Epoxyeicosatrienoic Acids Contribute With Altered Nitric Oxide and Endothelin-1 Pathways to Conduit Artery Endothelial Dysfunction in Essential Hypertension

Author:

Bellien Jeremy1,Iacob Michele1,Remy-Jouet Isabelle1,Lucas Daniele1,Monteil Christelle1,Gutierrez Laurence1,Vendeville Cathy1,Dreano Yvonne1,Mercier Alain1,Thuillez Christian1,Joannides Robinson1

Affiliation:

1. From the Department of Pharmacology, Rouen University Hospital, Rouen (J.B., M.I., C.T., R.J.); Institut National de la Sante et de la Recherche Medicale (INSERM) U1096, Rouen Medical School, University of Rouen, Rouen (J.B., M.I., I.R.-J., C.M., C.V., C.T., R.J.); Centre d'Investigation Clinique–INSERM 0204, Rouen University Hospital, Rouen (L.G.); Department of General Medicine, Rouen Medical School, University of Rouen, Institute for Research and Innovation in Biomedicine, Rouen (A.M.); and...

Abstract

Background— We sought to clarify, using functional and biological approaches, the role of epoxyeicosatrienoic acids, nitric oxide (NO)/reactive oxygen species balance, and endothelin-1 in conduit artery endothelial dysfunction during essential hypertension. Methods and Results— Radial artery diameter and mean wall shear stress were determined in 28 untreated patients with essential hypertension and 30 normotensive control subjects during endothelium-dependent flow-mediated dilatation induced by hand skin heating. The role of epoxyeicosatrienoic acids and NO was assessed with the brachial infusion of inhibitors of cytochrome P450 epoxygenases (fluconazole) and NO synthase ( N G -monomethyl- l -arginine [L-NMMA]). Compared with controls, hypertensive patients exhibited a decreased flow-mediated dilatation in response to postischemic hyperemia as well as to heating, as shown by the lesser slope of their diameter–shear stress relationship. In controls, heating-induced flow-mediated dilatation was reduced by fluconazole, L-NMMA, and, to a larger extent, by L-NMMA+fluconazole. In patients, flow-mediated dilatation was not affected by fluconazole and was reduced by L-NMMA and L-NMMA+fluconazole to a lesser extent than in controls. Furthermore, local plasma epoxyeicosatrienoic acids increased during heating in controls (an effect diminished by fluconazole) but not in patients. Plasma nitrite, an indicator of NO availability, increased during heating in controls (an effect abolished by L-NMMA) and, to a lesser extent, in patients, whereas, inversely, reactive oxygen species increased more in patients (an effect diminished by L-NMMA). Plasma endothelin-1 decreased during heating in controls but not in patients. Conclusions— These results show that an impaired role of epoxyeicosatrienoic acids contributes, together with an alteration in NO/reactive oxygen species balance and endothelin-1 pathway, to conduit artery endothelial dysfunction in essential hypertension. Clinical Trial Registration— https://www.eudract.ema.europa.eu . Unique identifier: RCB2007-A001–10-53.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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