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首页> 外文期刊>Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology >Widespread loss of neuronal populations in the spinal ventral horn in sporadic motor neuron disease. A morphometric study.
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Widespread loss of neuronal populations in the spinal ventral horn in sporadic motor neuron disease. A morphometric study.

机译:散发性运动神经元疾病在脊髓腹角神经元种群的广泛流失。形态计量学研究。

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摘要

The cytopathology and loss of neurons was studied in 7670 neurons from the ventral horn of the third lumbar segment of the spinal cord of six sporadic motor neuron disease (MND) patients compared with 7568 neurons in seven age matched control subjects. A modified Tomlinson et al. [Tomlinson BE, Irving D, Rebeiz JJ. Total numbers of limb motor neurones in the human lumbosacral cord and an analysis of the accuracy of various sampling procedures. J Neurol Sci 1973;20:313-27] sampling procedure was used for neuronal counts. The ventral horn was divided in quadrants. Neuronal populations were also classified by the maximum cell diameter through the nucleolus. There was widespread loss of neurons in all quadrants of the ventral horn in MND. Size distribution histograms showed similar neuron loss across all populations of neurons. The dorsomedial quadrant contains almost exclusively interneurons and the ventrolateral quadrant mostly motor neurons. The cytopathology of neurons in the dorsomedial quadrant and of large motorneurons in the ventrolateral quadrant MND was similar. In the dorsomedial quadrant, neuron loss (56.7%) was similar to the loss of large motor neurons in the ventrolateral quadrant (64.4%). The loss of presumed motor neurons and interneurons increased with increased disease duration. There was no evidence that loss of presumed interneurons occurred prior, or subsequent, to loss of motor neurons. We conclude that, in sporadic MND, all neuronal populations in the ventral horn are affected and that interneurons are involved to a similar extent and in parallel with motor neurons, as reported in the G86R transgenic mouse model of familial MND. The increasing evidence of loss of neurons other than motor neurons in MND suggests the need for revising the concept of selective motor neuron vulnerability.
机译:在六名散发性运动神经元疾病(MND)患者的脊髓第三腰节腹侧角的7670个神经元中研究了7670个神经元的细胞病理学和损失,而在7个年龄匹配的对照组中,则为7568个神经元。修改的汤姆林森等。 [汤姆林森(Tomlinson BE),欧文(Irving),丽贝兹(Rebeiz JJ)。人腰s部肢体运动神经元总数以及各种采样程序的准确性分析。 [J Neurol Sci 1973; 20:313-27]采样程序用于神经元计数。腹角分为四象限。还通过通过核仁的最大细胞直径对神经元群体进行分类。在MND腹角的所有象限中神经元普遍丢失。大小分布直方图显示在所有神经元种群中相似的神经元丢失。背侧象限几乎只包含中间神经元,腹侧象限主要包含运动神经元。背侧象限中神经元的细胞病理学和腹侧象限MND中大型运动神经元的细胞病理学相似。在背侧象限中,神经元丢失(56.7%)与腹侧象限中大型运动神经元的丢失(64.4%)相似。推测的运动神经元和中间神经元的丧失随着疾病持续时间的增加而增加。没有证据表明假定的中间神经元丢失发生在运动神经元丢失之前或之后。我们得出的结论是,在散发性MND中,腹角中的所有神经元种群均受到影响,并且在家族性MND的G86R转基因小鼠模型中报道,中间神经元的参与程度与运动神经元相似,且与运动神经元平行。 MND中除运动神经元以外的其他神经元丧失的证据越来越多,这表明需要修订选择性运动神经元易损性的概念。

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