Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan, USA; Department of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan Medical School, Ann Arbor, Michigan, USA; Department of Surgery, Division of Vascular Surgery, University of Michigan Medical School, Ann Arbor, Michigan, USA.
J Thromb Haemost. 2023 Dec;21(12):3317-3328. doi: 10.1016/j.jtha.2023.09.013.
Antiplatelet therapy plays a critical role in the prevention and treatment of major cardiovascular diseases triggered by thrombosis. Since the 1900s, significant progress in reducing morbidity and death caused by cardiovascular diseases has been made. However, despite the development and approval of drugs that specifically target the platelet, including inhibitors for cycloxygenase-1, P2Y receptor, integrin αIIbβ3, phosphodiesterases, and protease-activated receptor 1, the risk of recurrent thrombotic events remains high, and the increased risk of bleeding is a major concern. Scientific advances in our understanding of the role of platelets in haemostasis and thrombosis have revealed novel targets, such as protease-activated receptor 4 (PAR4), glycoprotein Ib (GPIb)-V-IX complex, glycoprotein VI, and 12-lipoxygenase. The antithrombotic effects and safety of the pharmacologic inhibition of these targets are currently under investigation in clinical studies. This review provides an overview of drugs in early development to target the platelet and those in current use in clinical practice. Furthermore, it describes the emerging drug targets being developed and studied to reduce platelet activity and outlines potential novel therapeutic targets in the platelet.
抗血小板治疗在预防和治疗由血栓引起的主要心血管疾病方面起着关键作用。自 20 世纪以来,降低心血管疾病发病率和死亡率方面取得了重大进展。然而,尽管针对血小板的药物,包括环氧化酶-1、P2Y 受体、整合素 αIIbβ3、磷酸二酯酶和蛋白酶激活受体 1 的抑制剂已经开发和批准,但复发性血栓事件的风险仍然很高,出血风险增加是一个主要关注点。我们对血小板在止血和血栓形成中的作用的科学认识的进步揭示了新的靶点,如蛋白酶激活受体 4(PAR4)、糖蛋白 Ib(GPIb)-V-IX 复合物、糖蛋白 VI 和 12-脂氧合酶。目前正在临床研究中研究这些靶点的药理学抑制的抗血栓作用和安全性。本综述概述了早期开发的针对血小板的药物和目前在临床实践中使用的药物,还描述了正在开发和研究以降低血小板活性的新兴药物靶点,并概述了血小板中潜在的新型治疗靶点。