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Flash visual evoked potentials in the hypomyelinated mutant mouse shiverer

机译:下髓鞘突变的小鼠颤抖中的闪光视觉诱发电位

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摘要

Myelin basic protein (MBP) is an essential component of central nervous system (CNS) myelin, as demonstrated by shiverer mutant mice that have deletions of most of the Mbp structural gene. These mutants do not produce detectable MBP protein, and their CNS is hypomyelinated. Although the function of the visual pathway is presumed to be adversely affected by hypomyelination of the optic nerve, it has never been studied. We compared flash visual evoked potentials (FVEPs) of shiverer homozygotes with those of their wild-type littermates in order to characterize any dysfunction. There was a statistically significant delay in the implicit times of a negative component peaking at 85 ms and a large positive component peaking at 170 ms in the FVEPs of the shiverer mice. The amplitudes of the two components did not differ significantly in the shiverers and wild-type controls. Barring a retinal pathology, which cannot be excluded by these data, the delayed FVEP of the shiverer can likely be attributed to effects of hypomyelination of the optic nerve, optic tract and visual radiations on conduction time in the visual pathway and subsequent further post-synaptic delays.
机译:髓鞘碱性蛋白(MBP)是中枢神经系统(CNS)髓鞘的重要组成部分,这是由颤抖的突变小鼠所证实的,该小鼠具有大部分Mbp结构基因的缺失。这些突变体不产生可检测的MBP蛋白,并且它们的CNS是低髓鞘的。尽管假定视觉通路的功能受到视神经髓鞘不足的不利影响,但从未对其进行过研究。我们比较了颤抖纯合子与野生型同窝动物的闪光视觉诱发电位(FVEP),以表征任何功能障碍。在颤抖小鼠的FVEP中,负组分在85 ms处达到峰值,而大的正组分在170 ms处达到峰值,隐式时间存在统计学上的显着延迟。在颤抖和野生型对照中,这两个分量的幅度没有显着差异。除非这些数据不能排除视网膜病理,否则颤抖的FVEP延迟可能归因于视神经,视神经束和视辐射的低髓鞘性对视路径中传导时间的影响,以及随后突触后的进一步影响。延误。

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