Journal
CELL METABOLISM
Volume 8, Issue 3, Pages 249-256Publisher
CELL PRESS
DOI: 10.1016/j.cmet.2008.07.006
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Funding
- Muscular Dystrophy Association
- PHS [NS041777, EY10804]
- United Mitochondrial Disease Foundation
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Neuromuscular disorders with defects in the mitochondrial ATP-generating system affect a large number of children and adults worldwide, but remain without treatment. We used a mouse model of mitochondrial myopathy, caused by a cytochrome c oxidase deficiency, to evaluate the effect of induced mitochondrial biogenesis on the course of the disease' Mitochondrial biogenesis was induced either by transgenic expression of peroxisome proliferator-activated receptor gamma (PPAR gamma) coactivator alpha (PGC-1 alpha) in skeletal muscle or by administration of bezafibrate, a PPAR panagonist. Both strategies successfully stimulated residual respiratory capacity in muscle tissue. Mitochondrial proliferation resulted in an enhanced OXPHOS capacity per muscle mass. As a consequence, ATP levels were conserved resulting in a delayed onset of the myopathy and a markedly prolonged life span. Thus, induction of mitochondrial biogenesis through pharmacological or metabolic modulation of the PPAR/PGC-1 alpha pathway promises to be an effective therapeutic approach for mitochondrial disorders.
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