In the United States, nearly a tenth of the population has type 2 diabetes mellitus (T2DM). The chronic hyperglycemia found in this disease causes angiopathy, leading to kidney failure, blindness, amputation, stroke, and heart attack. Some of the medicines used to treat T2DM have an adverse side effect profile, underscoring the need to develop new anti-hyperglycemic agents. The recently discovered Palmitic Acid esters of HydroxyStearic Acids (PAHSAs) have been shown to improve blood glucose levels by increasing insulin release and insulin sensitivity through their activity on free fatty acid receptors-1 and -4. However, the effect that the chemical structure has on biological activity and the origins of PAHSAs remain unknown.
The Specific Aims of this proposal are to: 1) develop a synthetic platform for PAHSAs and determine the relationship between PAHSA structure and anti-diabetic activity and 2) determine the biosynthetic origins of PAHSAs. Uncovering the structural elements responsible for the anti-diabetic activity of PAHSAs may provide a lead structure for a novel treatment in the fight against diabetes. Furthermore, elucidation of the biosynthesis of PAHSAs may spur future studies that would allow for treatment of this disease by helping patients with diabetes increase their own endogenous PAHSA synthesis.

Public Health Relevance

Type 2 diabetes mellitus is a major contributor to human death, suffering, and healthcare costs both in the UnitedStatesandaroundtheworld.Thisprojectwillhelpcombatthisdiseasebylayingthefoundationfora newtreatment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
1F30DK112622-01
Application #
9258617
Study Section
Special Emphasis Panel (ZDK1-GRB-R (O1)L)
Program Officer
Castle, Arthur
Project Start
2016-09-14
Project End
2020-09-13
Budget Start
2016-09-14
Budget End
2017-09-13
Support Year
1
Fiscal Year
2016
Total Cost
$33,677
Indirect Cost
Name
University of Texas Austin
Department
Type
Schools of Pharmacy
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78712
Kolar, Matthew J; Nelson, Andrew T; Chang, Tina et al. (2018) Faster Protocol for Endogenous Fatty Acid Esters of Hydroxy Fatty Acid (FAHFA) Measurements. Anal Chem 90:5358-5365
Nelson, Andrew T; Kolar, Matthew J; Chu, Qian et al. (2017) Stereochemistry of Endogenous Palmitic Acid Ester of 9-Hydroxystearic Acid and Relevance of Absolute Configuration to Regulation. J Am Chem Soc 139:4943-4947