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线粒体靶向抗氧化补充剂可提高中年训练有素男性自行车运动员 8 公里计时赛成绩。

Mitochondria-targeted antioxidant supplementation improves 8 km time trial performance in middle-aged trained male cyclists.

机构信息

Discipline of Nutrition, School of Medical Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand.

School of Kinesiology, University of British Columbia, Vancouver, Canada.

出版信息

J Int Soc Sports Nutr. 2021 Aug 21;18(1):58. doi: 10.1186/s12970-021-00454-0.

Abstract

BACKGROUND

Exercise increases skeletal muscle reactive oxygen species (ROS) production, which may contribute to the onset of muscular fatigue and impair athletic performance. Mitochondria-targeted antioxidants such as MitoQ, which contains a ubiquinone moiety and is targeted to mitochondria through the addition of a lipophilic triphenylphosphonium cation, are becoming popular amongst active individuals as they are designed to accumulate within mitochondria and may provide targeted protection against exercise-induced oxidative stress. However, the effect of MitoQ supplementation on cycling performance is currently unknown. Here, we investigate whether MitoQ supplementation can improve cycling performance measured as time to complete an 8 km time trial.

METHOD

In a randomized, double-blind, placebo-controlled crossover study, 19 middle-aged (age: 44 ± 4 years) recreationally trained (VO: 58.5 ± 6.2 ml·kg·min, distance cycled per week during 6 months prior to study enrollment: 158.3 ± 58.4 km) male cyclists completed 45 min cycling at 70% VO followed by an 8 km time trial after 28 days of supplementation with MitoQ (20 mg·day) and a placebo. Free F-isoprostanes were measured in plasma samples collected at rest, after 45 min cycling at 70% VO and after completion of the time trial. Respiratory gases and measures of rating of perceived exertion (RPE) were also collected.

RESULTS

Mean completion time for the time trial was 1.3% faster with MitoQ (12.91 ± 0.94 min) compared to placebo (13.09 ± 0.95 min, p = 0.04, 95% CI [0.05, 2.64], d = 0.2). There was no difference in RPE during the time trial between conditions (p = 0.82) despite there being a 4.4% increase in average power output during the time trial following MitoQ supplementation compared to placebo (placebo; 270 ± 51 W, MitoQ; 280 ± 53 W, p = 0.04, 95% CI [0.49, 8.22], d = 0.2). Plasma F-isoprostanes were lower on completion of the time trial following MitoQ supplementation (35.89 ± 13.6 pg·ml) compared to placebo (44.7 ± 16.9 pg·ml p = 0.03).

CONCLUSION

These data suggest that MitoQ supplementation may be an effective nutritional strategy to attenuate exercise-induced increases in oxidative damage to lipids and improve cycling performance.

摘要

背景

运动增加骨骼肌活性氧(ROS)的产生,这可能导致肌肉疲劳的发生,并损害运动表现。线粒体靶向抗氧化剂,如 MitoQ,它含有一个泛醌部分,并通过添加亲脂性三苯基膦阳离子靶向线粒体,在活跃人群中越来越受欢迎,因为它们被设计在线粒体中积累,并可能对运动引起的氧化应激提供有针对性的保护。然而,MitoQ 补充剂对自行车运动表现的影响目前尚不清楚。在这里,我们研究了 MitoQ 补充剂是否可以提高作为完成 8 公里计时赛时间的自行车运动表现。

方法

在一项随机、双盲、安慰剂对照交叉研究中,19 名中年(年龄:44±4 岁)有规律运动的(VO:58.5±6.2ml·kg·min,在研究入组前的 6 个月内每周骑自行车的距离:158.3±58.4km)男性自行车运动员在 70% VO 下进行 45 分钟的自行车运动,然后在 28 天的 MitoQ(20mg·天)和安慰剂补充后完成 8 公里计时赛。在休息时、70% VO 自行车运动 45 分钟后和计时赛结束时采集血浆样本,测量游离 F-异前列烷。还收集了呼吸气体和感知用力程度(RPE)的测量值。

结果

与安慰剂(13.09±0.95min,p=0.04,95%CI[0.05,2.64],d=0.2)相比,MitoQ(12.91±0.94min)使计时赛的平均完成时间快了 1.3%。尽管在 MitoQ 补充后,计时赛期间的平均功率输出增加了 4.4%(安慰剂:270±51W,MitoQ:280±53W,p=0.04,95%CI[0.49,8.22],d=0.2),但在计时赛期间 RPE 没有差异(p=0.82)。与安慰剂相比,MitoQ 补充后计时赛结束时的血浆 F-异前列烷水平较低(35.89±13.6pg·ml)(44.7±16.9pg·ml,p=0.03)。

结论

这些数据表明,MitoQ 补充剂可能是一种有效的营养策略,可以减轻运动引起的脂质氧化损伤的增加,并提高自行车运动表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd80/8379793/8f2a47c7ad44/12970_2021_454_Fig1_HTML.jpg

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