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The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study
INTRODUCTION: Krill oil supplementation has been shown to improve postexercise immune function; however, its effect on muscle hypertrophy is currently unknown. Therefore, the aim of present study was to investigate the ability of krill oil to stimulate mTOR signaling and its ability to augment resis...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944280/ https://www.ncbi.nlm.nih.gov/pubmed/29854443 http://dx.doi.org/10.1155/2018/7625981 |
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author | Georges, John Sharp, Matthew H. Lowery, Ryan P. Wilson, Jacob M. Purpura, Martin Hornberger, Troy A. Harding, Flint Johnson, James H. Peele, David M. Jäger, Ralf |
author_facet | Georges, John Sharp, Matthew H. Lowery, Ryan P. Wilson, Jacob M. Purpura, Martin Hornberger, Troy A. Harding, Flint Johnson, James H. Peele, David M. Jäger, Ralf |
author_sort | Georges, John |
collection | PubMed |
description | INTRODUCTION: Krill oil supplementation has been shown to improve postexercise immune function; however, its effect on muscle hypertrophy is currently unknown. Therefore, the aim of present study was to investigate the ability of krill oil to stimulate mTOR signaling and its ability to augment resistance training-induced changes in body composition and performance. METHODS: C(2)C(12) myoblasts cells were stimulated with krill oil or soy-derived phosphatidylcholine (S-PC), and then, the ratio of P-p70-389 to total p70 was used as readout for mTOR signaling. In double-blind, placebo-controlled study, resistance trained subjects consumed either 3 g krill oil daily or placebo, and each took part in an 8-week periodized resistance training program. Body composition, maximal strength, peak power, and rate of perceived recovery were assessed collectively at the end of weeks 0 and 8. In addition, safety parameters (comprehensive metabolic panel (CMP), complete blood count (CBC), and urine analysis (UA)) and cognitive performance were measured pre- and posttesting. RESULTS: Krill oil significantly stimulated mTOR signaling in comparison to S-PC and control. No differences for markers on the CMP, CBC, or UA were observed. Krill oil significantly increased lean body mass from baseline (p=0.021, 1.4 kg, +2.1%); however, there were no statistically significant differences between groups for any measures taken. CONCLUSION: Krill oil activates mTOR signaling. Krill oil supplementation in athletes is safe, and its effect on resistance exercise deserves further research. |
format | Online Article Text |
id | pubmed-5944280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-59442802018-05-31 The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study Georges, John Sharp, Matthew H. Lowery, Ryan P. Wilson, Jacob M. Purpura, Martin Hornberger, Troy A. Harding, Flint Johnson, James H. Peele, David M. Jäger, Ralf J Nutr Metab Research Article INTRODUCTION: Krill oil supplementation has been shown to improve postexercise immune function; however, its effect on muscle hypertrophy is currently unknown. Therefore, the aim of present study was to investigate the ability of krill oil to stimulate mTOR signaling and its ability to augment resistance training-induced changes in body composition and performance. METHODS: C(2)C(12) myoblasts cells were stimulated with krill oil or soy-derived phosphatidylcholine (S-PC), and then, the ratio of P-p70-389 to total p70 was used as readout for mTOR signaling. In double-blind, placebo-controlled study, resistance trained subjects consumed either 3 g krill oil daily or placebo, and each took part in an 8-week periodized resistance training program. Body composition, maximal strength, peak power, and rate of perceived recovery were assessed collectively at the end of weeks 0 and 8. In addition, safety parameters (comprehensive metabolic panel (CMP), complete blood count (CBC), and urine analysis (UA)) and cognitive performance were measured pre- and posttesting. RESULTS: Krill oil significantly stimulated mTOR signaling in comparison to S-PC and control. No differences for markers on the CMP, CBC, or UA were observed. Krill oil significantly increased lean body mass from baseline (p=0.021, 1.4 kg, +2.1%); however, there were no statistically significant differences between groups for any measures taken. CONCLUSION: Krill oil activates mTOR signaling. Krill oil supplementation in athletes is safe, and its effect on resistance exercise deserves further research. Hindawi 2018-04-26 /pmc/articles/PMC5944280/ /pubmed/29854443 http://dx.doi.org/10.1155/2018/7625981 Text en Copyright © 2018 John Georges et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Georges, John Sharp, Matthew H. Lowery, Ryan P. Wilson, Jacob M. Purpura, Martin Hornberger, Troy A. Harding, Flint Johnson, James H. Peele, David M. Jäger, Ralf The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study |
title | The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study |
title_full | The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study |
title_fullStr | The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study |
title_full_unstemmed | The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study |
title_short | The Effects of Krill Oil on mTOR Signaling and Resistance Exercise: A Pilot Study |
title_sort | effects of krill oil on mtor signaling and resistance exercise: a pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944280/ https://www.ncbi.nlm.nih.gov/pubmed/29854443 http://dx.doi.org/10.1155/2018/7625981 |
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