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NPY/AgRP Neurons Are Essential for Feeding in Adult Mice but Can Be Ablated in Neonates
Serge Luquet,Francisco A. Perez,Thomas S. Hnasko,Richard D. Palmiter*
Hypothalamic neurons that express neuropeptide Y (NPY) and agouti-relatedprotein (AgRP) are thought to be critical regulators of feedingbehavior and body weight. To determine whether NPY/AgRP neuronsare essential in mice, we targeted the human diphtheria toxinreceptor to the Agrp locus, which allows temporally controlledablation of NPY/AgRP neurons to occur after an injection ofdiphtheria toxin. Neonatal ablation of NPY/AgRP neurons hadminimal effects on feeding, whereas their ablation in adultscaused rapid starvation. These results suggest that network-basedcompensatory mechanisms can develop after the ablation of NPY/AgRPneurons in neonates but do not readily occur when these neuronsbecome essential in adults.
Howard Hughes Medical Institute and Department of Biochemistry, University of Washington, Box 357370, Seattle, WA 98195, USA.
Note added in proof: Two related papers (28, 29) were publishedonline while this Report was under review. In both cases, theauthors report that partial ablation of NPY/AgRP neurons resultsin smaller mice that eat less than controls do. The partialablation is probably the consequence of gradual ablation orpartial penetrance of transgene expression. Neither paper describesthe starvation phenotype nor the neonatal compensation reportedhere.
* To whom correspondence should be addressed. E-mail: palmiter{at}u.washington.edu
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