Regulation of Skeletal Muscle Function by Amino Acids

被引:182
作者
Kamei, Yasutomi [1 ]
Hatazawa, Yukino [1 ,2 ]
Uchitomi, Ran [1 ]
Yoshimura, Ryoji [1 ,3 ]
Miura, Shinji [4 ]
机构
[1] Kyoto Prefectural Univ, Grad Sch Life & Environm Sci, Kyoto 6068522, Japan
[2] Ajinomoto Co Inc, Kawasaki, Kanagawa 2108681, Japan
[3] Nagasaki Int Univ, Fac Hlth Management, Dept Hlth & Nutr, Nagasaki 8593298, Japan
[4] Univ Shizuoka, Grad Sch Nutr & Environm Sci, Shizuoka 4228526, Japan
关键词
amino acid; skeletal muscle; PGC1; alpha; exercise; energy expenditure; branched-chain amino acid (BCAA); leucine; beta-hydroxy-beta-methylbutyrate (HMB); beta-aminoisobutyric acid (BAIBA); metabolic diseases; BETA-AMINOISOBUTYRIC ACID; MYOFIBRILLAR PROTEIN; SLOW-TWITCH; SUPPLEMENTATION; METHYLBUTYRATE; LEUCINE; PHOSPHORYLATION; METABOLISM; CATABOLISM; EXPRESSION;
D O I
10.3390/nu12010261
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Amino acids are components of proteins that also exist free-form in the body; their functions can be divided into (1) nutritional, (2) sensory, and (3) biological regulatory roles. The skeletal muscle, which is the largest organ in the human body, representing similar to 40% of the total body weight, plays important roles in exercise, energy expenditure, and glucose/amino acid usage-processes that are modulated by various amino acids and their metabolites. In this review, we address the metabolism and function of amino acids in the skeletal muscle. The expression of PGC1 alpha, a transcriptional coactivator, is increased in the skeletal muscle during exercise. PGC1 alpha activates branched-chain amino acid (BCAA) metabolism and is used for energy in the tricarboxylic acid (TCA) cycle. Leucine, a BCAA, and its metabolite, beta-hydroxy-beta-methylbutyrate (HMB), both activate mammalian target of rapamycin complex 1 (mTORC1) and increase protein synthesis, but the mechanisms of activation appear to be different. The metabolite of valine (another BCAA), beta-aminoisobutyric acid (BAIBA), is increased by exercise, is secreted by the skeletal muscle, and acts on other tissues, such as white adipose tissue, to increase energy expenditure. In addition, several amino acid-related molecules reportedly activate skeletal muscle function. Oral 5-aminolevulinic acid (ALA) supplementation can protect against mild hyperglycemia and help prevent type 2 diabetes. beta-alanine levels are decreased in the skeletal muscles of aged mice. beta-alanine supplementation increased the physical performance and improved the executive function induced by endurance exercise in middle-aged individuals. Further studies focusing on the effects of amino acids and their metabolites on skeletal muscle function will provide data essential for the production of food supplements for older adults, athletes, and individuals with metabolic diseases.
引用
收藏
页数:11
相关论文
共 60 条
[41]   β-Hydroxy β-Methylbutyrate Improves Dexamethasone-Induced Muscle Atrophy by Modulating the Muscle Degradation Pathway in SD Rat [J].
Noh, Kyung Kyun ;
Chung, Ki Wung ;
Choi, Yeon Ja ;
Park, Min Hi ;
Jang, Eun Ji ;
Park, Chan Hum ;
Yoon, Changshin ;
Kim, Nam Deuk ;
Kim, Mi Kyung ;
Chung, Hae Young .
PLOS ONE, 2014, 9 (07)
[42]   The Effects of Leucine-Enriched Branched-Chain Amino Acid Supplementation on Recovery After High-Intensity Resistance Exercise [J].
Osmond, Adam D. ;
Directo, Dean J. ;
Elam, Marcus L. ;
Juache, Gabriela ;
Kreipke, Vince C. ;
Saralegui, Desiree E. ;
Wildman, Robert ;
Wong, Michael ;
Jo, Edward .
INTERNATIONAL JOURNAL OF SPORTS PHYSIOLOGY AND PERFORMANCE, 2019, 14 (08) :1081-1088
[43]   Leucine minimizes denervation-induced skeletal muscle atrophy of rats through akt/mtor signaling pathways [J].
Ribeiro, Carolina B. ;
Christofoletti, Daiane C. ;
Pezolato, Vitor A. ;
Marqueti Durigan, Rita de Cassia ;
Prestes, Jonato ;
Tibana, Ramires A. ;
Pereira, Elaine C. L. ;
de Sousa Neto, Ivo V. ;
Durigan, Joao L. Q. ;
da Silva, Carlos A. .
FRONTIERS IN PHYSIOLOGY, 2015, 6
[44]   β-Aminoisobutyric Acid Induces Browning of White Fat and Hepatic β-Oxidation and Is Inversely Correlated with Cardiometabolic Risk Factors [J].
Roberts, Lee D. ;
Bostrom, Pontus ;
O'Sullivan, John F. ;
Schinzel, Robert T. ;
Lewis, Gregory D. ;
Dejam, Andre ;
Lee, Youn-Kyoung ;
Palma, Melinda J. ;
Calhoun, Sondra ;
Georgiadi, Anastasia ;
Chen, Ming-Huei ;
Ramachandran, Vasan S. ;
Larson, Martin G. ;
Bouchard, Claude ;
Rankinen, Tuomo ;
Souza, Amanda L. ;
Clish, Clary B. ;
Wang, Thomas J. ;
Estall, Jennifer L. ;
Soukas, Alexander A. ;
Cowan, Chad A. ;
Spiegelman, Bruce M. ;
Gerszten, Robert E. .
CELL METABOLISM, 2014, 19 (01) :96-108
[45]   5-aminolevulinic acid (ALA) deficiency causes impaired glucose tolerance and insulin resistance coincident with an attenuation of mitochondrial function in aged mice [J].
Saitoh, Shinichi ;
Okano, Satoshi ;
Nohara, Hidekazu ;
Nakano, Hiroshi ;
Shirasawa, Nobuyuki ;
Naito, Akira ;
Yamamoto, Masayuki ;
Kelly, Vincent P. ;
Takahashi, Kiwamu ;
Tanaka, Tohru ;
Nakajima, Motowo ;
Nakajima, Osamu .
PLOS ONE, 2018, 13 (01)
[46]   LYSINE REQUIREMENTS AND WHOLE-BODY PROTEIN-TURNOVER IN GROWING PIGS [J].
SALTER, DN ;
MONTGOMERY, AI ;
HUDSON, A ;
QUELCH, DB ;
ELLIOTT, RJ .
BRITISH JOURNAL OF NUTRITION, 1990, 63 (03) :503-513
[47]   L-Lysine suppresses myofibrillar protein degradation and autophagy in skeletal muscles of senescence-accelerated mouse prone 8 [J].
Sato, Tomonori ;
Ito, Yoshiaki ;
Nagasawa, Takashi .
BIOGERONTOLOGY, 2017, 18 (01) :85-95
[48]   Skeletal Muscle-specific PGC-1α Overexpression Suppresses Atherosclerosis in Apolipoprotein E-Knockout Mice [J].
Shimba, Yuki ;
Togawa, Hanako ;
Senoo, Nanami ;
Ikeda, Masahiko ;
Miyoshi, Noriyuki ;
Morita, Akihito ;
Miura, Shinji .
SCIENTIFIC REPORTS, 2019, 9 (1)
[49]   Exercise promotes BCAA catabolism: Effects of BCAA supplementation on skeletal muscle during exercise [J].
Shimomura, Y ;
Murakami, T ;
Nakai, N ;
Nagasaki, M ;
Harris, RA .
JOURNAL OF NUTRITION, 2004, 134 (06) :1583S-1587S
[50]   Physiological and pathological roles of branched-chain amino acids in the regulation of protein and energy metabolism and neurological functions [J].
Shimomura, Yoshiharu ;
Kitaura, Yasuyuki .
PHARMACOLOGICAL RESEARCH, 2018, 133 :215-217