共 172 条
Soluble epoxide hydrolase: Gene structure, expression and deletion
被引:184
作者:

Harris, Todd R.
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h-index: 0
机构: Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA

Hammock, Bruce D.
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h-index: 0
机构:
Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
机构:
[1] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
来源:
关键词:
EPHX2;
Epoxyeicosatrienoic acid;
Lipid signaling;
Inflammation;
Hypertension;
ARACHIDONIC-ACID METABOLISM;
SPONTANEOUSLY HYPERTENSIVE-RATS;
INDUCED CARDIAC-HYPERTROPHY;
BLOOD-PRESSURE REGULATION;
INDUCED PULMONARY-HYPERTENSION;
ISCHEMIA-REPERFUSION INJURY;
ENDOTHELIUM IN-VITRO;
EPOXYEICOSATRIENOIC ACIDS;
MOUSE-LIVER;
PEROXISOME PROLIFERATOR;
D O I:
10.1016/j.gene.2013.05.008
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Mammalian soluble epoxide hydrolase (sEH) converts epoxides to their corresponding diols through the addition of a water molecule. sEH readily hydrolyzes lipid signaling molecules, including the epoxyeicosatrienoic acids (EETs), epoxidized lipids produced from arachidonic acid by the action of cytochrome p450s. Through its metabolism of the EETs and other lipid mediators, sEH contributes to the regulation of vascular tone, nociception, angiogenesis and the inflammatory response. Because of its central physiological role in disease states such as cardiac hypertrophy, diabetes, hypertension, and pain sEH is being investigated as a therapeutic target. This review begins with a brief introduction to sEH protein structure and function. sEH evolution and gene structure are then discussed before human small nucleotide polymorphisms and mammalian gene expression are described in the context of several disease models. The review ends with an overview of studies that have employed the sEH knockout mouse model. (c) 2013 Elsevier B.V. All rights reserved.
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页码:61 / 74
页数:14
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