Nano Chromium Picolinate Improves Gene Expression Associated with Insulin Signaling in Porcine Skeletal Muscle and Adipose Tissue

被引:5
作者
Hung, Alex T. [1 ]
Leury, Brian J. [1 ]
Sabin, Matthew A. [2 ]
Fahri, Fahri [1 ]
DiGiacomo, Kristy [1 ]
Lien, Tu-Fa [3 ]
Dunshea, Frank R. [1 ,4 ]
机构
[1] Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Murdoch Childrens Res Inst, Parkville, Vic 3010, Australia
[3] Natl Chiayi Univ, Dept Anim Sci, Chiayi 600, Taiwan
[4] Univ Leeds, Fac Biol Sci, Leeds LS2 9JT, W Yorkshire, England
关键词
chromium; nanotechnology; insulin sensitivity; cytokine; BODY-COMPOSITION; MOLECULAR-MECHANISMS; GLUCOSE-INTOLERANCE; LIPID-METABOLISM; RESISTANCE; ADIPONECTIN; SUPPLEMENTATION; SENSITIVITY; OBESE; PROTEIN;
D O I
10.3390/ani10091685
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Simple Summary Dietary chromium has been shown to reduce fat deposition and improve insulin action whereas dietary fat can increase fat deposition and cause insulin resistance. This study found that dietary nanoparticles of chromium picolinate, an organic form of chromium, caused changes in the genes involved in insulin action in both muscle and fat tissue that indicated improved insulin action. Conversely, a moderate increase in dietary fat caused changes consistent with increased fat deposition and reduced insulin action. In conclusion, nanoparticles of chromium picolinate offer a means of supplementing pigs diets to improve growth performance and carcass composition. The aim of this study was to investigate the interactive effects of dietary nano chromium picolinate (nCrPic) and dietary fat on genes involved in insulin signaling in skeletal muscle and subcutaneous adipose tissue of pigs. Forty-eight gilts were stratified on body weight into four blocks of four pens of three pigs and then within each block each pen was randomly allocated to four treatment groups in a 2 x 2 factorial design. The respective factors were dietary fat (22 or 57 g/kg) and dietary nCrPic (0 or 400 ppb nCrPic) fed for six weeks. Skeletal muscle samples were collected from theLongissimus thoracisand subcutaneous adipose tissue collected from above this muscle. Dietary nCrPic increased adiponectin, uncoupling protein 3 (UCP3) and serine/threonine protein kinase (AKT) mRNA expression, whereas dietary fat decreased adiponectin and increased leptin, tumor necrosis factor-alpha(TNF-alpha), peroxisome proliferator-activated receptors gamma(PPAR gamma) and CCAAT/enhancer-binding protein alpha(C/EBP alpha) mRNA expression in adipose tissue. In skeletal muscle, dietary nCrPic increased phosphatidylinositol 3 kinase (PI3K), AKT, UCP3 and interleukin-15 (IL-15), as well as decreased suppressor of cytokine signaling 3 (SOCS3) mRNA expression. The improvement in insulin signaling and muscle mass and the reduction in carcass fatness by dietary nCrPic may be via decreased SOCS3 and increased UCP3 and IL-15 in skeletal muscle and increased adiponectin in subcutaneous adipose tissue.
引用
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页码:1 / 14
页数:14
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