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J Physiol. 2015 Dec 15;593(24):5255-68. doi: 10.1113/JP271299.
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Mitochondrial dysfunction in diabetic neuropathy: a series of unfortunate metabolic events.糖尿病性神经病变中的线粒体功能障碍:一系列不幸的代谢事件。
Curr Diab Rep. 2015 Nov;15(11):89. doi: 10.1007/s11892-015-0671-9.
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Molecular insight and pharmacological approaches targeting mitochondrial dynamics in skeletal muscle during obesity.肥胖期间针对骨骼肌线粒体动力学的分子见解和药理学方法。
Ann N Y Acad Sci. 2015 Sep;1350:82-94. doi: 10.1111/nyas.12863. Epub 2015 Aug 24.
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Pharmacol Res. 2015 Sep;99:344-50. doi: 10.1016/j.phrs.2015.05.015. Epub 2015 Jul 2.
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Excision of Expanded GAA Repeats Alleviates the Molecular Phenotype of Friedreich's Ataxia.切除扩增的GAA重复序列可减轻弗里德赖希共济失调的分子表型。
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磷-31磁共振波谱:一种测量人体骨骼肌体内线粒体氧化磷酸化能力的工具。

Phosphorus-31 Magnetic Resonance Spectroscopy: A Tool for Measuring In Vivo Mitochondrial Oxidative Phosphorylation Capacity in Human Skeletal Muscle.

作者信息

Kumar Vidhya, Chang Henry, Reiter David A, Bradley David P, Belury Martha, McCormack Shana E, Raman Subha V

机构信息

Davis Heart and Lung Research Institute, The Ohio State University.

Laboratory of Clinical Investigation, National Institute on Aging.

出版信息

J Vis Exp. 2017 Jan 19(119):54977. doi: 10.3791/54977.

DOI:10.3791/54977
PMID:28190054
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5352276/
Abstract

Skeletal muscle mitochondrial oxidative phosphorylation (OXPHOS) capacity, which is critically important in health and disease, can be measured in vivo and noninvasively in humans via phosphorus-31 magnetic resonance spectroscopy (PMRS). However, the approach has not been widely adopted in translational and clinical research, with variations in methodology and limited guidance from the literature. Increased optimization, standardization, and dissemination of methods for in vivo PMRS would facilitate the development of targeted therapies to improve OXPHOS capacity and could ultimately favorably impact cardiovascular health. PMRS produces a noninvasive, in vivo measure of OXPHOS capacity in human skeletal muscle, as opposed to alternative measures obtained from explanted and potentially altered mitochondria via muscle biopsy. It relies upon only modest additional instrumentation beyond what is already in place on magnetic resonance scanners available for clinical and translational research at most institutions. In this work, we outline a method to measure in vivo skeletal muscle OXPHOS. The technique is demonstrated using a 1.5 Tesla whole-body MR scanner equipped with the suitable hardware and software for PMRS, and we explain a simple and robust protocol for in-magnet resistive exercise to rapidly fatigue the quadriceps muscle. Reproducibility and feasibility are demonstrated in volunteers as well as subjects over a wide range of functional capacities.

摘要

骨骼肌线粒体氧化磷酸化(OXPHOS)能力在健康和疾病中至关重要,可通过磷-31磁共振波谱(PMRS)在人体中进行无创的体内测量。然而,该方法在转化研究和临床研究中尚未得到广泛应用,存在方法学上的差异且文献指导有限。加强体内PMRS方法的优化、标准化和传播将有助于开发改善OXPHOS能力的靶向疗法,并最终对心血管健康产生积极影响。与通过肌肉活检从离体且可能发生改变的线粒体获得的替代测量方法不同,PMRS可对人体骨骼肌的OXPHOS能力进行无创的体内测量。它仅依赖于大多数机构用于临床和转化研究的磁共振扫描仪上已有的适度额外仪器设备。在这项工作中,我们概述了一种测量体内骨骼肌OXPHOS的方法。使用配备适合PMRS的硬件和软件的1.5特斯拉全身磁共振扫描仪演示了该技术,并且我们解释了一种简单且可靠的磁体内部电阻运动方案,以使股四头肌快速疲劳。在志愿者以及具有广泛功能能力的受试者中证明了该方法的可重复性和可行性。