Department of Human Health and Nutritional Sciences, University of Guelph, 491 Gordon St., Guelph, ON, N1G 2W1, Canada.
Sports Med. 2017 Mar;47(Suppl 1):13-21. doi: 10.1007/s40279-017-0693-3.
Since the seminal finding almost 50 years ago that exercise training increases mitochondrial content in skeletal muscle, a considerable amount of research has been dedicated to elucidate the mechanisms inducing mitochondrial biogenesis. The discovery of peroxisome proliferator-activated receptor γ co-activator 1α as a major regulator of exercise-induced gene transcription was instrumental in beginning to understand the signals regulating this process. However, almost two decades after its discovery, our understanding of the signals inducing mitochondrial biogenesis remain poorly defined, limiting our insights into possible novel training modalities in elite athletes that can increase the oxidative potential of muscle. In particular, the role of mitochondrial reactive oxygen species has received very little attention; however, several lifestyle interventions associated with an increase in mitochondrial reactive oxygen species coincide with the induction of mitochondrial biogenesis. Furthermore, the diminishing returns of exercise training are associated with reductions in exercise-induced, mitochondrial-derived reactive oxygen species. Therefore, research focused on altering redox signaling in elite athletes may prove to be effective at inducing mitochondrial biogenesis and augmenting training regimes. In the context of exercise performance, the biological effect of increasing mitochondrial content is an attenuated rise in free cytosolic adenosine diphosphate (ADP), and subsequently decreased carbohydrate flux at a given power output. Recent evidence has shown that mitochondrial ADP sensitivity is a regulated process influenced by nutritional interventions, acute exercise, and exercise training. This knowledge raises the potential to improve mitochondrial bioenergetics in the absence of changes in mitochondrial content. Elucidating the mechanisms influencing the acute regulation of mitochondrial ADP sensitivity could have performance benefits in athletes, especially as these individuals display high levels of mitochondria, and therefore are subjects in whom it is notoriously difficult to further induce mitochondrial adaptations. In addition to changes in ADP sensitivity, an increase in mitochondrial coupling would have a similar bioenergetic response, namely a reduction in free cytosolic ADP. While classically the stoichiometry of the electron transport chain has been considered rigid, recent evidence suggests that sodium nitrate can improve the efficiency of this process, creating the potential for dietary sources of nitrate (e.g., beetroot juice) to display similar improvements in exercise performance. The current review focuses on these processes, while also discussing the biological relevance in the context of exercise performance.
自近 50 年前发现运动训练可增加骨骼肌中线粒体含量以来,大量研究致力于阐明诱导线粒体生物发生的机制。过氧化物酶体增殖物激活受体 γ 共激活因子 1α(peroxisome proliferator-activated receptor γ co-activator 1α)作为运动诱导基因转录的主要调节因子的发现,对于开始理解调节这一过程的信号至关重要。然而,在发现它近 20 年后,我们对诱导线粒体生物发生的信号的理解仍然很不清楚,这限制了我们对精英运动员中可能增加肌肉氧化能力的新型训练方式的深入了解。特别是,线粒体活性氧的作用几乎没有受到关注;然而,与诱导线粒体生物发生同时发生的几种与线粒体活性氧增加相关的生活方式干预措施。此外,运动训练的收益递减与运动诱导的线粒体衍生活性氧的减少有关。因此,专注于改变精英运动员的氧化还原信号的研究可能会有效地诱导线粒体生物发生并增强训练方案。就运动表现而言,增加线粒体含量的生物学效应是自由细胞溶质 ADP(adenosine diphosphate)的升高幅度降低,随后在给定功率输出下碳水化合物通量减少。最近的证据表明,线粒体 ADP 敏感性是一个受营养干预、急性运动和运动训练影响的调节过程。这一知识提高了在不改变线粒体含量的情况下改善线粒体生物能的潜力。阐明影响线粒体 ADP 敏感性急性调节的机制可能会使运动员受益,尤其是因为这些个体表现出高水平的线粒体,并且因此是众所周知难以进一步诱导线粒体适应的对象。除了 ADP 敏感性的变化外,线粒体偶联的增加也会产生类似的生物能反应,即自由细胞溶质 ADP 的减少。虽然经典上电子传递链的化学计量被认为是刚性的,但最近的证据表明,硝酸钠可以提高这个过程的效率,从而为硝酸盐的饮食来源(例如,甜菜根汁)创造类似的改善运动表现的潜力。本综述重点讨论了这些过程,同时还讨论了它们在运动表现背景下的生物学意义。