Dillon Edgar L, Sheffield-Moore Melinda, Paddon-Jones Douglas, Gilkison Charles, Sanford Arthur P, Casperson Shanon L, Jiang Jie, Chinkes David L, Urban Randall J
Department of Internal Medicine, The University of Texas Medical Branch at Galveston, Galveston, Texas 77555-1060, USA.
J Clin Endocrinol Metab. 2009 May;94(5):1630-7. doi: 10.1210/jc.2008-1564. Epub 2009 Feb 10.
Inadequate dietary protein intake has been implicated in sarcopenia.
The objectives of this study were to determine whether: 1) chronic essential amino acid (EAA) supplementation improves postabsorptive muscle protein fractional synthesis rate (FSR), lean body mass (LBM), and one-repetition maximum muscle strength, and androgen receptor and IGF-I muscle protein expression; and 2) the acute anabolic response to EAA ingestion is preserved after a 3-month supplementation period. Using a randomized, double-blinded, placebo-controlled design, older women (68 +/- 2 yr) were assigned to receive either placebo (n = 7), or 15 g EAA/d [supplemented treatment group (SUP)] (n = 7) for 3 months. Metabolic outcomes were assessed in association with stable isotope studies conducted at 0 and 3 months.
The study was performed at The University of Texas Medical Branch General Clinical Research Center.
Ingestion of 7.5 g EAA acutely stimulated FSR in both groups at 0 months (P < 0.05). Basal FSR at 3 months was increased in SUP only. The magnitude of the acute response to EAA was unaltered after 3 months in SUP. LBM increased in SUP only (P < 0.05). One-repetition maximum strength remained unchanged in both groups. Basal IGF-I protein expression increased in SUP after 3 months (P = 0.05), with no changes in androgen receptor or total and phosphorylated Akt, mammalian target of rapamycin, S6 kinase, and 4E-binding protein.
EAA improved LBM and basal muscle protein synthesis in older individuals. The acute anabolic response to EAA supplementation is maintained over time and can improve LBM, possibly offsetting the debilitating effects of sarcopenia.
膳食蛋白质摄入不足与肌肉减少症有关。
本研究的目的是确定:1)长期补充必需氨基酸(EAA)是否能提高吸收后肌肉蛋白质的分数合成率(FSR)、去脂体重(LBM)和一次重复最大肌肉力量,以及雄激素受体和IGF-I肌肉蛋白表达;2)在3个月的补充期后,对EAA摄入的急性合成代谢反应是否得以保留。采用随机、双盲、安慰剂对照设计,将老年女性(68±2岁)分为两组,一组接受安慰剂(n = 7),另一组接受15 g EAA/天[补充治疗组(SUP)](n = 7),为期3个月。在0个月和3个月时进行稳定同位素研究,评估代谢结果。
该研究在德克萨斯大学医学分部综合临床研究中心进行。
0个月时,两组摄入7.5 g EAA均能急性刺激FSR(P < 0.05)。仅SUP组3个月时的基础FSR增加。SUP组在3个月后对EAA的急性反应幅度未改变。仅SUP组的LBM增加(P < 0.05)。两组的一次重复最大力量均保持不变。3个月后,SUP组的基础IGF-I蛋白表达增加(P = 0.05),雄激素受体、总Akt和磷酸化Akt、雷帕霉素靶蛋白、S6激酶及4E结合蛋白均无变化。
EAA可改善老年人的LBM和基础肌肉蛋白质合成。对EAA补充的急性合成代谢反应随时间持续存在,且可改善LBM,可能抵消肌肉减少症的衰弱影响。