NPY/AgRP neurons are not essential for feeding responses to glucoprivation

被引:107
作者
Luquet, Serge
Phillips, Colin T.
Palmiter, Richard D.
机构
[1] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
关键词
neuropeptide Y; agouti-related protein; glucopenia; ghrelin; neuron ablation; 2-deoxy-D-glucose; insulin; INSULIN-INDUCED HYPOGLYCEMIA; LACKING NEUROPEPTIDE-Y; AGOUTI-RELATED PROTEIN; ARCUATE NUCLEUS; MONOSODIUM GLUTAMATE; GLUCOSENSING NEURONS; BLOOD-GLUCOSE; FOOD-INTAKE; GROWTH-HORMONE; MICE LEADS;
D O I
10.1016/j.peptides.2006.08.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Animals respond to hypoglycemia by eating and by stimulating gluconeogenesis. These responses to glucose deprivation are initiated by glucose-sensing neurons in the brain, but the neural circuits that control feeding behavior are not well established. Neurons in the arcuate region of the hypothalamus that express neuropeptide Y (NPY) and agouti-related protein (AgRP) have been implicated in mediating the feeding response to glucoprivation. We devised a method to selectively ablate these neurons in neonatal mice and then tested adult mice for their feeding responses to fasting, mild hypoglycemia, 2-deOXY-D-glucose and a ghrelin receptor agonist. Whereas the feeding response to the ghrelin receptor agonist was completely abrogated, the feeding response to glucoprivation was normal. The feeding response after a fast was attenuated when standard chow was available but normal with more palatable solid or liquid diet. We conclude that NPY/AgRP neurons are not necessary for generating or mediating the orexigenic response to glucose deficiency, but they are essential for the feeding response to ghrelin and refeeding on standard chow after a fast. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:214 / 225
页数:12
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