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  Hypothalamic UDP Increases in Obesity and Promotes Feeding via P2Y6-Dependent Activation of AgRP Neurons

Steculorum, S. M., Paeger, L., Bremser, S., Evers, N., Hinze, Y., Idzko, M., et al. (2015). Hypothalamic UDP Increases in Obesity and Promotes Feeding via P2Y6-Dependent Activation of AgRP Neurons. Cell, 162(6), 1404-17. doi:10.1016/j.cell.2015.08.032.

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Steculorum, S. M., Author
Paeger, L., Author
Bremser, S., Author
Evers, N., Author
Hinze, Y.1, Author           
Idzko, M., Author
Kloppenburg, P., Author
Bruning, J. C., Author
Affiliations:
1Metabolomics, Core Facilities, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3394018              

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Free keywords: Agouti-Related Protein/metabolism Animals *Appetite Regulation Disease Models, Animal Hypothalamus/*metabolism In Vitro Techniques Male Mice Mice, Inbred C57BL Obesity/*metabolism Receptors, Purinergic P2/*metabolism Uridine Diphosphate/*metabolism
 Abstract: Activation of orexigenic AgRP-expressing neurons in the arcuate nucleus of the hypothalamus potently promotes feeding, thus defining new regulators of AgRP neuron activity could uncover potential novel targets for obesity treatment. Here, we demonstrate that AgRP neurons express the purinergic receptor 6 (P2Y6), which is activated by uridine-diphosphate (UDP). In vivo, UDP induces ERK phosphorylation and cFos expression in AgRP neurons and promotes action potential firing of these neurons in brain slice recordings. Consequently, central application of UDP promotes feeding, and this response is abrogated upon pharmacologic or genetic inhibition of P2Y6 as well as upon pharmacogenetic inhibition of AgRP neuron activity. In obese animals, hypothalamic UDP content is elevated as a consequence of increased circulating uridine concentrations. Collectively, these experiments reveal a potential regulatory pathway in obesity, where peripheral uridine increases hypothalamic UDP concentrations, which in turn can promote feeding via PY6-dependent activation of AgRP neurons.

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 Dates: 2015-09-102015-09-12
 Publication Status: Issued
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 Identifiers: Other: 26359991
DOI: 10.1016/j.cell.2015.08.032
ISSN: 1097-4172 (Electronic)0092-8674 (Linking)
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Title: Cell
Source Genre: Journal
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Pages: - Volume / Issue: 162 (6) Sequence Number: - Start / End Page: 1404 - 17 Identifier: -