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丙酮酸乙酯可维持 IGF-I 对 C2C12 肌管中 mTOR 底物和蛋白质合成的敏感性。

Ethyl pyruvate preserves IGF-I sensitivity toward mTOR substrates and protein synthesis in C2C12 myotubes.

机构信息

Department of Cellular and Molecular Physiology (H166), Pennsylvania State University College of Medicine, 500 University Drive, Hershey, Pennsylvania 17033, USA.

出版信息

Endocrinology. 2011 Jan;152(1):151-63. doi: 10.1210/en.2010-0248. Epub 2010 Nov 24.

Abstract

Bacterial infection decreases skeletal muscle protein synthesis via inhibition of the mammalian target of rapamycin (mTOR), a key regulator of translation initiation. To better define the mechanism by which muscle mTOR activity is decreased, we used an in vitro model of C2C12 myotubes treated with endotoxin [lipopolysaccharide (LPS)]and interferon (IFN)-γ to determine whether stable lipophilic pyruvate derivatives restore mTOR signaling. Myotubes treated with a combination of LPS and IFNγ down-regulated the phosphorylation of the mTOR substrates S6 kinase-1 and 4E binding protein-1. The phosphorylation of ribosomal protein S6 was decreased, whereas phosphorylation of elongation factor-2 was enhanced; all results consistent with defects in both translation initiation and elongation. LPS/IFNγ decreased protein synthesis 60% in myotubes. Treatment with methyl or ethyl pyruvate partially protected against the LPS/IFNγ-induced fall in mTOR signaling. The protective effect of ethyl and methyl pyruvate could not be replicated by an equimolar amount of sodium pyruvate. Although LPS/IFNγ treated myotubes were initially IGF-I responsive, prolonged exposure (≥ 17 h) resulted in IGF-I resistance at the level of mTOR despite normal IGF-I receptor phosphorylation. Ethyl pyruvate treatment restored IGF-I sensitivity as evidenced by the left shift in the IGF-I dose-response curve and maintained IGF-I responsiveness for a prolonged period of time. Ethyl pyruvate also restored IGF-I-stimulated protein synthesis in LPS/IFNγ-treated myotubes. Cotreatment with N-acetyl cysteine or ascorbic acid also preserved IGF-I sensitivity and mTOR activity. The data suggest that the combination of LPS and IFNγ inhibits mTOR activity and that prolonged exposure induces IGF-I resistance in myotubes. Lipophilic pyruvate derivatives and antioxidants show promise at rescuing mTOR activity and muscle protein synthesis by maintaining IGF-I sensitivity in this model.

摘要

细菌感染通过抑制哺乳动物雷帕霉素靶蛋白(mTOR)来减少骨骼肌蛋白合成,mTOR 是翻译起始的关键调节剂。为了更好地定义肌肉 mTOR 活性降低的机制,我们使用了用内毒素 [脂多糖(LPS)] 和干扰素(IFN)-γ处理的 C2C12 肌管的体外模型,以确定稳定的亲脂性丙酮酸盐衍生物是否恢复 mTOR 信号。用 LPS 和 IFNγ 处理的肌管下调了 mTOR 底物 S6 激酶-1 和 4E 结合蛋白-1 的磷酸化。核糖体蛋白 S6 的磷酸化减少,而伸长因子-2 的磷酸化增强;所有结果均与翻译起始和延伸均存在缺陷一致。LPS/IFNγ 使肌管中的蛋白质合成降低了 60%。用甲基或乙基丙酮酸盐处理可部分防止 LPS/IFNγ 引起的 mTOR 信号下降。LPS/IFNγ 处理的肌管最初对 IGF-I 有反应,但延长暴露(≥17 小时)导致 mTOR 对 IGF-I 产生抗性,尽管 IGF-I 受体磷酸化正常。尽管用等摩尔量的丙酮酸钠不能复制乙基和甲基丙酮酸的保护作用,但乙基丙酮酸处理可恢复 IGF-I 敏感性,表现为 IGF-I 剂量反应曲线向左移位,并可延长 IGF-I 敏感性。乙基丙酮酸还可恢复 LPS/IFNγ 处理的肌管中 IGF-I 刺激的蛋白质合成。用 N-乙酰半胱氨酸或抗坏血酸共同处理也可保持 IGF-I 敏感性和 mTOR 活性。数据表明,LPS 和 IFNγ 的组合抑制了 mTOR 活性,并且延长暴露会导致肌管中 IGF-I 产生抗性。亲脂性丙酮酸衍生物和抗氧化剂有望通过维持该模型中的 IGF-I 敏感性来恢复 mTOR 活性和肌肉蛋白质合成。

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