Med Sci Sports Exerc. 2023 Mar 1;55(3):398-408. doi: 10.1249/MSS.0000000000003061. Epub 2022 Oct 18.
Resistance exercise training (RET) attenuates age-related muscle and strength loss ("sarcopenia"). However, compared with machine-based RET, the efficacy of cost-effective, accessible elastic band RET (EB-RET) for muscle adaptive remodeling lacks supporting mechanistic evidence.
Eight young (YM; 24 ± 4 yr) and eight older (OM; 68 ± 6 yr) untrained males consumed an oral stable isotope tracer (D 2 O) combined with serial vastus lateralis muscle biopsies to measure integrated myofibrillar protein synthesis (iMyoPS) and regulatory signaling over ~48 h before (habitual) and after an acute bout of EB-RET (6 × 12 repetitions at ~70% of one-repetition maximum). iMyoPS was determined via gas chromatography-pyrolysis-isotope ratio mass spectroscopy and regulatory signaling expression by immunoblot.
Habitual iMyoPS did not differ between YM and OM (1.62% ± 0.21% vs 1.43% ± 0.47%·d -1 , respectively, P = 0.128). There was a significant increase in iMyoPS after EB-RET in YM (2.23% ± 0.69%·d -1 , P = 0.02), but not OM (1.75% ± 0.54%·d -1 , P = 0.30). EB-RET increased the phosphorylation of key anabolic signaling proteins similarly in YM and OM at 1 h postexercise, including p-IRS-1 Ser636/639 , p-Akt Ser473 , p-4EBP-1 Thr37/46 , p-P70S6K Thr389 , and p-RPS6 Ser240/244 , whereas p-TSC2 Thr1462 and p-mTOR Ser2448 increased only in YM (all P < 0.05). There were no differences in the expression of amino acid transporters/sensors or proteolytic markers after EB-RET.
iMyoPS was elevated after EB-RET in YM but not OM. However, the increase in acute anabolic signaling with EB-RET was largely similar between groups. In conclusion, the capacity for EB-RET to stimulate iMyoPS may be impaired in older age. Further work may be necessary to optimize prescriptive programming in YM and OM.
抗阻运动训练(RET)可减轻与年龄相关的肌肉和力量丧失(“肌肉减少症”)。然而,与基于器械的 RET 相比,经济实惠、易于获得的弹性带抗阻运动训练(EB-RET)对肌肉适应性重塑的效果缺乏支持的机制证据。
8 名年轻(YM;24 ± 4 岁)和 8 名年长(OM;68 ± 6 岁)未经训练的男性在进行急性 EB-RET(6 组×12 次,约为 1 次重复最大值的 70%)前和后(习惯),通过口服稳定同位素示踪剂(D2O)联合股外侧肌活检来测量整合肌纤维蛋白合成(iMyoPS)和调节信号,持续约 48 小时。通过气相色谱-热解-同位素比质谱法测定 iMyoPS,通过免疫印迹法测定调节信号表达。
YM 和 OM 的习惯 iMyoPS 没有差异(分别为 1.62%±0.21%和 1.43%±0.47%·d-1,P=0.128)。YM 在 EB-RET 后 iMyoPS 显著增加(2.23%±0.69%·d-1,P=0.02),而 OM 则没有增加(1.75%±0.54%·d-1,P=0.30)。YM 和 OM 在运动后 1 小时时,EB-RET 同样会增加关键合成代谢信号蛋白的磷酸化,包括 p-IRS-1 Ser636/639、p-Akt Ser473、p-4EBP-1 Thr37/46、p-P70S6K Thr389 和 p-RPS6 Ser240/244,而 p-TSC2 Thr1462 和 p-mTOR Ser2448 仅在 YM 中增加(均 P<0.05)。EB-RET 后氨基酸转运体/传感器或蛋白水解标志物的表达没有差异。
YM 在 EB-RET 后 iMyoPS 升高,但 OM 则没有。然而,EB-RET 后急性合成代谢信号的增加在两组之间基本相似。总之,EB-RET 刺激 iMyoPS 的能力可能在老年时受损。可能需要进一步的工作来优化 YM 和 OM 的处方编程。