Selective Insulin and Leptin Resistance in Metabolic Disorders

被引:246
作者
Koenner, A. Christine [1 ,2 ,3 ]
Bruening, Jens C. [1 ,2 ,3 ]
机构
[1] Univ Cologne, Dept Mouse Genet & Metab, Cologne Excellence Cluster Cellular Stress Respon, Inst Genet,CMMC, D-50674 Cologne, Germany
[2] Max Planck Inst Neurol Res, D-50931 Cologne, Germany
[3] Univ Hosp Cologne, Ctr Endocrinol Diabet & Prevent Med CEDP, D-50924 Cologne, Germany
关键词
DIET-INDUCED OBESITY; ENDOPLASMIC-RETICULUM STRESS; HEPATIC GLUCOSE-PRODUCTION; POMC-EXPRESSING CELLS; ENERGY HOMEOSTASIS; ADIPOSE-TISSUE; MELANOCORTIN SYSTEM; PERIPHERAL GLUCOSE; BODY-WEIGHT; FOOD-INTAKE;
D O I
10.1016/j.cmet.2012.07.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Obesity represents a major risk factor for the development of insulin and leptin resistance, ultimately leading to a pleiotropic spectrum of metabolic alterations. However, resistance to both hormones does not uniformly affect all target cells and intracellular signaling pathways. In contrast, numerous clinical phenotypes arise from selective hormone resistance, leading to inhibition of defined intracellular signaling pathways in some tissues, while in other cell types hormone action is maintained or even overactivated. Here, we review the molecular mechanisms and clinical outcomes resulting from selective insulin and leptin resistance, which should ultimately guide future strategies for the treatment of obesity-associated diseases.
引用
收藏
页码:144 / 152
页数:9
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