Laboratory of Molecular Biology, Nutrition and Biotechnology, Universitat de les Illes Balears and CIBER de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), E-07122 Palma de Mallorca, Spain.
J Nutr Biochem. 2011 Sep;22(9):828-34. doi: 10.1016/j.jnutbio.2010.07.007. Epub 2010 Dec 15.
Resveratrol is a naturally occurring polyphenol known to affect energy metabolism and insulin sensitivity in mice and lipogenic gene expression in adipocytes. Here, we sought to get further insight into the impact of resveratrol on adipocyte biology by studying its effects on oxidative metabolism and the expression of the insulin resistance-related adipokines resistin and Retinol-Binding Protein 4 (RBP4) in mature adipocytes. Effects were assessed in 3T3-L1 adipocytes and in adipocytes derived from primary mouse embryonic fibroblasts (MEF). Besides reducing triacylglycerol content and the mRNA levels of lipogenic genes, resveratrol treatment resulted in both models in increased mRNA levels of carnitine palmitoyltransferase 1 (a rate-limiting enzyme in mitochondrial fatty acid oxidation), reduced mRNA levels of receptor interacting protein 140 (a suppressor of oxidative metabolism), and signs of enhanced flux through the fatty acid beta-oxidation pathway. In primary MEF-derived adipocytes, the treatment also increased mitochondrial DNA content and the mRNA levels of subunit II of cytochrome oxidase (a component of the mitochondrial respiratory chain) and of uncoupling protein 1. Expression of resistin and RBP4 was reduced in both adipocyte models following resveratrol treatment. The results indicate that resveratrol directly acts in mature white adipocytes to favor a remodeling toward increased oxidative capacity and reduced lipogenesis, while down-regulating two putative insulin resistance factors. These results constitute novel insights into resveratrol action in adipocytes that add to the potential of this food phytochemical and its synthetic analogues for the control of obesity and related metabolic disorders.
白藜芦醇是一种天然存在的多酚,已知其可影响小鼠的能量代谢和胰岛素敏感性,以及脂肪细胞中的脂肪生成基因表达。在这里,我们通过研究白藜芦醇对氧化代谢的影响以及胰岛素抵抗相关脂肪因子抵抗素和视黄醇结合蛋白 4(RBP4)在成熟脂肪细胞中的表达,来进一步了解白藜芦醇对脂肪细胞生物学的影响。在 3T3-L1 脂肪细胞和源自原代小鼠胚胎成纤维细胞(MEF)的脂肪细胞中评估了这些影响。除了降低三酰基甘油含量和脂肪生成基因的 mRNA 水平外,白藜芦醇处理还导致两种模型中的肉碱棕榈酰转移酶 1(线粒体脂肪酸氧化的限速酶)的 mRNA 水平增加,受体相互作用蛋白 140(氧化代谢的抑制剂)的 mRNA 水平降低,并且脂肪酸β-氧化途径的通量增加。在原代 MEF 衍生的脂肪细胞中,该处理还增加了线粒体 DNA 含量和细胞色素氧化酶亚基 II(线粒体呼吸链的组成部分)和解偶联蛋白 1 的 mRNA 水平。在两种脂肪细胞模型中,抵抗素和 RBP4 的表达在白藜芦醇处理后均降低。这些结果表明,白藜芦醇直接作用于成熟的白色脂肪细胞,有利于增加氧化能力和减少脂肪生成,同时下调两个潜在的胰岛素抵抗因子。这些结果为白藜芦醇在脂肪细胞中的作用提供了新的见解,增加了这种食物植物化学物质及其合成类似物在控制肥胖和相关代谢紊乱方面的潜力。