Cyclooxygenase-2 inhibitors: Is there an association with coronary or renal events?

被引:18
作者
Richard J. Bing
机构
[1] Dept. of Experimental Cardiology, Huntington Med. Research Institutes, Pasadena, CA 91101
关键词
Nitric Oxide; Celecoxib; Naproxen; Prostacyclin; Rofecoxib;
D O I
10.1007/s11883-003-0082-2
中图分类号
学科分类号
摘要
The article is concerned with the effects of specific cyclooxygenase-2 (COX-2) inhibitors and their relationship to thrombotic cardiovascular events and to renal disease. Clinical and experimental aspects of COX-2-specific inhibitors are cited. A COX-2 inhibitor, celecoxib, interferes with myocardial prostacyclin production and also produces hypertension. Data have shown that in animal experiments, celecoxib also lowers myocardial prostaglandin concentration but fails to inhibit thromboxane concentration to the same degree. In the kidney, celecoxib can result in glomerular and interstitial nephritis or papillary necrosis. As in infarcted heart muscle, the COX-2-specific inhibitor celecoxib causes a significant decline in prostaglandin in the renal medulla. It was concluded from both clinical and experimental findings that COX-2 inhibitors can cause thrombotic cardiovascular events as well as renal disease. For these reasons, care should be exercised in administering specific COX-2 inhibitors to patients with pre-existing cardiac or renal disease. Copyright © 2003 by Current Science Inc.
引用
收藏
页码:114 / 117
页数:3
相关论文
共 30 条
[1]  
Vane J.R., Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like drugs, Nat. New Biol., 231, pp. 232-235, (1971)
[2]  
Smith W.L., Garavito R.M., DeWitt D.L., Prostaglandin endoperoxide H synthases (cyclooxygenases)-1 and -2, J. Biol. Chem., 271, pp. 33157-33160, (1996)
[3]  
Smith W.L., DeWitt D.L., Garavito R.M., Cyclooxygenases: Structural, cellular, and molecular biology, Annu. Rev. Biochem., 69, pp. 145-182, (2000)
[4]  
Kraemer S.A., Meade S.A., DeWitt D.L., Prostaglandin endoperoxide synthase gene structure: Identification of the transcriptional start side and 5′-flanking regulatory sequences, Arch. Biochem. Biophys., 293, pp. 391-400, (1992)
[5]  
Kujubu D.A., Herschman H.R., Dexamethasone inhibits mitogen induction of the TIS 10 prostaglandin synthase/cyclooxygenase gene, J. Biol. Chem., 267, pp. 7991-7994, (1992)
[6]  
Bing R.J., Myocardial ischemia and infarction: Growth of ideas, Cardiovasc. Res., 51, pp. 13-20, (2001)
[7]  
Bing R.J., Miyataka M., Rich K.A., Et al., Nitric oxide, prostanoids, cyclooxygenase and angiogenesis in colon and breast cancer, Clin. Cancer Res., 7, pp. 3385-3392, (2001)
[8]  
Allison M.C., Howatson A.G., Torrance C.J., Et al., Gastrointestinal damage associated with the use of nonsteroidal anti-inflammatory drugs, N. Engl. J. Med., 327, pp. 749-755, (1992)
[9]  
Bing R.J., Some aspects of biochemistry of myocardial infarction, Cell Mol. Life Sci., 58, pp. 1-5, (2001)
[10]  
Dudek R., Wildhirt S., Conforto A., Et al., Inducible nitric oxide synthase activity in myocardium after myocardial infarction in rabbit, Biochem. Biophys. Res. Commun., 205, pp. 1671-1680, (1994)