X-irradiation improves mdx mouse muscle as a model of myofiber loss in DMD
- Charing Cross and Westminster Medical School, London (England)
The mdx mouse, although a genetic and biochemical homologue of human Duchenne muscular dystrophy (DMD), presents a comparatively mild histopathological and clinical phenotype. These differences are partially attributable to the greater efficacy of regeneration in the mdx mouse than in DMD muscle. To lessen this disparity, we have used a single dose of X-irradiation (16 Gy) to inhibit regeneration in one leg of mdx mice. The result is an almost complete block of muscle fiber regeneration leading to progressive loss of muscle fibers and their replacement by loose connective tissue. Surviving fibers are mainly peripherally nucleated and, surprisingly, of large diameter. Thus, X-irradiation converts mdx muscle to a model system in which the degenerative process can be studied in isolation from the complicating effect of myofiber regeneration. This system should be of use for testing methods of alleviating the myofiber degeneration which is common to mdx and DMD.
- OSTI ID:
- 6005994
- Journal Information:
- Muscle and Nerve; (USA), Vol. 14:1; ISSN 0148-639X
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
MUSCLES
BIOLOGICAL RADIATION EFFECTS
BIOLOGICAL MODELS
BIOLOGICAL REGENERATION
MICE
NERVOUS SYSTEM DISEASES
PHENOTYPE
X RADIATION
ANIMALS
BIOLOGICAL EFFECTS
BIOLOGICAL RECOVERY
DISEASES
ELECTROMAGNETIC RADIATION
IONIZING RADIATIONS
MAMMALS
RADIATION EFFECTS
RADIATIONS
RECOVERY
RODENTS
VERTEBRATES
560152* - Radiation Effects on Animals- Animals