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.