Literature DB >> 21404300

Differential susceptibility of muscles to myotonia and force impairment in a mouse model of myotonic dystrophy.

Michelle Moyer1, Dara S Berger, Andrea N Ladd, Erik Van Lunteren.   

Abstract

INTRODUCTION: Myotonic dystrophy, or dystrophia myotonica (DM), is characterized by prominent muscle wasting and weakness as well as delayed muscle relaxation resulting from persistent electrical discharges.
METHODS: We hypothesized heterogeneity among muscles in degree of weakness and myotonia in an expanded [(CUG)(250)] repeats transgenic (HSA(LR)) mouse DM model. Muscle contraction was compared among diaphragm, extensor digitorum longus (EDL), and soleus muscles.
RESULTS: Myotonia was found only in EDL, as manifested by longer late-relaxation time and elevated myotonic index. EDL, but not the other two muscles, had impaired force over a wide range of stimulation frequencies. During fatigue-inducing stimulation, DM EDL muscle force per cross-sectional area was significantly impaired during 25-Hz stimulation, whereas there were no differences in fatigue response for DM diaphragm or soleus.
CONCLUSION: In an expanded repeats model of DM the EDL is more susceptible to myotonia and force impairment than muscles with lower proportions of fast-twitch fibers.
Copyright © 2010 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21404300     DOI: 10.1002/mus.21988

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


  6 in total

Review 1.  Molecular mechanisms of muscle atrophy in myotonic dystrophies.

Authors:  Lubov Timchenko
Journal:  Int J Biochem Cell Biol       Date:  2013-06-21       Impact factor: 5.085

2.  Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I.

Authors:  Marielle Brockhoff; Nathalie Rion; Kathrin Chojnowska; Tatiana Wiktorowicz; Christopher Eickhorst; Beat Erne; Stephan Frank; Corrado Angelini; Denis Furling; Markus A Rüegg; Michael Sinnreich; Perrine Castets
Journal:  J Clin Invest       Date:  2017-01-09       Impact factor: 14.808

3.  Transcriptional profiling reveals extraordinary diversity among skeletal muscle tissues.

Authors:  Erin E Terry; Xiping Zhang; Christy Hoffmann; Laura D Hughes; Scott A Lewis; Jiajia Li; Matthew J Wallace; Lance A Riley; Collin M Douglas; Miguel A Gutierrez-Monreal; Nicholas F Lahens; Ming C Gong; Francisco Andrade; Karyn A Esser; Michael E Hughes
Journal:  Elife       Date:  2018-05-29       Impact factor: 8.140

4.  Antisense oligonucleotide and adjuvant exercise therapy reverse fatigue in old mice with myotonic dystrophy.

Authors:  Ningyan Hu; Eunjoo Kim; Layal Antoury; Jia Li; Paloma González-Pérez; Seward B Rutkove; Thurman M Wheeler
Journal:  Mol Ther Nucleic Acids       Date:  2020-11-26       Impact factor: 8.886

5.  Muscleblind, BSF and TBPH are mislocalized in the muscle sarcomere of a Drosophila myotonic dystrophy model.

Authors:  Beatriz Llamusi; Ariadna Bargiela; Juan M Fernandez-Costa; Amparo Garcia-Lopez; Raffaella Klima; Fabian Feiguin; Ruben Artero
Journal:  Dis Model Mech       Date:  2012-11-01       Impact factor: 5.758

6.  Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.

Authors:  Aline Huguet; Fadia Medja; Annie Nicole; Alban Vignaud; Céline Guiraud-Dogan; Arnaud Ferry; Valérie Decostre; Jean-Yves Hogrel; Friedrich Metzger; Andreas Hoeflich; Martin Baraibar; Mário Gomes-Pereira; Jack Puymirat; Guillaume Bassez; Denis Furling; Arnold Munnich; Geneviève Gourdon
Journal:  PLoS Genet       Date:  2012-11-29       Impact factor: 5.917

  6 in total

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