In vivo GluCEST MRI: Reproducibility, background contribution and source of glutamate changes in the MPTP model of Parkinson's disease

被引:36
作者
Bagga, Puneet [1 ]
Pickup, Stephen [1 ]
Crescenzi, Rachelle [1 ]
Martinez, Daniel [2 ]
Borthakur, Arijitt [1 ]
D'Aquilla, Kevin [1 ]
Singh, Anup [4 ]
Verma, Gaurav [1 ]
Detre, John A. [1 ,3 ]
Greenberg, Joel [3 ]
Hariharan, Hari [1 ]
Reddy, Ravinder [1 ]
机构
[1] Univ Penn, Dept Radiol, Ctr Magnet Resonance & Opt Imaging, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[4] Indian Inst Technol, Ctr Biomed Engn, New Delhi, India
基金
美国国家卫生研究院;
关键词
MOUSE MODEL; NEURODEGENERATION; SPECTRA; MICE;
D O I
10.1038/s41598-018-21035-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glutamate Chemical Exchange Saturation Transfer (GluCEST) MRI is a recently developed technique to image glutamate. In the present study, we evaluated the reproducibility and background contamination to the GluCEST and source of the GluCEST changes in a mouse model of Parkinson's disease. Repeated measurements in five mice demonstrated an intra-animal coefficient of variation (CV) of GluCEST signal to be 2.3 +/- 1.3% and inter-animal CV of GluCEST to be 3.3 +/- 0.3%. Mice were treated with MPTP to create a localized striatal elevation of glutamate. We found an elevation in the GluCEST contrast of the striatum following MPTP treatment (Control: 23.3 +/- 0.8%, n = 16; MPTP: 26.2 +/- 0.8%, n = 19; p <= 0.001). Additionally, the positive association between glutamate concentration measured via H-1 MRS and GluCEST signal was used to estimate background contribution to the measured GluCEST. The contribution of signal from non-glutamate sources was found to be similar to 28% of the total GluCEST. Immunohistochemical analysis of the brain showed co-localization of glutamate with GFAP in the striatum. This suggests that the elevated glutamate present in the striatum in this mouse model reflects astroglial proliferation or reactivity due to the action of MPTP. The potential of GluCEST as a biomarker for imaging inflammation mediated gliosis is discussed.
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页数:9
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