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Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design
BACKGROUOND: The purpose of this study was to examine resting the metabolic response to the ingestion of a complex containing Citrus Aurantium + Caffeine (CA + C) and if its consumption influences metabolic recovery following a high-intensity anaerobic exercise bout in habitual caffeine users. METHO...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366059/ https://www.ncbi.nlm.nih.gov/pubmed/30728061 http://dx.doi.org/10.1186/s12970-019-0271-1 |
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author | Kliszczewicz, Brian Bechke, Emily Williamson, Cassie Green, Zackery Bailey, Paul McLester, John McLester, Cherilyn |
author_facet | Kliszczewicz, Brian Bechke, Emily Williamson, Cassie Green, Zackery Bailey, Paul McLester, John McLester, Cherilyn |
author_sort | Kliszczewicz, Brian |
collection | PubMed |
description | BACKGROUOND: The purpose of this study was to examine resting the metabolic response to the ingestion of a complex containing Citrus Aurantium + Caffeine (CA + C) and if its consumption influences metabolic recovery following a high-intensity anaerobic exercise bout in habitual caffeine users. METHODS: Ten physically active males (25.1 ± 3.9 years; weight 78.71 ± 9.53 kg; height 177.2 ± 4.6 cm; body fat 15.5 ± 3.13%) participated in this study. This study was performed in a double-blind, randomized crossover fashion consisting of two exhaustive exercise protocols. On each visit the participants consumed either a CA + C (100 mg of CA and 100 mg of C) or placebo (dextrose) capsule. After consumption, participants were monitored throughout a 45-min ingestion period, then completed a repeated Wingate protocol, and were then monitored throughout a 45-min recovery period. Metabolic function was measured through blood glucose, plasma insulin, plasma triglycerides, and plasma catecholamines: epinephrine (E) and norepinephrine (NE). Biomarkers were taken at four different time points; Ingestion period: baseline (I1), post-ingestion period (I2); Recovery period: immediately post-exercise (R1), post-recovery period (R2). RESULTS: A repeated measures ANOVA revealed significant time-dependent increases in plasma E and NE at I2 only in the CA + C trial (p < 0.05), and a significant decrease in blood glucose at I2 in the PLA trial (p < 0.05); however, no meaningful changes in glucose was observed following CA + C ingestion. No changes in insulin or triglycerides were observed during the ingestion period. No trial-dependent differences were observed in the Recovery period. All biomarkers of metabolic recovery were equivalent when evaluating R1 v R2. Participants recovered in a similar time-dependent manner in all markers of metabolism following the PLA and CA + C trials. CONCLUSION: The findings of this study suggested that normal recommended dosages of 100 mg CA + 100 mg C is sufficient to promote glucose sparing at rest, with modest increases in SNS activity; however, the individual role of CA or C in this response cannot be determined. |
format | Online Article Text |
id | pubmed-6366059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63660592019-02-15 Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design Kliszczewicz, Brian Bechke, Emily Williamson, Cassie Green, Zackery Bailey, Paul McLester, John McLester, Cherilyn J Int Soc Sports Nutr Research Article BACKGROUOND: The purpose of this study was to examine resting the metabolic response to the ingestion of a complex containing Citrus Aurantium + Caffeine (CA + C) and if its consumption influences metabolic recovery following a high-intensity anaerobic exercise bout in habitual caffeine users. METHODS: Ten physically active males (25.1 ± 3.9 years; weight 78.71 ± 9.53 kg; height 177.2 ± 4.6 cm; body fat 15.5 ± 3.13%) participated in this study. This study was performed in a double-blind, randomized crossover fashion consisting of two exhaustive exercise protocols. On each visit the participants consumed either a CA + C (100 mg of CA and 100 mg of C) or placebo (dextrose) capsule. After consumption, participants were monitored throughout a 45-min ingestion period, then completed a repeated Wingate protocol, and were then monitored throughout a 45-min recovery period. Metabolic function was measured through blood glucose, plasma insulin, plasma triglycerides, and plasma catecholamines: epinephrine (E) and norepinephrine (NE). Biomarkers were taken at four different time points; Ingestion period: baseline (I1), post-ingestion period (I2); Recovery period: immediately post-exercise (R1), post-recovery period (R2). RESULTS: A repeated measures ANOVA revealed significant time-dependent increases in plasma E and NE at I2 only in the CA + C trial (p < 0.05), and a significant decrease in blood glucose at I2 in the PLA trial (p < 0.05); however, no meaningful changes in glucose was observed following CA + C ingestion. No changes in insulin or triglycerides were observed during the ingestion period. No trial-dependent differences were observed in the Recovery period. All biomarkers of metabolic recovery were equivalent when evaluating R1 v R2. Participants recovered in a similar time-dependent manner in all markers of metabolism following the PLA and CA + C trials. CONCLUSION: The findings of this study suggested that normal recommended dosages of 100 mg CA + 100 mg C is sufficient to promote glucose sparing at rest, with modest increases in SNS activity; however, the individual role of CA or C in this response cannot be determined. BioMed Central 2019-02-06 /pmc/articles/PMC6366059/ /pubmed/30728061 http://dx.doi.org/10.1186/s12970-019-0271-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article Kliszczewicz, Brian Bechke, Emily Williamson, Cassie Green, Zackery Bailey, Paul McLester, John McLester, Cherilyn Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
title | Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
title_full | Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
title_fullStr | Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
title_full_unstemmed | Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
title_short | Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
title_sort | citrus aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366059/ https://www.ncbi.nlm.nih.gov/pubmed/30728061 http://dx.doi.org/10.1186/s12970-019-0271-1 |
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