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Regulation of Skeletal Muscle Function by Amino Acids
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 ~40% of the total body weight, plays im...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019684/ https://www.ncbi.nlm.nih.gov/pubmed/31963899 http://dx.doi.org/10.3390/nu12010261 |
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author | Kamei, Yasutomi Hatazawa, Yukino Uchitomi, Ran Yoshimura, Ryoji Miura, Shinji |
author_facet | Kamei, Yasutomi Hatazawa, Yukino Uchitomi, Ran Yoshimura, Ryoji Miura, Shinji |
author_sort | Kamei, Yasutomi |
collection | PubMed |
description | 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 ~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 PGC1α, a transcriptional coactivator, is increased in the skeletal muscle during exercise. PGC1α activates branched-chain amino acid (BCAA) metabolism and is used for energy in the tricarboxylic acid (TCA) cycle. Leucine, a BCAA, and its metabolite, β-hydroxy-β-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), β-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. β-alanine levels are decreased in the skeletal muscles of aged mice. β-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. |
format | Online Article Text |
id | pubmed-7019684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70196842020-03-09 Regulation of Skeletal Muscle Function by Amino Acids Kamei, Yasutomi Hatazawa, Yukino Uchitomi, Ran Yoshimura, Ryoji Miura, Shinji Nutrients Communication 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 ~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 PGC1α, a transcriptional coactivator, is increased in the skeletal muscle during exercise. PGC1α activates branched-chain amino acid (BCAA) metabolism and is used for energy in the tricarboxylic acid (TCA) cycle. Leucine, a BCAA, and its metabolite, β-hydroxy-β-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), β-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. β-alanine levels are decreased in the skeletal muscles of aged mice. β-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. MDPI 2020-01-19 /pmc/articles/PMC7019684/ /pubmed/31963899 http://dx.doi.org/10.3390/nu12010261 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Kamei, Yasutomi Hatazawa, Yukino Uchitomi, Ran Yoshimura, Ryoji Miura, Shinji Regulation of Skeletal Muscle Function by Amino Acids |
title | Regulation of Skeletal Muscle Function by Amino Acids |
title_full | Regulation of Skeletal Muscle Function by Amino Acids |
title_fullStr | Regulation of Skeletal Muscle Function by Amino Acids |
title_full_unstemmed | Regulation of Skeletal Muscle Function by Amino Acids |
title_short | Regulation of Skeletal Muscle Function by Amino Acids |
title_sort | regulation of skeletal muscle function by amino acids |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019684/ https://www.ncbi.nlm.nih.gov/pubmed/31963899 http://dx.doi.org/10.3390/nu12010261 |
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