIATED BY OXIDATIVE AND CA-2+-DEPENDENT MECHANISMS [J].
MIRABELLI, F ;
SALIS, A ;
VAIRETTI, M ;
BELLOMO, G ;
THOR, H ;
ORRENIUS, S .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1989, 270 (02) :478-488
[53]  
MONCADA S, 1991, PHARMACOL REV, V43, P109
[54]   ISOLATION OF NITRIC-OXIDE SYNTHASE FROM HUMAN PLATELETS [J].
MURUGANANDAM, A ;
MUTUS, B .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1994, 1200 (01) :1-6
[55]   OXYGEN-RADICAL-MEDIATED LIPID-PEROXIDATION AND INHIBITION OF ADP-INDUCED PLATELET-AGGREGATION [J].
OHYASHIKI, T ;
KOBAYASHI, M ;
MATSUI, K .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1991, 288 (01) :282-286
[56]  
POU S, 1992, J BIOL CHEM, V267, P24173
[57]  
PRATICO D, 1992, J LAB CLIN MED, V119, P364
[58]  
PRATICO D, 1991, HAEMOSTASIS, V21, P169
[59]   POLYMORPHONUCLEAR LEUKOCYTE-DERIVED O2-REACTIVE SPECIES ACTIVATE PRIMED PLATELETS IN HUMAN WHOLE-BLOOD [J].
PRATICO, D ;
IULIANO, L ;
ALESSANDRI, C ;
CAMASTRA, C ;
VIOLI, F .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :H1582-H1587
[60]  
PRITCHARD KA, 1986, THROMB HAEMOSTASIS, V55, P6