Laurent D, Schneider K E, Prusaczyk W K, Franklin C, Vogel S M, Krssak M, Petersen K F, Goforth H W, Shulman G I
Department of Internal Medicine and the Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Clin Endocrinol Metab. 2000 Jun;85(6):2170-5. doi: 10.1210/jcem.85.6.6655.
To examine the effect of caffeine ingestion on muscle glycogen utilization and the neuroendocrine axis during exercise, we studied 20 muscle glycogen-loaded subjects who were given placebo or caffeine (6 mg/kg) in a double blinded fashion 90 min before cycling for 2 h at 65% of their maximal oxygen consumption. Exercise-induced glycogen depletion in the thigh muscle was noninvasively measured by means of 13C nuclear magnetic resonance spectroscopy (NMR) spectroscopy, and plasma concentrations of substrates and neuroendocrine hormones, including beta-endorphins, were also assessed. Muscle glycogen content was increased 140% above normal values on the caffeine trial day (P < 0.001). After cycling for 2 h, caffeine ingestion was associated with a greater increase in plasma lactate (caffeine: +1.0 +/- 0.2 mmol/L; placebo, +0.1 +/- 0.2 mmol/L; P < 0.005), epinephrine (caffeine, +223 +/- 82 pg/mL; placebo, +56 +/- 26 pg/mL; P < 0.05), and cortisol (caffeine, +12 +/- 3 mg/mL; placebo, +2 +/- 2 mg/mL; P < 0.001) levels. However, plasma free fatty acid concentrations increased (caffeine, +814 +/- 133 mmol/L; placebo, +785 +/- 85 mmol/L; P = NS), and muscle glycogen content decreased (caffeine, -57 +/- 6 mmol/L muscle; placebo, -53 +/- 5 mmol/L muscle; P = NS) to the same extent in both groups. At the same time, plasma beta-endorphin levels almost doubled (from 30 +/- 5 to 53 +/- 13 pg/mL; P < 0.05) in the caffeine-treated group, whereas no change occurred in the placebo group. We conclude that caffeine ingestion 90 min before prolonged exercise does not exert a muscle glycogen-sparing effect in athletes with high muscle glycogen content. However, these data suggest that caffeine lowers the threshold for exercise-induced beta-endorphin and cortisol release, which may contribute to the reported benefits of caffeine on exercise endurance.
为了研究运动期间摄入咖啡因对肌肉糖原利用及神经内分泌轴的影响,我们对20名肌肉糖原储备充足的受试者进行了研究。在以最大耗氧量的65%进行2小时自行车运动前90分钟,以双盲方式给他们服用安慰剂或咖啡因(6毫克/千克)。通过13C核磁共振波谱法(NMR)无创测量运动诱导的大腿肌肉糖原消耗情况,并评估包括β-内啡肽在内的底物和神经内分泌激素的血浆浓度。在服用咖啡因试验日,肌肉糖原含量比正常值增加了140%(P<0.001)。在进行2小时自行车运动后,摄入咖啡因与血浆乳酸(咖啡因组:+1.0±0.2毫摩尔/升;安慰剂组:+0.1±0.2毫摩尔/升;P<0.005)、肾上腺素(咖啡因组:+223±82皮克/毫升;安慰剂组:+56±26皮克/毫升;P<0.05)和皮质醇(咖啡因组:+12±3毫克/毫升;安慰剂组:+2±2毫克/毫升;P<0.001)水平的更大升高相关。然而,两组的血浆游离脂肪酸浓度均升高(咖啡因组:+814±133毫摩尔/升;安慰剂组:+785±85毫摩尔/升;P=无显著性差异),且肌肉糖原含量下降程度相同(咖啡因组:-57±6毫摩尔/升肌肉;安慰剂组:-53±5毫摩尔/升肌肉;P=无显著性差异)。同时,咖啡因治疗组的血浆β-内啡肽水平几乎翻倍(从30±5皮克/毫升增至53±13皮克/毫升;P<0.05),而安慰剂组无变化。我们得出结论,在长时间运动前90分钟摄入咖啡因对肌肉糖原含量高的运动员没有肌肉糖原节省作用。然而,这些数据表明咖啡因降低了运动诱导的β-内啡肽和皮质醇释放的阈值,这可能有助于解释咖啡因对运动耐力有益的报道。