Affiliation:
1. Department of Biological Sciences California State Polytechnic University Pomona Pomona California USA
2. Department of Biology University of Virginia Charlottesville Virginia USA
3. Department of Physiology Michigan State University East Lansing Michigan USA
Abstract
AbstractObjectiveThis study aimed to determine a dopaminergic circuit required for diet‐induced obesity in mice.MethodsWe created conditional deletion mutants for tyrosine hydroxylase (TH) using neurotensin receptor 1 (Ntsr1) Cre and other Cre drivers and measured feeding and body weight on standard and high‐fat diets. We then used an adeno‐associated virus to selectively restore TH to the ventral tegmental area (VTA) Ntsr1 neurons in conditional knockout (cKO) mice.ResultsMice with cKO of Th using Vglut2‐Cre, Cck‐Cre, Calb1‐Cre, and Bdnf‐Cre were susceptible to obesity on a high‐fat diet; however, Ntsr1‐Cre Th cKO mice resisted weight gain on a high‐fat diet and did not experience an increase in day eating unlike their wild‐type littermate controls. Restoration of TH to the VTA Ntsr1 neurons of the Ntsr1‐Cre Th cKO mice using an adeno‐associated virus resulted in an increase in weight gain and day eating on a high‐fat diet.ConclusionsNtsr1‐Cre Th cKO mice failed to increase day eating on a high‐fat diet, offering a possible explanation for their resistance to diet‐induced obesity. These results implicate VTA Ntsr1 dopamine neurons as promoting out‐of‐phase feeding behavior on a high‐fat diet that could be an important contributor to diet‐induced obesity in humans.
Funder
Division of Diabetes, Endocrinology, and Metabolic Diseases