白藜芦醇
肌发生
肌肉萎缩
下调和上调
骨骼肌
内科学
内分泌学
C2C12型
心肌细胞
肾脏疾病
基因敲除
萎缩
生物
化学
肾
医学
细胞生物学
肌肉肥大
药理学
生物化学
细胞凋亡
基因
作者
Lijing Sun,Yanni Sun,Shun-Jie Chen,Shuang Liu,Gengru Jiang
标识
DOI:10.1016/j.bbrc.2017.04.022
摘要
Skeletal muscle atrophy is an important clinical characteristic of chronic kidney disease (CKD); however, at present, the therapeutic approaches to muscle atrophy induced by CKD are still at an early stage of development. Resveratrol is used to attenuate muscle atrophy in other experimental models, but the effects on a CKD model are largely unknown. Here, we showed that resveratrol prevented an increase in MuRF1 expression and attenuated muscle atrophy in vivo model of CKD. We also found that phosphorylation of NF-κB was inhibited at the same time. Dexamethasone-induced MuRF1 upregulation was significantly attenuated in C2C12 myotubes by resveratrol in vitro, but this effect on C2C12 myotubes was abrogated by a knockdown of NF-κB, suggesting that the beneficial effect of resveratrol was NF-κB dependent. Our findings provide novel information about the ability of resveratrol to prevent or treat muscle atrophy induced by CKD.
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