Citrus Aurantium and caffeine complex versus placebo on biomarkers of metabolism: a double blind crossover design
Autor: | John R. McLester, Emily Bechke, Brian Kliszczewicz, Zackery Green, Cherilyn N. McLester, Cassie Williamson, Paul Bailey |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Blood Glucose Male Citrus medicine.medical_treatment chemistry.chemical_compound Norepinephrine 0302 clinical medicine Ingestion Insulin Nutrition and Dietetics Cross-Over Studies P-synephrine Epinephrine lcsh:RC1200-1245 Caffeine lcsh:Nutrition. Foods and food supply Anaerobic exercise medicine.drug Research Article Adult medicine.medical_specialty lcsh:TX341-641 Placebo 03 medical and health sciences Young Adult Double-Blind Method Internal medicine medicine Humans lcsh:Sports medicine Exercise Triglycerides 030109 nutrition & dietetics business.industry Repeated measures design 030229 sport sciences Crossover study Endocrinology Metabolism Glucose chemistry Dietary Supplements Exercise Test business Energy Metabolism Biomarkers Food Science |
Zdroj: | Journal of the International Society of Sports Nutrition Journal of the International Society of Sports Nutrition, Vol 16, Iss 1, Pp 1-7 (2019) |
ISSN: | 1550-2783 |
Popis: | 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 |
Databáze: | OpenAIRE |
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