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Signal alterations of glutamate-weighted chemical exchange saturation transfer MRI in lysophosphatidylcholine-induced demyelination in the rat brain.
Lee, Do-Wan; Woo, Dong-Cheol; Heo, Hwon; Kim, Kyung Won; Kim, Jeong Kon; Lee, Dong-Hoon.
Afiliação
  • Lee DW; Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Woo DC; Department of Convergence Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea; Convergence Medicine Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Republic of Korea.
  • Heo H; Department of Convergence Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Kim KW; Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Kim JK; Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Lee DH; Departmet of Radiation Convergence Engineering, Yonsei University, Wonju, Gangwon, Republic of Korea. Electronic address: dlee1@yonsei.ac.kr.
Brain Res Bull ; 164: 334-338, 2020 11.
Article em En | MEDLINE | ID: mdl-32926951
ABSTRACT

PURPOSE:

To compare in vivo glutamate-weighted chemical exchange saturation transfer (GluCEST-weighted) signal changes between in a rat model of demyelinated multiple sclerosis and control groups. PROCEDURES Using a pre-clinical 7 T magnetic resonance imaging (MRI) system, CEST imaging was applied to a toxin (lysophosphatidylcholine; LPC) induced rat (MSLPC) and control (CTRL) groups to compare in vivo glutamate signal changes. The GluCEST-weighted signals were analyzed based on the magnetization transfer ratio asymmetry approach at 3.0 ppm on the region-of-interests (ROIs) in the corpus callosum and hippocampus at each hemispheric region.

RESULTS:

GluCEST-weighted signals were significantly changed between the CTRL and MSLPC groups, while higher glutamate signals were indicated in the MSLPC than the CTRL group ([MSLPC / CTRL]; hippocampus [6.159 ± 0.790 / 4.336 ± 0.446] and corpus callosum [-3.545 ± 0.945 / -6.038 ± 0.620], all p = 0.001).

CONCLUSIONS:

Our results show increased GluCEST-weighted signals in the LPC-induced demyelination rat brain compared with control. GluCEST-weighted imaging could be a useful tool for defining a biomarker to estimate the glutamate-related metabolism in MS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Lisofosfatidilcolinas / Doenças Desmielinizantes / Ácido Glutâmico Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Lisofosfatidilcolinas / Doenças Desmielinizantes / Ácido Glutâmico Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article