Cyclooxygenase-2 selective inhibitors

被引:19
作者
Cannon, GW
机构
[1] VAMC, Salt Lake City, UT 84148 USA
[2] Univ Utah, Div Rheumatol, Salt Lake City, UT USA
关键词
D O I
10.1358/dot.1999.35.7.548261
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The identification of two cyclooxygenase (COX) enzymes has been a tremendous advance in understanding the role of prostaglandins in inflammation and the actions of nonsteroidal antiinflammatory drugs (NSAIDs). COX-1 activity appears to be related to "constitutive" or "house-keeping" functions in the gastric mucosa, kidney and platelets. COX-2 activity is "inducible" and generally occurs in response to a specific stimulus to enhance inflammatory actions. Current NSAIDs inhibit both COX-1 and COX-2, although the clinical benefit of NSAIDs appears to be associated with inhibition of COX-2 activity. The inhibition of COX-1 activity by NSAIDs is related to adverse side effects in general, particularly gastrointestinal toxicity. Recently, COX-2 selective inhibitors have been developed. Current data would suggest that by inhibiting COX-2 action, these agents may have efficacy similar to that of standard NSAIDs and that by not inhibiting COX-I activity, they may have less toxicity than standard NSAIDs. Thus, these actions indicate that COX-2 selective inhibitors will have similar clinical efficacy to the traditional NSAIDs with fewer adverse side effects. (C) 1999 Prous Science: All rights reserved.
引用
收藏
页码:487 / 496
页数:10
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