Cellular and molecular mechanisms of endothelial dysfunction in diabetes

被引:170
作者
Roberts, Anna C. [1 ]
Porter, Karen E. [1 ,2 ]
机构
[1] Univ Leeds, LIGHT, Div Cardiovasc & Diabet Res, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, MCRC, Leeds LS2 9JT, W Yorkshire, England
关键词
Diabetes; endothelial function; endothelial dysfunction; metabolic memory; microRNA; novel therapies; NITRIC-OXIDE SYNTHASE; PROTEIN-KINASE-C; ALTERED GENE-EXPRESSION; GLYCATION END-PRODUCTS; INSULIN-RESISTANCE; DEPENDENT VASODILATION; CORONARY-ARTERY; HIGH GLUCOSE; MEDIATED VASODILATION; TNF-ALPHA;
D O I
10.1177/1479164113500680
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In healthy individuals, the vascular endothelium regulates an intricate balance of factors that maintain vascular homeostasis and normal arterial function. Functional disruption of the endothelium is known to be an early event that underlies the development of subsequent cardiovascular disease (CVD) including atherosclerosis and coronary heart disease. In addition, the rising global epidemic of type 2 diabetes is a significant problem conferring a significantly higher risk of CVD to individuals in whom endothelial dysfunction is also notable. This review first summarises the role of endothelium in health and explores and evaluates the impact of diabetes on endothelial function. The characteristic features of insulin resistance and other metabolic disturbances that may underlie long-term changes in vascular endothelial function (metabolic memory) are described along with proposed cellular, molecular and epigenetic mechanisms. Through understanding the underlying mechanisms, novel targets for future therapies to restore endothelial homeostasis and drive' a reparative cellular phenotype are explored.
引用
收藏
页码:472 / 482
页数:11
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