Literature DB >> 10366220

What does chronic electrical stimulation teach us about muscle plasticity?

D Pette1, G Vrbová.   

Abstract

The model of chronic low-frequency stimulation for the study of muscle plasticity was developed over 30 years ago. This protocol leads to a transformation of fast, fatigable muscles toward slower, fatigue-resistant ones. It involves qualitative and quantitative changes of all elements of the muscle fiber studied so far. The multitude of stimulation-induced changes makes it possible to establish the full adaptive potential of skeletal muscle. Both functional and structural alterations are caused by orchestrated exchanges of fast protein isoforms with their slow counterparts, as well as by altered levels of expression. This remodeling of the muscle fiber encompasses the major, myofibrillar proteins, membrane-bound and soluble proteins involved in Ca2+ dynamics, and mitochondrial and cytosolic enzymes of energy metabolism. Most transitions occur in a coordinated, time-dependent manner and result from altered gene expression, including transcriptional and posttranscriptional processes. This review summarizes the advantages of chronic low-frequency stimulation for studying activity-induced changes in phenotype, and its potential for investigating regulatory mechanisms of gene expression. The potential clinical relevance or utility of the technique is also considered.

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Year:  1999        PMID: 10366220     DOI: 10.1002/(sici)1097-4598(199906)22:6<666::aid-mus3>3.0.co;2-z

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


  56 in total

1.  Activation of MEF2 by muscle activity is mediated through a calcineurin-dependent pathway.

Authors:  H Wu; B Rothermel; S Kanatous; P Rosenberg; F J Naya; J M Shelton; K A Hutcheson; J M DiMaio; E N Olson; R Bassel-Duby; R S Williams
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

2.  Regulation of myosin heavy chain expression during rat skeletal muscle development in vitro.

Authors:  C E Torgan; M P Daniels
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

3.  Fast-to-slow transformation and nuclear import/export kinetics of the transcription factor NFATc1 during electrostimulation of rabbit muscle cells in culture.

Authors:  Hans-Peter Kubis; Renate J Scheibe; Joachim D Meissner; Gunther Hornung; Gerolf Gros
Journal:  J Physiol       Date:  2002-06-15       Impact factor: 5.182

4.  Proliferation of mitochondria in chronically stimulated rabbit skeletal muscle--transcription of mitochondrial genes and copy number of mitochondrial DNA.

Authors:  J Schultz; R J Wiesner
Journal:  J Bioenerg Biomembr       Date:  2000-12       Impact factor: 2.945

5.  Six1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotype.

Authors:  Raphaelle Grifone; Christine Laclef; François Spitz; Soledad Lopez; Josiane Demignon; Jacques-Emmanuel Guidotti; Kiyoshi Kawakami; Pin-Xian Xu; Robert Kelly; Basil J Petrof; Dominique Daegelen; Jean-Paul Concordet; Pascal Maire
Journal:  Mol Cell Biol       Date:  2004-07       Impact factor: 4.272

6.  Function induced modifications of gene expression: an alternative approach to gene therapy of Duchenne muscular dystrophy.

Authors:  Gerta Vrbová
Journal:  J Muscle Res Cell Motil       Date:  2004       Impact factor: 2.698

7.  Intercostal muscle pacing with high frequency spinal cord stimulation in dogs.

Authors:  Anthony F DiMarco; Krzysztof E Kowalski
Journal:  Respir Physiol Neurobiol       Date:  2010-03-23       Impact factor: 1.931

8.  Neuromuscular electrostimulation: a new therapeutic option to improve radio-cephalic arteriovenous fistula maturation in end-stage chronic kidney disease patients.

Authors:  Lucia Martinez; Vicent Esteve; Montserrat Yeste; Vicent Artigas; Secundino Llagostera
Journal:  Int Urol Nephrol       Date:  2017-04-21       Impact factor: 2.370

9.  Myosin light chain isoform expression among single mammalian skeletal muscle fibers: species variations.

Authors:  Sabahattin Bicer; Peter J Reiser
Journal:  J Muscle Res Cell Motil       Date:  2005-02-24       Impact factor: 2.698

10.  Inactivation of sarcoplasmic reticulum Ca(2+)-atpase in low-frequency stimulated rat muscle.

Authors:  S Matsunaga; S Harmon; B Gohlsch; K Ohlendieck; D Pette
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

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