COX-2 and beyond: Approaches to prostaglandin inhibition in human disease

被引:391
作者
FitzGerald, G [1 ]
机构
[1] Univ Penn, Ctr Expt Therapeut, Philadelphia, PA 19104 USA
关键词
D O I
10.1038/nrd1225
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Selective inhibitors of cyclooxygenase (COX)-2 afford relief from pain and inflammation. They could also prove useful in the chemoprevention of cancer and are being investigated in a range of neurological diseases. This novel class of drug is less likely to cause gastric ulceration than traditional nonsteroidal anti-inflammatory drugs (tNSAIDs). However, plausible mechanisms have been proposed whereby COX-2 inhibitors could cause thrombosis or renovascular hypertension in patients predisposed to these conditions. The limited data available with structurally distinct inhibitors in relevant populations are consistent with this possibility, although these might be partly explained by a cardioprotective effect of the NSAID naproxen. This article will review the role of COX-2 inhibitors in a number of indications, including cardiovascular disease, hypertension and atherosclerosis.
引用
收藏
页码:879 / 890
页数:12
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