Mechanism of action of aspirin-like drugs

被引:111
作者
Vane, JR
Botting, RM
机构
[1] William Harvey Research Institute, St Bartholomew's/Royal London Sch., Westfield College, London EC1M 6BQ, Charterhouse Square
关键词
cyclooxygenase; prostaglandins;
D O I
10.1016/S0049-0172(97)80046-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nonsteroid antiinflammatory drugs (NSAIDs) or aspirin-like drugs act by inhibiting the activity of the cyclooxygenase (COX) enzyme. Two isoforms of COX exist, COX-1, which is constitutively expressed, and COX-2, which is an inducible isoform. Prostaglandins synthesized by the constitutively expressed COX-1 are implicated in the maintenance of normal physiological function and have a 'cytoprotective' action in the stomach. COX-2 expression is normally low but is induced by inflammatory stimuli and cytokines, It is thought that the antiinflammatory actions of NSAIDs are caused by the inhibition of COX-2, whereas the unwanted side effects, such as gastrointestinal and renal toxicity, are caused by the inhibition of the constitutively expressed COX-1, Individual NSAIDs show different selectivities against the COX-1 and COX-2 isoforms. NSAIDs that are selective towards COX-2, such as meloxicam, may have an improved side-effect profile over current NSAIDs, In addition to their use as antiinflammatory agents in the treatment of rheumatoid arthritis and osteoarthritis, selective COX-2 inhibitors may also be beneficial in inhibiting colorectal tumor cell growth and in delaying premature labor. Copyright (C) 1997 by W.B. Saunders Company.
引用
收藏
页码:2 / 10
页数:9
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