Targeting endoplasmic reticulum stress in insulin resistance

被引:195
|
作者
Salvado, Laia [1 ,2 ]
Palomer, Xavier [1 ,2 ]
Barroso, Emma [1 ,2 ]
Vazquez-Carrera, Manuel [1 ,2 ]
机构
[1] Univ Barcelona, Fac Pharm, Dept Pharmacol & Therapeut Chem, IBUB, Barcelona, Spain
[2] Inst Salud Carlos III, Spanish Biomed Res Ctr Diabet & Associated Metab, Madrid, Spain
来源
关键词
endoplasmic reticulum stress; inflammation; insulin resistance; type 2 diabetes mellitus; unfolded protein response; UNFOLDED PROTEIN RESPONSE; THIOREDOXIN-INTERACTING PROTEIN; DENSITY-LIPOPROTEIN RECEPTOR; AMPK-DEPENDENT MECHANISM; PANCREATIC BETA-CELLS; SKELETAL-MUSCLE CELLS; FRUCTOSE-FED MICE; ER-STRESS; GLUCOSE-HOMEOSTASIS; ADIPOSE-TISSUE;
D O I
10.1016/j.tem.2015.05.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The endoplasmic reticulum (ER) is involved in the development of insulin resistance and progression to type 2 diabetes mellitus (T2DM). Disruption of ER homeostasis leads to ER stress, which activates the unfolded protein response (UPR). This response is linked to different processes involved in the development of insulin resistance (IR) and T2DM, including inflammation, lipid accumulation, insulin biosynthesis, and a-cell apoptosis. Understanding the mechanisms by which disruption of ER homeostasis leads to IR and its progression to T2DM may offer new pharmacological targets for the treatment and prevention of these diseases. Here, we examine ER stress, the UPR, and downstream pathways in insulin sensitive tissues, and in IR, and offer insights towards therapeutic strategies.
引用
收藏
页码:438 / 448
页数:11
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