Regulation of obesity and insulin resistance by nitric oxide

被引:193
作者
Sansbury, Brian E. [1 ,2 ]
Hill, Bradford G. [1 ,2 ,3 ]
机构
[1] Univ Louisville, Sch Med, Diabet & Obes Ctr, Inst Mol Cardiol, Louisville, KY 40202 USA
[2] Univ Louisville, Sch Med, Dept Physiol & Biophys, Louisville, KY 40202 USA
[3] Univ Louisville, Sch Med, Dept Biochem & Mol Biol, Louisville, KY 40202 USA
关键词
Nitric oxide; Diabetes; Insulin resistance; Obesity; eNOS; Mitochondria; Free radicals; NECROSIS-FACTOR-ALPHA; DIET-INDUCED OBESITY; ENDOTHELIUM-DEPENDENT RELAXATION; ACTIVATED-RECEPTOR-GAMMA; SYNTHASE MESSENGER-RNA; HIGH-FAT DIET; CENTRAL-NERVOUS-SYSTEM; BROWN ADIPOSE-TISSUE; L-ARGININE SUPPLEMENTATION; SENSITIZING SUBSTANCE HISS;
D O I
10.1016/j.freeradbiomed.2014.05.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Obesity is a risk factor for developing type 2 diabetes and cardiovascular disease and has quickly become a worldwide pandemic with few tangible and safe treatment options. Although it is generally accepted that the primary cause of obesity is energy imbalance, i.e., the calories consumed are greater than are utilized, understanding how caloric balance is regulated has proven a challenge. Many "distal" causes of obesity, such as the structural environment, occupation, and social influences, are exceedingly difficult to change or manipulate. Hence, molecular processes and pathways more proximal to the origins of obesity-those that directly regulate energy metabolism or caloric intake-seem to be more feasible targets for therapy. In particular, nitric oxide (NO) is emerging as a central regulator of energy metabolism and body composition. NO bioavailability is decreased in animal models of diet-induced obesity and in obese and insulin-resistant patients, and increasing NO output has remarkable effects on obesity and insulin resistance. This review discusses the role of NO in regulating adiposity and insulin sensitivity and places its modes of action into context with the known causes and consequences of metabolic disease. (C) 2014 The Authors. Published by Elsevier Inc.
引用
收藏
页码:383 / 399
页数:17
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