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A High-Fat Diet Coordinately Downregulates Genes Required for Mitochondrial Oxidative Phosphorylation in Skeletal Muscle

机译:高脂饮食会下调骨骼肌线粒体氧化磷酸化所需的基因。

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Obesity and type 2 diabetes have been associated with a high-fat diet (HFD) and reduced mitochondrial mass and function. We hypothesized a HFD may affect expression of genes involved in mitochondrial function and biogenesis. To test this hypothesis, we fed 10 insulin-sensitive males an isoenergetic HFD for 3 days with muscle biopsies before and after intervention. Oligonu-cleotide microarray analysis revealed 297 genes were differentially regulated by the HFD (Bonferonni adjusted P < 0.001). Six genes involved in oxidative phosphorylation (OXPHOS) decreased. Four were members of mitochondrial complex Ⅰ: NDUFB3, NDUFB5, NDUFS1, and NDUFV1; one was SDHB in complex Ⅱ and a mitochondrial carrier protein SLC25A12. Peroxisome proliferator-activated receptor γ coactivator-1 (PGC1) α and PGC1β mRNA were decreased by -20%, P < 0.01, and -25%, P < 0.01, respectively. In a separate experiment, we fed C57B1/6J mice a HFD for 3 weeks and found that the same OXPHOS and PGC1 mRNAs were downregulated by ~90%, cytochrome C and PGC1α protein by ~40%. Combined, these results suggest a mechanism whereby HFD downregulates genes necessary for OXPHOS and mitochondrial biogenesis. These changes mimic those observed in diabetes and insulin resistance and, if sustained, may result in mitochondrial dysfunction in the prediabetic/insulin-resistant state.
机译:肥胖和2型糖尿病与高脂饮食(HFD)和线粒体质量和功能降低有关。我们假设HFD可能会影响参与线粒体功能和生物发生的基因的表达。为了验证这一假设,我们在干预前后为10名胰岛素敏感性男性等能量HFD进行了3天的肌肉活检。寡核苷酸微阵列分析显示,有297个基因受到HFD的差异调节(Bonferonni调整P <0.001)。参与氧化磷酸化(OXPHOS)的六个基因减少。四个是线粒体复合体Ⅰ的成员:NDUFB3,NDUFB5,NDUFS1和NDUFV1;一种是复合物Ⅱ中的SDHB和线粒体载体蛋白SLC25A12。过氧化物酶体增殖物激活受体γcoactivator-1(PGC1)α和PGC1βmRNA分别降低了-20%,P <0.01和-25%,P <0.01。在一个单独的实验中,我们给C57B1 / 6J小鼠喂了HFD 3周,发现相同的OXPHOS和PGC1 mRNA下调约90%,细胞色素C和PGC1α蛋白下调约40%。结合起来,这些结果表明,HFD下调OXPHOS和线粒体生物发生所必需的基因的机制。这些变化模仿在糖尿病和胰岛素抵抗中观察到的变化,如果持续存在,则可能导致糖尿病前期/胰岛素抵抗状态下的线粒体功能障碍。

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