Open Access11,12‐Epoxyeicosatrienoic acid induces vasodilator response in the rat perfused mesenteric vasculature
Author(s) -
Bihzad S. M.,
Yousif M. H. M.
Publication year - 2017
Publication title -
autonomic and autacoid pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.44
H-Index - 21
eISSN - 1474-8673
pISSN - 1474-8665
DOI - 10.1111/aap.12052
Subject(s) - iberiotoxin , vasodilation , epoxide hydrolase 2 , chemistry , mesenteric arteries , nitric oxide , glibenclamide , epoxyeicosatrienoic acid , sodium nitroprusside , soluble guanylyl cyclase , apamin , endocrinology , medicine , cyclooxygenase , pharmacology , charybdotoxin , potassium channel , nitric oxide synthase , carbachol , receptor , biochemistry , arachidonic acid , enzyme , artery , diabetes mellitus , organic chemistry , guanylate cyclase
Summary Epoxyeicosatrienoic acids (EETs) are endogenous ligands that undergo hydrolysis by soluble epoxide hydrolase (sEH). The responses of 11, 12‐EET in comparison with other vasodilator agonists including carbachol and sodium nitroprusside (SNP) were investigated. The effect of 1‐cyclohexyl‐3‐dodecyl urea (CDU), a sEH, was tested on the vasodilator effect induced by 11, 12‐EET in the perfused mesenteric beds isolated from normo‐glycaemic and type‐1 STZ‐diabetic rats. In the perfused mesenteric beds of control and diabetic animals, 11, 12‐EET produced vasodilation in a dose‐dependent manner. The vasodilator response induced by 11, 12‐EET was significantly decreased in tissues obtained from diabetic animals, but this was significantly corrected through inhibition of sEH. The effects of nitric oxide synthase inhibitor, cyclo‐oxygenase inhibitor, specific potassium channel inhibitors, soluble guanylyl cyclase inhibitor and transient receptor potential channel V4 inhibitor, on vasodilator response to 11, 12‐EET were investigated. In tissues isolated from control animals, vasodilator responses to 11, 12‐EET were not inhibited by acute incubation with l ‐NAME, l ‐NAME with indomethacin, glibenclamide, iberiotoxin, charybdotoxin, apamin or ODQ. Incubation with the transient receptor potential channel V4 inhibitor ruthenium red caused significantly reduced vasodilator responses induced by 11, 12‐EET. In conclusion, results from this study indicate that 11, 12‐EET has a vasodilator effect in the perfused mesenteric bed, partly through activation of vanilloid receptor. A strategy to elevate the levels of EETs may have a significant impact in correcting microvascular abnormality associated with diabetes.