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首页> 外文期刊>NMR in biomedicine >Absolute quantification of phosphorus metabolite concentrations in human muscle in vivo by P-31 MRS: a quantitative review
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Absolute quantification of phosphorus metabolite concentrations in human muscle in vivo by P-31 MRS: a quantitative review

机译:P-31 MRS对人体肌肉中磷代谢物浓度的绝对定量:定量综述

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(31)p MRS offers a unique view of muscle metabolism in vivo, but correct quantification is important. Inter-study correlation of estimates of [Pi] and [phosphocreatine (PCr)] in a number of published studies suggest that the main technical problem in calibrated (31)p MRS studies is the measurement of PCr and Pi signal intensities, rather than absolute quantification of [ATP]. For comparison, we discuss the few published biopsy studies of calf muscle and a selection of the many studies of quadriceps muscle. The ATP concentration is close to the value that we obtained in calf muscle in our own study, presented here, on four healthy subjects, by localised P-31 MRS using a surface coil incorporating an internal reference and calibrated using an external phantom. However, the freeze-clamp biopsy PCr concentration is similar to 20% lower than the value obtained by (31)p MRS, consistent with PCr breakdown by creatine kinase during freezing. Finally, we illustrate some consequences of uncertainty in resting [PCr] for analysis of mitochondrial function from PCr kinetics using a published (31)p MRS study of exercise and recovery: the lower the assumed resting [PCr], the lower the absolute rate of oxidative ATP synthesis estimated from the PCr resynthesis rate; in addition, the lower the assumed resting [PCr], or the higher the assumed [total creatine], the higher the apparent resting [ADP], and therefore the more sigmoid the relationship between the rate of oxidative ATP synthesis and [ADP]. Correct quantification of resting metabolite concentrations is crucially important for this sort of analysis. Our own results ([PCr] = 33 +/- 2 mM, [Pi] = 4.5 +/- 0.2 mM, and [ATP] = 8.2 +/- 0.4 mM; mean SEM) are close to the overall mean values of the 10 published studies on calf muscle by 'calibrated, (31)p MRS (as in the present work), and of [PCr] and [Pi] in a representative selection of 'uncalibrated, (31)p MRS studies (i.e. from measured PCr/ATP and Pi/ATP ratios, assuming a literature value for [ATP]). Copyright (c) 2007 John Wiley & Sons, Ltd.
机译:(31)p MRS提供了体内肌肉代谢的独特视角,但是正确的量化很重要。在许多已发表的研究中,对Pi和[磷酸肌酸(PCr)]的估计之间的研究间相关性表明,校正的(31)p MRS研究中的主要技术问题是PCr和Pi信号强度的测量,而不是绝对的定量[ATP]。为了进行比较,我们讨论了一些已发表的小腿肌肉活检研究和许多股四头肌研究的选择。 ATP浓度接近于我们在本研究中针对四名健康受试者在小腿肌肉中获得的值,方法是使用结合有内部参照物的表面线圈对P-31 MRS进行定位,并使用外部体模进行校准。但是,冷冻钳活检的PCr浓度比通过(31)p MRS获得的值低约20%,这与冷冻过程中肌酸激酶对PCr的破坏相一致。最后,我们使用已发表的(31)p MRS运动和恢复研究对静息[PCr]不确定性的某些后果进行了分析,该结果来自于PCr动力学的线粒体功能分析:假定静息[PCr]越低,其绝对率就越低。由PCr再合成速率估算的氧化ATP合成;另外,假定的静息[PCr]越低,或假定的[总肌酸]越高,则表观静息[ADP]越高,因此氧化ATP合成速率与[ADP]之间的关系越呈S形。静止代谢产物浓度的正确定量对于此类分析至关重要。我们自己的结果([PCr] = 33 +/- 2 mM,[Pi] = 4.5 +/- 0.2 mM,[ATP] = 8.2 +/- 0.4 mM;平均SEM)接近于10篇关于“校准的(31)p MRS的小腿肌肉的研究(如本工作),以及[PCr]和[Pi]在“未校准的(31)p MRS的代表性研究中的选择(即从假设[ATP]的文献价值为PCr / ATP和Pi / ATP的比率)。版权所有(c)2007 John Wiley&Sons,Ltd.

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