High-fat diets cause insulin resistance despite an increase in muscle mitochondria

被引:426
作者
Hancock, Chad R. [1 ]
Han, Dong-Ho [1 ]
Chen, May [1 ]
Terada, Shin [1 ]
Yasuda, Toshihiro [1 ]
Wright, David C. [1 ]
Holloszy, John O. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Med, Div Geriatr & Nutr Sci, St Louis, MO 63110 USA
关键词
mitochondrial biogenesis; mitochondrial dysfunction; PPAR delta; skeletal muscle; PGC-1; alpha;
D O I
10.1073/pnas.0802057105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 1 alpha (PGC-1 alpha) protein expression. Similarly, overexpression of PPARS results in a large increase in PGC-1 alpha protein in the absence of any increase in FGC-1 alpha mRNA. We interpret our findings as evidence that raising free fatty acids results in an increase in mitochondria by activating PPAR delta, which mediates a posttranscriptional increase in PGC-1 alpha. Our findings argue against the concept that insulin resistance is mediated by a deficiency of muscle mitochondria.
引用
收藏
页码:7815 / 7820
页数:6
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