Department of Life Science and Applied Chemistry, Nagoya Institute of Technology, Nagoya, Japan;
Department of Life Sciences, The University of Tokyo, Tokyo, Japan; and.
J Appl Physiol (1985). 2017 Oct 1;123(4):710-716. doi: 10.1152/japplphysiol.01009.2016. Epub 2017 Jul 20.
Resistance exercise (RE) volume is recognized as an important factor that stimulates muscle protein synthesis (MPS) and is considered, at least in part, to be involved in the mammalian target of rapamycin complex 1 (mTORC1)-associated signaling. However, the effects of relatively high-volume RE on mTORC1 and MPS remain unclear. In the present study, we used an animal model of RE to investigate the relationship between RE volume and MPS. Male Sprague-Dawley rats were subjected to RE, and muscle samples were obtained 6 h after performing 1, 3, 5, 10, or 20 sets of RE. Although 1 set of RE did not increase MPS [measured by the surface sensing of translation (SUnSET) method], multiple sets (3, 5, 10, and 20 sets) significantly increased MPS. However, the increase in MPS reached a plateau after 3 or 5 sets of RE, and no further increase in MPS was observed with additional RE sets. In contrast to the MPS response, we observed that p70S6K phosphorylation at Thr389, a marker of mTORC1 activity, and Ser240/244 phosphorylation of rpS6, a downstream target of p70S6K, gradually increased with higher RE volume. The above results suggest that the relationship between RE volume and MPS was not linear. Thus the increase in MPS with increasing RE volume saturates before p70S6K phosphorylation, suggesting a threshold effect for the relationship between p70S6K activation and MPS. The aim of this study was to investigate the relationship between resistance exercise (RE) volume and muscle protein synthesis. We found that the relationship between RE volume and p70S6K phosphorylation was almost linear, but the increase in muscle protein synthesis began to plateau after approximately five sets of RE.
抗阻运动(RE)量被认为是刺激肌肉蛋白质合成(MPS)的一个重要因素,并且至少部分涉及雷帕霉素靶蛋白复合物 1(mTORC1)相关信号通路。然而,相对高量的 RE 对 mTORC1 和 MPS 的影响尚不清楚。在本研究中,我们使用了抗阻运动的动物模型来研究 RE 量与 MPS 之间的关系。雄性 Sprague-Dawley 大鼠接受抗阻运动,在进行 1、3、5、10 或 20 组抗阻运动后 6 小时获取肌肉样本。尽管 1 组抗阻运动不会增加 MPS[通过表面感应翻译(SUnSET)法测量],但多组(3、5、10 和 20 组)明显增加了 MPS。然而,在进行 3 或 5 组抗阻运动后,MPS 的增加达到了一个平台期,并且再增加抗阻运动组数不会导致 MPS 的进一步增加。与 MPS 反应相反,我们观察到 mTORC1 活性的标志物 Thr389 处的 p70S6K 磷酸化以及 p70S6K 的下游靶标 rpS6 的 Ser240/244 磷酸化随着更高的 RE 量逐渐增加。上述结果表明,RE 量与 MPS 之间的关系不是线性的。因此,随着 RE 量的增加,MPS 的增加在 p70S6K 磷酸化之前达到饱和,这表明 p70S6K 激活与 MPS 之间存在阈值效应。本研究旨在探讨抗阻运动(RE)量与肌肉蛋白质合成之间的关系。我们发现,RE 量与 p70S6K 磷酸化之间的关系几乎是线性的,但在进行大约五组 RE 后,肌肉蛋白质合成的增加开始趋于平稳。