EXCEED THE SPACE PROVIDED. The long-term goal of this project is to develop novel dietary strategies for the control of human obesity, the most prevalent nutrition-related disease in America. The objective of this application is to identify isomer- specific mechanisms by which conjugated linoleic acid (CLA), unsaturated fatty acids found in beef and dairy foods that reduce adiposity in certain animals and humans, alters lipid metabolism in cultures of human (pre)adipocytes. The central hypothesis for the proposed research is that the trans-10, cis-12 isomer of CLA attenuates triglyceride (TG) content and alters lipid droplet morphology by enhancing energy expenditure, lipolysis, and fatty acid oxidation, thereby down-regulating the expression of perilipin-A, a major regulator of adipocyte TG storage. This hypothesis was formulated based on our preliminary findings in human (pre)adipocyte cultures demonstrating that trans-10, cis-12, but not cis-9, trans-11, CLA decreased TG content, de novo lipogenesis, fatty acid esterification, and perilipin protein without affecting differentiation per se. The rationale for the proposed research is that once we understand how trans-10, cis-12 CLA prevents TG accumulation in (pre)adipocytes, effective strategies can be developed using CLA as an antiobesity nutrient in fortified foods or supplements for clinical trials. To accomplish this objective, the following specific aims will be examined in human cultures of differentiating preadipocytes and newly- differentiated adipocytes:
Aim #1. Determine the mechanism by which trans-10, cis-12 CLA decreases cellular TG content;
and Aim #2. Determine the mechanism by which trans-10, cis-12 CLA decreases the expression of perilipin-A.
In Aim #1, the impact of fatty acid type and dose on oxygen consumption, mitochondrial and peroxisomal beta-oxidation, lipolysis, fatty acid oxidation, and uncoupling protein expression will be determined.
In Aim #2, the influence of fatty acid type and dose on perilipin-A protein and gene expression will be evaluated. Using primary cultures of human adipocytes as our model is important, because there are clear differences between the lipid metabolism of human and animal adipocytes. The proposed studies are significant because they are expected to lead to the development of novel strategies for weight loss. Consequently, reductions in health problems and financial costs related to obesity are expected. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK063070-03S1
Application #
6968099
Study Section
Nutrition Study Section (NTN)
Program Officer
Yanovski, Susan Z
Project Start
2002-09-30
Project End
2006-06-30
Budget Start
2005-01-01
Budget End
2005-06-30
Support Year
3
Fiscal Year
2005
Total Cost
$17,931
Indirect Cost
Name
University of North Carolina Greensboro
Department
Nutrition
Type
Schools of Arts and Sciences
DUNS #
616152567
City
Greensboro
State
NC
Country
United States
Zip Code
27402
Shen, Wan; McIntosh, Michael K (2016) Nutrient Regulation: Conjugated Linoleic Acid's Inflammatory and Browning Properties in Adipose Tissue. Annu Rev Nutr 36:183-210
Shen, Wan; Baldwin, Jessie; Collins, Brian et al. (2015) Low level of trans-10, cis-12 conjugated linoleic acid decreases adiposity and increases browning independent of inflammatory signaling in overweight Sv129 mice. J Nutr Biochem 26:616-25
Shen, Wan; Martinez, Kristina; Chuang, Chia Chi et al. (2013) The phospholipase C inhibitor U73122 attenuates trans-10, cis-12 conjugated linoleic acid-mediated inflammatory signaling and insulin resistance in human adipocytes. J Nutr 143:584-90
Martinez, Kristina; Shyamasundar, Shruthi; Kennedy, Arion et al. (2013) Diacylglycerol kinase inhibitor R59022 attenuates conjugated linoleic acid-mediated inflammation in human adipocytes. J Lipid Res 54:662-70
Shen, Wan; Chuang, Chia-Chi; Martinez, Kristina et al. (2013) Conjugated linoleic acid reduces adiposity and increases markers of browning and inflammation in white adipose tissue of mice. J Lipid Res 54:909-22
Reardon, Meaghan; Gobern, Semone; Martinez, Kristina et al. (2012) Oleic acid attenuates trans-10,cis-12 conjugated linoleic acid-mediated inflammatory gene expression in human adipocytes. Lipids 47:1043-51
Obsen, Thomas; Faergeman, Nils J; Chung, Soonkyu et al. (2012) Trans-10, cis-12 conjugated linoleic acid decreases de novo lipid synthesis in human adipocytes. J Nutr Biochem 23:580-90
Schmidt, Soren F; Jorgensen, Mette; Sandelin, Albin et al. (2012) Cross-species ChIP-seq studies provide insights into regulatory strategies of PPARýý in adipocytes. Transcription 3:19-24
Schmidt, Søren F; Mandrup, Susanne (2011) Gene program-specific regulation of PGC-1{alpha} activity. Genes Dev 25:1453-8
Schmidt, Søren F; Jørgensen, Mette; Chen, Yun et al. (2011) Cross species comparison of C/EBP? and PPAR? profiles in mouse and human adipocytes reveals interdependent retention of binding sites. BMC Genomics 12:152

Showing the most recent 10 out of 23 publications