Molecular mechanisms and therapeutics of the deficit in specific force in ageing skeletal muscle

被引:54
作者
Delbono, O [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Dept Interna Med,Gerontol & Neurosci Program, Winston Salem, NC 27157 USA
关键词
ageing; calcium channels; calcium signaling; insulin-like growth factor 1; sarcopenia; skeletal muscle;
D O I
10.1023/A:1020189627325
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The age-related impairment in muscle force is only partially explained by the loss of muscle mass. The loss both in specific and absolute forces contributes to the muscle weakness measured in the elderly and in animal models of ageing. Successful interventions aimed at preventing age-associated functional deficits will require a better insight into the mechanisms underlying the decline in muscle-specific force. The present review article is focused on recent evidence supporting excitation-contraction uncoupling as a key factor underlying fast and slow muscle fiber impairment with ageing. The molecular, functional and structural factors supporting this theory and counteracting measures such as insulin-like growth factor 1 transgenic overexpression are discussed.
引用
收藏
页码:265 / 270
页数:6
相关论文
共 37 条
[1]   INTRAMEMBRANE CHARGE MOVEMENT RESTORED IN DYSGENIC SKELETAL-MUSCLE BY INJECTION OF DIHYDROPYRIDINE RECEPTOR CDNAS [J].
ADAMS, BA ;
TANABE, T ;
MIKAMI, A ;
NUMA, S ;
BEAM, KG .
NATURE, 1990, 346 (6284) :569-572
[2]   HIGH-AFFINITY [H-3] PN200-110 AND [H-3] RYANODINE BINDING TO RABBIT AND FROG SKELETAL-MUSCLE [J].
ANDERSON, K ;
COHN, AH ;
MEISSNER, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02) :C462-C466
[3]   THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1 [J].
ANGEL, P ;
HATTORI, K ;
SMEAL, T ;
KARIN, M .
CELL, 1988, 55 (05) :875-885
[4]   CA2+ AND ACTIVATION MECHANISMS IN SKELETAL-MUSCLE [J].
ASHLEY, CC ;
MULLIGAN, IP ;
LEA, TJ .
QUARTERLY REVIEWS OF BIOPHYSICS, 1991, 24 (01) :1-73
[5]   Viral mediated expression of insulin-like growth factor I blocks the aging-related loss of skeletal muscle function [J].
Barton-Davis, ER ;
Shoturma, DI ;
Musaro, A ;
Rosenthal, N ;
Sweeney, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15603-15607
[6]   CONTRACTION-INDUCED INJURY - RECOVERY OF SKELETAL-MUSCLES IN YOUNG AND OLD MICE [J].
BROOKS, SV ;
FAULKNER, JA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (03) :C436-C442
[7]   CONTRACTILE PROPERTIES OF SKELETAL-MUSCLES FROM YOUNG, ADULT AND AGED MICE [J].
BROOKS, SV ;
FAULKNER, JA .
JOURNAL OF PHYSIOLOGY-LONDON, 1988, 404 :71-82
[8]   ISOMETRIC, SHORTENING, AND LENGTHENING CONTRACTIONS OF MUSCLE-FIBER SEGMENTS FROM ADULT AND OLD MICE [J].
BROOKS, SV ;
FAULKNER, JA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02) :C507-C513
[9]  
BROOKS SV, 1994, MED SCI SPORT EXER, V26, P432
[10]   MYOGENIC VECTOR EXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-I STIMULATES MUSCLE-CELL DIFFERENTIATION AND MYOFIBER HYPERTROPHY IN TRANSGENIC MICE [J].
COLEMAN, ME ;
DEMAYO, F ;
YIN, KC ;
LEE, HM ;
GESKE, R ;
MONTGOMERY, C ;
SCHWARTZ, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) :12109-12116