Soluble epoxide hydrolase is a therapeutic target for acute inflammation

被引:392
作者
Schmelzer, KR
Kubala, L
Newman, JW
Kim, IH
Eiserich, JP
Hammock, BD [1 ]
机构
[1] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Internal Med, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Physiol & Membrane Biol, Davis, CA 95616 USA
[4] Univ Calif Davis, Canc Res Ctr, Davis, CA 95616 USA
关键词
cyclooxygenase; lipoxin A(4); lipoxygenase; proinflammatory mediators; epoxygenase;
D O I
10.1073/pnas.0503279102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
As of 2004, > 73 million people were prescribed anti inflammatory medication. Despite the extensive number of current products, many people still suffer from their diseases or the pharmacological properties (side effects) of the medications. Therefore, developing therapeutic strategies to treat inflammation remains an important endeavor. Here, we demonstrate that the soluble epoxide hydrolase (sEH) is a key pharmacologic target for treating acute systemic inflammation. Lipopolysaccharide-induced mortality, systemic hypotension, and histologically evaluated tissue injury were substantially diminished by administration of urea-based, small-molecule inhibitors of sEH to C57BL/6 mice. Moreover, sEH inhibitors decreased plasma levels of proinflammatory cytokines and nitric oxide metabolites while promoting the formation of lipoxins, thus supporting inflammatory resolution. These data suggest that sEH inhibitors have therapeutic efficacy in the treatment and management of acute inflammatory diseases.
引用
收藏
页码:9772 / 9777
页数:6
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