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不同剂量咖啡因对代谢、儿茶酚胺及运动表现的反应。

Metabolic, catecholamine, and exercise performance responses to various doses of caffeine.

作者信息

Graham T E, Spriet L L

机构信息

School of Human Biology, University of Guelph, Ontario, Canada.

出版信息

J Appl Physiol (1985). 1995 Mar;78(3):867-74. doi: 10.1152/jappl.1995.78.3.867.

DOI:10.1152/jappl.1995.78.3.867
PMID:7775331
Abstract

This study examined the exercise responses of well-trained endurance athletes to various doses of caffeine to evaluate the impact of the drug on exercise metabolism and endurance capacity. Subjects (n = 8) withdrew from all dietary sources of caffeine for 48 h before each of four tests. One hour before exercise they ingested capsules of placebo or caffeine (3, 6, or 9 mg/kg), rested quietly, and then ran at 85% of maximal O2 consumption to voluntary exhaustion. Blood samples for methylxanthine, catecholamine, glucose, lactate, free fatty acid, and glycerol analyses were taken every 15 min. Plasma caffeine concentration increased with each dose (P < 0.05). Its major metabolite, paraxanthine, did not increase between the 6 and 9 mg/kg doses, suggesting that hepatic caffeine metabolism was saturated. Endurance was enhanced with both 3 and 6 mg/kg of caffeine (increases of 22 +/- 9 and 22 +/- 7%, respectively; both P < 0.05) over the placebo time of 49.4 +/- 4.2 min, whereas there was no significant effect with 9 mg/kg of caffeine. In contrast, plasma epinephrine was not increased with 3 mg/kg of caffeine but was greater with the higher doses (P < 0.05). Similarly only the highest dose of caffeine resulted in increases in glycerol and free fatty acids (P < 0.05). Thus the highest dose had the greatest effect on epinephrine and blood-borne metabolites yet had the least effect on performance. The lowest dose had little or no effect on epinephrine and metabolites but did have an ergogenic effect. These results are not compatible with the traditional theory that caffeine mediates its ergogenic effect via enhanced catecholamines.

摘要

本研究检测了训练有素的耐力运动员对不同剂量咖啡因的运动反应,以评估该药物对运动代谢和耐力的影响。在四项测试的每一项之前,受试者(n = 8)停止从所有饮食来源摄入咖啡因48小时。运动前一小时,他们服用安慰剂或咖啡因(3、6或9毫克/千克)胶囊,安静休息,然后以最大耗氧量的85%跑步至自愿力竭。每15分钟采集一次血样,用于分析甲基黄嘌呤、儿茶酚胺、葡萄糖、乳酸、游离脂肪酸和甘油。血浆咖啡因浓度随每剂增加(P < 0.05)。其主要代谢物,副黄嘌呤,在6和9毫克/千克剂量之间没有增加,表明肝脏咖啡因代谢已饱和。与安慰剂组49.4 +/- 4.2分钟的时间相比,3和6毫克/千克的咖啡因均增强了耐力(分别增加22 +/- 9%和22 +/- 7%;两者P < 0.05),而9毫克/千克的咖啡因没有显著影响。相比之下,3毫克/千克的咖啡因没有使血浆肾上腺素增加,但较高剂量时增加更明显(P < 0.05)。同样,只有最高剂量的咖啡因导致甘油和游离脂肪酸增加(P < 0.05)。因此,最高剂量对肾上腺素和血源代谢物的影响最大,但对运动表现的影响最小。最低剂量对肾上腺素和代谢物几乎没有影响,但确实有促力作用。这些结果与咖啡因通过增强儿茶酚胺介导其促力作用的传统理论不一致。

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