Arachidonic acid metabolites as endothelium-derived hyperpolarizing factors

被引:163
作者
Campbell, William B.
Falck, John R.
机构
[1] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[2] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75230 USA
关键词
cytochrome P450 system; endothelium; arachidonic acid; vascular relaxation; endothelium-derived hyperpolarizing factor;
D O I
10.1161/01.HYP.0000255173.50317.fc
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The endothelium regulates vascular tone through the release of a number of soluble mediators, including NO, prostaglandin I-2, and endothelium-derived hyperpolarizing factor. Epoxyeicosatrienoic acids are cytochrome P450 epoxygenase metabolites of arachidonic acid. They are synthesized by the vascular endothelium and open calcium-activated potassium channels, hyperpolarize the membrane, and relax vascular smooth muscle. Endothelium-dependent relaxations to acetylcholine, bradykinin, and shear stress that are not inhibited by cyclooxygenase and NO synthase inhibitors are mediated by the endothelium-derived hyperpolarizing factor. In arteries from experimental animals and humans, the non-NO, non-prostaglandin-mediated relaxations and endothelium-dependent hyperpolarizations are blocked by cytochrome P450 inhibitors, calcium-activated potassium channel blockers, and epoxyeicosatrienoic acid antagonists. Acetylcholine and bradykinin stimulate epoxyeicosatrienoic acid release from endothelial cells and arteries. These findings indicate that epoxyeicosatrienoic acids act as endothelium-derived hyperpolarizing factors and regulate arterial tone.
引用
收藏
页码:590 / 596
页数:7
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