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首页> 外文期刊>NeuroImage >Dynamics of MRI lesion development in an animal model of viral-induced acute progressive CNS demyelination.
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Dynamics of MRI lesion development in an animal model of viral-induced acute progressive CNS demyelination.

机译:病毒诱发的急性进行性中枢神经系统脱髓鞘动物模型中MRI病变发展的动力学。

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摘要

Theiler's murine encephalitis virus (TMEV) infection in mice is an established model of CNS demyelinating diseases. The aim of the study was to determine the chronological pattern of lesion development in this model of monophasic fulminant demyelinating disease. We followed six highly susceptible interferon-gamma receptor knockout mice with serial in vivo brain magnetic resonance imaging (MRI) studies to determine changes in overall T2 lesion load and gadolinium enhancement. Altogether, 163 individual lesions were followed over 52 days. The number of lesions increased linearly with time. Four chronological patterns of lesion development were seen: (a) expanding lesions (48.5% of all lesions, 54.05% volume contribution); (b) expanding-retracting lesions (20.85% of all lesions, 15.03% volume contribution); (c) fluctuating lesions (16.6% of all lesions, 28.8% volume contribution); (d) stable lesions (14.05% of all lesions, 2.12% volume contribution). Gadolinium enhancement was not seen in the evolution ofevery lesion. Enhancement was both time- and lesion type-dependent. Early in the disease course (<43 days after infection), enhancement was almost always seen, later on (>43 days after infection) it was only seen in 8% of new lesions. All of fluctuating, 85.3% of expanding, 83.5% of expanding-retracting, and 56.5% of stable lesions were associated with gadolinium enhancement. We conclude that the MRI features of TMEV-induced demyelination in this model showed four unique chronological patterns, and inconsistent gadolinium enhancement. These novel findings may provide new insights into the pathogenesis of acute fulminant multiple sclerosis (MS).
机译:小鼠泰勒氏鼠脑炎病毒(TMEV)感染是中枢神经系统脱髓鞘疾病的公认模型。该研究的目的是确定这种单相暴发性脱髓鞘疾病模型中病变发展的时间顺序。我们跟踪了六只高度敏感的干扰素-γ受体敲除小鼠,进行了一系列体内脑磁共振成像(MRI)研究,以确定总体T2损伤负荷和g增强的变化。在52天内共追踪了163个个体病变。病变数目随时间线性增加。可见病灶发展的四种时间顺序:(a)病灶扩大(占所有病灶的48.5%,占体积的54.05%); (b)伸缩性病变(占所有病变的20.85%,体积贡献的15.03%); (c)波动的病变(占所有病变的16.6%,占体积的28.8%); (d)病灶稳定(占所有病灶的14.05%,占体积的2.12%)。在每个病变的演变过程中均未见d的增强。增强与时间和病变类型有关。在病程的早期(感染后<43天),几乎总是可见到增强,后来(感染后> 43天)仅在8%的新病灶中可见到增强。与g增强有关的所有波动,扩张的85.3%,扩张-收缩的83.5%和稳定的病变的56.5%。我们得出的结论是,在该模型中,TMEV引起的脱髓鞘的MRI特征显示出四种独特的时间顺序模式,以及enhancement增强不一致。这些新发现可能为急性暴发性多发性硬化症(MS)的发病机理提供新的见解。

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