Insulin and glucagon are critical components of metabolic pathways that regulate energy homeostasis in mammals. Dysfunction of these important pathways can result in disease states that are of growing public health concerns, such as diabetes and obesity. Model organisms are increasingly used as tools to gain further understanding of biochemical pathways that are conserved across species. Drosophila melanogaster has found increasing use as a model organism to understand metabolic disease and feeding behavior. Drosophila insulin-like peptides (DILPs) and adipokinetic hormone (AKH) are neuropeptides that have similar roles as mammalian insulin and glucagon, respectively. For example, removal of insulin secretion in a fly results in markedly elevated circulating carbohydrate levels;conversely, removal of AKH secretion results in lowered circulating carbohydrate levels. Several studies have been recently published revealing the importance of the insulin- and glucagon-like signaling pathways in Drosophila in controlling growth, metabolism, and feeding behavior. The primary focus of this proposal is to characterize the expression pattern and functional role of the AKH receptor in Drosophila, the functional homolog of the mammalian glucagon receptor.
Our specific aims are (1) to assess the role of the AKH receptor in mobilizing internal energy stores, (2) to determine the mechanisms by which the AKH receptor modulates food-searching locomotor behavior, and (3) to ascertain the functional role of the Drosophila AKH receptor in taste perception. We will also use a variety of genetic techniques to manipulate the expression of the AKH receptor, as well as generate mutants with altered expression patterns. We will also undertake a detailed characterization of the physiological and behavioral consequences of AKH receptor expression.

Public Health Relevance

We hope that results obtained from our investigations will yield insights into the regulation of energy balance and metabolism that are relevant to human disease. We are particularly interested in biochemical pathways that are involved in conditions that could lead to diabetes or obesity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08DK075922-03
Application #
8100238
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Hyde, James F
Project Start
2009-09-01
Project End
2011-10-28
Budget Start
2011-08-01
Budget End
2011-10-28
Support Year
3
Fiscal Year
2011
Total Cost
$30,037
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Pediatrics
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390