Systems-based Discovery of Tomatidine as a Natural Small Molecule Inhibitor of Skeletal Muscle Atrophy

被引:110
作者
Dyle, Michael C. [1 ,2 ,3 ]
Ebert, Scott M. [1 ,2 ,3 ]
Cook, Daniel P. [1 ,2 ,3 ]
Kunkel, Steven D. [1 ,2 ,3 ]
Fox, Daniel K. [1 ,2 ,3 ]
Bongers, Kale S. [1 ,2 ,3 ]
Bullard, Steven A. [1 ,2 ,3 ,4 ]
Dierdorff, Jason M. [1 ,2 ,3 ]
Adams, Christopher M. [1 ,2 ,3 ,4 ]
机构
[1] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
[3] Univ Iowa, Roy J & Lucille A Carver Coll Med, Fraternal Order Eagles Diabet Res Ctr, Iowa City, IA 52242 USA
[4] Iowa City Vet Affairs Med Ctr, Iowa City, IA 52246 USA
基金
美国国家卫生研究院;
关键词
ALPHA-TOMATINE; EXPRESSION SIGNATURES; DEFICIENT MICE; FAT MASS; SARCOPENIA; HYPERTROPHY; ACTIVATION; MANAGEMENT; PROTECTS; TOMATOES;
D O I
10.1074/jbc.M114.556241
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Skeletal muscle atrophy is a common and debilitating condition that lacks an effective therapy. To address this problem, we used a systems-based discovery strategy to search for a small molecule whose mRNA expression signature negatively correlates to mRNA expression signatures of human skeletal muscle atrophy. This strategy identified a natural small molecule from tomato plants, tomatidine. Using cultured skeletal myotubes from both humans and mice, we found that tomatidine stimulated mTORC1 signaling and anabolism, leading to accumulation of protein and mitochondria, and ultimately, cell growth. Furthermore, in mice, tomatidine increased skeletal muscle mTORC1 signaling, reduced skeletal muscle atrophy, enhanced recovery from skeletal muscle atrophy, stimulated skeletal muscle hypertrophy, and increased strength and exercise capacity. Collectively, these results identify tomatidine as a novel small molecule inhibitor of muscle atrophy. Tomatidine may have utility as a therapeutic agent or lead compound for skeletal muscle atrophy.
引用
收藏
页码:14913 / 14924
页数:12
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