Literature DB >> 11805861

Influence of ageing on the fatigability of isolated mouse skeletal muscles from mature and aged mice.

Marco A de Paula Brotto1, Thomas M Nosek, Ralph C Kolbeck.   

Abstract

We investigated the influence of ageing on the fatiguing characteristics of the mouse extensor digitorum longus (EDL) muscle as compared to those of the soleus muscle. Fatigue was produced by an intermittent stimulation protocol. We report for mature and aged animals the effects of fatigue on force produced during stimulation patterns that in non-fatigued muscle gave maximum force (T(max), high frequency stimulation) and approximately half-maximum force (1/2T(max), low frequency stimulation). In 15-month-old (mature) mice, fatiguing stimulation decreased T(max) in EDL and soleus muscle to 10.3 +/- 1.0 % and 33.4 +/- 3.0 % of control, respectively. In 30-month-old (aged) mice, the decrease in T(max) in EDL and soleus was statistically equal to that of the younger animals. Fatiguing stimulation decreased 1/2T(max) in EDL and soleus from 15-month-old animals to 22.5 +/- 2.9 % and 45.7 +/- 0.3 % of control, respectively. In 30-month-old animals, the 1/2T(max) in EDL and soleus muscle decreased to 18.2 +/- 1.3 % and 35.0 +/- 3.6 % of control, respectively. Under all conditions, the soleus fatigued significantly less. Contractile recovery from fatiguing stimulation was complete for the soleus in both age groups after 30 min, but incomplete for the EDL. The 1/2T(max)/T(max) ratio significantly increased in EDL and soleus muscle from 15-month-old animals after fatiguing stimulation. This increase was less significant in EDL, and absent in soleus muscle, from 30-month-old animals. These results indicate that fatiguing stimulation induces a leftward shift in the force-frequency relationship in the young animals; this shift is either significantly less (EDL) or absent (soleus) in the older animals. We speculate that the leftward shift of the force-frequency relationship may reflect a protective mechanism in younger animals against some of the damaging effects of fatiguing stimulation (i.e. oxidative stress).

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Year:  2002        PMID: 11805861     DOI: 10.1113/eph8702224

Source DB:  PubMed          Journal:  Exp Physiol        ISSN: 0958-0670            Impact factor:   2.969


  13 in total

1.  Rats genetically selected for low and high aerobic capacity exhibit altered soleus muscle myofilament functions.

Authors:  B J Biesiadecki; M A Brotto; L S Brotto; L G Koch; S L Britton; T M Nosek; J-P Jin
Journal:  Am J Physiol Cell Physiol       Date:  2019-12-25       Impact factor: 4.249

2.  Ex vivo assessment of contractility, fatigability and alternans in isolated skeletal muscles.

Authors:  Ki Ho Park; Leticia Brotto; Oanh Lehoang; Marco Brotto; Jianjie Ma; Xiaoli Zhao
Journal:  J Vis Exp       Date:  2012-11-01       Impact factor: 1.355

3.  Fibroblast growth factor 23 does not directly influence skeletal muscle cell proliferation and differentiation or ex vivo muscle contractility.

Authors:  Keith G Avin; Julian A Vallejo; Neal X Chen; Kun Wang; Chad D Touchberry; Marco Brotto; Sarah L Dallas; Sharon M Moe; Michael J Wacker
Journal:  Am J Physiol Endocrinol Metab       Date:  2018-03-20       Impact factor: 4.310

4.  Temporal adaptive changes in contractility and fatigability of diaphragm muscles from streptozotocin-diabetic rats.

Authors:  Marco Brotto; Leticia Brotto; J-P Jin; Thomas M Nosek; Andrea Romani
Journal:  J Biomed Biotechnol       Date:  2010-05-06

5.  Muscle-specific inositide phosphatase (MIP/MTMR14) is reduced with age and its loss accelerates skeletal muscle aging process by altering calcium homeostasis.

Authors:  Sandra Romero-Suarez; Jinhua Shen; Leticia Brotto; Todd Hall; Chenglin Mo; Héctor H Valdivia; Jon Andresen; Michael Wacker; Thomas M Nosek; Cheng-Kui Qu; Marco Brotto
Journal:  Aging (Albany NY)       Date:  2010-08       Impact factor: 5.682

6.  Original Research: Central and peripheral quadriceps fatigue in young and middle-aged untrained and endurance-trained men: A comparative study.

Authors:  Damien Bachasson; Nicolas Decorte; Bernard Wuyam; Guillaume Y Millet; Samuel Verges
Journal:  Exp Biol Med (Maywood)       Date:  2016-06-10

7.  Deficiency of MIP/MTMR14 phosphatase induces a muscle disorder by disrupting Ca(2+) homeostasis.

Authors:  Jinhua Shen; Wen-Mei Yu; Marco Brotto; Joseph A Scherman; Caiying Guo; Christopher Stoddard; Thomas M Nosek; Héctor H Valdivia; Cheng-Kui Qu
Journal:  Nat Cell Biol       Date:  2009-05-24       Impact factor: 28.824

8.  Store-operated Ca(2+) entry (SOCE) contributes to normal skeletal muscle contractility in young but not in aged skeletal muscle.

Authors:  Angela M Thornton; Xiaoli Zhao; Noah Weisleder; Leticia S Brotto; Sylvain Bougoin; Thomas M Nosek; Michael Reid; Brian Hardin; Zui Pan; Jianjie Ma; Jerome Parness; Marco Brotto
Journal:  Aging (Albany NY)       Date:  2011-06       Impact factor: 5.682

9.  Muscle aging is associated with compromised Ca2+ spark signaling and segregated intracellular Ca2+ release.

Authors:  Noah Weisleder; Marco Brotto; Shinji Komazaki; Zui Pan; Xiaoli Zhao; Thomas Nosek; Jerome Parness; Hiroshi Takeshima; Jianjie Ma
Journal:  J Cell Biol       Date:  2006-08-28       Impact factor: 10.539

Review 10.  Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy-new hopes for treatment of musculoskeletal diseases.

Authors:  Heather Manring; Eduardo Abreu; Leticia Brotto; Noah Weisleder; Marco Brotto
Journal:  Front Physiol       Date:  2014-02-18       Impact factor: 4.566

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