Literature DB >> 9536444

Rapid recovery following contraction-induced injury to in situ skeletal muscles in mdx mice.

S V Brooks1.   

Abstract

The muscles of mdx mice lack the subsarcolemmal protein dystrophin, and as a consequence may be more susceptible to damage induced by contractions. The purpose of this study was to characterize the response of muscles in mdx mice to contraction-induced injury in situ. The hypothesis tested was that following a protocol of repeated stretches of maximally activated muscles, the magnitude of the injury is greater for muscles in mdx mice than for muscles in C57BL/10 control mice, and consequently, the muscles in mdx mice recover more slowly. Each stretch was of 20% strain relative to muscle fibre length (Lf) at 0.5 Lf s-1 and was initiated from the force plateau of an isometric contraction. The protocol consisted of a total of ten contractions, with one contraction occurring every ten seconds. The time-course of injury and recovery was determined through measurements of in situ force production at 10, 30, 45 and 60 minutes, and either 12, 24, 48 or 72 hours after the contraction protocol. The initial injury, as assessed by the decrease in force production both immediately and 60 minutes after the contraction protocol, was significantly greater for the muscles in mdx mice compared with those in control mice. Over the next three days, a value for maximum isometric force of approximately 80% of the pre-injury value was maintained for muscles in control mice, whereas within three days muscles in mdx mice showed complete recovery of force. For muscles in mdx mice, the greater decrease in force during the contraction protocol and the more rapid recovery indicates an increased susceptibility to contraction-induced injury but an enhanced rate of recovery.

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Mesh:

Year:  1998        PMID: 9536444     DOI: 10.1023/a:1005364713451

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  31 in total

1.  Sarcomere dynamics and contraction-induced injury to maximally activated single muscle fibres from soleus muscles of rats.

Authors:  P C Macpherson; R G Dennis; J A Faulkner
Journal:  J Physiol       Date:  1997-04-15       Impact factor: 5.182

2.  Contraction-induced injury: recovery of skeletal muscles in young and old mice.

Authors:  S V Brooks; J A Faulkner
Journal:  Am J Physiol       Date:  1990-03

3.  Skeletal muscle regeneration after crush injury in dystrophic mdx mice: an autoradiographic study.

Authors:  M D Grounds; J K McGeachie
Journal:  Muscle Nerve       Date:  1992-05       Impact factor: 3.217

4.  Injury to muscle fibres after single stretches of passive and maximally stimulated muscles in mice.

Authors:  S V Brooks; E Zerba; J A Faulkner
Journal:  J Physiol       Date:  1995-10-15       Impact factor: 5.182

5.  Experimental mouse muscle damage: the importance of external calcium.

Authors:  D A Jones; M J Jackson; G McPhail; R H Edwards
Journal:  Clin Sci (Lond)       Date:  1984-03       Impact factor: 6.124

6.  The use of A23187 to demonstrate the role of intracellular calcium in causing ultrastructural damage in mammalian muscle.

Authors:  S J Publicover; C J Duncan; J L Smith
Journal:  J Neuropathol Exp Neurol       Date:  1978-09       Impact factor: 3.685

7.  Differential expression of muscular dystrophy in diaphragm versus hindlimb muscles of mdx mice.

Authors:  E E Dupont-Versteegden; R J McCarter
Journal:  Muscle Nerve       Date:  1992-10       Impact factor: 3.217

8.  Role of calcium in triggering rapid ultrastructural damage in muscle: a study with chemically skinned fibres.

Authors:  C J Duncan
Journal:  J Cell Sci       Date:  1987-05       Impact factor: 5.285

9.  Loss of cytoplasmic basic fibroblast growth factor from physiologically wounded myofibers of normal and dystrophic muscle.

Authors:  M S Clarke; R Khakee; P L McNeil
Journal:  J Cell Sci       Date:  1993-09       Impact factor: 5.285

10.  Mechanical function of dystrophin in muscle cells.

Authors:  C Pasternak; S Wong; E L Elson
Journal:  J Cell Biol       Date:  1995-02       Impact factor: 10.539

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  33 in total

Review 1.  Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse.

Authors:  J M Gillis
Journal:  J Muscle Res Cell Motil       Date:  1999-10       Impact factor: 2.698

2.  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

3.  Muscle injury induced by different types of contractions in dystrophic mdx mice.

Authors:  Jianwei Lou; Wenbo Bi; Wei Li; Yuying Zhao; Shuping Liu; Jinfan Zheng; Chuanzhu Yan
Journal:  J Muscle Res Cell Motil       Date:  2012-02-11       Impact factor: 2.698

4.  Adaptive strength gains in dystrophic muscle exposed to repeated bouts of eccentric contraction.

Authors:  Jarrod A Call; Michael D Eckhoff; Kristen A Baltgalvis; Gordon L Warren; Dawn A Lowe
Journal:  J Appl Physiol (1985)       Date:  2011-09-29

5.  Modulation of insulin-like growth factor (IGF)-I and IGF-binding protein interactions enhances skeletal muscle regeneration and ameliorates the dystrophic pathology in mdx mice.

Authors:  Jonathan D Schertzer; Stefan M Gehrig; James G Ryall; Gordon S Lynch
Journal:  Am J Pathol       Date:  2007-09-06       Impact factor: 4.307

Review 6.  Eccentric exercise in aging and diseased skeletal muscle: good or bad?

Authors:  Richard M Lovering; Susan V Brooks
Journal:  J Appl Physiol (1985)       Date:  2013-03-07

7.  A new immuno-, dystrophin-deficient model, the NSG-mdx(4Cv) mouse, provides evidence for functional improvement following allogeneic satellite cell transplantation.

Authors:  Robert W Arpke; Radbod Darabi; Tara L Mader; Yu Zhang; Akira Toyama; Cara-Lin Lonetree; Nardina Nash; Dawn A Lowe; Rita C R Perlingeiro; Michael Kyba
Journal:  Stem Cells       Date:  2013-08       Impact factor: 6.277

Review 8.  Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy.

Authors:  Miranda D Grounds; Hannah G Radley; Gordon S Lynch; Kanneboyina Nagaraju; Annamaria De Luca
Journal:  Neurobiol Dis       Date:  2008-04-09       Impact factor: 5.996

9.  Poloxamer 188 reduces the contraction-induced force decline in lumbrical muscles from mdx mice.

Authors:  Rainer Ng; Joseph M Metzger; Dennis R Claflin; John A Faulkner
Journal:  Am J Physiol Cell Physiol       Date:  2008-05-21       Impact factor: 4.249

10.  Loss of nNOS inhibits compensatory muscle hypertrophy and exacerbates inflammation and eccentric contraction-induced damage in mdx mice.

Authors:  Stanley C Froehner; Sarah M Reed; Kendra N Anderson; Paul L Huang; Justin M Percival
Journal:  Hum Mol Genet       Date:  2014-09-11       Impact factor: 6.150

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