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Mitochondrial Dysfunction as an Underlying Cause of Skeletal Muscle Disorders.

Tsung-Hsien ChenKok-Yean KohKurt Ming-Chao LinChu-Kuang Chou
Published in: International journal of molecular sciences (2022)
Mitochondria are an important energy source in skeletal muscle. A main function of mitochondria is the generation of ATP for energy through oxidative phosphorylation (OXPHOS). Mitochondrial defects or abnormalities can lead to muscle disease or multisystem disease. Mitochondrial dysfunction can be caused by defective mitochondrial OXPHOS, mtDNA mutations, Ca 2+ imbalances, mitochondrial-related proteins, mitochondrial chaperone proteins, and ultrastructural defects. In addition, an imbalance between mitochondrial fusion and fission, lysosomal dysfunction due to insufficient biosynthesis, and/or defects in mitophagy can result in mitochondrial damage. In this review, we explore the association between impaired mitochondrial function and skeletal muscle disorders. Furthermore, we emphasize the need for more research to determine the specific clinical benefits of mitochondrial therapy in the treatment of skeletal muscle disorders.
Keyphrases
  • skeletal muscle
  • oxidative stress
  • insulin resistance
  • cell death
  • bone marrow
  • gene expression
  • metabolic syndrome
  • adipose tissue
  • reactive oxygen species
  • mitochondrial dna
  • endoplasmic reticulum
  • smoking cessation