Robertson Caroline V, Immink Maarten A, Marino Frank E
School of Exercise Science, Sport and Health, Faculty of Science, Charles Sturt University Bathurst, NSW, Australia.
School of Health Sciences, Alliance for Research in Exercise, Nutrition and Activity (ARENA) and Cognitive Neuroscience Laboratory, University of South Australia Adelaide, SA, Australia.
Front Physiol. 2016 Dec 27;7:640. doi: 10.3389/fphys.2016.00640. eCollection 2016.
Exogenous cortisol is a modulator of behavior related to increased motivated decision making (Putman et al., 2010), where risky choices yield potentially big reward. Making risk based judgments has been shown to be important to athletes in optimizing pacing during endurance events (Renfree et al., 2014; Micklewright et al., 2015). Therefore, the aims of this study were to examine the effect of 50 mg exogenous cortisol on neurophysiological responses and risk taking behavior in nine healthy men. Further to this, to examine the effect of exogenous cortisol on exercise performance. Using a double blind counterbalanced design, cyclists completed a placebo (PLA), and a cortisol (COR) trial (50 mg cortisol), with drug ingestion at 0 min. Each trial consisted of a rest period from 0 to 60 min, followed by a risk taking behavior task, a 30 min time trial (TT) with 5 × 30 s sprints at the following time intervals; 5, 11, 17, 23, and 29 min. Salivary cortisol (SaCOR), Electroencephalography (EEG) and Near Infrared Spectroscopy (NIRs) were measured at 15, 30, 45, and 60 min post-ingestion. Glucose and lactate samples were taken at 0 and 60 min post-ingestion. During exercise, power output (PO), heart rate (HR), EEG, and NIRS were measured. SaCOR was measured 10 min post-exercise. Cortisol increased risk taking behavior from baseline testing. This was in line with significant neurophysiological changes at rest and during exercise. At rest, SaCOR levels were higher ( < 0.01) in COR compared to PLA (29.7 ± 22.7 and 3.27 ± 0.7 nmol/l, respectively). At 60 min alpha slow EEG response was higher in COR than PLA in the PFC (5.5 ± 6.4 vs. -0.02 ± 8.7% change; < 0.01). During the TT there was no difference in total km, average power or average sprint power, although Peak power (PP) achieved was lower in COR than PLA (465.3 ± 83.4 and 499.8 ± 104.3; < 0.05) and cerebral oxygenation was lower in COR ( < 0.05). This is the first study to examine the effect of exogenous cortisol on exercise performance. These results are in line with previous research showing altered risk taking behavior following exogenous cortisol, however the altered behavior did not translate into changes in exercise performance.
外源性皮质醇是一种与增强动机性决策相关行为的调节因子(普特曼等人,2010年),在这种情况下,冒险选择会带来潜在的巨大回报。已证明基于风险的判断对运动员在耐力项目中优化节奏很重要(伦弗里等人,2014年;米克勒赖特等人,2015年)。因此,本研究的目的是检验50毫克外源性皮质醇对九名健康男性神经生理反应和冒险行为的影响。此外,还要检验外源性皮质醇对运动表现的影响。采用双盲平衡设计,自行车运动员完成了一次安慰剂(PLA)试验和一次皮质醇(COR)试验(50毫克皮质醇),在0分钟时摄入药物。每次试验包括从0到60分钟的休息期,随后是一个冒险行为任务、一个30分钟的计时赛(TT),在以下时间间隔进行5次30秒冲刺;5、11、17、23和29分钟。在摄入后15、30、45和60分钟测量唾液皮质醇(SaCOR)、脑电图(EEG)和近红外光谱(NIRs)。在摄入后0和60分钟采集葡萄糖和乳酸样本。在运动过程中,测量功率输出(PO)、心率(HR)、EEG和NIRS。运动后10分钟测量SaCOR。皮质醇使冒险行为较基线测试有所增加。这与休息和运动期间显著的神经生理变化一致。休息时,COR组的SaCOR水平高于PLA组(<0.01)(分别为29.7±22.7和3.27±0.7纳摩尔/升)。在60分钟时,COR组在PFC中的α慢EEG反应高于PLA组(5.5±6.4与-0.02±8.7%变化;<0.01)。在计时赛期间,总公里数、平均功率或平均冲刺功率没有差异,尽管COR组达到的峰值功率(PP)低于PLA组(465.3±83.4和499.8±104.3;<0.05),且COR组的脑氧合较低(<0.05)。这是第一项研究外源性皮质醇对运动表现影响的研究。这些结果与之前关于外源性皮质醇后冒险行为改变的研究一致,然而行为的改变并未转化为运动表现的变化。