Comparative response of casein protein hydrolysate-fed young and older human serum on in vitro muscle protein metabolism and myotube size.

IF 5 2区 生物学 Q2 CELL BIOLOGY American journal of physiology. Cell physiology Pub Date : 2025-02-01 Epub Date: 2025-01-13 DOI:10.1152/ajpcell.00117.2024
Martina Pauk, Miryam Amigo-Benavent, Bijal Patel, Philip M Jakeman, Brian P Carson
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Abstract

In this study, we used an ex vivo-in vitro model to assess the effect of feeding older (50-70 yr) adults a casein protein hydrolysate (CPH) compared with nonbioactive nonessential amino acid (NEAA) supplement on muscle protein synthesis (MPS) and markers of muscle protein breakdown (MPB). As a secondary objective, to assess any attenuation with aging, we compared the anabolic response to CPH-fed serum from older and young adults. Serum from seven healthy older and seven young men following overnight fast and 60-min postprandial ingestion of CPH or NEAA (0.33 g·kg-1 body mass) was used to condition C2C12 myotube media. Analysis by two-way ANOVA of the fed relative to fasted MPS response revealed a main effect for protein type in pmTOR (P = 0.009), p70S6K (P = 0.031), p4E-BP1 (P = 0.047), and MPS (P = 0.041) with a greater response to CPH-fed serum, and interaction effects (age × protein) between young and old serum for pmTOR (P = 0.009) and p70S6K (P = 0.016). In addition, significant changes in myotube diameter (P = 0.049), atrogin-1 (P = 0.004), and MuRF-1 (P = 0.012) in response to CPH-fed compared with fasted serum were observed with no differences between young and old serum. In conclusion, this study demonstrated that CPH-fed serum from both young and older (50-70 yr) adults can stimulate MPS and muscle growth and can suppress biomarkers of muscle protein breakdown processes.NEW & NOTEWORTHY This study extended previously developed coculture models and found that treating skeletal muscle cells with ex vivo human serum following feeding with a casein protein hydrolysate resulted in greater protein signaling, muscle protein synthesis, muscle growth, and lower expression of genes related to muscle protein breakdown compared with feeding with a nonessential amino acid control. These findings were similar using serum from young and older adults.

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酪蛋白水解物饲喂年轻人和老年人血清对体外肌肉蛋白质代谢和肌管大小的比较反应。
在本研究中,我们采用离体体外模型来评估饲喂老年(50 - 70岁)成人酪蛋白水解物(CPH)与非生物活性非必需氨基酸(NEAA)对肌肉蛋白合成(MPS)和肌肉蛋白分解(MPB)标志物的影响。作为次要目标,为了评估随年龄增长的衰减,我们比较了老年人和年轻人对cph血清的合成代谢反应。7名健康老年男性和7名年轻男性在禁食过夜和餐后60分钟摄入CPH或NEAA (0.33 g.kg-1体重)后的血清用于调节C2C12肌管培养基。双因素方差分析显示,pmTOR (p=0.009)、p70S6K (p=0.031)、p4E-BP1 (p=0.047)和MPS (p=0.041)中的蛋白类型是主要影响因素,cph喂养的血清对pmTOR (p=0.009)和p70S6K (p=0.016)的交互作用(AgeXProtein)是年轻和年老血清对pmTOR (p=0.009)和p70S6K的交互作用。此外,与空腹血清相比,cph喂养组肌管直径(p=0.049)、Atrogin-1 (p=0.004)和MuRF-1 (p=0.012)均有显著变化,而年轻和年老血清之间无差异。总之,本研究表明,年轻和老年(50 - 70岁)成年人的cph血清可以刺激MPS,肌肉生长并抑制肌肉蛋白分解过程的生物标志物。
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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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