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慢性脱髓鞘性颈髓斑块中的轴突变化

Axonal changes in chronic demyelinated cervical spinal cord plaques.

作者信息

Lovas G, Szilágyi N, Majtényi K, Palkovits M, Komoly S

机构信息

Department of Neurology, 'Jahn Ferenc' Teaching Hospital, Laboratory of Neuromorphology, Semmelweis University Medical School, Budapest, Hungary.

出版信息

Brain. 2000 Feb;123 ( Pt 2):308-17. doi: 10.1093/brain/123.2.308.

Abstract

Imaging and pathomorphological studies in multiple sclerosis suggest that axonal injury and axonal loss are playing a crucial role in those with persistent disability and long-standing disease. Although the existence of axonal injury in multiple sclerosis is proven, especially in the zone of active inflammation, the effect of chronic inflammation on the axons remains elusive. The aim of this study was to perform a quantitative morphometrical analysis, estimating axonal loss and evaluating axonal degenerative changes in cervical spinal cord samples of patients suffering from secondary progressive multiple sclerosis. Completely demyelinated plaques, normal appearing white matter (NAWM) and control material from anatomically identical regions of the cord have been compared. Neurofilament immunostaining was used for identification of the axons. We observed a significant reduction of axonal density (number of axons/mm(2)) in multiple sclerosis, both in the plaque and in the NAWM compared with the control cases. Axons under approximately 3.3 microm diameter seemed to be more affected. The intensity of the immunostaining was significantly reduced in the plaque compared with either NAWM or control. Our results on the cervical cord combined with other observations support the concept of slow axonal degeneration rather than acute damage as a cause of chronic disability in multiple sclerosis.

摘要

多发性硬化症的影像学和病理形态学研究表明,轴突损伤和轴突丧失在那些存在持续性残疾和病程较长的患者中起着关键作用。尽管多发性硬化症中轴突损伤的存在已得到证实,尤其是在炎症活跃区域,但慢性炎症对轴突的影响仍不清楚。本研究的目的是进行定量形态计量分析,估计轴突丧失情况,并评估继发进展型多发性硬化症患者颈髓样本中的轴突退行性变化。对完全脱髓鞘斑块、外观正常的白质(NAWM)以及来自脊髓解剖结构相同区域的对照材料进行了比较。使用神经丝免疫染色来识别轴突。我们观察到,与对照病例相比,多发性硬化症患者的斑块和NAWM中的轴突密度(每平方毫米轴突数量)均显著降低。直径约3.3微米以下的轴突似乎受影响更大。与NAWM或对照相比,斑块中的免疫染色强度显著降低。我们在颈髓上的研究结果与其他观察结果相结合,支持了轴突缓慢退化而非急性损伤是多发性硬化症慢性残疾原因的观点。

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