Vane's discovery of the mechanism of action of aspirin changed our understanding of its clinical pharmacology

被引:99
作者
Botting, Regina M. [1 ]
机构
[1] St Bartholomews Hosp, William Harvey Res Inst, Coll Med, London EC1M 6BQ, England
关键词
cyclooxygenase-1; cyclooxygenase-2; cyclooxygenase-3; paracetamol; diclofenac; analgesia; hypothermia; PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; INDUCIBLE CYCLOOXYGENASE; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; ACETAMINOPHEN; INDOMETHACIN; PURIFICATION; PARACETAMOL; INHIBITION;
D O I
10.1016/S1734-1140(10)70308-X
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Aspirin exerts its analgesic, antipyretic and anti-inflammatory actions by inhibiting the enzyme cyclooxygenase and thus preventing the formation and release of prostaglandins. The elucidation by John Vane of the mechanism of action of aspirin in 1971 was followed twenty years later by the discovery of a second cyclooxygenase enzyme, COX-2 and the rapid development of selective inhibitors of this enzyme. The COX-2 inhibitors are potent anti-inflammatory drugs without the damaging side effects on the stomach mucosa of the non-selective aspirin-like inhibitors. More recently, two enzymes have been identified inhibition of which may explain the mechanism of action of paracetamol. These are a putative cyclooxygenase-3 which is a variant of cyclooxygenase-1 and derives from the same gene, and a COX-2 variant, induced with diclofenac, which may be involved in the resolution of inflammation.
引用
收藏
页码:518 / 525
页数:8
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