Vascular Endothelial Regulation of Obesity-Associated Insulin Resistance

被引:19
作者
Li, Manna [1 ]
Qian, Ming [1 ]
Xu, Jian [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Harold Hamm Diabet Ctr, Dept Med, Oklahoma City, OK 73106 USA
来源
FRONTIERS IN CARDIOVASCULAR MEDICINE | 2017年 / 4卷
基金
美国国家卫生研究院;
关键词
endothelial function; adipose; liver; skeletal muscle; obesity; insulin resistance; diabetes; metabolism; FATTY LIVER-DISEASE; ADIPOSE-TISSUE ANGIOGENESIS; FIBROBLAST GROWTH-FACTORS; SKELETAL-MUSCLE; LIPID-METABOLISM; PHENOTYPIC HETEROGENEITY; MOLECULAR-MECHANISMS; CELLS; DYSFUNCTION; ACTIVATION;
D O I
10.3389/fcvm.2017.00051
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is a worldwide epidemic that predisposes individuals to metabolic complications, such as type 2 diabetes mellitus and non-alcoholic fatty liver disease, all of which are related to an imbalance between food intake and energy expenditure. Identification of the pathogenic molecular mechanisms and effective therapeutic approaches are urgently needed. A well-accepted paradigm is that crosstalk between organs/tissues contributes to diseases. Endothelial dysfunction characterizes metabolic disorders and the related vascular complications. Over the past two decades, overwhelming studies have focused on mechanisms that lead to endothelial dysfunction. New investigations, however, have begun to appreciate the opposite direction of the crosstalk: endothelial regulation of metabolism, although the underlying mechanisms remain to be elucidated. This review summarizes the evidence that supports the concept of endothelial regulation of obesity and the associated insulin resistance in fat, liver, and skeletal muscles, the classic targets of insulin. Outstanding questions and future research directions are highlighted. Identification of the mechanisms of vascular endothelial regulation of metabolism may offer strategies for prevention and treatment of obesity and the related metabolic complications.
引用
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页数:9
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