Literature DB >> 6543918

Muscle development in mdx mutant mice.

J Dangain, G Vrbova.   

Abstract

Mechanical and contractile properties of tibialis anterior (TA) muscles from X-linked muscular dystrophic (mdx) mutant mice at different stages of development are compared to those of muscles from normal control animals. There is no difference between the tension output, speeds of contraction and relaxation, and weight of TA muscles from mutant adults and normal control animals. However, it is found that in 3-4-week-old mutant animals, tension output and muscle weight are very much reduced, and half relaxation time is prolonged. Thus, during this stage of development, muscles from mdx mice do not function properly. Histological examination of these muscles provides further evidence that, in these animals, rapid muscle destruction occurs at a particular time of development and that it is followed by complete recovery. This new mutant therefore presents an interesting case of muscle destruction and rapid regeneration. However, it is not an adequate model for Duchenne muscular dystrophy.

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Year:  1984        PMID: 6543918     DOI: 10.1002/mus.880070903

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  92 in total

1.  Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old.

Authors:  G S Lynch; R T Hinkle; J S Chamberlain; S V Brooks; J A Faulkner
Journal:  J Physiol       Date:  2001-09-01       Impact factor: 5.182

Review 2.  Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies.

Authors:  C A Collins; J E Morgan
Journal:  Int J Exp Pathol       Date:  2003-08       Impact factor: 1.925

Review 3.  The muscular dystrophies.

Authors:  V Dubowitz
Journal:  Postgrad Med J       Date:  1992-07       Impact factor: 2.401

Review 4.  Animal models of muscular dystrophy.

Authors:  Rainer Ng; Glen B Banks; John K Hall; Lindsey A Muir; Julian N Ramos; Jacqueline Wicki; Guy L Odom; Patryk Konieczny; Jane Seto; Joel R Chamberlain; Jeffrey S Chamberlain
Journal:  Prog Mol Biol Transl Sci       Date:  2012       Impact factor: 3.622

5.  Expression of HGF and IGF-1 during regeneration of masseter muscle in mdx mice.

Authors:  Hidemitsu Honda; Shinichi Abe; Ryo Ishida; Yutaka Watanabe; Osamu Iwanuma; Koji Sakiyama; Yoshinobu Ide
Journal:  J Muscle Res Cell Motil       Date:  2010-05-28       Impact factor: 2.698

6.  Characteristics of muscle fibers reconstituted in the regeneration process of masseter muscle in an mdx mouse model of muscular dystrophy.

Authors:  Won-Hyung Lee; Shinichi Abe; Hee-Jin Kim; Akinobu Usami; Atsuro Honda; Koji Sakiyama; Yoshinobu Ide
Journal:  J Muscle Res Cell Motil       Date:  2006-06-04       Impact factor: 2.698

Review 7.  What has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease?

Authors:  Jennifer Manning; Dervla O'Malley
Journal:  J Muscle Res Cell Motil       Date:  2015-02-11       Impact factor: 2.698

8.  Increased density of satellite cells in the absence of fibre degeneration in muscle of myotonic mice.

Authors:  J Schimmelpfeng; H Jockusch; P Heimann
Journal:  Cell Tissue Res       Date:  1987-08       Impact factor: 5.249

9.  Contractile properties of skinned muscle fibres from young and adult normal and dystrophic (mdx) mice.

Authors:  D A Williams; S I Head; G S Lynch; D G Stephenson
Journal:  J Physiol       Date:  1993-01       Impact factor: 5.182

10.  Immunoproteasome in animal models of Duchenne muscular dystrophy.

Authors:  Chiao-Nan Joyce Chen; Ted G Graber; Wendy M Bratten; Deborah A Ferrington; LaDora V Thompson
Journal:  J Muscle Res Cell Motil       Date:  2014-06-17       Impact factor: 2.698

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