Protein synthesis and the expression of growth-related genes are altered by running in human vastus lateralis and soleus muscles

被引:94
|
作者
Harber, Matthew P. [1 ]
Crane, Justin D. [1 ]
Dickinson, Jared M. [1 ]
Jemiolo, Bozena [1 ]
Raue, Ulrika [1 ]
Trappe, Todd A. [1 ]
Trappe, Scott W. [1 ]
机构
[1] Ball State Univ, Human Performance Lab, Muncie, IN 47306 USA
基金
美国国家航空航天局;
关键词
fractional synthesis rate; myogenic; proteolytic; exercise; myostatin; SKELETAL-MUSCLE; BED-REST; NUTRITION COUNTERMEASURES; RESISTANCE EXERCISE; FIBER FUNCTION; MYOSTATIN EXPRESSION; CONCURRENT EXERCISE; QUANTITATIVE PCR; TRICEPS SURAE; TIME-COURSE;
D O I
10.1152/ajpregu.90906.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Harber MP, Crane JD, Dickinson JM, Jemiolo B, Raue U, Trappe TA, Trappe SW. Protein synthesis and the expression of growth-related genes are altered by running in human vastus lateralis and soleus muscles. Am J Physiol Regul Integr Comp Physiol 296: R708-R714, 2009. First published December 31, 2008; doi:10.1152/ajpregu.90906.2008.-Recent evidence suggests aerobic exercise may help preserve soleus muscle mass during unloading. The purpose of this investigation was to examine the muscle-specific metabolic response to running as it relates to muscle growth. Mixed-muscle protein synthesis [fractional synthetic rate (FSR)] and gene expression (GE) were examined in the vastus lateralis (VL) and soleus (SOL) muscles from eight men (26 +/- 2 yr; V(over dot)O-2max 63 +/- 2 ml.kg(-1).min(-1)) before and after a 45-min level-grade treadmill run at 77 +/- 1% intensity. Muscle glycogen utilization was similar between muscles. Resting FSR was similar between the VL (0.080 +/- 0.007 %/h) and SOL (0.086 +/- 0.008 %/h) and was higher (P < 0.05) 24 h postexercise compared with rest for both muscles. The absolute change in FSR was not different between muscles (0.030 +/- 0.007 vs. 0.037 +/- 0.012 %/h for VL and SOL). At baseline, myostatin GE was approximately twofold higher (P < 0.05) in SOL compared with VL, while no other muscle-specific differences in GE were present. After running, myostatin GE was suppressed (P < 0.05) in both muscles at 4 h and was higher (P < 0.05) than baseline at 24 h for VL only. Muscle regulatory factor 4 mRNA was elevated (P < 0.05) at 4 h in both SOL and VL; MyoD and peroxisome-proliferator-activated receptor-gamma coactivator-1 alpha (PGC-1 alpha) were higher (P < 0.05) at 4 h, and forkhead box [FOXO]3A was higher at 24 h in SOL only, while muscle-RING-finger protein-1 (MuRF-1) was higher (P < 0.05) at 4 h in VL only. Myogenin and atrogin-1 GE were unaltered. The similar increases between muscles in FSR support running as part of the exercise countermeasure to preserve soleus mass during unloading. The subtle differences in GE suggest a potential mechanism for muscle-specific adaptations to chronic run training.
引用
收藏
页码:R708 / R714
页数:7
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