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本文引用的文献

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Reduced coupling of oxidative phosphorylation in vivo precedes electron transport chain defects due to mild oxidative stress in mice.体内氧化磷酸化偶联减少先于因轻度氧化应激导致的电子传递链缺陷在小鼠中发生。
PLoS One. 2011;6(11):e26963. doi: 10.1371/journal.pone.0026963. Epub 2011 Nov 22.
2
Skeletal muscle mitochondrial capacity and insulin resistance in type 2 diabetes.2 型糖尿病患者的骨骼肌线粒体容量与胰岛素抵抗。
J Clin Endocrinol Metab. 2011 Apr;96(4):1160-8. doi: 10.1210/jc.2010-1621. Epub 2011 Feb 9.
3
Dietary inorganic nitrate improves mitochondrial efficiency in humans.饮食中的无机硝酸盐可提高人体的线粒体效率。
Cell Metab. 2011 Feb 2;13(2):149-59. doi: 10.1016/j.cmet.2011.01.004.
4
Effect of 5-week moderate intensity endurance training on the oxidative stress, muscle specific uncoupling protein (UCP3) and superoxide dismutase (SOD2) contents in vastus lateralis of young, healthy men.为期 5 周的中等强度耐力训练对年轻健康男性股外侧肌氧化应激、肌肉特异性解偶联蛋白(UCP3)和超氧化物歧化酶(SOD2)含量的影响。
J Physiol Pharmacol. 2010 Dec;61(6):743-51.
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Mitochondrial proton and electron leaks.线粒体质子和电子渗漏。
Essays Biochem. 2010;47:53-67. doi: 10.1042/bse0470053.
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Mitochondrial function in vivo: spectroscopy provides window on cellular energetics.体内线粒体功能:光谱学为细胞能量学提供了窗口。
Methods. 2008 Dec;46(4):312-8. doi: 10.1016/j.ymeth.2008.10.001. Epub 2008 Oct 16.
7
Mild mitochondrial uncoupling impacts cellular aging in human muscles in vivo.轻度线粒体解偶联在体内影响人类肌肉细胞衰老。
Proc Natl Acad Sci U S A. 2007 Jan 16;104(3):1057-62. doi: 10.1073/pnas.0610131104. Epub 2007 Jan 10.
8
Mitochondrial coupling in humans: assessment of the P/O2 ratio at the onset of calf exercise.人体线粒体偶联:小腿运动开始时P/O2比值的评估。
Eur J Appl Physiol. 2007 Apr;99(6):593-604. doi: 10.1007/s00421-006-0382-7. Epub 2007 Jan 6.
9
Cycling efficiency in humans is related to low UCP3 content and to type I fibres but not to mitochondrial efficiency.人类的骑行效率与低水平的解偶联蛋白3含量及I型纤维有关,而与线粒体效率无关。
J Physiol. 2006 Mar 15;571(Pt 3):669-81. doi: 10.1113/jphysiol.2005.101691. Epub 2006 Jan 19.
10
Reduced mitochondrial coupling in vivo alters cellular energetics in aged mouse skeletal muscle.体内线粒体偶联减少会改变老年小鼠骨骼肌的细胞能量代谢。
J Physiol. 2005 Dec 1;569(Pt 2):467-73. doi: 10.1113/jphysiol.2005.097782. Epub 2005 Oct 27.

与久坐者相比,活跃受试者的肌肉中线粒体呼吸和解偶联增加,电子传递链含量减少。

Higher mitochondrial respiration and uncoupling with reduced electron transport chain content in vivo in muscle of sedentary versus active subjects.

机构信息

Department of Radiology, University of Washington Medical Center, Box 357115, Seattle, Washington 98195-7115, USA.

出版信息

J Clin Endocrinol Metab. 2013 Jan;98(1):129-36. doi: 10.1210/jc.2012-2967. Epub 2012 Nov 12.

DOI:10.1210/jc.2012-2967
PMID:23150693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3537085/
Abstract

OBJECTIVE

This study investigated the disparity between muscle metabolic rate and mitochondrial metabolism in human muscle of sedentary vs. active individuals.

RESEARCH DESIGN AND METHODS

Chronic activity level was characterized by a physical activity questionnaire and a triaxial accelerometer as well as a maximal oxygen uptake test. The ATP and O(2) fluxes and mitochondrial coupling (ATP/O(2) or P/O) in resting muscle as well as mitochondrial capacity (ATP(max)) were determined in vivo in human vastus lateralis muscle using magnetic resonance and optical spectroscopy on 24 sedentary and seven active subjects. Muscle biopsies were analyzed for electron transport chain content (using complex III as a representative marker) and mitochondrial proteins associated with antioxidant protection.

RESULTS

Sedentary muscle had lower electron transport chain complex content (65% of the active group) in proportion to the reduction in ATP(max) (0.69 ± 0.07 vs. 1.07 ± 0.06 mM sec(-1)) as compared with active subjects. This lower ATP(max) paired with an unchanged O(2) flux in resting muscle between groups resulted in a doubling of O(2) flux per ATP(max) (3.3 ± 0.3 vs. 1.7 ± 0.2 μM O(2) per mM ATP) that reflected mitochondrial uncoupling (P/O = 1.41 ± 0.1 vs. 2.1 ± 0.3) and greater UCP3/complex III (6.0 ± 0.7 vs. 3.8 ± 0.3) in sedentary vs. active subjects.

CONCLUSION

A smaller mitochondrial pool serving the same O(2) flux resulted in elevated mitochondrial respiration in sedentary muscle. In addition, uncoupling contributed to this higher mitochondrial respiration. This finding resolves the paradox of stable muscle metabolism but greater mitochondrial respiration in muscle of inactive vs. active subjects.

摘要

目的

本研究旨在探讨久坐与活跃个体的肌肉代谢率和线粒体代谢之间的差异。

研究设计与方法

通过体力活动问卷、三轴加速度计和最大摄氧量测试来描述慢性活动水平。使用磁共振和光学光谱技术,在 24 名久坐和 7 名活跃受试者的股外侧肌中,测定静息状态下肌肉的 ATP 和 O(2)通量以及线粒体偶联(ATP/O(2)或 P/O),以及线粒体容量(ATP(max))。对肌肉活检进行电子传递链含量分析(以复合物 III 作为代表性标志物)和与抗氧化保护相关的线粒体蛋白。

结果

与活跃组相比,久坐组的电子传递链复合物含量较低(为活跃组的 65%),与 ATP(max)的降低(0.69 ± 0.07 与 1.07 ± 0.06 mM sec(-1)) 成比例。这种较低的 ATP(max)与两组间静息肌肉中 O(2)通量不变相匹配,导致每单位 ATP(max)的 O(2)通量增加一倍(3.3 ± 0.3 与 1.7 ± 0.2 μM O(2) per mM ATP),反映线粒体解偶联(P/O = 1.41 ± 0.1 与 2.1 ± 0.3)和 UCP3/复合物 III 增加(6.0 ± 0.7 与 3.8 ± 0.3)。

结论

为相同的 O(2)通量服务的较小线粒体池导致久坐肌肉中的线粒体呼吸增加。此外,解偶联有助于这种更高的线粒体呼吸。这一发现解决了肌肉代谢率稳定但肌肉中活跃个体的线粒体呼吸更大的悖论。