Pharmacology of manipulating lean body mass

被引:12
作者
Sepulveda, Patricio V. [1 ]
Bush, Ernest D. [2 ]
Baar, Keith [3 ,4 ,5 ]
机构
[1] Monash Univ, Dept Physiol, Melbourne, Vic 3168, Australia
[2] Akashi Therapeut, Cambridge, MA USA
[3] Univ Calif Davis, Dept Neurobiol, Davis, CA 95616 USA
[4] Univ Calif Davis, Dept Physiol & Behav, Davis, CA 95616 USA
[5] Univ Calif Davis, Dept Physiol & Membrane Biol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
atrophy; cachexia; Duchenne muscular dystrophy; exercise; hypertrophy; regeneration; skeletal muscle; SKELETAL-MUSCLE HYPERTROPHY; ANDROGEN RECEPTOR MODULATORS; PROTEIN-SYNTHESIS; GENE-EXPRESSION; MUSCULAR-DYSTROPHY; RESISTANCE EXERCISE; MAMMALIAN TARGET; IIB RECEPTOR; CANCER CACHEXIA; DOUBLE-BLIND;
D O I
10.1111/1440-1681.12320
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dysfunction and wasting of skeletal muscle as a consequence of illness decreases the length and quality of life. Currently, there are few, if any, effective treatments available to address these conditions. Hence, the existence of this unmet medical need has fuelled large scientific efforts. Fortunately, these efforts have shown many of the underlying mechanisms adversely affecting skeletal muscle health. With increased understanding have come breakthrough disease-specific and broad spectrum interventions, some progressing through clinical development. The present review focuses its attention on the role of the antagonistic process regulating skeletal muscle mass before branching into prospective promising therapeutic targets and interventions. Special attention is given to therapies in development against cancer cachexia and Duchenne muscular dystrophy before closing remarks on design and conceptualization of future therapies are presented to the reader.
引用
收藏
页码:1 / 13
页数:13
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