Literature DB >> 1311662

Contractile properties and susceptibility to exercise-induced damage of normal and mdx mouse tibialis anterior muscle.

P Sacco1, D A Jones, J R Dick, G Vrbová.   

Abstract

1. The functional properties of tibialis anterior muscles of normal adult (C57BL/10) and age-matched dystrophin-deficient (C57BL/10 mdx) mice have been investigated in situ. Comparisons were made between tibialis anterior muscle strength, rates of force development and relaxation, force-frequency responses and fatiguability. Subjecting mdx and C57 muscles to a regimen of eccentric exercise allowed the hypothesis to be tested that dystrophin-deficient muscles are more susceptible to exercise-induced muscle damage. 2. mdx muscles were, on average, 30% stronger than C57 muscles and almost 80% heavier, but both had similar muscle lengths. Thus, although mdx muscles were stronger in absolute terms, their estimated force per unit cross-sectional area was significantly less than that of C57 muscles. 3. The force-frequency relationships of C57 and mdx muscles differed in that whilst, at 40 Hz, the former developed 70% of the force developed at 100 Hz, the latter developed only 55% of the maximal force. Twitch force was normal in mdx muscles, but contraction time was shortened, and the consequent reduction in fusion frequency probably explains the force-frequency differences observed between the two groups. 4. mdx muscles were less fatiguable than normal muscles when stimulated repeatedly at a frequency of 40 Hz. It is possible that the lower relative force at 40 Hz in mdx muscles entailed a lower energy demand and thus a slower rate of fatigue than seen in normal muscles. 5. Eccentrically exercised C57 muscles showed a large loss of maximal force for up to 12 days after exercise. Maximal force loss occurred 3 days after exercise (55% of non-exercised tibialis anterior muscle), which also corresponded with the period of greatest fibre necrosis. C57 muscles showed a significantly reduced 40 Hz/100 Hz force-frequency ratio at 1 and 3 days after exercise. This was primarily due to a reduced twitch amplitude rather than to a change in the time course of the twitch. It is unlikely, therefore, that the altered contractile characteristics of mdx muscle were a result of the presence of damaged but otherwise normal fibres. 6. C57 and mdx tibialis anterior muscles displayed similar degrees of force loss after exercise. Furthermore, the rate of recovery after the nadir of force loss was very similar for the two groups. By 12 days after exercise, force recovered to 76% and 80% of control in C57 and mdx muscles, respectively. Our findings do not support the hypothesis that dystrophin-deficient muscle is more susceptible to exercise-induced muscle damage.

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Year:  1992        PMID: 1311662     DOI: 10.1042/cs0820227

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  35 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.  Posttetanic potentiation in mdx muscle.

Authors:  Ian Curtis Smith; Jian Huang; Joe Quadrilatero; Allan Russell Tupling; Rene Vandenboom
Journal:  J Muscle Res Cell Motil       Date:  2010-10-23       Impact factor: 2.698

3.  Muscle damage, metabolism, and oxidative stress in mdx mice: Impact of aerobic running.

Authors:  Kevin E Schill; Alex R Altenberger; Jeovanna Lowe; Muthu Periasamy; Frederick A Villamena; JIll A Rafael-Fortney; Steven T Devor
Journal:  Muscle Nerve       Date:  2016-06       Impact factor: 3.217

Review 4.  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

5.  Adaptive and nonadaptive responses to voluntary wheel running by mdx mice.

Authors:  Rachel M Landisch; Allison M Kosir; Steven A Nelson; Kristen A Baltgalvis; Dawn A Lowe
Journal:  Muscle Nerve       Date:  2008-10       Impact factor: 3.217

Review 6.  The membrane hypothesis of Duchenne muscular dystrophy: quest for functional evidence.

Authors:  O F Hutter
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

7.  The chondrogenic response to exercise in the proximal femur of normal and mdx mice.

Authors:  David J Nye; Jeffrey M Costas; Jessica B Henley; Jin-Kwang Kim; Jeffrey H Plochocki
Journal:  BMC Musculoskelet Disord       Date:  2010-09-03       Impact factor: 2.362

8.  Full-length dystrophin expression in half of the heart cells ameliorates beta-isoproterenol-induced cardiomyopathy in mdx mice.

Authors:  Yongping Yue; Jeffrey W Skimming; Mingju Liu; Tammy Strawn; Dongsheng Duan
Journal:  Hum Mol Genet       Date:  2004-06-09       Impact factor: 6.150

9.  Time course study of the isometric contractile properties of mdx mouse striated muscles.

Authors:  C Pastoret; A Sebille
Journal:  J Muscle Res Cell Motil       Date:  1993-08       Impact factor: 2.698

Review 10.  Therapeutics for Duchenne muscular dystrophy: current approaches and future directions.

Authors:  Sasha Bogdanovich; Kelly J Perkins; Thomas O B Krag; Tejvir S Khurana
Journal:  J Mol Med (Berl)       Date:  2003-12-12       Impact factor: 4.599

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