Zürich Center for Integrative Human Physiology, Institute of Physiology, University of Zürich, Zürich, Switzerland.
Department of Biology, University of Colorado, Denver, CO, USA.
Acta Physiol (Oxf). 2018 Jan;222(1). doi: 10.1111/apha.12905. Epub 2017 Jul 6.
(i) To determine whether exercise-induced increases in muscle mitochondrial volume density (Mito ) are related to enlargement of existing mitochondria or de novo biogenesis and (ii) to establish whether measures of mitochondrial-specific enzymatic activities are valid biomarkers for exercise-induced increases in Mito .
Skeletal muscle samples were collected from 21 healthy males prior to and following 6 weeks of endurance training. Transmission electron microscopy was used for the estimation of mitochondrial densities and profiles. Biochemical assays, western blotting and high-resolution respirometry were applied to detect changes in specific mitochondrial functions.
Mito increased with 55 ± 9% (P < 0.001), whereas the number of mitochondrial profiles per area of skeletal muscle remained unchanged following training. Citrate synthase activity (CS) increased (44 ± 12%, P < 0.001); however, there were no functional changes in oxidative phosphorylation capacity (OXPHOS, CI+II ) or cytochrome c oxidase (COX) activity. Correlations were found between Mito and CS (P = 0.01; r = 0.58), OXPHOS, CI+CIIP (P = 0.01; R = 0.58) and COX (P = 0.02; R = 0.52) before training; after training, a correlation was found between Mito and CS activity only (P = 0.04; R = 0.49). Intrinsic respiratory capacities decreased (P < 0.05) with training when respiration was normalized to Mito This was not the case when normalized to CS activity although the percentage change was comparable CONCLUSIONS: Mito was increased by inducing mitochondrial enlargement rather than de novo biogenesis. CS activity may be appropriate to track training-induced changes in Mito
(一)确定运动引起的肌肉线粒体体积密度(Mito)增加与现有线粒体的扩大或新生物合成有关;(二)确定线粒体特异性酶活性的测量是否是运动引起的 Mito 增加的有效生物标志物。
在进行 6 周的耐力训练之前和之后,从 21 名健康男性中采集骨骼肌样本。使用透射电子显微镜估计线粒体密度和形态。应用生化测定、western blot 和高分辨率呼吸测定法来检测特定线粒体功能的变化。
Mito 增加了 55±9%(P<0.001),而训练后骨骼肌面积的线粒体形态数量保持不变。柠檬酸合酶活性(CS)增加(44±12%,P<0.001);然而,氧化磷酸化能力(OXPHOS,CI+II)或细胞色素 c 氧化酶(COX)活性没有功能变化。在训练前,Mito 与 CS(P=0.01;r=0.58)、OXPHOS、CI+CIIP(P=0.01;R=0.58)和 COX(P=0.02;R=0.52)之间存在相关性;训练后,Mito 仅与 CS 活性之间存在相关性(P=0.04;R=0.49)。当呼吸作用与 Mito 相匹配时,内在呼吸能力会随着训练而降低(P<0.05),而当与 CS 活性相匹配时则不会发生这种情况,尽管变化百分比是可比的。
Mito 的增加是通过诱导线粒体扩大而不是新生物合成来实现的。CS 活性可能适合追踪训练引起的 Mito 变化。