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Research Article

Increase in insulin-induced relaxation of consecutive arterial segments toward the periphery: Role of vascular oxidative state

, , , , , , & show all
Pages 749-757 | Received 09 Dec 2013, Accepted 11 Mar 2014, Published online: 10 Apr 2014
 

Abstract

Rationale. The oxidative state has been implicated in the signaling of various vasomotor functions, yet its role regarding the vasomotor action of insulin is less known. Objective. To investigate the insulin-evoked relaxations of consecutive arterial segments of different oxidative state and the role of extracellular signal-regulated kinase (ERK) pathway. Methods and Results. The oxidative state, as assessed by the level of ortho-tyrosine, was higher in the thoracic aorta of rats than in the abdominal aorta, and was the lowest in the femoral artery. The vasomotor function of vessels of same origin was studied using a small-vessel myograph. Insulin-induced relaxations increased toward the periphery (i.e., thoracic < abdominal < femoral). Aortic banding and hydrogen peroxide/aminotriazole increased the oxidative state of the thoracic aorta that was accompanied by ERK activation and decreased relaxation to insulin, and vice versa, acutely lowered oxidative state by superoxide dismutase/catalase improved relaxation. In contrast, insulin-induced relaxation of the femoral artery could be enhanced with a higher oxidative state, and reduced with a lower state. Conclusions. Oxidative state of vessels modulates the magnitude of vasomotor responses to insulin, which appears to be mediated via the ERK signaling pathway.

Acknowledgments

We express our sincere thanks to Dr. Sámikné Varga Ilona and Fábián Ildikó for their excellent technical assistance. The Deutsche Akademische Austauschdienst (DAAD) supported the work of I.A. Szijártó.

Sources of founding

Sources of Support of Akos Koller: Hungarian National Science Research Fund (OTKA) K 108444; SROP-4.2.2. A-11/1/KONV-2012-0024; SROP-4.2.2.A-11/1/KONV-2012-0017, American Heart Association, Founders Affiliate, 0855910D. Research of G.A. Molnar was supported by the European Union and the State of Hungary, co-financed by the European Social Fund in the framework of TÁMOP-4.2.4.A/2-11/1-2012-0001 ‘National Excellence Program’.

Declaration of interest

The authors report no declarations of interest. The authors alone are responsible for the content and writing of the paper.

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