High-fat diets cause insulin resistance despite an increase in muscle mitochondria.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 18509063.
- Also identified by DOI 10.1073/pnas.0802057105 and PMC identifier 2409421.
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Abstract
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.
Medical subject headings
- Dietary Fats
- Fatty Acids, Nonesterified
- Insulin Resistance
- Mitochondria, Muscle
- Muscle, Skeletal