Sucralose Promotes Food Intake through NPY and a Neuronal Fasting Response

Cell Metab. 2016 Jul 12;24(1):75-90. doi: 10.1016/j.cmet.2016.06.010.

Abstract

Non-nutritive sweeteners like sucralose are consumed by billions of people. While animal and human studies have demonstrated a link between synthetic sweetener consumption and metabolic dysregulation, the mechanisms responsible remain unknown. Here we use a diet supplemented with sucralose to investigate the long-term effects of sweet/energy imbalance. In flies, chronic sweet/energy imbalance promoted hyperactivity, insomnia, glucose intolerance, enhanced sweet taste perception, and a sustained increase in food and calories consumed, effects that are reversed upon sucralose removal. Mechanistically, this response was mapped to the ancient insulin, catecholamine, and NPF/NPY systems and the energy sensor AMPK, which together comprise a novel neuronal starvation response pathway. Interestingly, chronic sweet/energy imbalance promoted increased food intake in mammals as well, and this also occurs through an NPY-dependent mechanism. Together, our data show that chronic consumption of a sweet/energy imbalanced diet triggers a conserved neuronal fasting response and increases the motivation to eat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylate Kinase / metabolism
  • Animals
  • Appetite / drug effects
  • Dopamine / metabolism
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / drug effects
  • Drosophila melanogaster / physiology
  • Eating / drug effects*
  • Energy Intake / drug effects
  • Enzyme Activation / drug effects
  • Fasting*
  • Homeostasis / drug effects
  • Hunger / drug effects
  • Insulin / metabolism
  • Male
  • Neurons / drug effects
  • Neurons / metabolism*
  • Neuropeptide Y / metabolism*
  • Octopamine / metabolism
  • Receptors, Cell Surface / metabolism
  • Sucrose / analogs & derivatives*
  • Sucrose / pharmacology
  • Sweetening Agents / pharmacology
  • Taste / drug effects

Substances

  • Drosophila Proteins
  • Insulin
  • Neuropeptide Y
  • Receptors, Cell Surface
  • Sweetening Agents
  • gustatory receptor, Drosophila
  • Octopamine
  • Sucrose
  • trichlorosucrose
  • Adenylate Kinase
  • Dopamine