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血小板受体作为治疗靶点:过去、现在和未来。

Platelet receptors as therapeutic targets: Past, present and future.

机构信息

Dr. Wolfgang Siess, Institut für Prophylaxe und Epidemiologie der Kreislaufkrankheiten, Klinikum Innenstadt, Ludwig-Maximilians Universität München, Pettenkoferstr. 9, D-80336 München, Germany, Tel.: +49 89 4400 54380, Fax: +49 89 440054382, E-mail:

出版信息

Thromb Haemost. 2017 Jun 28;117(7):1249-1257. doi: 10.1160/TH16-12-0911. Epub 2017 Jun 9.

Abstract

Anti-platelet drugs reduce arterial thrombosis after plaque rupture and erosion, prevent stent thrombosis and are used to prevent and treat myocardial infarction and ischaemic stroke. Some of them may also be helpful in treating less frequent diseases such as thrombotic thrombocytopenic purpura. The present concise review aims to cover current and future developments of anti-platelet drugs interfering with the interaction of von Willebrand factor (VWF) with glycoprotein (GP) Ibα, and directed against GPVI, GPIIb/IIIa (integrin αβ), the thrombin receptor PAR-1, and the ADP receptor P2Y. The high expectations of having novel antiplatelet drugs which selectively inhibit arterial thrombosis without interfering with normal haemostasis could possibly be met in the near future.

摘要

抗血小板药物可减少斑块破裂和侵蚀后的动脉血栓形成,预防支架内血栓形成,并用于预防和治疗心肌梗死和缺血性中风。其中一些药物也可能对治疗血栓性血小板减少性紫癜等不太常见的疾病有帮助。本简明综述旨在涵盖目前和未来抗血小板药物在干扰血管性血友病因子(VWF)与糖蛋白(GP)Ibα相互作用以及针对 GPVI、GPIIb/IIIa(整合素αβ)、凝血酶受体 PAR-1 和 ADP 受体 P2Y 方面的新进展。人们期望在不久的将来能够获得新型的抗血小板药物,这些药物选择性地抑制动脉血栓形成,而不干扰正常的止血功能。

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