One size may not fit all: anti-aging therapies and sarcopenia

被引:22
作者
Burks, Tyesha N. [2 ]
Cohn, Ronald D. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pediat & Neurol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
来源
AGING-US | 2011年 / 3卷 / 12期
关键词
sarcopenia; therapy; caloric restriction; caloric restriction mimetics; anti-aging; skeletal muscle; GROWTH-FACTOR-I; SKELETAL-MUSCLE ATROPHY; ANDROGEN RECEPTOR MODULATORS; LIFELONG CALORIE RESTRICTION; SATELLITE-CELL-PROLIFERATION; AGE-RELATED DECLINE; AGING-RELATED LOSS; OXIDATIVE STRESS; DIETARY RESTRICTION; PHYSICAL FUNCTION;
D O I
10.18632/aging.100409
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sarcopenia refers to age-related loss of muscle mass and function. Several age-related changes occur in skeletal muscle including a decrease in myofiber size and number and a diminished ability of satellite cells to activate and proliferate upon injury leading to impaired muscle remodeling. Although the molecular mechanisms underlying sarcopenia are unknown, it is tempting to hypothesize that interplay between biological and environmental factors cooperate in a positive feedback cycle contributing to the progression of sarcopenia. Indeed many essential biological mechanisms such as apoptosis and autophagy and critical signaling pathways involved in skeletal muscle homeostasis are altered during aging and have been linked to loss of muscle mass. Moreover, the environmental effects of the sedentary lifestyle of older people further promote and contribute the loss of muscle mass. There are currently no widely accepted therapeutic strategies to halt or reverse the progression of sarcopenia. Caloric restriction has been shown to be beneficial as a sarcopenia and aging antagonist. Such results have made the search for caloric restriction mimetics (CRM) a priority. However given the mechanisms of action, some of the currently investigated CRMs may not combat sarcopenia. Thus, sarcopenia may represent a unique phenotypic feature of aging that requires specific and individually tailored therapeutic strategies.
引用
收藏
页码:1142 / 1153
页数:12
相关论文
共 139 条
  • [1] ADNITT PI, 1973, BRIT J PHARMACOL, V47, pP617
  • [2] ADNITT PI, 1972, BRIT J PHARMACOL, V45, pP152
  • [3] REGULATION OF SKELETAL-MUSCLE SATELLITE CELL-PROLIFERATION AND DIFFERENTIATION BY TRANSFORMING GROWTH FACTOR-BETA, INSULIN-LIKE GROWTH FACTOR-I, AND FIBROBLAST GROWTH-FACTOR
    ALLEN, RE
    BOXHORN, LK
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 138 (02) : 311 - 315
  • [4] INHIBITION OF SKELETAL-MUSCLE SATELLITE CELL-DIFFERENTIATION BY TRANSFORMING GROWTH-FACTOR-BETA
    ALLEN, RE
    BOXHORN, LK
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1987, 133 (03) : 567 - 572
  • [5] Muscle Wasting in Aged, Sarcopenic Rats Is Associated with Enhanced Activity of the Ubiquitin Proteasome Pathway
    Altun, Mikael
    Besche, Henrike C.
    Overkleeft, Herman S.
    Piccirillo, Rosanna
    Edelmann, Mariola J.
    Kessler, Benedikt M.
    Goldberg, Alfred L.
    Ulfhake, Brun
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (51) : 39597 - 39608
  • [6] Ryanodine Receptor Oxidation Causes Intracellular Calcium Leak and Muscle Weakness in Aging
    Andersson, Daniel C.
    Betzenhauser, Matthew J.
    Reiken, Steven
    Meli, Albano C.
    Umanskaya, Alisa
    Xie, Wenjun
    Shiomi, Takayuki
    Zalk, Ran
    Lacampagne, Alain
    Marks, Andrew R.
    [J]. CELL METABOLISM, 2011, 14 (02) : 196 - 207
  • [7] [Anonymous], HOME CARE PROVID
  • [8] The AMP-activated protein kinase AAK-2 links energy levels and insulin-like signals to lifespan in C-elegans
    Apfeld, J
    O'Connor, G
    McDonagh, T
    DiStefano, PS
    Curtis, R
    [J]. GENES & DEVELOPMENT, 2004, 18 (24) : 3004 - 3009
  • [9] Inhibition of mammalian S6 kinase by resveratrol suppresses autophagy
    Armour, Sean M.
    Baur, Joseph A.
    Hsieh, Sherry N.
    Land-Bracha, Abigail
    Thomas, Sheila M.
    Sinclair, David A.
    [J]. AGING-US, 2009, 1 (06): : 515 - 528
  • [10] Rapamycin and FK506 reduce skeletal muscle voltage sensor expression and function
    Avila, G
    Dirksen, RT
    [J]. CELL CALCIUM, 2005, 38 (01) : 35 - 44