Department of Community and Preventive Medicine, University of Rochester School of Medicine, P. O. Box 644, 601 Elmwood Avenue, Rochester, NY 14642, USA.
J Cardiovasc Transl Res. 2010 Oct;3(5):538-46. doi: 10.1007/s12265-010-9213-7. Epub 2010 Jul 27.
Platelets are the primary cell mediator of thrombosis. A deficiency of platelets can result in severe bleeding defects. "Overactive" platelets contribute to life-threatening outcomes in diseases such as heart attack, stroke, and cancer. The use of platelet inhibitors for thrombosis prevention must therefore seek a delicate balance between inhibiting platelet activation and an associated increased bleeding risk. There are currently few platelet inhibitors clinically available, making the search for novel anti-platelet drug targets a major research priority. Several newly identified pathways of platelet activation may hold hope in this area. In addition, important roles for platelets beyond hemostasis have been discovered. Platelets have recently been described as mediators of diverse inflammatory diseases such as arthritis, hepatitis, malaria, and atherosclerosis. This has heightened the need to broaden our understanding of platelet functions and platelet-derived inflammatory mediators. It has also heightened interest in a continued search for new platelet inhibitors and presents new opportunities for platelet inhibitors to be used in a wide array of disease treatment strategies.
血小板是血栓形成的主要细胞介质。血小板缺乏会导致严重的出血缺陷。“过度活跃”的血小板会导致心脏病发作、中风和癌症等危及生命的后果。因此,血小板抑制剂的使用必须在抑制血小板激活和相关的出血风险增加之间寻求微妙的平衡。目前临床上可用的血小板抑制剂很少,因此寻找新的抗血小板药物靶点是一个主要的研究重点。几个新发现的血小板激活途径在这方面可能有希望。此外,血小板在止血以外的重要作用也已被发现。血小板最近被描述为关节炎、肝炎、疟疾和动脉粥样硬化等多种炎症性疾病的介质。这就需要我们更广泛地了解血小板的功能和血小板衍生的炎症介质。这也增加了对继续寻找新的血小板抑制剂的兴趣,并为血小板抑制剂在广泛的疾病治疗策略中使用提供了新的机会。