Obesity causes selective and long-lasting desensitization of AgRP neurons to dietary fat

被引:82
作者
Beutler, Lisa R. [1 ]
Corpuz, Timothy, V [2 ]
Ahn, Jamie S. [2 ]
Kosar, Seher [2 ]
Song, Weimin [3 ]
Chen, Yiming [4 ,5 ]
Knight, Zachary A. [2 ,4 ,5 ,6 ]
机构
[1] UCSF Dept Med, San Francisco, CA USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[3] Northwestern Univ, Feinberg Sch Med, Comprehens Metab Core, Chicago, IL 60611 USA
[4] UCSF Dept Physiol, San Francisco, CA 94115 USA
[5] UCSF, Neurosci Grad Program, San Francisco, CA 94115 USA
[6] Kavli Inst Fundamental Neurosci, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
CAUSES GHRELIN RESISTANCE; ARCUATE NUCLEUS; NEUROPEPTIDE-Y; FOOD-INTAKE; INTRINSIC EXCITABILITY; LEPTIN RESISTANCE; NPY/AGRP NEURONS; WEIGHT-LOSS; MICE; RECEPTORS;
D O I
10.7554/eLife.55909
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Body weight is regulated by interoceptive neural circuits that track energy need, but how the activity of these circuits is altered in obesity remains poorly understood. Here we describe the in vivo dynamics of hunger-promoting AgRP neurons during the development of diet-induced obesity in mice. We show that high-fat diet attenuates the response of AgRP neurons to an array of nutritionally-relevant stimuli including food cues, intragastric nutrients, cholecystokinin and ghrelin. These alterations are specific to dietary fat but not carbohydrate or protein. Subsequent weight loss restores the responsiveness of AgRP neurons to exterosensory cues but fails to rescue their sensitivity to gastrointestinal hormones or nutrients. These findings reveal that obesity triggers broad dysregulation of hypothalamic hunger neurons that is incompletely reversed by weight loss and may contribute to the difficulty of maintaining a reduced weight.
引用
收藏
页码:1 / 21
页数:21
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