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Paradoxical effect of IKKβ inhibition on the expression of E3 ubiquitin ligases and unloading‐induced skeletal muscle atrophy

机译:IKKβ抑制对E3泛素连接酶表达和空腹诱导的骨骼肌萎缩的悖论作用

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摘要

We tested whether NF‐κB pathway is indispensable for the increase in expression of E3‐ligases and unloading‐induced muscle atrophy using IKKβ inhibitor IMD‐0354. Three groups of rats were used: nontreated control (C), 3 days of unloading/hindlimb suspension with (HS+IMD) or without (HS) IMD‐0354. Levels of IκBα were higher in HS+IMD (1.16‐fold) and lower in HS (0.82‐fold) when compared with C group. IMD‐0354 treatment during unloading: had no effect on loss of muscle mass; increased mRNA levels of MuRF1 and MAFbx; increased levels of pFoxO3; and had no effect on levels of Bcl‐3, p105, and p50 proteins. Our study for the first time showed that inhibiting IKK β in vivo during 3‐day unloading failed to diminish expression of ubiquitin ligases and prevent muscle atrophy.
机译:我们使用IKKβ抑制剂IMD-0354测试了NF-κB通路对于E3连接酶表达的增加和空腹诱导的肌肉萎缩是否必不可少。使用三组大鼠:未经处理的对照组(C),有(HS + IMD)或无(HS)IMD-0354的三天卸载/后肢悬吊。与C组相比,HS + IMD中IκBα的水平较高(1.16倍),HS中较低(0.82倍)。卸载过程中的IMD-0354治疗:对肌肉质量的损失没有影响; MuRF1和MAFbx的mRNA水平升高; pFoxO3的 s 水平升高;且对Bcl-3,p105和p50蛋白的水平没有影响。我们的研究首次显示,在3天的卸载过程中抑制体内的IKKβ不能减少泛素连接酶的表达并防止肌肉萎缩。

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