Increased Activity of Endogenous Endothelin in Patients With Type II Diabetes Mellitus

Abstract

Background— Endothelial dysfunction may contribute to the risk of premature atherosclerosis in patients with diabetes. Endothelin (ET-1) may be involved in this process by activating smooth muscle cell mitogenesis and leukocyte adhesion. We sought to assess the activity of endogenous ET-1 in a group of patients with type II diabetes mellitus with the use of antagonists of ET-1 receptors. Methods and Results— Forearm blood flow (FBF) responses (strain gauge plethysmography) to intraarterial infusion of a selective blocker of ET A receptors (BQ-123) and, on a different occasion, to ET-1, were measured in 15 patients with diabetes and 12 healthy controls. In addition, 5 patients with diabetes received coinfusion of BQ-123 and BQ-788 (a selective blocker of ET B receptors). In normal subjects, BQ-123 did not significantly modify FBF from baseline ( P =0.16). In contrast, BQ-123 administration resulted in a significant vasodilator response in patients with diabetes ( P <0.001). Infusion of exogenous ET-1 resulted in lower vasoconstrictor responses in patients with diabetes than in controls ( P =0.001), whereas the vasoconstrictor response to norepinephrine was similar in the 2 groups ( P =0.78). In patients with diabetes, the vasodilator response to selective ET A blockade was not significantly modified by nonselective blockade of ET-1 receptors obtained by coinfusion of BQ-123 and BQ-788. Conclusions— The activity of endogenous ET-1 on ET A receptors is enhanced in the resistance vessels of patients with diabetes, whereas their sensitivity to exogenous ET-1 is blunted. This abnormality may participate in the pathophysiology of vascular complications associated with diabetes.