Hausman G J, Poulos S P, Pringle T D, Azain M J
USDA, ARS, APRU, Athens, GA 30605, USA.
J Anim Sci. 2008 Apr;86(14 Suppl):E236-43. doi: 10.2527/jas.2007-0219. Epub 2007 Aug 8.
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 (PPARgamma), 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 TZD, induces marbling adipogenesis without inhibiting myogenesis when cells are grown on laminin precoated 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.
噻唑烷二酮类药物(TZD)是目前用于治疗2型糖尿病的胰岛素增敏剂,由于它们是过氧化物酶体增殖物激活受体γ(PPARγ,一种关键的脂肪生成转录因子)的配体,因此被广泛用作脂肪生成剂。本文综述了TZD作为肌肉内或大理石花纹脂肪生成潜在调节剂的体内和体外研究。在许多细胞培养系统中都报道了噻唑烷二酮诱导的脂肪生成,包括啮齿动物、人类、牛和猪的脂肪组织基质血管(S-V)细胞培养。对源自半腱肌的猪S-V细胞培养物的研究表明,TZD可能会改变肌肉内或大理石花纹脂肪生成。在肌肉S-V培养物中,前脂肪细胞的募集依赖于TZD,但在脂肪S-V培养物中则不依赖于TZD。肌肉和皮下脂肪组织中的脂肪细胞之间似乎存在差异,这让人想起在不同脂肪组织库的脂肪细胞中观察到的差异。当细胞在层粘连蛋白预包被的培养皿上生长时,一种TZD——曲格列酮可诱导大理石花纹脂肪生成而不抑制肌生成。此外,曲格列酮处理不会增加猪脂肪组织或肌肉S-V细胞培养物中的脂质含量。噻唑烷二酮处理可增加啮齿动物和人类肌肉中的脂质含量;然而,在猪中用罗格列酮处理49天并未影响肌肉脂质含量和肉质,但观察到肌肉脂肪酸组成有几个显著变化。尽管需要优化TZD的治疗时机,但有证据表明这些化合物可能会增强猪的大理石花纹沉积。