Treatment of inflammatory diseases by selective eicosanoid inhibition: a double-edged sword?

被引:39
|
作者
Yedgar, Saul
Krimsky, Miron
Cohen, Yuval
Flower, Roderick J.
机构
[1] Univ London, William Harvey Res Inst, Biochem Pharmacol Ctr, London EC1M 6BQ, England
[2] Morria Biopharmaceut Plc, London W1K 5JH, England
[3] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Biochem, IL-91120 Jerusalem, Israel
基金
英国惠康基金;
关键词
D O I
10.1016/j.tips.2007.07.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eicosanoids are generally considered to be potent pro-inflammatory mediators, and their suppression has, therefore, been a desirable therapeutic goal. However, analysis of the literature reveals that inhibition of specific eicosanoids per se is a simplistic approach because it overlooks the fact that net pathophysiological effects of these lipid mediators arise from a complex balance between eicosanoids derived from different pathways, which might exhibit both pro-and anti-inflammatory activities (depending on organs and disease stage), or which might have essential physiological roles. An alternative strategy, discussed in this review, might be to control inflammatory lipid mediators in such a way as to avoid disrupting this intricate inter-eicosanoid balance and its physiological sequelae.
引用
收藏
页码:459 / 464
页数:6
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