Sobaniec-Lotowska Maria E
Department of Clinical Pathomorphology, Medical University of Bialystok, Poland.
Int J Exp Pathol. 2003 Jun;84(3):115-25. doi: 10.1046/j.1365-2613.2003.00343.x.
The aim of the study was to analyse the astrocyte ultrastructure within the hippocampal gyre cortex and neocortex of the temporal lobe in valproate encephalopathy induced by chronic administration of an anti-epileptic drug - sodium valproate (VPA) to rats for 1, 3, 6, 9 and 12 months, once daily intragastrically, in a dose of 200 mg/kg b.w. and after its withdrawal for 1 and 3 months. Prolonged application of VPA caused damage to protoplasmic astrocytes of the cortex regions examined, mainly in the pyramidal layer, which intensified in the later stages of the experiment, especially after 9 and 12 months. Ultrastructural alterations in astroglia during this experiment did not differ significantly between the hippocampal cortex and neocortex. The most pronounced astroglial abnormalities, concerning about 2/3 of protoplasmic astrocytes after 9 and 12 months, were characterized by considerable swelling of cells, with the presence of empty vacuolar structures in the cytoplasm, a substantial decrease in the number of gliofilaments or even their complete loss, which indicated fibrillopoietic failure of the cell, and the appearance of astrocytes showing phagocytic activity. The astrocytic changes coexisted with distinct damage to neurones and structural elements of the blood-brain barrier. One month after termination of chronic exposure to the drug, the abnormalities did not subside, whereas after 3 months features of distinct normalization could be observed in a considerable number, more than a half, of astrocytes. In valproate encephalopathy, apart from any direct effect of VPA and/or its metabolites on astrocytes, the main cause of the protoplasmic astroglial damage in the cortex of the CNS structures examined could be associated with changes in microcirculation in the cortex (vasogenic factor), leading to its ischaemia.
本研究的目的是分析在给大鼠每日一次胃内注射剂量为200mg/kg体重的抗癫痫药物丙戊酸钠(VPA)1、3、6、9和12个月,以及停药1和3个月后,丙戊酸脑病大鼠海马回皮质和颞叶新皮质内星形胶质细胞的超微结构。长期应用VPA导致所检查皮质区域的原浆性星形胶质细胞受损,主要在锥体细胞层,在实验后期这种损伤加剧,尤其是在9和12个月后。在此实验中,海马皮质和新皮质的星形胶质细胞超微结构改变无显著差异。最明显的星形胶质细胞异常,在9和12个月时约2/3的原浆性星形胶质细胞出现,其特征为细胞明显肿胀,细胞质中存在空泡结构,胶质丝数量大幅减少甚至完全消失,这表明细胞的纤维形成功能衰竭,并且出现了具有吞噬活性的星形胶质细胞。星形胶质细胞的变化与神经元和血脑屏障结构成分的明显损伤同时存在。慢性药物暴露终止1个月后,异常并未消退,而在3个月后,相当数量(超过一半)的星形胶质细胞可观察到明显的正常化特征。在丙戊酸脑病中,除了VPA和/或其代谢产物对星形胶质细胞的任何直接作用外,所检查的中枢神经系统结构皮质中原浆性星形胶质细胞损伤的主要原因可能与皮质微循环变化(血管源性因素)有关,导致其缺血。