Vascular Biology |
From the Department of Pathophysiology, Semmelweis University, H-1445, Budapest, Hungary, and the Department of Physiology, New York Medical College, Valhalla, NY.
Correspondence to Akos Koller, MD, PhD, Department of Physiology, New York Medical College, Valhalla, NY 10595. E-mail koller{at}nymc.edu
We hypothesized that in hyperhomocysteinemia (HHcy), flow-induced arteriolar constriction is due to an enhanced generation of reactive oxygen and/or nitrogen species, causing an impairment of nitric oxide (NO) and prostaglandin mediation of the response. Changes in diameter of isolated, pressurized (at 80 mm Hg) gracilis muscle arterioles (diameter
170 µm) from control and methionine dietinduced HHcy rats were measured by videomicroscopy. Increases in intraluminal flow (from 0 to 25 µL/min) resulted in NO- and prostaglandin-mediated dilations of control arterioles (maximum, control, 30±4 µm) but elicited significant constrictions of HHcy arterioles (maximum, HHcy, -32±3 µm), which were abolished by the thromboxane A2 receptor blocker SQ 29,548. Intraluminal administration of superoxide dismutase plus catalase did not affect flow-mediated dilations of control arterioles, but in HHcy arterioles, it reversed the flow-induced constrictions to dilations (maximum 18±4 µm), which were abolished by an NO synthase inhibitor. Flow-induced constrictions of HHcy arterioles were prevented by the presence of the xanthine oxidase inhibitor oxypurinol [but not by the NAD(P)H-oxidase inhibitor diphenyleneiodonium] and by urate, a known peroxynitrite scavenger. Also, authentic peroxynitrite elicited arteriolar constrictions (-31±8 µm) that were eliminated by urate and SQ 29,548. Thus, we suggest that in HHcy, xanthine oxidasederived superoxide scavenges NO released to flow, forming peroxynitrite, which promotes release of thromboxane A2, resulting in arteriolar constriction.
Key Words: homocysteine arterioles flow-induced constriction thromboxane A2 reactive oxygen species xanthine oxidase
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