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      Endothelial dysfunction - a major mediator of diabetic vascular disease.

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          Abstract

          The vascular endothelium is a multifunctional organ and is critically involved in modulating vascular tone and structure. Endothelial cells produce a wide range of factors that also regulate cellular adhesion, thromboresistance, smooth muscle cell proliferation, and vessel wall inflammation. Thus, endothelial function is important for the homeostasis of the body and its dysfunction is associated with several pathophysiological conditions, including atherosclerosis, hypertension and diabetes. Patients with diabetes invariably show an impairment of endothelium-dependent vasodilation. Therefore, understanding and treating endothelial dysfunction is a major focus in the prevention of vascular complications associated with all forms of diabetes mellitus. The mechanisms of endothelial dysfunction in diabetes may point to new management strategies for the prevention of cardiovascular disease in diabetes. This review will focus on the mechanisms and therapeutics that specifically target endothelial dysfunction in the context of a diabetic setting. Mechanisms including altered glucose metabolism, impaired insulin signaling, low-grade inflammatory state, and increased reactive oxygen species generation will be discussed. The importance of developing new pharmacological approaches that upregulate endothelium-derived nitric oxide synthesis and target key vascular ROS-producing enzymes will be highlighted and new strategies that might prove clinically relevant in preventing the development and/or retarding the progression of diabetes associated vascular complications.

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          Author and article information

          Journal
          Biochim Biophys Acta
          Biochimica et biophysica acta
          Elsevier BV
          0006-3002
          0006-3002
          Dec 2013
          : 1832
          : 12
          Affiliations
          [1 ] Institute of Physiology, Faculty of Medicine, University of Coimbra, Portugal; IBILI, Faculty of Medicine, University of Coimbra, Portugal. Electronic address: csena@ci.uc.pt.
          Article
          S0925-4439(13)00271-8
          10.1016/j.bbadis.2013.08.006
          23994612
          dbc85952-56c9-47a8-abf3-6fbdb5621257
          © 2013.
          History

          Diabetes,Endothelial dysfunction,Endothelium,Oxidative stress,Potential therapeutic target,Vascular function

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