What does chronic electrical stimulation teach us about muscle plasticity?

被引:1
作者
Pette, D [1 ]
Vrbová, G
机构
[1] Univ Konstanz, Fac Biol, D-78457 Constance, Germany
[2] UCL, Dept Anat & Dev Biol, London, England
关键词
chronic low-frequency stimulation; contractile activity; gene expression; muscle transformation;
D O I
10.1002/(SICI)1097-4598(199906)22:6<666::AID-MUS3>3.0.CO;2-Z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (C) 1999 John Wiley & Sons, Inc.
引用
收藏
页码:666 / 677
页数:12
相关论文
共 193 条
[1]   LONG-TERM ELECTRICAL-STIMULATION OF RABBIT SKELETAL-MUSCLE INCREASES GROWTH OF PAIRED ARTERIES AND VEINS [J].
ADAIR, TH ;
HANG, J ;
WELLS, ML ;
MCGEE, FD ;
MONTANI, JP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 269 (02) :H717-H724
[2]   FAST MYOSIN HEAVY-CHAIN DIVERSITY IN SKELETAL-MUSCLES OF THE RABBIT - HEAVY CHAIN-IID, NOT CHAIN-IIB PREDOMINATES [J].
AIGNER, S ;
GOHLSCH, B ;
HAMALAINEN, N ;
STARON, RS ;
UBER, A ;
WEHRLE, U ;
PETTE, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 211 (1-2) :367-372
[3]   THE ROLE OF FREQUENCY IN THE EFFECTS OF LONG-TERM INTERMITTENT STIMULATION OF DENERVATED SLOW-TWITCH MUSCLE IN THE RAT [J].
ALAMOOD, WS ;
LEWIS, DM .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 392 :377-395
[4]   EFFECTS OF CHRONIC ELECTRICAL-STIMULATION ON CONTRACTILE PROPERTIES OF LONG-TERM DENERVATED RAT SKELETAL-MUSCLE [J].
ALAMOOD, WS ;
LEWIS, DM ;
SCHMALBRUCH, H .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 441 :243-256
[5]   Myosin heavy chain isoform transformation in single fibres from m vastus lateralis in spinal cord injured individuals: Effects of long-term functional electrical stimulation (FES) [J].
Andersen, JL ;
Mohr, T ;
BieringSorensen, F ;
Galbo, H ;
Kjaer, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1996, 431 (04) :513-518
[6]   Induction and maintenance of increased VEGF protein by chronic motor nerve stimulation in skeletal muscle [J].
Annex, BH ;
Torgan, CE ;
Lin, PN ;
Taylor, DA ;
Thompson, MA ;
Peters, KG ;
Kraus, WE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 274 (03) :H860-H867
[7]   MITOCHONDRIAL BIOGENESIS IN STRIATED MUSCLES - RAPID INDUCTION OF CITRATE SYNTHASE MESSENGER-RNA BY NERVE-STIMULATION [J].
ANNEX, BH ;
KRAUS, WE ;
DOHM, GL ;
WILLIAMS, RS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (02) :C266-C270
[8]   MUSCLE LIM PROTEIN, A NOVEL ESSENTIAL REGULATOR OF MYOGENESIS, PROMOTES MYOGENIC DIFFERENTIATION [J].
ARBER, S ;
HALDER, G ;
CARONI, P .
CELL, 1994, 79 (02) :221-231
[9]   MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure [J].
Arber, S ;
Hunter, JJ ;
Ross, J ;
Hongo, M ;
Sansig, G ;
Borg, J ;
Perriard, JC ;
Chien, KR ;
Caroni, P .
CELL, 1997, 88 (03) :393-403
[10]  
AUSONI S, 1990, J NEUROSCI, V10, P153