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在长时间运动期间,伪麻黄碱没有增强体能的作用。

Pseudoephedrine is without ergogenic effects during prolonged exercise.

作者信息

Gillies H, Derman W E, Noakes T D, Smith P, Evans A, Gabriels G

机构信息

Liberty Life Chair of Exercise and Sports Science, Medical Research Council/University of Cape Town Bioenergetics of Exercise Research Unit, Observatory, South Africa.

出版信息

J Appl Physiol (1985). 1996 Dec;81(6):2611-7. doi: 10.1152/jappl.1996.81.6.2611.

Abstract

This study was designed to measure whether a single dose of 120 mg pseudoephedrine ingested 120 min before exercise influences performance during 1 h of high-intensity exercise. The effects of exercise on urinary excretion of the drug were also studied. Ten healthy male cyclists were tested on two occasions, separated by at least 7 days, by using a randomly assigned, double-blind, placebo-controlled, crossover design. Exercise performance was tested during a 40-km trial on a laboratory cycle ergometer, and skeletal muscle function was measured during isometric contractions. On a third occasion, subjects ingested 120 mg pseudoephedrine but did not exercise [control (C)]. Pseudoephedrine did not influence either time trial performance [drug (D) vs. placebo: 58.1 +/- 1.4 (SE) vs. 58.7 +/- 1.5 min] or isometric muscle function. Urinary pseudoephedrine concentrations were significantly increased 1 h after exercise (D vs. C: 114.3 +/- 27.2 vs. 35.4 +/- 13.1 micrograms/ml; P < 0.05). Peak plasma pseudoephedrine concentrations (P < 0.05) but not time taken to reach peak plasma concentrations or the area under the plasma pseudoephedrine concentration vs. time curve was significantly increased in the total group with exercise (D vs. C). In three subjects, plasma pseudoephedrine concentrations were not influenced by exercise. Only these subjects showed increased urinary pseudoephedrine excretion during exercise. We conclude that a single therapeutic dose of pseudoephedrine did not have a measurable ergogenic effect during high-intensity exercise of 1-h duration, but plasma drug concentrations and urinary excretion were altered by exercise. These findings have practical relevance to doping control regulations in international sporting competitions.

摘要

本研究旨在测定在运动前120分钟摄入单剂量120毫克伪麻黄碱是否会影响1小时高强度运动期间的表现。同时还研究了运动对该药物尿排泄的影响。采用随机分配、双盲、安慰剂对照、交叉设计,对10名健康男性自行车运动员进行了两次测试,两次测试间隔至少7天。在实验室自行车测力计上进行40公里试验时测试运动表现,并在等长收缩期间测量骨骼肌功能。在第三次测试中,受试者摄入120毫克伪麻黄碱但不进行运动[对照组(C)]。伪麻黄碱对计时赛表现[药物组(D)与安慰剂组:58.1±1.4(标准误)对58.7±1.5分钟]或等长肌肉功能均无影响。运动1小时后尿伪麻黄碱浓度显著升高(D组与C组:114.3±27.2对35.4±13.1微克/毫升;P<0.05)。运动组整体血浆伪麻黄碱峰值浓度显著升高(P<0.05),但达到血浆峰值浓度的时间或血浆伪麻黄碱浓度-时间曲线下面积不受影响(D组与C组)。在三名受试者中,血浆伪麻黄碱浓度不受运动影响。只有这些受试者在运动期间尿伪麻黄碱排泄增加。我们得出结论,单剂量治疗量的伪麻黄碱在1小时的高强度运动期间没有可测量的促力作用,但运动可改变血浆药物浓度和尿排泄。这些发现与国际体育比赛中的兴奋剂控制规定具有实际相关性。

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