4 公里自行车计时赛不同阶段后的血清代谢组概况:随机对照试验的二次分析

Rafael A. Azevedo, Ramon Cruz, Marcos D. Silva-Cavalcante, Adriano E. Lima-Silva, Romulo Bertuzzi
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引用次数: 0

摘要

人们一直认为,在整个自行车计时赛(TT)过程中,运动强度的变化会与各种代谢变化相一致,以防止任务过早失败。然而,这一假设是基于目标代谢物的反应,这限制了我们对运动过程中代谢反应复杂的相互联系的理解。目前的研究描述了自行车 4 公里 TT 特定阶段后的代谢组特征,即非目标代谢分析。11 名男性自行车运动员在交叉平衡设计中进行了三次分开的 TT,分别在快速起跑(FS,600 ± 205 米)、匀速(EP,3600 ± 190 米)或终点冲刺(ES,4000 米)阶段结束时中断。在任何运动前和运动停止后 5 分钟采集血液样本,并使用核磁共振代谢组学进行代谢组学特征描述。功率输出(PO)也被持续记录。与 EP 相比,FS 和 ES 期间的 PO 值更高(均 p <0.05),同时伴有不同的代谢组学特征。FS 显示了 TCA 循环及其相关途径(如谷氨酸、柠檬酸和缬氨酸代谢)中代谢物的高表达量;而 EP 则引起了与抗氧化作用和氧输送调整相关的变化。最后,ES 与参与 NAD 转化和血清素代谢的途径有关。这些研究结果表明,自行车 TT 的特定阶段伴随着不同的代谢组学特征,为特定代谢途径与运动强度调节过程的相关性提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The blood serum metabolome profile after different phases of a 4-km cycling time trial: Secondary analysis of a randomized controlled trial

The blood serum metabolome profile after different phases of a 4-km cycling time trial: Secondary analysis of a randomized controlled trial

It has been assumed that exercise intensity variation throughout a cycling time trial (TT) occurs in alignment of various metabolic changes to prevent premature task failure. However, this assumption is based on target metabolite responses, which limits our understanding of the complex interconnection of metabolic responses during exercise. The current study characterized the metabolomic profile, an untargeted metabolic analysis, after specific phases of a cycling 4-km TT. Eleven male cyclists performed three separated TTs in a crossover counterbalanced design, which were interrupted at the end of the fast-start (FS, 600 ± 205 m), even-pace (EP, 3600 ± 190 m), or end-spurt (ES, 4000 m) phases. Blood samples were taken before any exercise and 5 min after exercise cessation, and the metabolomic profile characterization was performed using Nuclear Magnetic Resonance metabolomics. Power output (PO) was also continually recorded. There were higher PO values during the FS and ES compared to the EP (all p < 0.05), which were accompanied by distinct metabolomic profiles. FS showed high metabolite expression in TCA cycle and its related pathways (e.g., glutamate, citric acid, and valine metabolism); whereas, the EP elicited changes associated with antioxidant effects and oxygen delivery adjustment. Finally, ES was related to pathways involved in NAD turnover and serotonin metabolism. These findings suggest that the specific phases of a cycling TT are accompanied by distinct metabolomic profiles, providing novel insights regarding the relevance of specific metabolic pathways on the process of exercise intensity regulation.

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