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UTE MRI for assessing demyelination in an mTBI mouse model: An open-field low-intensity blast study. | LitMetric

UTE MRI for assessing demyelination in an mTBI mouse model: An open-field low-intensity blast study.

Neuroimage

Department of Radiology, University of California San Diego, CA, USA; Radiology Service, VA San Diego Healthcare System, CA, USA; Department of Bioengineering, University of California San Diego, CA, USA. Electronic address:

Published: February 2025

Mild traumatic brain injury (mTBI) is a leading cause of long-term disability. Following mTBI, secondary chemical cascades and neuroinflammation can result in myelin damage, significantly impairing cognitive function. This study aims to assess demyelination in mice with mTBI induced by open-field low-intensity blast (LIB) using a novel three-dimensional short repetition time adiabatic inversion recovery UTE (3D STAIR-UTE) magnetic resonance imaging (MRI) sequence. Thirty male C57BL/6 mice, with 15 experiencing mTBI and 15 serving as sham controls, were included in this study. Behavioral tests were performed starting at 5 days post-injury to assess motor activity and anxiety-like responses followed by STAIR-UTE imaging using a pre-clinical 3T MRI scanner. Additionally, a proton density-weighted UTE sequence was scanned alongside the STAIR-UTE for quantification of myelin proton fraction (MPF). Luxol fast blue (LFB) staining was performed to evaluate myelin changes between the mTBI group and the control group. The behavioral tests indicated decreased motor activity in the center zone and increased anxiety-like response in the mTBI mice compared to sham controls. The STAIR-UTE sequence revealed significantly lower MPFs in the corpus callosum of mTBI mice (8.4 ± 0.4 % vs. 8.7 ± 0.4 %; P = 0.003), consistent with the myelin reduction observed in the LFB staining (0.77 ± 0.22 vs. 1.09 ± 0.15; P = 0.004). Our findings demonstrate that the STAIR-UTE sequence facilitates quantitative myelin imaging at 3T MRI, enabling the detection of demyelination in the white matter of the mouse brain associated with alterations in motor and anxiety domains post-LIB exposure.

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Source
http://dx.doi.org/10.1016/j.neuroimage.2025.121103DOI Listing

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