Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice.

Abstract

Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene, leading to the absence of the dystrophin protein in striated muscle. A significant number of these mutations are premature stop codons. On the basis of the observation that aminoglycoside treatment can suppress stop codons in cultured cells, we tested the effect of gentamicin on cultured muscle cells from the mdx mouse - an animal model for DMD that possesses a premature stop codon in the dystrophin gene. Exposure of mdx myotubes to gentamicin led to the expression and localization of dystrophin to the cell membrane. We then evaluated the effects of differing dosages of gentamicin on expression and functional protection of the muscles of mdx mice. We identified a treatment regimen that resulted in the presence of dystrophin in the cell membrane in all striated muscles examined and that provided functional protection against muscular injury. To our knowledge, our results are the first to demonstrate that aminoglycosides can suppress stop codons not only in vitro but also in vivo. Furthermore, these results raise the possibility of a novel treatment regimen for muscular dystrophy and other diseases caused by premature stop codon mutations. This treatment could prove effective in up to 15% of patients with DMD.

• Authors: E R Barton-Davis, L Cordier, D I Shoturma, S E Leland, H L Sweeney
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 104 Issue 4 Pg. 375-81 (Aug 1999) ISSN: 0021-9738 [Print] United States
• PMID: 10449429 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Anti-Bacterial Agents
• Codon, Terminator
• Dystrophin
• Gentamicins

Topics

• Animals
• Anti-Bacterial Agents (administration & dosage, pharmacology, toxicity)
• Cell Membrane (metabolism)
• Cells, Cultured
• Codon, Terminator (drug effects)
• Dose-Response Relationship, Drug
• Dystrophin (genetics, physiology)
• Gene Expression (drug effects)
• Gentamicins (administration & dosage, pharmacology, toxicity)
• Hearing (drug effects)
• Humans
• Kidney (drug effects)
• Male
• Mice
• Mice, Inbred mdx
• Muscle Contraction (drug effects)
• Muscle, Skeletal (drug effects, physiopathology)
• Muscular Dystrophy, Animal (drug therapy, genetics, physiopathology)
• Mutation