Silk Peptide Ameliorates Sarcopenia through the Regulation of Akt/mTOR/FoxO3a Signaling Pathways and the Inhibition of Low-Grade Chronic Inflammation in Aged Mice

被引:9
作者
Oh, Hyun-Ji [1 ]
Jin, Heegu [1 ]
Lee, Jeong-Yong [2 ]
Lee, Boo-Yong [1 ]
机构
[1] CHA Univ, Dept Food Sci & Biotechnol, Coll Life Sci, Seongnam 13488, South Korea
[2] Worldway Co Ltd, Sejong 30003, South Korea
关键词
acid-hydrolyzed silk peptide; sarcopenia; Akt; mTOR; FoxO3a; signaling pathway; aging; oxidative stress; inflammation; UBIQUITIN-LIGASES MURF-1; SKELETAL-MUSCLE ATROPHY; OXIDATIVE STRESS; AUTOPHAGY; FOXO;
D O I
10.3390/cells12182257
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As populations around the world age, interest in healthy aging is growing. One of the first physical changes that occurs with aging is the loss of muscle mass and strength, termed sarcopenia. Sarcopenia limits the activity of older people, reduces their quality of life, and increases the likelihood of their developing disease. In the present study, we aimed to evaluate the effects of the ingestion of acid-hydrolyzed silk peptide (SP) on the muscle mass and strength of mice of >22 months of age with naturally occurring sarcopenia, and to identify the mechanisms involved. The daily administration of SP for 8 weeks increased the activation of the Akt/mTOR/FoxO3a signaling pathways and increased the muscle mass and strength of the old mice. In addition, SP inhibited oxidative stress and inflammation in muscle, which are direct causes of sarcopenia. Therefore, SP represents a promising potential treatment for sarcopenia that may improve the healthy lifespan and quality of life of older people.
引用
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页数:14
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