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Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy
INTRODUCTION: The lipid messenger phosphatidic acid (PA) plays a critical role in the stimulation of mTOR signaling. However, the mechanism by which PA stimulates mTOR is currently unknown. Therefore, the purpose of this study was to compare the effects of various PA precursors and phospholipids on...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066292/ https://www.ncbi.nlm.nih.gov/pubmed/24959196 http://dx.doi.org/10.1186/1743-7075-11-29 |
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author | Joy, Jordan M Gundermann, David M Lowery, Ryan P Jäger, Ralf McCleary, Sean A Purpura, Martin Roberts, Michael D Wilson, Stephanie MC Hornberger, Troy A Wilson, Jacob M |
author_facet | Joy, Jordan M Gundermann, David M Lowery, Ryan P Jäger, Ralf McCleary, Sean A Purpura, Martin Roberts, Michael D Wilson, Stephanie MC Hornberger, Troy A Wilson, Jacob M |
author_sort | Joy, Jordan M |
collection | PubMed |
description | INTRODUCTION: The lipid messenger phosphatidic acid (PA) plays a critical role in the stimulation of mTOR signaling. However, the mechanism by which PA stimulates mTOR is currently unknown. Therefore, the purpose of this study was to compare the effects of various PA precursors and phospholipids on their ability to stimulate mTOR signaling and its ability to augment resistance training-induced changes in body composition and performance. METHODS: In phase one, C(2)C(12) myoblasts cells were stimulated with different phospholipids and phospholipid precursors derived from soy and egg sources. The ratio of phosphorylated p70 (P-p70-389) to total p70 was then used as readout for mTOR signaling. In phase two, resistance trained subjects (n = 28, 21 ± 3 years, 77 ± 4 kg, 176 ± 9 cm) consumed either 750 mg PA daily or placebo and each took part in an 8 week periodized resistance training program. RESULTS: In phase one, soy-phosphatidylserine, soy-Lyso-PA, egg-PA, and soy-PA stimulated mTOR signaling, and the effects of soy-PA (+636%) were significantly greater than egg-PA (+221%). In phase two, PA significantly increased lean body mass (+2.4 kg), cross sectional area (+1.0 cm), and leg press strength (+51.9 kg) over placebo. CONCLUSION: PA significantly activates mTOR and significantly improved responses in skeletal muscle hypertrophy, lean body mass, and maximal strength to resistance exercise. |
format | Online Article Text |
id | pubmed-4066292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40662922014-06-24 Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy Joy, Jordan M Gundermann, David M Lowery, Ryan P Jäger, Ralf McCleary, Sean A Purpura, Martin Roberts, Michael D Wilson, Stephanie MC Hornberger, Troy A Wilson, Jacob M Nutr Metab (Lond) Research INTRODUCTION: The lipid messenger phosphatidic acid (PA) plays a critical role in the stimulation of mTOR signaling. However, the mechanism by which PA stimulates mTOR is currently unknown. Therefore, the purpose of this study was to compare the effects of various PA precursors and phospholipids on their ability to stimulate mTOR signaling and its ability to augment resistance training-induced changes in body composition and performance. METHODS: In phase one, C(2)C(12) myoblasts cells were stimulated with different phospholipids and phospholipid precursors derived from soy and egg sources. The ratio of phosphorylated p70 (P-p70-389) to total p70 was then used as readout for mTOR signaling. In phase two, resistance trained subjects (n = 28, 21 ± 3 years, 77 ± 4 kg, 176 ± 9 cm) consumed either 750 mg PA daily or placebo and each took part in an 8 week periodized resistance training program. RESULTS: In phase one, soy-phosphatidylserine, soy-Lyso-PA, egg-PA, and soy-PA stimulated mTOR signaling, and the effects of soy-PA (+636%) were significantly greater than egg-PA (+221%). In phase two, PA significantly increased lean body mass (+2.4 kg), cross sectional area (+1.0 cm), and leg press strength (+51.9 kg) over placebo. CONCLUSION: PA significantly activates mTOR and significantly improved responses in skeletal muscle hypertrophy, lean body mass, and maximal strength to resistance exercise. BioMed Central 2014-06-16 /pmc/articles/PMC4066292/ /pubmed/24959196 http://dx.doi.org/10.1186/1743-7075-11-29 Text en Copyright © 2014 Joy et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Joy, Jordan M Gundermann, David M Lowery, Ryan P Jäger, Ralf McCleary, Sean A Purpura, Martin Roberts, Michael D Wilson, Stephanie MC Hornberger, Troy A Wilson, Jacob M Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy |
title | Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy |
title_full | Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy |
title_fullStr | Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy |
title_full_unstemmed | Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy |
title_short | Phosphatidic acid enhances mTOR signaling and resistance exercise induced hypertrophy |
title_sort | phosphatidic acid enhances mtor signaling and resistance exercise induced hypertrophy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066292/ https://www.ncbi.nlm.nih.gov/pubmed/24959196 http://dx.doi.org/10.1186/1743-7075-11-29 |
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