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Quantification of unsaturated fatty acids by PRESS localized-DEPT enhanced 13C MRS and ERETIC in human skeletal muscle

机译:通过pREss本地化DEpT增强13C mRs和ERETIC对人骨骼肌中不饱和脂肪酸的定量

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摘要

Introduction: The in vivo concentration and composition of unsaturated fatty acids (UFA), which are an important source of fuel in skeletal muscle, is a valid measure to assess dietary intake [1]. Some studies have demonstrated that the fatty acid contents are tissue specific [2]. In this work, we combine DEPT (Distortionless Enhancement of Polarization Transfer) and PRESS localization on protons [3] to achieve muscle group specifc in vivo detection of UFA. ERETIC (Electric Reference To access In vivo Concentrations) is used as a reference standard for absolute quantification [4]. Methods: To compose the proton-localized carbon acquired PRESS DEPT sequence, two slice selective 180 o pulses on I spins were inserted after the first 90 o pulse to realize PRESS localization and the residual part of the DEPT sequence was implemented subsequently, as plotted in figure 1. The sequence was tested on a DMSO (Dimethyl Sulfoxide) phantom and UFA in a large muscle volume. UFA signals from different calf and thigh muscle compartments were obtained and compared among healthy subjects. UFA quantification by using ERETIC method was cross-validated against internal creatine and external reference standards on five subjects. The experiments were carried out on 3T and 7T human MRI scanner. Results: In Figure 2 PRESS acquisition, PRESS-localized DEPT and PRESS-localized DEPT with proton decoupling on a DMSO phantom and a muscle volume are compared. UFA signals obtained from different muscle compartments are shown in Figure 3. Slightly different absolute concentrations and relative ratios between mono- and polyunsaturated fatty (MUFA, PUFA) acids are found (Figure 4). The MUFA/PUFA ratios are muscle compartments dependent and the average values are related to the dietary intakes. Cross-validation results shown in Figure 5, demonstrate that UFA concentrations measured with the ERETIC method are in excellent agreement with internal creatine and external reference methods. Conclusion: The sequence which combined PRESS and DEPT was imple- mented to achieve the first in vivo results for 13 C MRS. The in vivo experiments together with ERETIC reference show its feasibility to be applied to assess UFA in specific muscle compartments.
机译:简介:体内不饱和脂肪酸(UFA)的浓度和组成是骨骼肌重要的燃料来源,是评估饮食摄入的有效方法[1]。一些研究表明脂肪酸含量是组织特异性的[2]。在这项工作中,我们结合了DEPT(无畸变极化转移增强)和PRESS在质子上的定位[3],以实现UFA在体内肌群特异性检测。 ERETIC(访问体内浓度的电子参考)被用作绝对定量的参考标准[4]。方法:为构成质子定位的碳获得的PRESS DEPT序列,在第一个90 o脉冲后在I自旋上插入两个切片选择性的180 o脉冲以实现PRESS定位,并随后实现DEPT序列的剩余部分,如图所示图1.在大肌肉量的DMSO(二甲基亚砜)体模和UFA上测试了序列。从不同的小腿和大腿肌肉区室获得了UFA信号,并在健康受试者之间进行了比较。使用ERETIC方法进行的UFA定量针对五个受试者的内部肌酸和外部参考标准进行了交叉验证。实验是在3T和7T人体MRI扫描仪上进行的。结果:在图2中,PRESS采集中,比较了DMSO体模上质子去耦的PRESS定位DEPT和PRESS定位DEPT和肌肉体积。从不同的肌肉区室获得的UFA信号如图3所示。发现单不饱和脂肪酸和多不饱和脂肪酸(MUFA,PUFA)之间的绝对浓度和相对比例略有不同(图4)。 MUFA / PUFA比值取决于肌肉区室,平均值与饮食摄入量有关。图5所示的交叉验证结果表明,使用ERETIC方法测得的UFA浓度与内部肌酸和外部参照法非常吻合。结论:将PRESS和DEPT相结合的序列已实现,以实现13 C MRS的首次体内结果。体内实验与ERETIC参考文献一起显示了其可用于评估特定肌肉区室中的UFA的可行性。

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