神经突定向弥散和密度成像可以检测ALS小鼠脊髓症状前轴突变性。

Q2 Medicine
Functional neurology Pub Date : 2018-07-01
R G Gatto, S M Mustafi, M Y Amin, T H Mareci, Yu-Chien Wu, R L Magin
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引用次数: 0

摘要

神经突定向弥散和密度成像(NODDI)是一种MRI多壳扩散技术,为研究神经退行性疾病的微结构变化提供了新的见解。本研究主要旨在确定noddi衍生参数与肌萎缩侧索硬化症(ALS)早期白质(WM)异常变化之间的关系。在Bruker Avance III HD 17.6T磁铁中扫描ALS小鼠(G93A-SOD1小鼠)的脊髓。采用荧光轴突标记小鼠(YFP, G93A-SOD1小鼠)进行定量组织学分析。NODDI细胞内体积分数降低(-24%),取向弥散指数增加(+35%),各向同性体积分数增加(+33%)。此外,组织病理学结果显示轴突面积减少(-11%),髓磷脂含量减少(-29%)。WM在轴突内间隙减少(-71%),轴突外间隙增加(+22%)。我们的研究表明,NODDI可能是一种检测ALS症状前脊髓WM微结构变性的合适技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neurite orientation dispersion and density imaging can detect presymptomatic axonal degeneration in the spinal cord of ALS mice.

Neurite orientation dispersion and density imaging can detect presymptomatic axonal degeneration in the spinal cord of ALS mice.

Neurite orientation dispersion and density imaging can detect presymptomatic axonal degeneration in the spinal cord of ALS mice.

Neurite orientation dispersion and density imaging (NODDI), a MRI multi-shell diffusion technique, has offered new insights for the study of microstructural changes in neurodegenerative diseases. Mainly, the present study aimed to determine the connection between NODDI-derived parameters and changes in white matter (WM) abnormalities at early stages of amyotrophic lateral sclerosis (ALS). Spinal cords from ALS mice (G93A-SOD1 mice) were scanned in a Bruker Avance III HD 17.6T magnet. Fluorescent axonal-tagged mice (YFP, G93A-SOD1 mice) were used for quantitative histological analysis. NODDI showed a decrease in intra-cellular volume fraction (-24%) and increases in orientation dispersion index (+35%) and isotropic volume fraction (+33%). In addition, histoathological results demonstrated a reductions in axonal area (-11%) and myelin content (-29%). A histological decrease in WM intra-axonal space (-71%) and an increase in the extra-axonal compartment (+22%) were also detected. Our studies demonstrate that NODDI may be a suitable technique for detecting presymptomatic spinal cord WM microstructural degeneration in ALS.

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来源期刊
Functional neurology
Functional neurology 医学-神经科学
CiteScore
3.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Information not localized
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