Top-down control of conditioned overconsumption is mediated by insular cortex Nos1 neurons

Cell Metab. 2021 Jul 6;33(7):1418-1432.e6. doi: 10.1016/j.cmet.2021.03.001. Epub 2021 Mar 23.

Abstract

Associative learning allows animals to adapt their behavior in response to environmental cues. For example, sensory cues associated with food availability can trigger overconsumption even in sated animals. However, the neural mechanisms mediating cue-driven non-homeostatic feeding are poorly understood. To study this, we recently developed a behavioral task in which contextual cues increase feeding even in sated mice. Here, we show that an insular cortex to central amygdala circuit is necessary for conditioned overconsumption, but not for homeostatic feeding. This projection is marked by a population of glutamatergic nitric oxide synthase-1 (Nos1)-expressing neurons, which are specifically active during feeding bouts. Finally, we show that activation of insular cortex Nos1 neurons suppresses satiety signals in the central amygdala. The data, thus, indicate that the insular cortex provides top-down control of homeostatic circuits to promote overconsumption in response to learned cues.

Keywords: RNA sequencing; amygdala; associative learning; feeding; insular cortex; nitric oxide synthase-1.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Clozapine / analogs & derivatives
  • Clozapine / pharmacology
  • Conditioning, Psychological / drug effects
  • Conditioning, Psychological / physiology
  • Cues
  • Eating / drug effects
  • Eating / physiology
  • Feeding Behavior / drug effects
  • Feeding Behavior / physiology*
  • Female
  • Insular Cortex / drug effects
  • Insular Cortex / metabolism
  • Insular Cortex / pathology
  • Insular Cortex / physiology*
  • Learning / drug effects
  • Learning / physiology
  • Male
  • Mice
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / physiology*
  • Nitric Oxide Synthase Type I / genetics*
  • Nitric Oxide Synthase Type I / metabolism
  • Overnutrition / etiology*
  • Overnutrition / genetics
  • Overnutrition / metabolism
  • Overnutrition / pathology

Substances

  • Nitric Oxide Synthase Type I
  • Nos1 protein, mouse
  • Clozapine
  • clozapine N-oxide