Title of article :
The function of porcine PPARγ and dietary fish oil effect on the expression of lipid and glucose metabolism related genes
Author/Authors :
Yu-Hsiang Yu، نويسنده , , Shinn-Chih Wu، نويسنده , , Winston Teng-Kuei Cheng، نويسنده , , Harry J. Mersmann، نويسنده , , Tang-Long Shen، نويسنده , , Shih-Torng Ding، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
8
From page :
179
To page :
186
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.
Keywords :
Adiponectin , Fish oil , Polyunsaturated fatty acids , Insulin sensitivity , Mice , Peroxisome proliferator-activated receptor ?
Journal title :
The Journal of Nutritional Biochemistry
Serial Year :
2011
Journal title :
The Journal of Nutritional Biochemistry
Record number :
1299761
Link To Document :
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