Removal of high-fat diet after chronic exposure drives binge behavior and dopaminergic dysregulation in female mice

Neuroscience. 2016 Jun 21:326:170-179. doi: 10.1016/j.neuroscience.2016.04.002. Epub 2016 Apr 8.

Abstract

A significant contributor to the obesity epidemic is the overconsumption of highly palatable, energy dense foods. Chronic intake of palatable foods is associated with neuroadaptations within the mesocorticolimbic dopamine system adaptations which may lead to behavioral changes, such as overconsumption or bingeing. We examined behavioral and molecular outcomes in mice that were given chronic exposure to a high-fat diet (HFD; 12weeks), with the onset of the diet either in adolescence or adulthood. To examine whether observed effects could be reversed upon removal of the HFD, animals were also studied 4weeks after a return to chow feeding. Most notably, female mice, particularly those exposed to HFD starting in adolescence, demonstrated the emergence of binge-like behavior when given restricted access to a palatable food. Further, changes in dopamine-related gene expression and dopamine content in the prefrontal cortex were observed. Some of these HFD-driven phenotypes reversed upon removal of the diet, whereas others were initiated by removal of the diet. These findings have implications for obesity management and interventions, as both pharmacological and behavioral therapies are often combined with dietary interventions (e.g., reduction in calorie dense foods).

Keywords: adolescence; binge; dopamine; high-fat diet; reward; sex difference.

MeSH terms

  • Adipose Tissue / metabolism
  • Animals
  • Body Weight
  • Brain / metabolism*
  • Bulimia / metabolism*
  • Diet, High-Fat / adverse effects*
  • Dopamine / metabolism*
  • Dopamine Plasma Membrane Transport Proteins / metabolism
  • Eating
  • Female
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Nucleus Accumbens / metabolism
  • Prefrontal Cortex / metabolism
  • Receptors, Dopamine D1 / metabolism
  • Receptors, Dopamine D2 / metabolism
  • Reward
  • Tyrosine 3-Monooxygenase / metabolism
  • Ventral Tegmental Area / metabolism

Substances

  • DRD2 protein, mouse
  • Dopamine Plasma Membrane Transport Proteins
  • Drd1 protein, mouse
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Tyrosine 3-Monooxygenase
  • Dopamine