Hindbrain Double-Negative Feedback Mediates Palatability-Guided Food and Water Consumption

Cell. 2020 Sep 17;182(6):1589-1605.e22. doi: 10.1016/j.cell.2020.07.031. Epub 2020 Aug 24.

Abstract

Hunger and thirst have distinct goals but control similar ingestive behaviors, and little is known about neural processes that are shared between these behavioral states. We identify glutamatergic neurons in the peri-locus coeruleus (periLCVGLUT2 neurons) as a polysynaptic convergence node from separate energy-sensitive and hydration-sensitive cell populations. We develop methods for stable hindbrain calcium imaging in free-moving mice, which show that periLCVGLUT2 neurons are tuned to ingestive behaviors and respond similarly to food or water consumption. PeriLCVGLUT2 neurons are scalably inhibited by palatability and homeostatic need during consumption. Inhibition of periLCVGLUT2 neurons is rewarding and increases consumption by enhancing palatability and prolonging ingestion duration. These properties comprise a double-negative feedback relationship that sustains food or water consumption without affecting food- or water-seeking. PeriLCVGLUT2 neurons are a hub between hunger and thirst that specifically controls motivation for food and water ingestion, which is a factor that contributes to hedonic overeating and obesity.

Keywords: GRIN lens; appetite; hunger; in vivo calcium imaging; ingestive behavior; locus ceruleus; locus coeruleus; palatability; periLC; thirst.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Appetite / physiology
  • Appetite Regulation / physiology*
  • Behavior Rating Scale
  • Drinking / physiology*
  • Eating / physiology*
  • Feedback
  • Feeding Behavior / physiology
  • Female
  • Glutamine / metabolism
  • Glutamine / physiology
  • Homeostasis / physiology
  • Hunger / physiology
  • Locus Coeruleus / cytology*
  • Male
  • Mice
  • Mice, Knockout
  • Motivation / physiology
  • Nerve Net / physiology*
  • Neurons / drug effects
  • Neurons / physiology*
  • Recombinant Proteins
  • Reward
  • Rhombencephalon / cytology
  • Rhombencephalon / diagnostic imaging
  • Rhombencephalon / physiology*
  • Single-Cell Analysis / methods*
  • Taste / physiology
  • Thirst / physiology

Substances

  • Recombinant Proteins
  • Glutamine