14,15-Dihydroxyeicosatrienoic acid activates peroxisome proliferator-activated receptor-α

Epoxyeicosatrienoic acids (EETs), lipid mediators synthesized from arachidonic acid by cytochrome P-450 epoxygenases, are converted by soluble epoxide hydrolase (SEH) to the corresponding dihydroxyeicosatrienoic acids (DHETs). Originally considered as inactive degradation products of EETs, DHETs have biological activity in some systems. Here we examined the capacity of EETs and DHETs to activate peroxisome proliferator-activated receptor-alpha (PPAR alpha). We find that among the EET and DHET regioisomers, 14,15-DHET is the most potent PPAR alpha activator in a COS-7 cell expression system. Incubation with 10 mu M 14,15- DHET produced a 12-fold increase in PPAR alpha-mediated luciferase activity, an increase similar to that produced by the PPAR alpha agonist Wy-14643 (20 mu M). Although 10 mu M 14,15-EET produced a threefold increase in luciferase activity, this was abrogated by the SEH inhibitor dicyclohexylurea. 14- Hexyloxytetradec-5(Z)-enoic acid, a 14,15-EET analog that cannot be converted to a DHET, did not activate PPAR alpha. However, PPAR alpha was activated by 2-(14,15- epoxyeicosatrienoyl) glycerol, which was hydrolyzed and the released 14,15- EET converted to 14,15- DHET. COS-7 cells incorporated 14,15-[H-3] DHET from the medium, and the cells also retained a small amount of the DHET formed during incubation with 14,15-[H-3] EET. Binding studies indicated that 14,15[H-3] DHET binds to the ligand binding domain of PPAR alpha with a Kd of 1.4 mu M. Furthermore, 14,15- DHET increased the expression of carnitine palmitoyltransferase 1A, a PPAR alpha- responsive gene, in transfected HepG2 cells. These findings suggest that 14,15-DHET, produced from 14,15-EET by the action of SEH, may function as an endogenous activator of PPAR alpha.