Protease-activated receptors as targets for antiplatelet therapy

被引:31
作者
Hamilton, Justin R. [1 ]
机构
[1] Monash Univ L6, Australian Ctr Blood Dis, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
Antiplatelet agents; Arterial thrombosis; Platelets; Protease-activated receptors; Thrombin; FUNCTIONAL THROMBIN RECEPTOR; PLATELET-ADHESION; ASPIRIN; ANTAGONISTS; VARIABILITY; CLOPIDOGREL; HEMOSTASIS; PROTECTION; RESISTANCE; FIBRINOGEN;
D O I
10.1016/j.blre.2008.06.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Arterial thrombosis, manifesting as acute myocardial infarction or ischaemic stroke, is the single most common cause of morbidity and mortality in industrialised societies. Platelets are a pre-requisite for the formation of arterial thrombi and, as a consequence, novel antiplatelet agents are sought to meet the significant clinical need for a potent, safe, and orally available therapy for the management of cardiovascular disease. Platelet thrombin receptors, termed protease-activated receptors (PARs), represent one promising candidate for the development of such therapy. This review outlines the role of platelet PARs in haemostasis and thrombosis and discusses the preclinical and clinical evidence supporting the potential of PAR antagonists as novel antiplatelet therapy. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:61 / 65
页数:5
相关论文
共 42 条
  • [1] [Anonymous], HEART DIS STROK STAT
  • [2] Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
  • [3] Clopidogrel and aspirin versus aspirin alone for the prevention of atherothrombotic events
    Bhatt, DL
    Fox, KAA
    Hacke, W
    Berger, PB
    Black, HR
    Boden, WE
    Cacoub, P
    Cohen, EA
    Creager, MA
    Easton, JD
    Flather, MD
    Haffner, SM
    Hamm, CW
    Hankey, GJ
    Johnston, SC
    Mak, KH
    Mas, JL
    Montalescot, G
    Pearson, TA
    Steg, PG
    Steinhubl, SR
    Weber, MA
    Brennan, DM
    Fabry-Ribaudo, L
    Booth, J
    Topol, EJ
    Frye, RL
    Amarenco, P
    Brass, LM
    Buyse, M
    Cohen, LS
    DeMets, DL
    Fuster, V
    Hart, RG
    Marler, JR
    McCarthy, C
    Schoemig, A
    Lincoff, AM
    Brener, SJ
    Sila, CA
    Albuquerque, A
    Aroutiounov, G
    Artemiev, D
    Atkeson, BG
    Bartel, T
    Basart, DCG
    Lima, AB
    Belli, G
    Bordalo e Sa, AL
    Bosch, X
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (16) : 1706 - 1717
  • [4] Thrombus formation: stability matters
    Brass, Lawrence F.
    [J]. BLOOD, 2006, 108 (09) : 2883 - 2884
  • [5] Contact-dependent signaling events that promote thrombus formation
    Brass, LF
    Jiang, H
    Wu, J
    Stalker, TJ
    Zhu, L
    [J]. BLOOD CELLS MOLECULES AND DISEASES, 2006, 36 (02) : 157 - 161
  • [6] Combined deficiency of protease-activated receptor-4 and fibrinogen recapitulates the hemostatic defect but not the embryonic lethality of prothrombin deficiency
    Camerer, E
    Duong, DN
    Hamilton, JR
    Coughlin, SR
    [J]. BLOOD, 2004, 103 (01) : 152 - 154
  • [7] Discovery of potent orally active thrombin receptor (protease activated receptor 1) antagonists as novel antithrombotic agents
    Chackalamannil, S
    Xia, Y
    Greenlee, WJ
    Clasby, M
    Doller, D
    Tsai, H
    Asberom, T
    Czarniecki, M
    Ahn, HS
    Boykow, G
    Foster, C
    Agans-Fantuzzi, J
    Bryant, M
    Lau, J
    Chintala, M
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (19) : 5884 - 5887
  • [8] Heterotricyclic himbacine analogs as potent, orally active thrombin receptor (protease activated receptor-1) antagonists
    Chelliah, Mariappan V.
    Chackalamannil, Samuel
    Xia, Yan
    Eagen, Keith
    Clasby, Martin C.
    Gao, Xiaobang
    Greenlee, William
    Ahn, Ho-Sani
    Agans-Fantuzzi, Jacqueline
    Boykow, George
    Hsieh, Yunsheng
    Bryant, Matthew
    Palamanda, Jairam
    Chan, Tze-Ming
    Hesk, David
    Chintala, Madbu
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (21) : 5147 - 5160
  • [9] Chew DP, 2001, CIRCULATION, V103, P201
  • [10] Coma-Canella Isabel, 2007, Cardiovascular & Hematological Disorders - Drug Targets, V7, P274, DOI 10.2174/187152907782793590