Astragalus polysaccharides decrease muscle wasting through Akt/mTOR, ubiquitin proteasome and autophagy signalling in 5/6 nephrectomised rats

被引:37
作者
Lu, Lu [1 ,2 ,3 ]
Huang, Yan-Feng [4 ]
Chen, De-Xiu [1 ,2 ,3 ]
Wang, Ming [1 ]
Zou, Yu-Cong [2 ]
Wan, Heng [5 ]
Wei, Lian-Bo [1 ,2 ,3 ]
机构
[1] Southern Med Univ, ZhuJiang Hosp, Dept Tradit Chinese Med, Guangzhou 510280, Guangdong, Peoples R China
[2] Southern Med Univ, Sch Tradit Chinese Med, Guangzhou 510515, Guangdong, Peoples R China
[3] Southern Med Univ, TCM Integrated Hosp, Dept Nephrol, Guangzhou 510515, Guangdong, Peoples R China
[4] Southern Med Univ, Peoples Hosp Shunde 1, Dept Tradit Chinese Med, Guangzhou 528300, Guangdong, Peoples R China
[5] Southern Med Univ, Affiliated Hosp 3, Dept Endocrinol, Guangzhou 510280, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
Muscle wasting; Astragalus polysaccharides; Chronic kidney disease; Protein metabolism; CHRONIC KIDNEY-DISEASE; PEROXIDE-INDUCED INJURY; SKELETAL-MUSCLE; OXIDATIVE STRESS; IN-VITRO; NEUROPEPTIDE-Y; PROTEIN; ATROPHY; MICE; APOPTOSIS;
D O I
10.1016/j.jep.2016.03.068
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Existing evidences suggest that Radix Astragali and its polysaccharides composition (APS) can improve muscle mass, but the mechanisms need more research. Aim of the study: In this study, we aimed to examine the effects of APS on muscle wasting at molecular level in 5/6 nephrectomised rats. Materials and methods: We performed 5/6 nephrectomy or sham operation in 160 6-week-old SpragueDawley rats, and feed animals with or without 2% APS for 155 days. After treatment, we compared the change of weight, muscle fibre, protein metabolism, pro-inflammatory factors (TNF-alpha, IL-15, CRP) and oxidative factors (MDA, SOD) among each group. In addition, we detected the Akt/mTOR, ubiquitin proteasome, autophagy signalling and AA transporters in vivo and in vitro. Results: Data in vivo show 2% APS could alleviate weight loss and improve protein metabolism in nephrectomised rats. The levels of serum pro-inflammatory factors and oxidative factors were restored by APS treatment. In molecular levels, APS restored Akt/mTOR, MAFbx, MuRF1, Atg7, LC3B-II/LC3B-I and SLC38A2 which changed in nephrectomised rats. Data in vitro show the optimal dose of APS is 0.2 mg/mL, and SLC38A2 siRNA attenuated the effects of 0.2 mg/mL APS on atrophy and autophagy. Conclusions: Our results suggested APS could improve muscle wasting through Akt/mTOR, ubiquitin proteasome and autophagy signalling, and SLC38A2 may be one of potential targets. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:125 / 135
页数:11
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