| Literature DB >> 28753423 |
Alexander R Nectow1, Marc Schneeberger2, Hongxing Zhang3, Bianca C Field2, Nicolas Renier4, Estefania Azevedo2, Bindiben Patel5, Yupu Liang6, Siddhartha Mitra6, Marc Tessier-Lavigne7, Ming-Hu Han3, Jeffrey M Friedman8.
Abstract
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, DRNVgat and DRNVGLUT3 neurons), are reciprocally activated by changes in energy balance and that modulating their activity has opposite effects on feeding-DRNVgat neurons increase, whereas DRNVGLUT3 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.Entities:
Keywords: body weight; dorsal raphe nucleus; energy homeostasis; feeding; leptin resistance; locomotor activity; obesity
Mesh:
Year: 2017 PMID: 28753423 DOI: 10.1016/j.cell.2017.06.045
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582