The Role of Muscle Insulin Resistance in the Pathogenesis of Atherogenic Dyslipidemia and Nonalcoholic Fatty Liver Disease Associated with the Metabolic Syndrome

被引:97
作者
Jornayvaz, Francois R. [1 ]
Samuel, Varman T. [1 ,4 ]
Shulman, Gerald I. [1 ,2 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06536 USA
[3] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06536 USA
[4] Vet Affairs Med Ctr, West Haven, CT 06516 USA
来源
ANNUAL REVIEW OF NUTRITION, VOL 30 | 2010年 / 30卷
关键词
intramyocellular lipids; muscle glycogen synthesis; hepatic de novo lipogenesis; mitochondrial dysfunction; physical activity; GLUCOSE-TRANSPORT-PHOSPHORYLATION; SKELETAL-MUSCLE; GLYCOGEN-SYNTHESIS; HEPATIC STEATOSIS; DIACYLGLYCEROL ACYLTRANSFERASE; ROSIGLITAZONE TREATMENT; CARDIOVASCULAR-DISEASE; PROVISIONAL REPORT; DIABETES-MELLITUS; LIPID-CONTENT;
D O I
10.1146/annurev.nutr.012809.104726
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The metabolic syndrome is a clustering of cardiovascular risk factors, including insulin resistance, abdominal obesity, dyslipidemia, and hypertension, and is associated with other comorbidities such as a proinflammatory state and nonalcoholic fatty liver disease (NAFLD). Its prevalence is high, especially among developed countries, and mainly reflects overnutrition and sedentary lifestyle. Moreover, the developing countries are not spared, as obesity and its related problems such as the metabolic syndrome are increasing quickly. We review the potential primary role of skeletal muscle insulin resistance in the pathophysiology of the metabolic syndrome, showing that in lean, young, insulin-resistant individuals, impaired muscle glucose transport and glycogen synthesis redirect energy derived from carbohydrate into hepatic de novo lipogenesis, promoting the development of atherogenic dyslipidemia and NAFLD. The demonstration of a link between skeletal muscle insulin resistance and the metabolic syndrome offers opportunities in targeting early defects in muscle insulin action in order to counteract the development of the disease and its related complications.
引用
收藏
页码:273 / 290
页数:18
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