PNOCARC Neurons Promote Hyperphagia and Obesity upon High-Fat-Diet Feeding

Neuron. 2020 Jun 17;106(6):1009-1025.e10. doi: 10.1016/j.neuron.2020.03.022. Epub 2020 Apr 16.

Abstract

Calorie-rich diets induce hyperphagia and promote obesity, although the underlying mechanisms remain poorly defined. We find that short-term high-fat-diet (HFD) feeding of mice activates prepronociceptin (PNOC)-expressing neurons in the arcuate nucleus of the hypothalamus (ARC). PNOCARC neurons represent a previously unrecognized GABAergic population of ARC neurons distinct from well-defined feeding regulatory AgRP or POMC neurons. PNOCARC neurons arborize densely in the ARC and provide inhibitory synaptic input to nearby anorexigenic POMC neurons. Optogenetic activation of PNOCARC neurons in the ARC and their projections to the bed nucleus of the stria terminalis promotes feeding. Selective ablation of these cells promotes the activation of POMC neurons upon HFD exposure, reduces feeding, and protects from obesity, but it does not affect food intake or body weight under normal chow consumption. We characterize PNOCARC neurons as a novel ARC neuron population activated upon palatable food consumption to promote hyperphagia.

Keywords: PNOC neurons; acute high-fat-diet feeding; arcuate nucleus; food intake; hypothalamus; neuropeptide; nociceptin; obesity; orphanin FQ; prepronociceptin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arcuate Nucleus of Hypothalamus / cytology
  • Arcuate Nucleus of Hypothalamus / metabolism
  • Arcuate Nucleus of Hypothalamus / physiology*
  • Diet, High-Fat*
  • Feeding Behavior / physiology*
  • GABAergic Neurons / metabolism
  • GABAergic Neurons / physiology*
  • Hyperphagia*
  • Mice
  • Neural Inhibition / physiology
  • Neurons / metabolism
  • Neurons / physiology
  • Obesity*
  • Optogenetics
  • Pro-Opiomelanocortin / metabolism
  • Protein Precursors / metabolism
  • Receptors, Opioid / metabolism
  • Septal Nuclei / physiology
  • Weight Gain / physiology*

Substances

  • Protein Precursors
  • Receptors, Opioid
  • prepronociceptin
  • Pro-Opiomelanocortin