doi: 10.1161/01.HYP.0000018041.48432.B5
(Hypertension. 2002;39:1088.)
© 2002 American Heart Association, Inc.
Scientific Contributions |
Nitric Oxide Modulates Superoxide Release and Peroxynitrite Formation in Human Blood Vessels
From the Departments of Cardiovascular Medicine (T.J.G., N.E.J.W., K.M.C.) and Cardiac Surgery (R.P., D.T.), University of Oxford, John Radcliffe Hospital, United Kingdom.
Correspondence to Dr Keith M. Channon, Department of Cardiovascular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK. E-mail keith.channon{at}cardiov.ox.ac.uk
Abstract— Nitric oxide and superoxide have important roles as vascular signaling molecules. Nitric oxide (NO) reacts rapidly with superoxide, producing peroxynitrite. The relative balance between these radicals has important implications for vascular pathophysiology in hypertension and other vascular disease states. However, the relationships between superoxide, NO, and peroxynitrite formation in human blood vessels remain unclear. Accordingly, we systematically measured NO, superoxide, and peroxynitrite production from human internal mammary arteries, radial arteries, and saphenous veins from 78 patients undergoing coronary bypass surgery. Basal superoxide release was detected in all vessels at similar levels. However, endothelial removal or nitric oxide synthase inhibition increased mean superoxide release, with a corresponding reduction in peroxynitrite formation. Conversely, NO donors and superoxide scavengers both reduced superoxide release, whereas only NO donors increased peroxynitrite formation. These changes were much larger in arteries that in veins, but there were striking correlations between superoxide production, NO bioavailability, and peroxynitrite formation between the vessel types. Our findings provide direct evidence for coordinated vascular signaling mediated by interactions between NO, superoxide, and peroxynitrite and have important implications for studies of the functional effects of these radicals in human blood vessels.
Key Words: endothelium • oxidative stress • vascular diseases • nitric oxide • human
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