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2,5 -己二酮性神经病中的施万细胞异常

Schwann cell abnormalities in 2,5-hexanedione neuropathy.

作者信息

Powell H C, Koch T, Garrett R, Lampert P W

出版信息

J Neurocytol. 1978 Aug;7(4):517-28. doi: 10.1007/BF01173995.

Abstract

Distinctive cytoplasmic alterations of Schwann cells were observed by electron microscopy in rats and mice with peripheral neuropathy induced by chronic exposure to 2,5-hexanedione. Pronounced enlargement of Schwann cells was due to accumulation of 100 angstrom cytoplasmic filaments and endoplasmic reticulum and was most often observed after 12--15 weeks exposure to 2,5-hexanedione. Examination of teased nerve fibres revealed segmental demyelination and remyelination involving axons of normal diameter as well as giant axons. The filament disorder induced by 2,5-hexanedione administration is not limited solely to axoplasmic contents. Possible mechanisms of demyelination are discussed and the changes are compared to those observed in human neuropathy for which 2,5-hexanedione appears to be the closest experimental model.

摘要

通过电子显微镜观察发现,长期接触2,5 -己二酮诱导周围神经病变的大鼠和小鼠的施万细胞存在独特的细胞质改变。施万细胞明显肿大是由于100埃的细胞质细丝和内质网积聚所致,最常在接触2,5 -己二酮12 - 15周后观察到。对 teased 神经纤维的检查显示,节段性脱髓鞘和髓鞘再生涉及正常直径的轴突以及巨大轴突。2,5 -己二酮给药诱导的细丝紊乱不仅限于轴浆内容物。文中讨论了脱髓鞘的可能机制,并将这些变化与在人类神经病变中观察到的变化进行了比较,2,5 -己二酮似乎是最接近的实验模型。

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