首页> 美国卫生研究院文献>Journal of Zhejiang University. Science. B >A high-fat diet increases body fat mass and up-regulates expression of genes related to adipogenesis and inflammation in a genetically lean pig
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A high-fat diet increases body fat mass and up-regulates expression of genes related to adipogenesis and inflammation in a genetically lean pig

机译:高脂饮食会增加体脂量并上调与遗传瘦肉猪脂肪形成和炎症相关的基因的表达

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摘要

Because of their physiological similarity to humans, pigs provide an excellent model for the study of obesity. This study evaluated diet-induced adiposity in genetically lean pigs and found that body weight and energy intake did not differ between controls and pigs fed the high-fat (HF) diet for three months. However, fat mass percentage, adipocyte size, concentrations of total cholesterol (TC), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C), insulin, and leptin in plasma were significantly higher in HF pigs than in controls. The HF diet increased the expression in backfat tissue of genes responsible for cholesterol synthesis such as Insig-1 and Insig-2. Lipid metabolism-related genes including sterol regulatory element binding protein 1c (SREBP-1c), fatty acid synthase 1 (FASN1), diacylglycerol O-acyltransferase 2 (DGAT2), and fatty acid binding protein 4 (FABP4) were significantly up-regulated in backfat tissue, while the expression of proliferator-activated receptor-α (PPAR-α) and carnitine palmitoyl transferase 2 (CPT2), both involved in fatty acid oxidation, was reduced. In liver tissue, HF feeding significantly elevated the expression of SREBP-1c, FASN1, DGAT2, and hepatocyte nuclear factor-4α (HNF-4α) mRNAs. Microarray analysis further showed that the HF diet had a significant effect on the expression of 576 genes. Among these, 108 genes were related to 21 pathways, with 20 genes involved in adiposity deposition and 26 related to immune response. Our results suggest that an HF diet can induce genetically lean pigs into obesity with body fat mass expansion and adipose-related inflammation.
机译:由于其与人的生理相似性,猪为肥胖研究提供了极好的模型。这项研究评估了基因瘦肉猪的饮食诱导的肥胖症,发现对照组和体重高,饲喂三个月的猪的体重和能量摄入没有差异。但是,血浆中的脂肪质量百分比,脂肪细胞大小,总胆固醇(TC),甘油三酸酯(TG),高密度脂蛋白胆固醇(HDL-C)和低密度脂蛋白胆固醇(LDL-C),胰岛素和瘦素的浓度HF猪的血脂显着高于对照组。 HF饮食增加了脂肪合成中负责胆固醇合成的基因如Insig-1和Insig-2的表达。脂代谢相关基因包括固醇调节元件结合蛋白1c(SREBP-1c),脂肪酸合酶1(FASN1),二酰基甘油O-酰基转移酶2(DGAT2)和脂肪酸结合蛋白4(FABP4)上调。脂肪组织中,虽然都参与了脂肪酸氧化,但增殖物激活受体-α(PPAR-α)和肉碱棕榈酰转移酶2(CPT2)的表达却降低了。在肝组织中,HF喂养显着提高了SREBP-1c,FASN1,DGAT2和肝细胞核因子4α(HNF-4α)mRNA的表达。微阵列分析进一步表明,HF饮食对576个基因的表达有显着影响。在这些基因中,有108个基因与21种途径有关,其中20个基因与肥胖沉积有关,有26个基因与免疫反应有关。我们的结果表明,HF饮食可导致遗传瘦肉的猪肥胖,并伴有体内脂肪膨胀和脂肪相关的炎症。

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