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ARTICLE |
1 USDA, ARS, APRU, Athens, GA, 30605
2 The Coca-Cola Company, Innovation, Ingredient Science, Atlanta, GA, 30313
3 Animal and Dairy Science Department, University of Georgia, Athens, GA. 30602
* To whom correspondence should be addressed. E-mail: Gary.Hausman{at}ARS.USDA.GOV.
| Abstract |
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Thiazolidinediones (TZD) are insulin sensitizing agents currently used for the treatment of type 2 diabetes and are widely used as adipogenic agents because they are ligands of peroxisome proliferator-activated receptor gamma (PPAR
), a key adipogenic transcription factor. In vivo and in vitro studies of TZD as potential modifiers of intramuscular or marbling adipogenesis are reviewed. Thiazolidinedione-induced adipogenesis has been reported in numerous cell culture systems including rodent, human, bovine and porcine adipose tissue stromal-vascular (S-V) cell cultures. Studies of porcine S-V cell cultures derived from semitendinosus muscle show that TZD can potentially modify intramuscular or marbling adipogenesis. Preadipocyte recruitment was TZD dependent in muscle (S-V) cultures but TZD independent in adipose S-V cultures. There appear to be differences between adipocytes in muscle and subcutaneous adipose tissue, reminiscent of differences observed in adipocytes from different adipose tissue depots. Troglitazone, a thiazolidinedione, induces marbling adipogenesis without inhibiting myogenesis when cells are grown on laminin pre-coated culture dishes. Additionally, troglitazone treatment does not increase lipid content in porcine adipose tissue or muscle S-V cell cultures. Thiazolidinedione treatment increases lipid content of muscle in rodents and humans; however, rosiglitazone treatment for 49 d in pigs did not influence muscle lipid content and meat quality, but several significant changes in muscle fatty acid composition were observed. Although timing of treatment with TZD needs to be optimized, evidence suggests these compounds may enhance marbling deposition in swine.
Key Words: Thiazolidinedione, Porcine, Marbling, Adipogenesis, Skeletal muscle, Adipose, CCAAT/Enhancer binding protein alpha, Peroxisome proliferator-activated receptor gamma
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