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瓜尤萨叶提取物对情绪、认知和运动认知表现以及血压、心率和心室复极化的急性剂量反应效应。

Acute, dose-response effects of guayusa leaf extract on mood, cognitive and motor-cognitive performance, and blood pressure, heart rate, and ventricular repolarization.

作者信息

Helwig Nathaniel J, Schwager Laura E, Berry Alexander C, Zucker Anna C, Venenga Jacob S, Sterbenz Samantha C, Jenkins Nathaniel D M

机构信息

University of Iowa, Department of Health and Human Physiology, Iowa City, IA, USA.

University of Iowa, Abboud Cardiovascular Research Center, Iowa City, IA, USA.

出版信息

J Int Soc Sports Nutr. 2024 Dec;21(1):2379424. doi: 10.1080/15502783.2024.2379424. Epub 2024 Jul 16.

DOI:10.1080/15502783.2024.2379424
PMID:39014963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11257001/
Abstract

PURPOSE

We conducted a randomized, double-blind, placebo-controlled crossover trial in young adults to examine the dose-dependent (600 mg versus 1200 mg), acute effects of consumption of an tea extract (GLE) on mood, cognitive and motor-cognitive performance, as well as its acute cardiovascular effects.

METHODS

Twenty-five adults (mean ± SD, age = 28 ± 7 y; 9 M/16 F) completed familiarization and then three randomly ordered experimental visits where they consumed either 600 mg (GLE) or 1200 mg (GLE) GLE or placebo (PLA). Following supplement consumption, participants completed a mood state survey, assessments of perceived jitteriness, energy, and focus, and neurocognitive and motor-cognitive testing. Blood pressure (BP), heart rate, and QT interval length were determined before and after supplementation.

RESULTS

GLE significantly improved total mood disturbance (mean ± SE difference = -6.9 ± 2.6 au,  = 0.034), fatigue-inertia (-2.84 ± 0.89 au,  = 0.008), perceived energy (+13.00 ± 4.49 au;  = 0.02), motor speed (+4.52 ± 1.42 au,  = 0.008), and psychomotor speed (+7.20 ± 2.16 au,  = 0.005) relative to PLA. GLE also improved psychomotor speed (+5.08 ± 2.16 ms,  = 0.045) and uniquely increased motor-cognitive performance as reflected by a decrease in reaction time (-0.106 ± 0.04 ms,  = 0.026) during a neurocognitive hop test. The effect of GLE on jitteriness was both dose- and sex-dependent. Jitteriness increased with increasing GLE dose in women only ( < 0.001). Both GLE and GLE similarly increased systolic and diastolic BP by 4-5 mmHg ( ≤ 0.022). Neither GLE nor GLE acutely influenced QTc length ( = 0.31).

CONCLUSIONS

The goal of GLE supplementation should be considered when selecting a dosing strategy. Lower dosages of GLE (e.g. 600 mg) appear to optimize cognitive and mood-related outcomes while limiting side-effects such as jitteriness in women, and higher dosages may be necessary (e.g. 1200 mg) to promote improvements in motor-cognitive performance.

摘要

目的

我们在年轻成年人中进行了一项随机、双盲、安慰剂对照的交叉试验,以研究绿茶提取物(GLE)摄入量(600毫克与1200毫克)对情绪、认知和运动认知表现的剂量依赖性急性影响,以及其急性心血管效应。

方法

25名成年人(平均±标准差,年龄=28±7岁;9名男性/16名女性)完成了预实验,然后进行了三次随机排序的实验访视,期间他们分别服用600毫克(GLE)或1200毫克(GLE)的GLE或安慰剂(PLA)。补充剂服用后,参与者完成了情绪状态调查、对紧张感、精力和注意力的感知评估,以及神经认知和运动认知测试。在补充前后测定血压(BP)、心率和QT间期长度。

结果

与PLA相比,GLE显著改善了总情绪紊乱(平均±标准误差异=-6.9±2.6au,P=0.034)、疲劳-惰性(-2.84±0.89au,P=0.008)、感知精力(+13.00±4.49au;P=0.02)、运动速度(+4.52±1.42au,P=0.008)和心理运动速度(+7.20±2.16au,P=0.005)。GLE还改善了心理运动速度(+5.08±2.16毫秒,P=0.045),并独特地提高了运动认知表现,这在神经认知单脚跳测试中反应时间的减少(-0.106±0.04毫秒,P=0.026)中得到体现。GLE对紧张感的影响具有剂量和性别依赖性。仅在女性中,紧张感随GLE剂量增加而增加(P<0.001)。GLE和GLE均使收缩压和舒张压类似地升高4-5mmHg(P≤0.022)。GLE和GLE均未急性影响QTc长度(P=0.31)。

结论

在选择给药策略时应考虑补充GLE的目标。较低剂量的GLE(例如600毫克)似乎能优化认知和情绪相关结果,同时限制女性的紧张感等副作用,而较高剂量(例如1200毫克)可能是促进运动认知表现改善所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/10e6f9d80b3a/RSSN_A_2379424_F0008_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/90dcfc7cc77e/RSSN_A_2379424_F0001_B.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/bc361a8cbc03/RSSN_A_2379424_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/70a4fff8e6b3/RSSN_A_2379424_F0006_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/a7a512e15253/RSSN_A_2379424_F0007_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/10e6f9d80b3a/RSSN_A_2379424_F0008_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/90dcfc7cc77e/RSSN_A_2379424_F0001_B.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/e684afc3197e/RSSN_A_2379424_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/74cc44914812/RSSN_A_2379424_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/bc361a8cbc03/RSSN_A_2379424_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0079/11257001/70a4fff8e6b3/RSSN_A_2379424_F0006_B.jpg
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