Obesity and metabolic syndrome are rapidly growing worldwide, leading to high morbidity and mortality. Fundamental to these pathologies is adipose tissue. Chronic tissue inflammation, especially in adipose tissue, is a crucial feature of obesity and links to systemic insulin resistance and Type 2 diabetes (T2D). Although activation of brown adipose tissue (BAT) can increase energy expenditure and fuel utilization, leading to improvement of insulin sensitivity, little is known about whether the potential insulin-sensitizing effect of BAT is linked to resolution of inflammation. Specialized pro-resolving lipid mediators (SPM), such as the maresins, are novel mediators that resolve inflammation and trigger tissue regeneration. In work in progress, we discovered that activation of BAT by cold significantly reduces inflammation and improves systemic metabolism in obesity. Interestingly, we found that cold exposure selectively increases BAT production of maresins that are produced from ?-3 polyunsaturated fatty acid, docosahexaenoic acid (DHA). Based on these exciting findings, we hypothesize that the activation of BAT leads to increased production of maresins that act locally and systemically in resolving inflammation, leading to improved insulin sensitivity in obesity. The objectives of this proposal are to determine the role of maresins in the resolution of inflammation and improvement of insulin sensitivity in response to cold exposure and to investigate the molecular mechanisms mediating cold or ?3- adrenergic stimulation-induced maresin biosynthesis. We will determine the role of a potential lipid transporter as well as key enzymes that regulate the maresin production. Completion of the proposed studies will lead to an entirely new understanding of the beneficial effects of BAT activation in obesity and could lead to novel biomimicry-based therapeutic approaches of obesity and T2D.

Public Health Relevance

Obesity and diabetes are the two most prominent health burdens in the United States. The proposed research aims to understand the mechanisms of action of brown fat-derived lipid mediators that exert anti- inflammatory and anti-obesity effects. The success of the proposed studies will improve our knowledge of resolution of inflammation and provide promising therapeutic approaches for the treatment and prevention of obesity and diabetes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK122808-02
Application #
10136594
Study Section
Integrative Physiology of Obesity and Diabetes Study Section (IPOD)
Program Officer
Haft, Carol R
Project Start
2020-04-01
Project End
2024-01-31
Budget Start
2021-02-01
Budget End
2022-01-31
Support Year
2
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215