Rodríguez Ana M, Sánchez Juana, Tobaruela Aixa, Priego Teresa, Picó Catalina, Palou Andreu
Laboratory of Molecular Biology, Nutrition and Biotechnology (Nutrigenomics). University of the Balearic Islands (UIB) and CIBER Fisiopatología de la Obesidad y Nutrición (CIBEROBN), 07122 Palma de Mallorca, Spain.
Cell Physiol Biochem. 2010;25(2-3):337-46. doi: 10.1159/000276566. Epub 2010 Jan 12.
Fatty acid (FA) oversupply in skeletal muscle is related with metabolic disorders associated to obesity, and also with normal physiological responses. We studied, in vivo and in vitro, the chronological response to physiological increases of FA, analyzing the expression of selected genes important for glucose/lipid metabolism. An in vivo sequential model of fasting (known to increase circulating FA) and refeeding was used in male Wistar rats to study soleus (more oxidative) and gastrocnemius (more glycolytic) muscles, and a chronological study was made in C2C12 muscle cells under treatment of oleic/linoleic FA mixture, at physiological concentration. Body weight, muscle glycogen and blood parameters (glucose, insulin, free fatty acids -FFA-, triglycerides) were monitored. mRNA levels of muscle carnitine palmitoyl transferase 1 (mCPT1), GLUT 4, insulin receptor (InsR), MyoD1, peroxisome proliferator activated receptor (PPAR) gamma coactivator 1alpha (PGC1alpha) and beta (PGC1beta), PPARalpha, PPARdelta, pyruvate dehydrogenase kinase 4 (PDK4) and uncoupling proteins (UCPs) 2 and 3 were analyzed by quantitative RT-PCR. The main results were the quick induction of PGC1alpha, UCP3 and PDK4 in vivo (more marked in gastrocnemius) and of PGC1alpha, PGC1beta, InsR, PDK4, UCP2 and UCP3 in vitro. It is concluded that FA are able to rapidly induce the expression in muscle cells of key genes involved in their catabolism and that the oleic/linoleic acid mixture has a positive role increasing the expression of master metabolic regulators and their downstream target genes, facilitating the transition from a more glycolytic to a more lipid-oxidative metabolism.
骨骼肌中脂肪酸(FA)供应过剩与肥胖相关的代谢紊乱以及正常生理反应有关。我们在体内和体外研究了对FA生理增加的时间顺序反应,分析了对葡萄糖/脂质代谢重要的选定基因的表达。在雄性Wistar大鼠中使用禁食(已知会增加循环FA)和再喂养的体内顺序模型来研究比目鱼肌(氧化能力更强)和腓肠肌(糖酵解能力更强),并在生理浓度的油酸/亚油酸FA混合物处理下对C2C12肌肉细胞进行了时间顺序研究。监测体重、肌肉糖原和血液参数(葡萄糖、胰岛素、游离脂肪酸 -FFA-、甘油三酯)。通过定量RT-PCR分析肌肉肉碱棕榈酰转移酶1(mCPT1)、GLUT 4、胰岛素受体(InsR)、MyoD1、过氧化物酶体增殖物激活受体(PPAR)γ共激活因子1α(PGC1α)和β(PGC1β)、PPARα、PPARδ、丙酮酸脱氢酶激酶4(PDK4)和解偶联蛋白(UCPs)2和3的mRNA水平。主要结果是体内PGC1α、UCP3和PDK4的快速诱导(在腓肠肌中更明显)以及体外PGC1α、PGC1β、InsR、PDK4、UCP2和UCP3的快速诱导。结论是FA能够迅速诱导参与其分解代谢的关键基因在肌肉细胞中的表达,并且油酸/亚油酸混合物在增加主要代谢调节因子及其下游靶基因的表达方面具有积极作用促进从更多糖酵解代谢向更多脂质氧化代谢的转变。