The assessment of platelet activation in antiplatelet drug development

被引:5
作者
Tan, KT [1 ]
Lip, GYH [1 ]
机构
[1] Univ Birmingham, Dept Med, Haemostasis Thrombosis & Vasc Biol Unit, City Hosp, Birmingham B18 7QH, W Midlands, England
关键词
platelets; platelet activation; flow cytometer; enzyme-linked immumosorbent assay; P-selectin; platelet microparticles; clopidogrel; aspirin;
D O I
10.2174/092986705774933399
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
Platelet activation plays an important role in a wide range of pathological conditions. For example, platelet activation has been shown to be involved in the defence against parasitic infection, the pathogenesis of atherosclerotic disease, and various arterial and venous thrombotic diseases. Indeed, there is considerable interest in the manipulation of platelet function for therapeutic gain. It is for these reasons that there is considerable interest in developing assays measuring in vivo platelet activation. Current modalities in the measurement of platelet activation include Enzyme-linked Immunosorbent Assays (ELISA), platelet flow cytometry and electron microscopy. It is proposed that methods in measuring platelet activation can also be classified into 'direct' and 'indirect' modalities, both of which have their distinct advantages and disadvantages. Unfortunately, there is at present no consensus on the ideal method of measuring platelet activation. Thus, studies on platelet activation should ideally include at least one of each of direct and indirect modality of studying platelet activation. This review provides an overview of basic platelet biology and the various methods of measuring platelet activation, with an emphasis on their role in drug development.
引用
收藏
页码:3117 / 3125
页数:9
相关论文
共 78 条
[71]   Platelet-derived microparticles stimulate coronary artery smooth muscle cell mitogenesis by a PDGF-independent mechanism [J].
Weber, AA ;
Köppen, O ;
Schrör, K .
THROMBOSIS RESEARCH, 2000, 98 (05) :461-466
[72]  
WHITE JG, 1969, AM J PATHOL, V56, P267
[73]  
WHITE JG, 1968, AM J PATHOL, V53, P567
[74]  
WHITE JG, 1990, BLOOD, V76, pA481
[75]  
WHITE JG, 1971, PLATELETS, P83
[76]   Inhibition of platelet glycoprotein Ib, glycoprotein IIb/IIIa, or both by monoclonal antibodies prevents arterial thrombosis in baboons [J].
Wu, DM ;
Meiring, M ;
Kotze, HF ;
Deckmyn, H ;
Cauwenberghs, N .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (02) :323-328
[77]   Pathophysiologic implications of membrane phospholipid asymmetry in blood cells [J].
Zwaal, RFA ;
Schroit, AJ .
BLOOD, 1997, 89 (04) :1121-1132
[78]  
1998, SEM THROMB HAEMOST, V24, P163