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The effects of phosphatidylserine on endocrine response to moderate intensity exercise

BACKGROUND: Previous research has indicated that phosphatidylserine (PS) supplementation has the potential to attenuate the serum cortisol response to acute exercise stress. Equivocal findings suggest that this effect might be dose dependent. This study aimed to examine the influence of short-term s...

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Autores principales: Starks, Michael A, Starks, Stacy L, Kingsley, Michael, Purpura, Martin, Jäger, Ralf
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2503954/
https://www.ncbi.nlm.nih.gov/pubmed/18662395
http://dx.doi.org/10.1186/1550-2783-5-11
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author Starks, Michael A
Starks, Stacy L
Kingsley, Michael
Purpura, Martin
Jäger, Ralf
author_facet Starks, Michael A
Starks, Stacy L
Kingsley, Michael
Purpura, Martin
Jäger, Ralf
author_sort Starks, Michael A
collection PubMed
description BACKGROUND: Previous research has indicated that phosphatidylserine (PS) supplementation has the potential to attenuate the serum cortisol response to acute exercise stress. Equivocal findings suggest that this effect might be dose dependent. This study aimed to examine the influence of short-term supplementation with a moderate dose of PS (600 mg per day) on plasma concentrations of cortisol, lactate, growth hormone and testosterone before, during, and following moderate intensity exercise in healthy males. METHODS: 10 healthy male subjects participated in the study. Each subject was assigned to ingest 600 mg PS or placebo per day for 10 days using a double-blind, placebo-controlled, crossover design. Serial venous blood samples were taken at rest, after a 15 minute moderate intensity exercise protocol on a cycle ergometer that consisted of five 3-minute incremental stages beginning at 65% and ending at 85% VO(2 max), and during a 65 minute passive recovery. Plasma samples were assessed for cortisol, growth hormone, testosterone, lactate and testosterone to cortisol ratio for treatment (PS or placebo). RESULTS: Mean peak cortisol concentrations and area under the curve (AUC) were lower following PS (39 ± 1% and 35 ± 0%, respectively) when compared to placebo (p < 0.05). PS increased AUC for testosterone to cortisol ratio (184 ± 5%) when compared to placebo (p < 0.05). PS and placebo supplementation had no effect on lactate or growth hormone levels. CONCLUSION: The findings suggest that PS is an effective supplement for combating exercise-induced stress and preventing the physiological deterioration that can accompany too much exercise. PS supplementation promotes a desired hormonal status for athletes by blunting increases in cortisol levels.
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spelling pubmed-25039542008-08-08 The effects of phosphatidylserine on endocrine response to moderate intensity exercise Starks, Michael A Starks, Stacy L Kingsley, Michael Purpura, Martin Jäger, Ralf J Int Soc Sports Nutr Research Article BACKGROUND: Previous research has indicated that phosphatidylserine (PS) supplementation has the potential to attenuate the serum cortisol response to acute exercise stress. Equivocal findings suggest that this effect might be dose dependent. This study aimed to examine the influence of short-term supplementation with a moderate dose of PS (600 mg per day) on plasma concentrations of cortisol, lactate, growth hormone and testosterone before, during, and following moderate intensity exercise in healthy males. METHODS: 10 healthy male subjects participated in the study. Each subject was assigned to ingest 600 mg PS or placebo per day for 10 days using a double-blind, placebo-controlled, crossover design. Serial venous blood samples were taken at rest, after a 15 minute moderate intensity exercise protocol on a cycle ergometer that consisted of five 3-minute incremental stages beginning at 65% and ending at 85% VO(2 max), and during a 65 minute passive recovery. Plasma samples were assessed for cortisol, growth hormone, testosterone, lactate and testosterone to cortisol ratio for treatment (PS or placebo). RESULTS: Mean peak cortisol concentrations and area under the curve (AUC) were lower following PS (39 ± 1% and 35 ± 0%, respectively) when compared to placebo (p < 0.05). PS increased AUC for testosterone to cortisol ratio (184 ± 5%) when compared to placebo (p < 0.05). PS and placebo supplementation had no effect on lactate or growth hormone levels. CONCLUSION: The findings suggest that PS is an effective supplement for combating exercise-induced stress and preventing the physiological deterioration that can accompany too much exercise. PS supplementation promotes a desired hormonal status for athletes by blunting increases in cortisol levels. BioMed Central 2008-07-28 /pmc/articles/PMC2503954/ /pubmed/18662395 http://dx.doi.org/10.1186/1550-2783-5-11 Text en Copyright © 2008 Starks et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Starks, Michael A
Starks, Stacy L
Kingsley, Michael
Purpura, Martin
Jäger, Ralf
The effects of phosphatidylserine on endocrine response to moderate intensity exercise
title The effects of phosphatidylserine on endocrine response to moderate intensity exercise
title_full The effects of phosphatidylserine on endocrine response to moderate intensity exercise
title_fullStr The effects of phosphatidylserine on endocrine response to moderate intensity exercise
title_full_unstemmed The effects of phosphatidylserine on endocrine response to moderate intensity exercise
title_short The effects of phosphatidylserine on endocrine response to moderate intensity exercise
title_sort effects of phosphatidylserine on endocrine response to moderate intensity exercise
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2503954/
https://www.ncbi.nlm.nih.gov/pubmed/18662395
http://dx.doi.org/10.1186/1550-2783-5-11
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