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  4. The function of porcine PPARγ and dietary fish oil effect on the expression of lipid and glucose metabolism related genes
 
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The function of porcine PPARγ and dietary fish oil effect on the expression of lipid and glucose metabolism related genes

Resource
The Journal of Nutritional Biochemistry, 22(2), 179-186
Journal
The Journal of Nutritional Biochemistry
Journal Volume
22
Journal Issue
2
Pages
179-186
Date Issued
2011
Date
2011
Author(s)
Yu, Yu-Hsiang
Wu, Shinn-Chih  
Cheng, Winston Teng-Kuei
Mersmann, Harry J.
Shen, Tang-Long  
Ding, Shih-Torng  
DOI
10.1016/j.jnutbio.2010.01.006
URI
http://ntur.lib.ntu.edu.tw//handle/246246/233220
http://ntur.lib.ntu.edu.tw/bitstream/246246/233220/-1/02.pdf
Abstract
Peroxisome-proliferator-activated receptor γ (PPARγ) plays a critical role in regulation of adipocyte differentiation and insulin sensitivity. To become functional, PPARγ must be activated by binding an appropriate ligand. Polyunsaturated fatty acids (PUFA) are potential ligands for PPARγ. The current experiment was designed to determine the potential for PUFA, particularly eicosapentaenoic acid and docosahexaenoic acid, to activate the function of porcine PPARγ in vivo. Transgenic mice, expressing porcine PPARγ in skeletal muscle were generated and fed with a high-saturated fat (beef tallow) or high-unsaturated fat (fish oil) diet for 4 months. When transgenic mice were fed a fish oil supplemented diet, the expression of adipogenic and glucose uptake genes was increased, leading to reduced plasma glucose concentration. The PPARγ transgene increased the expression of Glut4 in the muscle. This result suggests that there was increased glucose utilization and, therefore, a reduced blood glucose concentration in the transgenic mice. Also, the plasma adiponectin was elevated by fish oil treatment, suggesting a role of adiponectin in mediating the PUFA effect. These results suggest that PUFA may serve as a natural regulator of glucose uptake in vivo and these effects are mainly through PPARγ function. © 2011 Elsevier Inc.
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