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辣椒素摄入对静息和运动时能量消耗和脂肪氧化的影响。

Effects of capsinoid ingestion on energy expenditure and lipid oxidation at rest and during exercise.

机构信息

Exercise Metabolism Research Group, Department of Kinesiology, McMaster University, 1280 Main Street West, Hamilton, Ontario, L8S 4K1, Canada.

出版信息

Nutr Metab (Lond). 2010 Aug 3;7:65. doi: 10.1186/1743-7075-7-65.


DOI:10.1186/1743-7075-7-65
PMID:20682072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2922296/
Abstract

BACKGROUND: The thermogenic and metabolic properties of capsinoids appear to mimic those of the more pungent sister compound capsaicin. However, few data exist on how capsinoid ingestion affects energy expenditure in humans and no data exist on its interaction with exercise. We aimed to determine how ingestion of capsinoids affected energy expenditure, lipid oxidation and blood metabolites at rest and during moderate intensity exercise. METHODS: Twelve healthy young men (age = 24.3 +/- 3 yr, BMI = 25.5 +/- 1.7 kg.m-2) were studied on two occasions in a double-blind design following ingestion of either placebo or 10 mg of purified capsinoids at rest, after 90 min of cycling at 55% VO2 peak, and for 30 min into recovery. Subjects ingested the capsules 30 min prior to exercise. RESULTS: At rest, following ingestion of capsinoids, we observed increases in VO2 and plasma norepinephrine levels, and decreases in concentrations of serum free fatty acids, plasma glycerol and the respiratory exchange ratio (all P < 0.05). At exercise onset, we observed a blunted accumulation of blood lactate with capsinoid ingestion vs. placebo (P < 0.05). There were no other significant differences between the conditions during or post-exercise. CONCLUSION: The ingestion of 10 mg of capsinoids increased adrenergic activity, energy expenditure, and resulted in a shift in substrate utilization toward lipid at rest but had little effect during exercise or recovery. The changes we observed confirm previous data on the thermogenic and metabolic effects of capsinoids at rest and further promote its potential role as an adjunct weight loss aid, in addition to diet and exercise.

摘要

背景:辣椒素类似物具有产热和代谢特性,似乎模仿了更辣的同源化合物辣椒素。然而,关于辣椒素类似物摄入如何影响人体能量消耗的数据很少,其与运动的相互作用也没有数据。我们旨在确定辣椒素类似物的摄入如何影响静息和中等强度运动时的能量消耗、脂肪氧化和血液代谢物。

方法:在双盲设计中,12 名健康年轻男性(年龄=24.3±3 岁,BMI=25.5±1.7kg.m-2)在两次试验中进行研究,分别在静息时、90 分钟 55%峰值摄氧量自行车运动后和恢复 30 分钟后摄入安慰剂或 10mg 纯化辣椒素。受试者在运动前 30 分钟内服用胶囊。

结果:在静息状态下,摄入辣椒素后,我们观察到 VO2 和血浆去甲肾上腺素水平升高,血清游离脂肪酸、血浆甘油和呼吸交换率降低(均 P<0.05)。在运动开始时,我们观察到与安慰剂相比,摄入辣椒素后血液乳酸的积累减少(P<0.05)。在运动中和运动后,其他条件没有明显差异。

结论:摄入 10mg 辣椒素可增加肾上腺素能活性和能量消耗,并导致静息时底物利用向脂肪转移,但在运动或恢复期间影响不大。我们观察到的变化证实了先前关于辣椒素在静息时的产热和代谢作用的研究数据,并进一步促进了其作为减肥辅助剂的潜在作用,除了饮食和运动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/db100a562937/1743-7075-7-65-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/e9a3a98d4643/1743-7075-7-65-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/190586080fe0/1743-7075-7-65-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/73206f060b86/1743-7075-7-65-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/a01066e341b1/1743-7075-7-65-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/db100a562937/1743-7075-7-65-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/e9a3a98d4643/1743-7075-7-65-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/190586080fe0/1743-7075-7-65-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/73206f060b86/1743-7075-7-65-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/a01066e341b1/1743-7075-7-65-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/331a/2922296/db100a562937/1743-7075-7-65-5.jpg

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本文引用的文献

[1]
Effect of capsinoids on energy metabolism in human subjects.

Br J Nutr. 2009-8-12

[2]
Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications.

Am J Clin Nutr. 2009-1

[3]
200th anniversary of lactate research in muscle.

Exerc Sport Sci Rev. 2008-7

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Cochrane Database Syst Rev. 2007-7-18

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Use of nonprescription dietary supplements for weight loss is common among Americans.

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Biosci Biotechnol Biochem. 2006-12

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Cochrane Database Syst Rev. 2006-10-18

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