Food hoarding and associated neuronal activation in brain reward circuitry in Mongolian gerbils

Physiol Behav. 2011 Sep 1;104(3):429-36. doi: 10.1016/j.physbeh.2011.04.062. Epub 2011 May 5.

Abstract

Mongolian gerbils (Meriones unguiculatus) display food hoarding and thus provide an opportunity to study the neuromechanisms underlying this behavior. In the present study, male gerbils exhibited a bimodal expression of food hoarding behavior-some displayed high levels of food hoarding whereas others virtually lacked this behavior under normal laboratory conditions with free access to food. Food hoarding was found to be associated with an increase in neuronal activation, indicated by Fos immunoreactive (ir) staining, in several brain areas including the nucleus accumbens, ventral tegmental area (VTA), and lateral hypothalamus. Food hoarding was also associated with increases in the number of cells labeled for tyrosine hydroxylase (TH-ir), the rate limiting enzyme for dopamine conversion, and the number of cells co-labeled for TH-ir/Fos-ir in the VTA, suggesting that dopamine in the brain reward circuitry may be involved in food hoarding. Further, we found that 22 h of food deprivation induced food hoarding in some, but not all, males that naturally did not display food hoarding. In these males, however, food hoarding did not increase TH-ir or TH-ir/Fos-ir expression in the VTA. Together, these data indicate that male Mongolian gerbils display diverse phenotypes of food hoarding behavior and that dopamine in the brain reward circuitry may be involved in the control of naturally occurring, but not food deprivation-induced, food hoarding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal
  • Body Weight / physiology
  • Brain / metabolism*
  • Eating / physiology
  • Fats / metabolism
  • Feeding Behavior / physiology*
  • Food Deprivation / physiology
  • Gene Expression Regulation
  • Gerbillinae / physiology*
  • Leptin / blood
  • Male
  • Neural Pathways / physiology
  • Proto-Oncogene Proteins c-fos / metabolism
  • Reward*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Fats
  • Leptin
  • Proto-Oncogene Proteins c-fos
  • Tyrosine 3-Monooxygenase