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运动训练通过扩大现有线粒体而不是从头生物合成来增加骨骼肌线粒体的体积密度。

Exercise training increases skeletal muscle mitochondrial volume density by enlargement of existing mitochondria and not de novo biogenesis.

机构信息

Zürich Center for Integrative Human Physiology, Institute of Physiology, University of Zürich, Zürich, Switzerland.

Department of Biology, University of Colorado, Denver, CO, USA.

出版信息

Acta Physiol (Oxf). 2018 Jan;222(1). doi: 10.1111/apha.12905. Epub 2017 Jul 6.

Abstract

AIMS

(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 .

METHOD

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.

RESULT

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

摘要

目的

(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。

方法

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。

结果

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。

结论

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。

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