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Myostatin Inhibition-Induced Increase in Muscle Mass and Strength Was Amplified by Resistance Exercise Training, and Dietary Essential Amino Acids Improved Muscle Quality in Mice

Authors
Jang, JiwoongPark, SangheeKim, YeongminJung, JiyeonLee, JinseokChang, YewonLee, Sang PilPark, Bum-ChanWolfe, Robert R.Choi, Cheol SooKim, Il-Young
Issue Date
May-2021
Publisher
MDPI
Keywords
deuterium oxide; essential amino acids; mass spectrometry; protein turnover; resistance exercise training; soluble activin receptor type IIB
Citation
NUTRIENTS, v.13, no.5
Journal Title
NUTRIENTS
Volume
13
Number
5
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/81383
DOI
10.3390/nu13051508
ISSN
2072-6643
Abstract
It has been frequently reported that myostatin inhibition increases muscle mass, but decreases muscle quality (i.e., strength/muscle mass). Resistance exercise training (RT) and essential amino acids (EAAs) are potent anabolic stimuli that synergistically increase muscle mass through changes in muscle protein turnover. In addition, EAAs are known to stimulate mitochondrial biogenesis. We have investigated if RT amplifies the anabolic potential of myostatin inhibition while EAAs enhance muscle quality through stimulations of mitochondrial biogenesis and/or muscle protein turnover. Mice were assigned into ACV (myostatin inhibitor), ACV+EAA, ACV+RT, ACV+EAA +RT, or control (CON) over 4 weeks. RT, but not EAA, increased muscle mass above ACV. Despite differences in muscle mass gain, myofibrillar protein synthesis was stimulated similarly in all vs. CON, suggesting a role for changes in protein breakdown in muscle mass gains. There were increases in MyoD expression but decreases in Atrogin-1/MAFbx expression in ACV+EAA, ACV+RT, and ACV+EAA+RT vs. CON. EAA increased muscle quality (e.g., grip strength and maximal carrying load) without corresponding changes in markers of mitochondrial biogenesis and neuromuscular junction stability. In conclusion, RT amplifies muscle mass and strength through changes in muscle protein turnover in conjunction with changes in implicated signaling, while EAAs enhance muscle quality through unknown mechanisms.
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