Hancock Chad R, Han Dong-Ho, Chen May, Terada Shin, Yasuda Toshihiro, Wright David C, Holloszy John O
Division of Geriatrics and Nutritional Sciences, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Proc Natl Acad Sci U S A. 2008 Jun 3;105(22):7815-20. doi: 10.1073/pnas.0802057105. Epub 2008 May 28.
It has been hypothesized that insulin resistance is mediated by a deficiency of mitochondria in skeletal muscle. In keeping with this hypothesis, high-fat diets that cause insulin resistance have been reported to result in a decrease in muscle mitochondria. In contrast, we found that feeding rats high-fat diets that cause muscle insulin resistance results in a concomitant gradual increase in muscle mitochondria. This adaptation appears to be mediated by activation of peroxisome proliferator-activated receptor (PPAR)delta by fatty acids, which results in a gradual, posttranscriptionally regulated increase in PPAR gamma coactivator 1alpha (PGC-1alpha) protein expression. Similarly, overexpression of PPARdelta results in a large increase in PGC-1alpha protein in the absence of any increase in PGC-1alpha mRNA. We interpret our findings as evidence that raising free fatty acids results in an increase in mitochondria by activating PPARdelta, which mediates a posttranscriptional increase in PGC-1alpha. Our findings argue against the concept that insulin resistance is mediated by a deficiency of muscle mitochondria.
有假说认为,胰岛素抵抗是由骨骼肌中线粒体缺乏介导的。与这一假说一致的是,据报道,导致胰岛素抵抗的高脂饮食会导致肌肉线粒体减少。相比之下,我们发现给大鼠喂食导致肌肉胰岛素抵抗的高脂饮食会导致肌肉线粒体随之逐渐增加。这种适应性变化似乎是由脂肪酸激活过氧化物酶体增殖物激活受体(PPAR)δ介导的,这导致PPARγ共激活因子1α(PGC-1α)蛋白表达在转录后受到调节而逐渐增加。同样,在PGC-1α mRNA没有任何增加的情况下,PPARδ的过表达会导致PGC-1α蛋白大幅增加。我们将我们的研究结果解释为证据,即游离脂肪酸的升高通过激活PPARδ导致线粒体增加,PPARδ介导PGC-1α在转录后的增加。我们的研究结果与胰岛素抵抗是由肌肉线粒体缺乏介导的这一概念相悖。