Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design

Abstract 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 user...

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Main Authors: Brian Kliszczewicz, Emily Bechke, Cassie Williamson, Zackery Green, Paul Bailey, John McLester, Cherilyn McLester
Format: Article
Language:English
Published: BMC 2019-02-01
Series:Journal of the International Society of Sports Nutrition
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12970-019-0271-1
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spelling doaj-da0626e687fd4a2e8b094596d1620f542020-11-25T03:20:12ZengBMCJournal of the International Society of Sports Nutrition1550-27832019-02-011611710.1186/s12970-019-0271-1Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover designBrian Kliszczewicz0Emily Bechke1Cassie Williamson2Zackery Green3Paul Bailey4John McLester5Cherilyn McLester6Department of Exercise Science and Sport Management, Kennesaw State UniversityDepartment of Exercise Science and Sport Management, Kennesaw State UniversityDepartment of Exercise Science and Sport Management, Kennesaw State UniversityDepartment of Exercise Science and Sport Management, Kennesaw State UniversityDepartment of Exercise Science and Sport Management, Kennesaw State UniversityDepartment of Exercise Science and Sport Management, Kennesaw State UniversityDepartment of Exercise Science and Sport Management, Kennesaw State UniversityAbstract 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.http://link.springer.com/article/10.1186/s12970-019-0271-1P-synephrineMetabolismCaffeineGlucoseInsulin
collection DOAJ
language English
format Article
sources DOAJ
author Brian Kliszczewicz
Emily Bechke
Cassie Williamson
Zackery Green
Paul Bailey
John McLester
Cherilyn McLester
spellingShingle Brian Kliszczewicz
Emily Bechke
Cassie Williamson
Zackery Green
Paul Bailey
John McLester
Cherilyn McLester
Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design
Journal of the International Society of Sports Nutrition
P-synephrine
Metabolism
Caffeine
Glucose
Insulin
author_facet Brian Kliszczewicz
Emily Bechke
Cassie Williamson
Zackery Green
Paul Bailey
John McLester
Cherilyn McLester
author_sort Brian Kliszczewicz
title 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_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_sort citrus aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design
publisher BMC
series Journal of the International Society of Sports Nutrition
issn 1550-2783
publishDate 2019-02-01
description Abstract 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.
topic P-synephrine
Metabolism
Caffeine
Glucose
Insulin
url http://link.springer.com/article/10.1186/s12970-019-0271-1
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