14,15-EPOXYEICOSATRIENOIC ACID METABOLISM IN ENDOTHELIAL-CELLS

Citation
M. Vanrollins et al., 14,15-EPOXYEICOSATRIENOIC ACID METABOLISM IN ENDOTHELIAL-CELLS, Journal of lipid research, 34(11), 1993, pp. 1931-1942
Citations number
65
Categorie Soggetti
Biology
Journal title
ISSN journal
00222275
Volume
34
Issue
11
Year of publication
1993
Pages
1931 - 1942
Database
ISI
SICI code
0022-2275(1993)34:11<1931:1AMIE>2.0.ZU;2-D
Abstract
Epoxyeicosatrienoic acid (EET) metabolism was studied in endothelial c ells to determine whether this tissue influence their vasoactive prope rties. Porcine aortic endothelial cells rapidly took up all four EET r egioisomers. The uptake of [1-C-14]14,15-EET reached a maximum in 15-3 0 min, and saturation was not observed with concentrations up to 5 muM . More than 70% of the incorporated 14,15-EET was contained in choline and inositol glycerophospholipids, most of it in the form of an EET e ster. A metabolite, 14,15-dihydroxyeicosatrienoic acid (14,15-DHET), a ccumulated in the medium during incubation, and products with similar chromatographic properties also were formed from 5,6-, 8,9-, and 11,12 -EET Much of the 14,15-EET taken up was only temporarily retained by t he cells, and in 2 h half was released into the medium as 14,15-DHET. Bovine aortic and human umbilical vein endothelial cells also took up 14,15-EET, incorporated it into choline glycerophospholipids, and conv erted it to 14,15-DHET. These findings suggest that the endothelium ma y limit the vascular actions of EETs through rapid uptake, hydration, and release of DHETs into the circulation. Some vasoactive effects of EETs may result from their temporary accumulation in endothelial phosp holipids involved in stimulus-response coupling.