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环孢素对接受溴化乙锭脱髓鞘模型的Wistar大鼠脑干影响的超微结构研究

Ultrastructural study of the effects of cyclosporine in the brainstem of Wistar rats submitted to the ethidium bromide demyelinating model.

作者信息

Bondan Eduardo Fernandes, Lallo Maria Anete, Graça Dominguita Lühers

机构信息

Universidade Paulista, São Paulo, SP, Brazil.

出版信息

Arq Neuropsiquiatr. 2008 Jun;66(2B):378-84. doi: 10.1590/s0004-282x2008000300019.

DOI:10.1590/s0004-282x2008000300019
PMID:18641876
Abstract

The ethidium bromide-demyelinating model (EB) was used to study remyelination in the brainstem under the use of cyclosporine (CsA). Wistar rats were submitted to intracisternal injection of 0.1% EB or 0.9% saline solution, and others were taken as histologic controls (group I). Within those injected with EB, some have not received immunosuppressive treatment (II); some were treated by intraperitonial route with CsA (III.E-10 mg/kg/day). Rats from group III.C were injected with saline solution and treated with CsA. The animals were perfused from 15 to 31 days post-injection collecting brainstem sections for light and transmission electron microscopy studies. After EB injection it was noted the presence of macrophages and non-degraded myelin debris, demyelinated axons, oligodendrocyte or Schwann cell remyelinated axons, groups of infiltrating pial cells, hypertrophic astrocytes and few lymphocytes. Tissue repair of EB-induced lesions in group III.E was similar to that of group II, but with the presence of a higher density of oligodendrocytes near remyelinating areas.

摘要

采用溴化乙锭脱髓鞘模型(EB),在使用环孢素(CsA)的情况下研究脑干的髓鞘再生。将Wistar大鼠经脑池内注射0.1% EB或0.9%盐溶液,其他大鼠作为组织学对照(I组)。在注射EB的大鼠中,一些未接受免疫抑制治疗(II组);一些经腹腔途径用CsA治疗(III.E组 - 10 mg/kg/天)。III.C组大鼠注射盐溶液并用CsA治疗。在注射后15至31天对动物进行灌注,收集脑干切片用于光镜和透射电镜研究。注射EB后,观察到存在巨噬细胞和未降解的髓鞘碎片、脱髓鞘轴突、少突胶质细胞或施万细胞再髓鞘化的轴突、浸润的软膜细胞群、肥大的星形胶质细胞和少量淋巴细胞。III.E组中EB诱导损伤的组织修复与II组相似,但在再髓鞘化区域附近少突胶质细胞密度更高。

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