Relationship between cyclooxygenase-2 inhibition and thrombogenesis

被引:9
作者
Dai, WD [1 ]
Kloner, RA [1 ]
机构
[1] Univ So Calif, Inst Heart, Good Samaritan Hosp, Los Angeles, CA 90017 USA
关键词
cyclooxygenase-2; thrombogenesis; myocardial infarction;
D O I
10.1177/107424840400900i108
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Recently there has been considerable interest in the role of cyclooxygenase-2 (COX-2) in thrombosis and myocardial infarction. A large number of clinical and basic studies have focused on whether COX-2 inhibitors can induce a prothrombotic disorder and increase the risk of cardiovascular thrombosis. This article reviews (1) the roles of COX-2 in the metabolism of prostaglandins; (2) the influence of COX-2 inhibition in the platelet aggregation and the antithrombotic function of vascular endothelium; (3) the roles of COX-2 inhibition in atherothrombosis; and (4) clinical trials that examine COX-2 inhibition in relationship to the risk of myocardial infarction. Based on the published data, this review suggests that COX-2 plays varying and sometimes conflicting roles in thrombogenesis, in prostaglandins' metabolism of endothelium in healthy or dysfunctional conditions, and in atherothrombosis. Future investigations under different pathologic conditions are needed to fully understand the net effect of COX-2 inhibition on thrombogenesis. The roles of COX-2 in the pathophysiologic process of cardiovascular thrombosis are diverse and controversial, and need to be further studied to guide clinical practice.
引用
收藏
页码:51 / 59
页数:9
相关论文
共 59 条
[1]
Role of anti-inflammatory drugs in the treatment of acute coronary syndromes. From athero-inflammation to athero-thrombosis [J].
Altman, R ;
Scazziota, A .
REVISTA ESPANOLA DE CARDIOLOGIA, 2003, 56 (01) :9-15
[2]
Efficacy assessment of meloxicam, a preferential cyclooxygenase-2 inhibitor, in acute coronary syndromes without ST-segment elevation - The nonsteroidal anti-inflammatory drugs in unstable angina treatment-2 (NUT-2) pilot study [J].
Altman, R ;
Luciardi, HL ;
Muntaner, J ;
Del Rio, F ;
Berman, SG ;
Lopez, R ;
Gonzalez, C .
CIRCULATION, 2002, 106 (02) :191-195
[3]
SYSTEMIC NATURE OF ENDOTHELIAL DYSFUNCTION IN ATHEROSCLEROSIS [J].
ANDERSON, TJ ;
GERHARD, MD ;
MEREDITH, IT ;
CHARBONNEAU, F ;
DELAGRANGE, D ;
CREAGER, MA ;
SELWYN, AP ;
GANZ, P .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (06) :B71-B74
[4]
ANGGARD E, 1965, J BIOL CHEM, V240, P3518
[5]
Cyclooxygenase-2 is widely expressed in atherosclerotic lesions affecting native and transplanted human coronary arteries and colocalizes with inducible nitric oxide synthase and nitrotyrosine particularly in macrophages [J].
Baker, CSR ;
Hall, RJC ;
Evans, TJ ;
Pomerance, A ;
Maclouf, J ;
Creminon, C ;
Yacoub, MH ;
Polak, JM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (03) :646-655
[6]
Adverse events associated with rofecoxib therapy -: Results of a large study in community-derived osteoarthritic patients [J].
Bannwarth, B ;
Trèves, R ;
Euller-Ziegler, L ;
Rolland, D ;
Ravaud, P ;
Dougados, M .
DRUG SAFETY, 2003, 26 (01) :49-54
[7]
Comparison of upper gastrointestinal toxicity of rofecoxib and naproxen in patients with rheumatoid arthritis. [J].
Bombardier, C ;
Laine, L ;
Reicin, A ;
Shapiro, D ;
Burgos-Vargas, R ;
Davis, B ;
Day, R ;
Ferraz, MB ;
Hawkey, CJ ;
Hochberg, MC ;
Kvien, TK ;
Schnitzer, TJ ;
Weaver, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (21) :1520-1528
[8]
THE PROSTACYCLIN-THROMBOXANE-A2 BALANCE - PATHOPHYSIOLOGICAL AND THERAPEUTIC IMPLICATIONS [J].
BUNTING, S ;
MONCADA, S ;
VANE, JR .
BRITISH MEDICAL BULLETIN, 1983, 39 (03) :271-276
[9]
Modulation of eicosanoid metabolism in endothelial cells in a xenograft model - Role of cyclooxygenase-2 [J].
Bustos, M ;
Coffman, TM ;
Saadi, S ;
Platt, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) :1150-1158
[10]
Vascular biology of thrombosis - Platelet-vessel wall interactions and aspirin effects [J].
Catella-Lawson, F .
NEUROLOGY, 2001, 57 (05) :S5-S7