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Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation

Recent investigations have suggested that highly trained athletes may be less responsive to the ergogenic effects of β-alanine (BA) supplementation than recreationally active individuals due to their elevated muscle buffering capacity. We investigated whether training status influences the effect of...

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Autores principales: de Salles Painelli, Vitor, Saunders, Bryan, Sale, Craig, Harris, Roger Charles, Solis, Marina Yázigi, Roschel, Hamilton, Gualano, Bruno, Artioli, Guilherme Giannini, Lancha Jr., Antonio Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984416/
https://www.ncbi.nlm.nih.gov/pubmed/24500111
http://dx.doi.org/10.1007/s00726-014-1678-2
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author de Salles Painelli, Vitor
Saunders, Bryan
Sale, Craig
Harris, Roger Charles
Solis, Marina Yázigi
Roschel, Hamilton
Gualano, Bruno
Artioli, Guilherme Giannini
Lancha Jr., Antonio Herbert
author_facet de Salles Painelli, Vitor
Saunders, Bryan
Sale, Craig
Harris, Roger Charles
Solis, Marina Yázigi
Roschel, Hamilton
Gualano, Bruno
Artioli, Guilherme Giannini
Lancha Jr., Antonio Herbert
author_sort de Salles Painelli, Vitor
collection PubMed
description Recent investigations have suggested that highly trained athletes may be less responsive to the ergogenic effects of β-alanine (BA) supplementation than recreationally active individuals due to their elevated muscle buffering capacity. We investigated whether training status influences the effect of BA on repeated Wingate performance. Forty young males were divided into two groups according to their training status (trained: T, and non-trained: NT cyclists) and were randomly allocated to BA and a dextrose-based placebo (PL) groups, providing four experimental conditions: NTPL, NTBA, TPL, TBA. BA (6.4 g day(−1)) or PL was ingested for 4 weeks, with participants completing four 30-s lower-body Wingate bouts, separated by 3 min, before and after supplementation. Total work done was significantly increased following supplementation in both NTBA (p = 0.03) and TBA (p = 0.002), and it was significantly reduced in NTPL (p = 0.03) with no difference for TPL (p = 0.73). BA supplementation increased mean power output (MPO) in bout 4 for the NTBA group (p = 0.0004) and in bouts 1, 2 and 4 for the TBA group (p ≤ 0.05). No differences were observed in MPO for NTPL and TPL. BA supplementation was effective at improving repeated high-intensity cycling performance in both trained and non-trained individuals, highlighting the efficacy of BA as an ergogenic aid for high-intensity exercise regardless of the training status of the individual.
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spelling pubmed-39844162014-04-22 Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation de Salles Painelli, Vitor Saunders, Bryan Sale, Craig Harris, Roger Charles Solis, Marina Yázigi Roschel, Hamilton Gualano, Bruno Artioli, Guilherme Giannini Lancha Jr., Antonio Herbert Amino Acids Original Article Recent investigations have suggested that highly trained athletes may be less responsive to the ergogenic effects of β-alanine (BA) supplementation than recreationally active individuals due to their elevated muscle buffering capacity. We investigated whether training status influences the effect of BA on repeated Wingate performance. Forty young males were divided into two groups according to their training status (trained: T, and non-trained: NT cyclists) and were randomly allocated to BA and a dextrose-based placebo (PL) groups, providing four experimental conditions: NTPL, NTBA, TPL, TBA. BA (6.4 g day(−1)) or PL was ingested for 4 weeks, with participants completing four 30-s lower-body Wingate bouts, separated by 3 min, before and after supplementation. Total work done was significantly increased following supplementation in both NTBA (p = 0.03) and TBA (p = 0.002), and it was significantly reduced in NTPL (p = 0.03) with no difference for TPL (p = 0.73). BA supplementation increased mean power output (MPO) in bout 4 for the NTBA group (p = 0.0004) and in bouts 1, 2 and 4 for the TBA group (p ≤ 0.05). No differences were observed in MPO for NTPL and TPL. BA supplementation was effective at improving repeated high-intensity cycling performance in both trained and non-trained individuals, highlighting the efficacy of BA as an ergogenic aid for high-intensity exercise regardless of the training status of the individual. Springer Vienna 2014-02-06 2014 /pmc/articles/PMC3984416/ /pubmed/24500111 http://dx.doi.org/10.1007/s00726-014-1678-2 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
de Salles Painelli, Vitor
Saunders, Bryan
Sale, Craig
Harris, Roger Charles
Solis, Marina Yázigi
Roschel, Hamilton
Gualano, Bruno
Artioli, Guilherme Giannini
Lancha Jr., Antonio Herbert
Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
title Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
title_full Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
title_fullStr Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
title_full_unstemmed Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
title_short Influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
title_sort influence of training status on high-intensity intermittent performance in response to β-alanine supplementation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984416/
https://www.ncbi.nlm.nih.gov/pubmed/24500111
http://dx.doi.org/10.1007/s00726-014-1678-2
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