Diet-Induced Obesity Attenuates Fasting-Induced Hyperphagia

被引:34
作者
Briggs, D. I. [1 ]
Lemus, M. B. [1 ]
Kua, E. [1 ]
Andrews, Z. B. [1 ]
机构
[1] Monash Univ, Dept Physiol, Clayton, Vic 3168, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
refeeding; hypothalamus; energy balance; NPY; AgRP; arcuate nucleus; GROWTH-HORMONE SECRETAGOGUE; HYPOTHALAMIC NEUROPEPTIDE-Y; ARCUATE NUCLEUS; GHRELIN; LEPTIN; NEURONS; RECEPTOR; MICE; BRAIN; SENSITIVITY;
D O I
10.1111/j.1365-2826.2011.02148.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity impairs arcuate (ARC) neuropeptide Y (NPY)/agouti-releated peptide (AgRP) neuronal function and renders these homeostatic neurones unresponsive to the orexigenic hormone ghrelin. In the present study, we investigated the effect of diet-induced obesity (DIO) on feeding behaviour, ARC neuronal activation and mRNA expression following another orexigenic stimulus, an overnight fast. We show that 9 weeks of high-fat feeding attenuates fasting-induced hyperphagia by suppressing ARC neuronal activation and hypothalamic NPY/AgRP mRNA expression. Thus, the lack of appropriate feeding responses in DIO mice to a fast is caused by failure ARC neurones to recognise and/or respond to orexigenic cues. We propose that fasting-induced hyperphagia is regulated not by homeostatic control of appetite in DIO mice, but rather by changes in the reward circuitry.
引用
收藏
页码:620 / 626
页数:7
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