Caloric Restriction Normalizes Obesity-Induced Alterations on Regulators of Skeletal Muscle Growth Signaling

被引:13
|
作者
Dungan, Cory M. [1 ]
Li, Ji [2 ]
Williamson, David L. [1 ,3 ]
机构
[1] SUNY Buffalo, Sch Publ Hlth & Hlth Profess, Dept Exercise & Nutr Sci, Univ Buffalo, 2 Sherman Hall Off,5 Sherman Hall, Buffalo, NY 14214 USA
[2] Univ Buffalo, Sch Med, Dept Pharmacol & Toxicol, Buffalo, NY USA
[3] Penn State Harrisburg, Kinesiol Program, Sch Behav Sci & Educ, Middletown, PA USA
关键词
mTORC1; SREBP1; Apoptosis; DIET-INDUCED OBESITY; MTORC1; REPRESSOR; INSULIN SENSITIVITY; PROTEIN-SYNTHESIS; INDUCED AUTOPHAGY; REDD1; EXPRESSION; AMINO-ACIDS; PHOSPHORYLATION; GENE; TRANSLATION;
D O I
10.1007/s11745-016-4168-3
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
The objective of this study was to establish the impact of caloric restriction on high fat diet-induced alterations on regulators of skeletal muscle growth. We hypothesized that caloric restriction would reverse the negative effects of high fat diet-induced obesity on REDD1 and mTOR-related signaling. Following an initial 8 week period of HF diet-induced obesity, caloric restriction (CR similar to 30 %) was employed while mice continued to consume either a low (LF) or high fat (HF) diet for 8 weeks. Western analysis of skeletal muscle showed that CR reduced (p < 0.05) the obesity-related effects on the lipogenic protein, SREBP1. Likewise, CR reduced (p < 0.05) the obesity-related effects on the hyperactivation of mTORC1 and ERK1/2 signaling to levels comparable to the LF mice. CR also reduced (p < 0.05) obesity-induced expression of negative regulators of growth, REDD1 and cleaved caspase 3. These findings have implications for on the reversibility of dysregulated growth signaling in obese skeletal muscle, using short-term caloric restriction.
引用
收藏
页码:905 / 912
页数:8
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