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- W2002858464 abstract "Abstract In muscular dystrophies (MD) the loss of muscle and its ability to function are associated with fibrosis. We evaluated the efficacy of halofuginone in reducing fibrosis in the dy 2J / dy 2J mouse model of congenital MD. Mice were injected intraperitoneally with 5 μg of halofuginone 3 times a week for 5 or 15 weeks, starting at the age of 3 weeks. Halofuginone caused a reduction in collagen synthesis in hindlimb muscles. This was associated with reductions in the degenerated area, in cell proliferation, in the number of myofibers with central nuclei, with increased myofiber diameter, and with enhanced motor coordination and balance. Halofuginone caused a reduction in infiltrating fibroblasts that were located close to centrally nucleated myofibers. Our results suggest that halofuginone reduced the deleterious effects of fibrosis, thus improving muscle integrity. Halofuginone meets the criteria for a novel antifibrotic therapy for MD patients. Muscle Nerve, 2010" @default.
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- W2002858464 date "2010-07-19" @default.
- W2002858464 modified "2023-10-18" @default.
- W2002858464 title "Fibrosis inhibition and muscle histopathology improvement in laminin-α2-deficient mice" @default.
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- W2002858464 doi "https://doi.org/10.1002/mus.21706" @default.
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