Neurite定向分散和密度成像可以检测ALS小鼠脊髓的症状前轴突变性。

Q2 Medicine Functional neurology Pub Date : 2018-07-01 DOI:10.11138/FNEUR/2018.33.3.155
Rodolfo Gabriel Gatto, S. M. Mustafi, M. Amin, T. Mareci, Yu-chien Wu, R. Magin
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引用次数: 24

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。
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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
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0.00%
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>12 weeks
期刊介绍: Information not localized
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