Department of Mouse Genetics and Metabolism, Institute for Genetics, Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases, Center of Molecular Medicine Cologne, University of Cologne, D-50674 Cologne, Germany.
Cell Metab. 2012 Aug 8;16(2):144-52. doi: 10.1016/j.cmet.2012.07.004.
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.
肥胖是胰岛素和瘦素抵抗发展的主要危险因素,最终导致多种代谢紊乱。然而,两种激素的抵抗并不均匀地影响所有靶细胞和细胞内信号通路。相比之下,许多临床表型源于激素的选择性抵抗,导致一些组织中特定细胞内信号通路被抑制,而在其他细胞类型中激素作用被维持甚至过度激活。在这里,我们综述了选择性胰岛素和瘦素抵抗的分子机制和临床结果,这将最终指导治疗肥胖相关疾病的未来策略。