Visualizing obesity-induced changes in dopamine reinforcement - PROJECT SUMMARY/ABSTRACT
Obesity is significant public health problem in the US and globally. Diet and exercise continue to be the
primary treatment for obesity, but behavioral change is often difficult and long-term success limited by relapse
to overconsumption and weight regain. The highly palatable and energy rich food that are readily available in
modern culture has been hypothesized to drive overeating through dopamine-mediated reinforcement that
generates hedonic hunger and addiction-like, compulsive consumption. Understanding dopamine mediated
compulsive overeating is important for understanding and addressing the behavioral inflexibility that makes
obesity so difficult to treat in the long-term. However, how dopamine may mediate compulsive consumption
remains unclear. While the basic premise of dopamine theories of obesity is that dopamine activity reinforces
consumption of tasty food, considerable evidence suggest that obesity actually induces impairments in
dopamine function. Thus, although theories on dopamine in obesity are crucial, a clear picture of how
dopamine is altered in obesity and how these changes mediate inflexible eating behavior has not emerged.
Direct observation of dopamine signaling during behavioral tasks in awake, behaving animals would
provide insight into how dopamine function changes in obesity and how those changes correspond to behavior.
However, one challenge in studying behavior in obesity in animals is that in order to get the animal to
participate in the experiment, for example to do a lever-pressing task, food restriction is typically required to
induce participatory motivation. In dietary induced obesity, however, food restriction interferes with the basic
condition being tested by, effectively, putting the animals on a calorie restricted diet. In this proposal, we will
use fiber photometry to directly measure dopamine release in awake, behaving mice comparing obese and
lean mice. We will use an optical self-stimulation paradigm that does not require food restriction to avoid the
problems of food restriction in obesity studies as well as to examine ‘pure’ dopamine reinforcement, i.e.,
reinforcement via dopamine activation absent actual reward or need/deprivation state. We will examine the
timecourse of obesity-induced alterations in dopamine and associated reinforcement efficacy. Finally, we will
provide a weight-loss dietary intervention with the obese mice to assess the extent to which weight-loss
correlates with potential normalization of dopamine. By providing a direct window onto dopamine signaling and
reinforcement in obesity, the proposed work will serve as a reference or touchstone for interpreting diverse,
sometimes disparate data on dopamine and obesity and for evaluating associated theories.