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mVps34通过一次急性抗阻运动激活。

mVps34 is activated by an acute bout of resistance exercise.

作者信息

Mackenzie M G, Hamilton D L, Murray J T, Baar K

机构信息

James Black Centre, University of Dundee, 28 Dow Street, Dundee DD15EH, U.K.

出版信息

Biochem Soc Trans. 2007 Nov;35(Pt 5):1314-6. doi: 10.1042/BST0351314.

Abstract

Resistance-exercise training results in a progressive increase in muscle mass and force production. Following an acute bout of resistance exercise, the rate of protein synthesis increases proportionally with the increase in protein degradation, correlating at 3 h in the starved state. Amino acids taken immediately before or immediately after exercise increase the post-exercise rate of protein synthesis. Therefore a protein that controls protein degradation and amino acid-sensitivity would be a potential candidate for controlling the activation of protein synthesis following resistance exercise. One such candidate is the class III PI3K (phosphoinositide 3-kinase) Vps34 (vacuolar protein sorting mutant 34). Vps34 controls both autophagy and amino acid signalling to mTOR (mammalian target of rapamycin) and its downstream target p70 S6K1 (S6 kinase 1). We have identified a significant increase in mVps34 (mammalian Vps34) activity 3 h after resistance exercise, continuing for at least 6 h, and propose a mechanism whereby mVps34 could act as an internal amino acid sensor to mTOR after resistance exercise.

摘要

抗阻训练会使肌肉量和力量产生逐渐增加。进行一次急性抗阻训练后,蛋白质合成速率会随着蛋白质降解的增加而成比例增加,在饥饿状态下3小时时两者相关。运动前或运动后立即摄入氨基酸会提高运动后蛋白质合成速率。因此,一种控制蛋白质降解和氨基酸敏感性的蛋白质可能是控制抗阻训练后蛋白质合成激活的潜在候选物。其中一个候选物是III类磷脂酰肌醇3激酶(PI3K)Vps34(液泡蛋白分选突变体34)。Vps34既控制自噬,也控制向雷帕霉素哺乳动物靶标(mTOR)及其下游靶标p70 S6激酶1(S6K1)的氨基酸信号传导。我们已经确定,抗阻训练3小时后mVps34(哺乳动物Vps34)活性显著增加,并持续至少6小时,我们提出了一种机制,通过该机制mVps34在抗阻训练后可作为mTOR的内部氨基酸传感器。

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