Suppr超能文献

抗血小板策略:过去、现在和未来。

Antiplatelet strategies: past, present, and future.

机构信息

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.

出版信息

J Thromb Haemost. 2023 Dec;21(12):3317-3328. doi: 10.1016/j.jtha.2023.09.013.

Abstract

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.

摘要

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。

相似文献

1
Antiplatelet strategies: past, present, and future.
J Thromb Haemost. 2023 Dec;21(12):3317-3328. doi: 10.1016/j.jtha.2023.09.013.
2
Platelet receptors as therapeutic targets: Past, present and future.
Thromb Haemost. 2017 Jun 28;117(7):1249-1257. doi: 10.1160/TH16-12-0911. Epub 2017 Jun 9.
3
LIM kinase-1 selectively promotes glycoprotein Ib-IX-mediated TXA2 synthesis, platelet activation, and thrombosis.
Blood. 2013 May 30;121(22):4586-94. doi: 10.1182/blood-2012-12-470765. Epub 2013 Apr 25.
4
Therapeutic strategies for thrombosis: new targets and approaches.
Nat Rev Drug Discov. 2020 May;19(5):333-352. doi: 10.1038/s41573-020-0061-0. Epub 2020 Mar 4.
5
Current and future antiplatelet therapies: emphasis on preserving haemostasis.
Nat Rev Cardiol. 2018 Mar;15(3):181-191. doi: 10.1038/nrcardio.2017.206. Epub 2018 Jan 3.
6
Progress in the development of antiplatelet agents: Focus on the targeted molecular pathway from bench to clinic.
Pharmacol Ther. 2019 Nov;203:107393. doi: 10.1016/j.pharmthera.2019.107393. Epub 2019 Jul 26.
7
Glycoprotein VI - novel target in antiplatelet medication.
Pharmacol Ther. 2021 Jan;217:107630. doi: 10.1016/j.pharmthera.2020.107630. Epub 2020 Jul 16.
9
Clinical use of clopidogrel.
Curr Pharm Des. 2012;18(33):5224-39. doi: 10.2174/138161212803251853.
10
GPVI inhibition: Advancing antithrombotic therapy in cardiovascular disease.
Eur Heart J Cardiovasc Pharmacother. 2024 Aug 14;10(5):465-473. doi: 10.1093/ehjcvp/pvae018.

引用本文的文献

2
Platelets and diseases: signal transduction and advances in targeted therapy.
Signal Transduct Target Ther. 2025 May 16;10(1):159. doi: 10.1038/s41392-025-02198-8.
3
Platelet signaling in immune landscape: comprehensive mechanism and clinical therapy.
Biomark Res. 2024 Dec 31;12(1):164. doi: 10.1186/s40364-024-00700-y.
4
Observational Analyses of Ex Vivo Native American Platelet Responses.
Int J Mol Sci. 2024 Nov 8;25(22):11990. doi: 10.3390/ijms252211990.
5
Evolving of treatment options for cerebral infarction.
World J Clin Cases. 2024 Nov 16;12(32):6534-6537. doi: 10.12998/wjcc.v12.i32.6534.
6
Roles of G proteins and their GTPase-activating proteins in platelets.
Biosci Rep. 2024 May 29;44(5). doi: 10.1042/BSR20231420.

本文引用的文献

2
Amplified inhibition of atherosclerotic plaque-induced platelet activation by glenzocimab with dual antiplatelet therapy.
J Thromb Haemost. 2023 Nov;21(11):3236-3251. doi: 10.1016/j.jtha.2023.07.018. Epub 2023 Aug 3.
4
Novel Strategy to Combat the Procoagulant Phenotype in Heparin-Induced Thrombocytopenia Using 12-LOX Inhibition.
Arterioscler Thromb Vasc Biol. 2023 Oct;43(10):1808-1817. doi: 10.1161/ATVBAHA.123.319434. Epub 2023 Jun 22.
5
Current concepts and novel targets for antiplatelet therapy.
Nat Rev Cardiol. 2023 Sep;20(9):583-599. doi: 10.1038/s41569-023-00854-6. Epub 2023 Apr 4.
6
Heart Disease and Stroke Statistics-2023 Update: A Report From the American Heart Association.
Circulation. 2023 Feb 21;147(8):e93-e621. doi: 10.1161/CIR.0000000000001123. Epub 2023 Jan 25.
7
An Updated Review on Glycoprotein IIb/IIIa Inhibitors as Antiplatelet Agents: Basic and Clinical Perspectives.
High Blood Press Cardiovasc Prev. 2023 Mar;30(2):93-107. doi: 10.1007/s40292-023-00562-9. Epub 2023 Jan 13.
9
Fifty years with aspirin and platelets.
Br J Pharmacol. 2023 Jan;180(1):25-43. doi: 10.1111/bph.15966. Epub 2022 Nov 3.
10
Glenzocimab: A GPVI (Glycoprotein VI)-Targeted Potential Antiplatelet Agent for the Treatment of Acute Ischemic Stroke.
Stroke. 2022 Nov;53(11):3506-3513. doi: 10.1161/STROKEAHA.122.039790. Epub 2022 Sep 21.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验