Increased insulin-stimulated endothelin-1 release is a distinct vascular phenotype distinguishing Cushing's disease from metabolic syndrome

Authors: Setola, Emanuela1; Losa, Marco2; Lanzi, Roberto1; Lucotti, Pietro1; Monti, Lucilla D.3; Castrignanò, Tristana2; Galluccio, Elena3; Giovanelli, Massimo2; Piatti, PierMarco1

Source: Clinical Endocrinology, Volume 66, Number 4, April 2007 , pp. 586-592(7)

Publisher: Blackwell Publishing

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Abstract:

Summary Objective 

Although much is known about the anti-inflammatory effects of an acute corticosteroid therapy, little is known about the effects on chronic hypercortisolism on endothelial dysfunction and proinflammatory alterations in patients with Cushing's disease (CD). Patients and methods 

We studied 9 patients with CD, 10 patients with metabolic syndrome and 27 normal controls. The tests consisted of an intravenous bolus of 0·1 U/kg insulin combined with a euglycaemic clamp technique with an arterialized forearm and assessment of the training parameters deep-venous balance of forearm glucose uptake (as an index of insulin sensitivity); NOx (nitric oxide end-products), c-GMP (second messenger of nitric oxide) and endothelin-1 release, as indices of endothelial function and proinflammatory systemic markers. Results 

Forearm glucose uptake incremental area was significantly lower in Cushing's disease and in the metabolic syndrome than in controls, suggesting a state of severe insulin resistance. Compared to controls and to the metabolic syndrome, basal and insulin-stimulated NOx release incremental areas were significantly reduced in Cushing's disease, while forearm c-GMP release was similarly decreased in CD and metabolic syndrome. By contrast, endothelin-1 incremental areas after insulin bolus were significantly higher in CD than in controls and the metabolic syndrome, in the presence of increased TNF-alpha, IL-6 and CRP levels. Forearm glucose uptake incremental area significantly correlated with NOx incremental area, forearm c-GMP release incremental area, TNF-alpha levels and ET-1 incremental area. Conclusions 

In patients with CD, supraphysiological insulin levels are not able to overcome the insulin resistance due to chronic hypercortisolism. Furthermore, an increased proatherogenic risk profile is characterized by decreased nitric oxide synthesis and activity, enhanced endothelin-1 levels and increased proinflammatory markers.

Document Type: Research article

DOI: 10.1111/j.1365-2265.2007.02774.x

Affiliations: 1: Diabetology, Endocrinology and Metabolic Disease Unit, 2: Pituitary Unit, Department of Neurosurgery, Scientific Institute San Raffaele, Università Vita-Salute San Raffaele, Milan, Italy 3: Core Laboratory, Diabetology, Endocrinology and Metabolic Disease Unit and

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