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2
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NMR Biomed. 2017 Jul;30(7). doi: 10.1002/nbm.3716. Epub 2017 Mar 8.
3
Creatine CEST MRI for Differentiating Gliomas with Different Degrees of Aggressiveness.用于鉴别不同侵袭程度胶质瘤的肌酸化学交换饱和转移磁共振成像
Mol Imaging Biol. 2017 Apr;19(2):225-232. doi: 10.1007/s11307-016-0995-0.
4
Downfield-NOE-suppressed amide-CEST-MRI at 7 Tesla provides a unique contrast in human glioblastoma.7特斯拉下的场下NOE抑制酰胺CEST-MRI在人类胶质母细胞瘤中提供了独特的对比。
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5
Investigating GluCEST and its specificity for pH mapping at low temperatures.研究低温下的GluCEST及其对pH值成像的特异性。
NMR Biomed. 2015 Nov;28(11):1507-17. doi: 10.1002/nbm.3416. Epub 2015 Sep 28.
6
Relaxation-compensated CEST-MRI of the human brain at 7T: Unbiased insight into NOE and amide signal changes in human glioblastoma.7T下人脑的弛豫补偿CEST-MRI:对人类胶质母细胞瘤中NOE和酰胺信号变化的无偏见解
Neuroimage. 2015 May 15;112:180-188. doi: 10.1016/j.neuroimage.2015.02.040. Epub 2015 Feb 26.
7
A combined analytical solution for chemical exchange saturation transfer and semi-solid magnetization transfer.化学交换饱和转移与半固体磁化转移的联合解析解
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Mol Imaging. 2014;13. doi: 10.2310/7290.2014.00046.
9
CEST signal at 2ppm (CEST@2ppm) from Z-spectral fitting correlates with creatine distribution in brain tumor.来自Z谱拟合的2ppm处的化学交换饱和转移(CEST)信号(CEST@2ppm)与脑肿瘤中的肌酸分布相关。
NMR Biomed. 2015 Jan;28(1):1-8. doi: 10.1002/nbm.3216. Epub 2014 Oct 8.
10
On the origins of chemical exchange saturation transfer (CEST) contrast in tumors at 9.4 T.在 9.4T 下肿瘤中化学交换饱和转移(CEST)对比的起源。
NMR Biomed. 2014 Apr;27(4):406-16. doi: 10.1002/nbm.3075. Epub 2014 Jan 29.

大鼠脑内 2 ppm 处 CEST 信号的分子起源分配。

Assignment of the molecular origins of CEST signals at 2 ppm in rat brain.

机构信息

Vanderbilt University Institute of Imaging Science, Nashville, Tennessee, USA.

Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, Tennessee, USA.

出版信息

Magn Reson Med. 2017 Sep;78(3):881-887. doi: 10.1002/mrm.26802. Epub 2017 Jun 26.

DOI:10.1002/mrm.26802
PMID:28653349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5561473/
Abstract

PURPOSE

Chemical exchange saturation transfer effects at 2 ppm (CEST@2ppm) in brain have previously been interpreted as originating from creatine. However, protein guanidino amine protons may also contribute to CEST@2ppm. This study aims to investigate the molecular origins and specificity of CEST@2ppm in brain.

METHODS

Two experiments were performed: (i) samples containing egg white albumin and creatine were dialyzed using a semipermeable membrane to demonstrate that proteins and creatine can be separated by this method; and (ii) tissue homogenates of rat brain with and without dialysis to remove creatine were studied to measure the relative contributions of proteins and creatine to CEST@2ppm.

RESULTS

The experiments indicate that dialysis can successfully remove creatine from proteins. Measurements on tissue homogenates show that, with the removal of creatine via dialysis, CEST@2ppm decreases to approximately 34% of its value before dialysis, which indicates that proteins and creatine have comparable contribution to the CEST@2ppm in brain. However, considering the contribution from peptides and amino acids to CEST@2ppm, creatine may have much less contribution to CEST@2ppm.

CONCLUSIONS

The contribution of proteins, peptides, and amino acids to CEST@2ppm cannot be neglected. The CEST@2ppm measurements of creatine in rat brain should be interpreted with caution. Magn Reson Med 78:881-887, 2017. © 2017 International Society for Magnetic Resonance in Medicine.

摘要

目的

此前,在 2 ppm(CEST@2ppm)处脑内的化学交换饱和转移效应被解释为来源于肌酸。然而,蛋白质胍基胺质子也可能对 CEST@2ppm 有贡献。本研究旨在探讨脑内 CEST@2ppm 的分子起源和特异性。

方法

进行了两项实验:(i)使用半透膜对含有蛋清白蛋白和肌酸的样品进行透析,以证明该方法可以将蛋白质和肌酸分离;(ii)研究了未经透析和经透析去除肌酸的大鼠脑匀浆,以测量蛋白质和肌酸对 CEST@2ppm 的相对贡献。

结果

实验表明,透析可以成功地将肌酸从蛋白质中去除。对组织匀浆的测量表明,通过透析去除肌酸后,CEST@2ppm 降低至透析前的约 34%,这表明蛋白质和肌酸对脑内 CEST@2ppm 的贡献相当。然而,考虑到肽和氨基酸对 CEST@2ppm 的贡献,肌酸对 CEST@2ppm 的贡献可能要小得多。

结论

蛋白质、肽和氨基酸对 CEST@2ppm 的贡献不容忽视。在解释大鼠脑内 CEST@2ppm 测量值时应谨慎。磁共振医学 78:881-887,2017。© 2017 国际磁共振学会。