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Autophagy in hypothalamic AgRP neurons regulates food intake and energy balance.

Abstract
Macroautophagy is a lysosomal degradative pathway that maintains cellular homeostasis by turning over cellular components. Here we demonstrate a role for autophagy in hypothalamic agouti-related peptide (AgRP) neurons in the regulation of food intake and energy balance. We show that starvation-induced hypothalamic autophagy mobilizes neuron-intrinsic lipids to generate endogenous free fatty acids, which in turn regulate AgRP levels. The functional consequences of inhibiting autophagy are the failure to upregulate AgRP in response to starvation, and constitutive increases in hypothalamic levels of pro-opiomelanocortin and its cleavage product α-melanocyte-stimulating hormone that typically contribute to a lean phenotype. We propose a conceptual framework for considering how autophagy-regulated lipid metabolism within hypothalamic neurons may modulate neuropeptide levels to have immediate effects on food intake, as well as long-term effects on energy homeostasis. Regulation of hypothalamic autophagy could become an effective intervention in conditions such as obesity and the metabolic syndrome.
AuthorsSusmita Kaushik, Jose Antonio Rodriguez-Navarro, Esperanza Arias, Roberta Kiffin, Srabani Sahu, Gary J Schwartz, Ana Maria Cuervo, Rajat Singh
JournalCell metabolism (Cell Metab) Vol. 14 Issue 2 Pg. 173-83 (Aug 03 2011) ISSN: 1932-7420 [Electronic] United States
PMID21803288 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2011 Elsevier Inc. All rights reserved.
Chemical References
  • Agouti-Related Protein
  • Agrp protein, mouse
  • Atg7 protein, mouse
  • Fatty Acids
  • Lipids
  • Microtubule-Associated Proteins
  • alpha-MSH
  • Pro-Opiomelanocortin
  • Autophagy-Related Protein 7
Topics
  • Agouti-Related Protein (metabolism)
  • Animals
  • Autophagy (physiology)
  • Autophagy-Related Protein 7
  • Cells, Cultured
  • Eating
  • Energy Metabolism
  • Fatty Acids (biosynthesis)
  • Hypothalamus (metabolism, physiology)
  • Lipids (biosynthesis)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microtubule-Associated Proteins (genetics)
  • Neurons (metabolism)
  • Pro-Opiomelanocortin (genetics, metabolism)
  • Starvation
  • alpha-MSH (biosynthesis)

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