Literature DB >> 9227435

Contractile properties of diaphragm muscle segments from old mdx and old transgenic mdx mice.

G S Lynch1, J A Rafael, R T Hinkle, N M Cole, J S Chamberlain, J A Faulkner.   

Abstract

Diaphragm muscles of young (4- to 6-mo-old) mdx mice show severe fiber necrosis and have normalized forces and powers 60 and 46% of the values for control C57BL/10 mice. In contrast, microinjection of mdx mouse embryos with a truncated dystrophin minigene has produced young transgenic mdx (tg-mdx) mice with a level of dystrophin expression and structural and functional properties of diaphragm muscle strips measured in vitro not different from those of control mice. Whether dystrophin expression and functional corrections persist for the life span of these animals is not know. We tested the null hypothesis that, in old (24 mo) tg-mdx mice, dystrophin expression is adequate and diaphragm muscle strips have forces and powers not different from values for diaphragm muscle strips from young tg-mdx mice or control mice. Compared with control values, diaphragm muscle strips from old mdx mice had normalized forces and powers of 48 and 31%, respectively. Expression of dystrophin persisted in diaphragm muscles of old tg-mdx mice, and functional properties were not different from diaphragm muscles of young tg-mdx or young or old control mice. These results suggest that, with a transgenic animal approach, dystrophin expression and functional corrections persist for the life span of the animals.

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Year:  1997        PMID: 9227435     DOI: 10.1152/ajpcell.1997.272.6.C2063

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  30 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

2.  Improved contractile function of the mdx dystrophic mouse diaphragm muscle after insulin-like growth factor-I administration.

Authors:  Paul Gregorevic; David R Plant; Kerri S Leeding; Leon A Bach; Gordon S Lynch
Journal:  Am J Pathol       Date:  2002-12       Impact factor: 4.307

Review 3.  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

4.  Ventilation during air breathing and in response to hypercapnia in 5 and 16 month-old mdx and C57 mice.

Authors:  Jerome Gayraud; Stefan Matecki; Karim Hnia; Dominique Mornet; Christian Prefaut; Jacques Mercier; Alain Michel; Michele Ramonatxo
Journal:  J Muscle Res Cell Motil       Date:  2007-04-13       Impact factor: 2.698

5.  Antibody-directed myostatin inhibition improves diaphragm pathology in young but not adult dystrophic mdx mice.

Authors:  Kate T Murphy; James G Ryall; Sarah M Snell; Lawrence Nair; René Koopman; Philip A Krasney; Chikwendu Ibebunjo; Kathryn S Holden; Paula M Loria; Christopher T Salatto; Gordon S Lynch
Journal:  Am J Pathol       Date:  2010-04-02       Impact factor: 4.307

Review 6.  Mechanisms of resistance to pathogenesis in muscular dystrophies.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1999-05       Impact factor: 3.396

7.  Interleukin-15 administration improves diaphragm muscle pathology and function in dystrophic mdx mice.

Authors:  Leah J Harcourt; Anna Greer Holmes; Paul Gregorevic; Jonathan D Schertzer; Nicole Stupka; David R Plant; Gordon S Lynch
Journal:  Am J Pathol       Date:  2005-04       Impact factor: 4.307

8.  Advanced aging causes diaphragm functional abnormalities, global proteome remodeling, and loss of mitochondrial cysteine redox flexibility in mice.

Authors:  Rachel C Kelley; Brian McDonagh; Leonardo F Ferreira
Journal:  Exp Gerontol       Date:  2017-12-28       Impact factor: 4.032

9.  Systemic delivery of NEMO binding domain/IKKγ inhibitory peptide to young mdx mice improves dystrophic skeletal muscle histopathology.

Authors:  Daniel P Reay; Michele Yang; Jon F Watchko; Molly Daood; Terrence L O'Day; Khaleel K Rehman; Denis C Guttridge; Paul D Robbins; Paula R Clemens
Journal:  Neurobiol Dis       Date:  2011-05-23       Impact factor: 5.996

10.  Systemic microdystrophin gene delivery improves skeletal muscle structure and function in old dystrophic mdx mice.

Authors:  Paul Gregorevic; Michael J Blankinship; James M Allen; Jeffrey S Chamberlain
Journal:  Mol Ther       Date:  2008-03-04       Impact factor: 11.454

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