Mrakic-Sposta Simona, Gussoni Maristella, Moretti Sarah, Pratali Lorenza, Giardini Guido, Tacchini Philippe, Dellanoce Cinzia, Tonacci Alessandro, Mastorci Francesca, Borghini Andrea, Montorsi Michela, Vezzoli Alessandra
Institute of Bioimaging and Molecular Physiology, National Council of Research (CNR), Segrate (Milan), Italy.
Department of Pathophysiology and Transplantation-Physiology Section, University of Milan, Milan, Italy.
PLoS One. 2015 Nov 5;10(11):e0141780. doi: 10.1371/journal.pone.0141780. eCollection 2015.
Aiming to gain a detailed insight into the physiological mechanisms involved under extreme conditions, a group of experienced ultra-marathon runners, performing the mountain Tor des Géants® ultra-marathon: 330 km trail-run in Valle d'Aosta, 24000 m of positive and negative elevation changes, was monitored. ROS production rate, antioxidant capacity, oxidative damage and inflammation markers were assessed, adopting micro-invasive analytic techniques.
Forty-six male athletes (45.04±8.75 yr, 72.6±8.4 kg, 1.76±0.05 m) were tested. Capillary blood and urine were collected before (Pre-), in the middle (Middle-) and immediately after (Post-) Race. Samples were analyzed for: Reactive Oxygen Species (ROS) production by Electron Paramagnetic Resonance; Antioxidant Capacity by Electrochemistry; oxidative damage (8-hydroxy-2-deoxy Guanosine: 8-OH-dG; 8-isoprostane: 8-isoPGF2α) and nitric oxide metabolites by enzymatic assays; inflammatory biomarkers (plasma and urine interleukin-6: IL-6-P and IL-6-U) by enzyme-linked immunosorbent assays (ELISA); Creatinine and Neopterin by HPLC, hematologic (lactate, glucose and hematocrit) and urine parameters by standard analyses.
Twenty-five athletes finished the race, while twenty-one dropped out of it. A significant increase (Post-Race vs Pre) of the ROS production rate (2.20±0.27 vs 1.65±0.22 μmol.min-1), oxidative damage biomarkers (8-OH-dG: 6.32±2.38 vs 4.16±1.25 ng.mg-1 Creatinine and 8-isoPGF2α: 1404.0±518.30 vs 822.51±448.91 pg.mg-1Creatinine), inflammatory state (IL-6-P: 66.42±36.92 vs 1.29±0.54 pg.mL-1 and IL-6-U: 1.33±0.56 vs 0.71±0.17 pg.mL1) and lactate production (+190%), associated with a decrease of both antioxidant capacity (-7%) and renal function (i.e. Creatinine level +76%) was found.
The used micro-invasive analytic methods allowed us to perform most of them before, during and immediately after the race directly in the field, by passing the need of storing and transporting samples for further analysis. Considered altogether the investigated variables showed up that exhaustive and prolonged exercise not only promotes the generation of ROS but also induces oxidative stress, transient renal impairment and inflammation.
为深入了解极端条件下的生理机制,对一组经验丰富的超级马拉松运动员进行了监测,他们参加了巨人之旅超马拉松赛:在奥斯塔山谷进行的330公里越野跑,累计海拔上升和下降24000米。采用微创分析技术评估了活性氧生成速率、抗氧化能力、氧化损伤和炎症标志物。
测试了46名男性运动员(45.04±8.75岁,72.6±8.4千克,身高1.76±0.05米)。在比赛前(赛前)、比赛中(赛中)和比赛结束后立即(赛后)采集毛细血管血和尿液样本。对样本进行以下分析:通过电子顺磁共振检测活性氧(ROS)生成;通过电化学检测抗氧化能力;通过酶促测定法检测氧化损伤(8-羟基-2-脱氧鸟苷:8-OH-dG;8-异前列腺素:8-isoPGF2α)和一氧化氮代谢产物;通过酶联免疫吸附测定法(ELISA)检测炎症生物标志物(血浆和尿液白细胞介素-6:IL-6-P和IL-6-U);通过高效液相色谱法检测肌酐和新蝶呤,通过标准分析法检测血液学指标(乳酸、葡萄糖和血细胞比容)和尿液参数。
25名运动员完成了比赛,21名退出。发现赛后活性氧生成速率(2.20±0.27对1.65±0.22微摩尔·分钟-1)、氧化损伤生物标志物(8-OH-dG:6.32±2.38对4.16±1.25纳克·毫克-1肌酐和8-isoPGF2α:1404.0±518.30对822.51±448.91皮克·毫克-1肌酐)、炎症状态(IL-6-P:66.42±36.92对1.29±0.54皮克·毫升-1和IL-6-U:1.33±0.56对0.71±0.17皮克·毫升-1)和乳酸生成(增加190%)显著增加,同时抗氧化能力(下降7%)和肾功能(即肌酐水平增加76%)下降。
所采用的微创分析方法使我们能够在比赛前、比赛期间和比赛结束后立即在现场直接进行大部分检测,无需储存和运输样本进行进一步分析。综合考虑所有研究变量表明,力竭性长时间运动不仅促进活性氧的生成,还会诱导氧化应激、短暂性肾功能损害和炎症。