The effect of caffeine dose on caffeine and paraxanthine changes in serum and saliva and CYP1A2 enzyme activity in athletes: a randomized placebo-controlled crossover trial.

IF 3.9 2区 医学 Q2 NUTRITION & DIETETICS Nutrition & Metabolism Pub Date : 2024-11-11 DOI:10.1186/s12986-024-00863-3
Natalia Główka, Jakub Malik, Jacek Anioła, Emilia E Zawieja, Agata Chmurzynska, Krzysztof Durkalec-Michalski
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Abstract

Background: Although caffeine (CAF) supplementation has been shown to improve exercise performance, its dose-dependent effect on CAF metabolism has not been sufficiently investigated. The aim of this study was to evaluate the effects of 3, 6 and 9 mg of CAF/kgBM on changes of CAF and paraxanthine (PRX) in the serum and saliva at four time-points.

Methods: In a randomized, double-blind, placebo-controlled crossover design, acute pre-exercise supplementation in 26 moderately-trained athletes, participating in high-intensity functional training (HIFT), was examined. The study protocol involved CAF/PRX biochemical analyses of serum and saliva with respect to CYP1A2 polymorphism and CYP1A2 enzyme activity.

Results: Despite significant differences between the serum and saliva levels of CAF and PRX, there was no difference in the PRX/CAF ratio. The interaction effect of dose and time-points for PRX concentration was revealed. The main effects of dose were observed for CAF and the PRX/CAF ratio. The main effect of time-points was registered only for serum CAF.

Conclusions: Dose- and time-dependent effect of CAF supplementation on CAF and PRX in the serum and saliva of athletes was confirmed, but there was no effect of the CAF dose on CYP1A2 enzyme activity, nor was there an interaction of CYP1A2 with enzyme inducibility. The CAF/PRX correlation indicated the possibility of interchangeable use of serum and/or saliva analyses in exercise studies.

Clinical trial registration: This trial was registered prospectively at ClinicalTrials.gov (NCT03822663, registration date: 30/01/2019).

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咖啡因剂量对运动员血清和唾液中咖啡因和副黄嘌呤变化以及 CYP1A2 酶活性的影响:随机安慰剂对照交叉试验。
背景:虽然咖啡因(CAF)补充剂已被证明可提高运动表现,但其对CAF代谢的剂量依赖性影响尚未得到充分研究。本研究旨在评估 3、6 和 9 毫克 CAF/kgBM 在四个时间点对血清和唾液中 CAF 和副黄嘌呤(PRX)变化的影响:采用随机、双盲、安慰剂对照交叉设计,对参加高强度功能训练(HIFT)的 26 名中度训练运动员进行急性运动前补充。研究方案包括对血清和唾液中的 CYP1A2 多态性和 CYP1A2 酶活性进行 CAF/PRX 生化分析:结果:尽管血清和唾液中的 CAF 和 PRX 含量存在明显差异,但 PRX/CAF 比率却没有差异。剂量和时间点对 PRX 浓度的交互效应显现出来。剂量对 CAF 和 PRX/CAF 比率有主效应。只有血清 CAF 存在时间点的主要效应:结论:补充 CAF 对运动员血清和唾液中 CAF 和 PRX 的剂量和时间依赖性效应得到证实,但 CAF 剂量对 CYP1A2 酶活性没有影响,CYP1A2 与酶诱导性之间也没有相互作用。CAF/PRX的相关性表明,在运动研究中可以互换使用血清和/或唾液分析:本试验在 ClinicalTrials.gov 进行了前瞻性注册(NCT03822663,注册日期:2019 年 1 月 30 日)。
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来源期刊
Nutrition & Metabolism
Nutrition & Metabolism 医学-营养学
CiteScore
8.40
自引率
0.00%
发文量
78
审稿时长
4-8 weeks
期刊介绍: Nutrition & Metabolism publishes studies with a clear focus on nutrition and metabolism with applications ranging from nutrition needs, exercise physiology, clinical and population studies, as well as the underlying mechanisms in these aspects. The areas of interest for Nutrition & Metabolism encompass studies in molecular nutrition in the context of obesity, diabetes, lipedemias, metabolic syndrome and exercise physiology. Manuscripts related to molecular, cellular and human metabolism, nutrient sensing and nutrient–gene interactions are also in interest, as are submissions that have employed new and innovative strategies like metabolomics/lipidomics or other omic-based biomarkers to predict nutritional status and metabolic diseases. Key areas we wish to encourage submissions from include: -how diet and specific nutrients interact with genes, proteins or metabolites to influence metabolic phenotypes and disease outcomes; -the role of epigenetic factors and the microbiome in the pathogenesis of metabolic diseases and their influence on metabolic responses to diet and food components; -how diet and other environmental factors affect epigenetics and microbiota; the extent to which genetic and nongenetic factors modify personal metabolic responses to diet and food compositions and the mechanisms involved; -how specific biologic networks and nutrient sensing mechanisms attribute to metabolic variability.
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