Cyclooxygenase-dependent signalling: molecular events and consequences

被引:39
作者
Versteeg, HH
Henegouwen, PMPVE
van Deventer, SJH
Peppelenbosch, MP
机构
[1] Univ Amsterdam, Acad Med Ctr, Lab Expt Internal Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Utrecht, Dept Mol Cell Biol, Inst Biomembranes & Lipid Biol, NL-3584 CH Utrecht, Netherlands
关键词
prostaglandin; non-steroidal anti-inflammatory drug; G protein-coupled receptor; peroxisome proliferator; activated receptor; signal transduction;
D O I
10.1016/S0014-5793(99)00105-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-steroidal anti-inflammatory drugs (NSAIDS) currently attract large interest. Next to pain relief, NSAIDs have important anti-thrombotic and anti-oncogenic effects. NSAIDs exert their action by inhibition of cyclooxygenase, the enzyme responsible for the production of prostanoids, Prostanoid signal transduction is still poorly understood, but it has become clear that these inflammatory lipids influence cellular physiology at three different levels: (1) activation of a 7X transmembrane receptor coupled to heterotrimeric G proteins, (2) the inhibition of inflammation by activating corticosteroid-like receptors, (3) participation in receptor protein tyrosine kinase signal transduction. In this review prostanoid signalling at these three different levels will be reviewed and the relevance in (patho)physiological processes will be evaluated. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:1 / 5
页数:5
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