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Identification of a Brainstem Circuit Controlling Feeding
Author(s) -
Alexander R. Nectow,
Marc Schneeberger,
Hongxing Zhang,
Bianca C. Field,
Nicolas Renier,
Estefania P. Azevedo,
Bindiben Patel,
Yupu Liang,
Siddhartha Mitra,
Marc TessierLavigne,
MingHu Han,
Jeffrey M. Friedman
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.06.045
Subject(s) - biology , brainstem , dorsal raphe nucleus , neuroscience , hypothalamus , glutamate receptor , druggability , food intake , nucleus , receptor , midbrain , endocrinology , central nervous system , gene , serotonin , biochemistry , serotonergic
Hunger, driven by negative energy balance, elicits the search for and consumption of food. While this response is in part mediated by neurons in the hypothalamus, the role of specific cell types in other brain regions is less well defined. Here, we show that neurons in the dorsal raphe nucleus, expressing vesicular transporters for GABA or glutamate (hereafter, DRN Vga and DRN VGLUT3 neurons), are reciprocally activated by changes in energy balance and that modulating their activity has opposite effects on feeding-DRN Vga neurons increase, whereas DRN VGLUT3 neurons suppress, food intake. Furthermore, modulation of these neurons in obese (ob/ob) mice suppresses food intake and body weight and normalizes locomotor activity. Finally, using molecular profiling, we identify druggable targets in these neurons and show that local infusion of agonists for specific receptors on these neurons has potent effects on feeding. These data establish the DRN as an important node controlling energy balance. PAPERCLIP.

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