New insights in leptin resistance mechanisms in mice

被引:75
作者
Balland, Eglantine [1 ]
Cowley, Michael A. [1 ]
机构
[1] Monash Univ, Monash Obes & Diabet Inst, Dept Physiol, Clayton, Vic 3800, Australia
基金
英国医学研究理事会;
关键词
Leptin; Leptin resistance; Obesity; Cellular signaling; Hypothalamus; Inflammation; DIET-INDUCED OBESITY; 3B-CYCLIC AMP PATHWAY; BLOOD-BRAIN-BARRIER; BODY-WEIGHT; DORSOMEDIAL HYPOTHALAMUS; CONFERS RESISTANCE; PARTIAL SATURATION; ER STRESS; RECEPTOR; TRANSPORT;
D O I
10.1016/j.yfrne.2015.09.004
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Leptin resistance is one of the main challenges of obesity. To date, two levels of resistance have been identified, first a decreased rate of leptin uptake into the brain and secondly a diminished central response to leptin. New findings have identified the mechanisms of leptin transport and demonstrated that it can be rescued in obesity, but it did not overcome the problem of central resistance. Alteration in the actions of leptin following diet-induced obesity (DIO) appears to be a multifactorial condition. Several phosphatases are inhibiting leptin signaling pathways in a pathological way. Besides, hypothalamic inflammation alters the neuronal circuits that control metabolism. Recent studies describing both mechanisms (inhibition of leptin signaling and inflammation), have provided key insights to potential new targets for treatment. However, recent data showing that DIO mice may conserve a cellular and physiological response to endogenous leptin, highlights the need to redefine the concept of "leptin resistance". Crown Copyright (C) 2015 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 65
页数:7
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