Inhibition of ADRP prevents diet-induced insulin resistance

被引:95
作者
Varela, Gladys M. [1 ,2 ]
Antwi, Daniel A. [1 ,2 ]
Dhir, Ravindra [1 ,2 ]
Yin, Xiaoyan [1 ,2 ]
Singhal, Neel S. [1 ,2 ]
Graham, Mark J. [3 ]
Crooke, Roseanne M. [3 ]
Ahima, Rexford S. [1 ,2 ]
机构
[1] Univ Penn, Sch Med, Div Endocrinol Diabet & Metab, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[3] ISIS Pharmaceut, Carlsbad, CA USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2008年 / 295卷 / 03期
关键词
adipose differentiation-related protein; liver; steatosis;
D O I
10.1152/ajpgi.90204.2008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Diets with high fat content induce steatosis, insulin resistance, and type 2 diabetes. The lipid droplet protein adipose differentiation-related protein (ADRP) mediates hepatic steatosis, but whether this affects insulin action in the liver or peripheral organs in diet-induced obesity is uncertain. We fed C57BL/6J mice a high-fat diet and simultaneously treated them with an antisense oligonucleotide (ASO) against ADRP for 4 wk. Glucose homeostasis was assessed with clamp and tracer techniques. ADRP ASO decreased the levels of triglycerides and diacylglycerol in the liver, but fatty acids, long-chain fatty acyl CoAs, ceramides, and cholesterol were unchanged. Insulin action in the liver was enhanced after ADRP ASO treatment, whereas muscle and adipose tissue were not affected. ADRP ASO increased the phosphorylation of insulin receptor substrate (IRS)1, IRS2, and Akt, and decreased gluconeogenic enzymes and PKC epsilon, consistent with its insulin-sensitizing action. These results demonstrate an important role for ADRP in the pathogenesis of diet-induced insulin resistance.
引用
收藏
页码:G621 / G628
页数:8
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