RETRACTED: Alpha-ketoglutarate promotes skeletal muscle hypertrophy and protein synthesis through Akt/mTOR signaling pathways (Retracted Article)

被引:64
作者
Cai, Xingcai [1 ]
Zhu, Canjun [1 ]
Xu, Yaqiong [1 ]
Jing, Yuanyuan [1 ]
Yuan, Yexian [1 ]
Wang, Lina [1 ]
Wang, Songbo [1 ]
Zhu, Xiaotong [1 ]
Gao, Ping [1 ]
Zhang, Yongliang [1 ]
Jiang, Qingyan [1 ,2 ]
Shu, Gang [1 ,2 ]
机构
[1] South China Agr Univ, Natl Engn Res Ctr Breeding Swine Ind, Coll Anim Sci, Guangzhou 510642, Guangdong, Peoples R China
[2] South China Agr Univ, ALLTECH SCAU Anim Nutr Control Res Alliance, Guangzhou 510642, Guangdong, Peoples R China
关键词
AMINO-ACIDS; NEONATAL PIGS; ATROPHY; MTOR; GLUTAMINE; GROWTH; METABOLISM; RECEPTORS; NUTRITION; LEUCINE;
D O I
10.1038/srep26802
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Skeletal muscle weight loss is accompanied by small fiber size and low protein content. Alpha-ketoglutarate (AKG) participates in protein and nitrogen metabolism. The effect of AKG on skeletal muscle hypertrophy has not yet been tested, and its underlying mechanism is yet to be determined. In this study, we demonstrated that AKG (2%) increased the gastrocnemius muscle weight and fiber diameter in mice. Our in vitro study also confirmed that AKG dose increased protein synthesis in C2C12 myotubes, which could be effectively blocked by the antagonists of Akt and mTOR. The effects of AKG on skeletal muscle protein synthesis were independent of glutamate, its metabolite. We tested the expression of GPR91 and GPR99. The result demonstrated that C2C12 cells expressed GPR91, which could be upregulated by AKG. GPR91 knockdown abolished the effect of AKG on protein synthesis but failed to inhibit protein degradation. These findings demonstrated that AKG promoted skeletal muscle hypertrophy via Akt/mTOR signaling pathway. In addition, GPR91 might be partially attributed to AKG-induced skeletal muscle protein synthesis.
引用
收藏
页数:11
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