慢性匹罗卡品和微毒素癫痫模型的丘脑神经病理学研究

Clement Hamani, Luiz E.A.M Mello
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引用次数: 5

摘要

分别给成年雄性Wistar大鼠注射150/0.5、75/1.5和50/2.0 mg/kg的匹罗卡品(Pilo)和picrotoxin (PTX) (Pilo/PTX mg/kg)。绝大多数动物出现癫痫持续状态(SE),之后观察120-131天自发性复发性癫痫发作(SRS)的发生。实验结束后,对动物进行深度麻醉,灌注10%甲醛固定液,用甲酚紫、珀尔斯和冯·科萨技术对其大脑进行加工。细胞计数是在一个规则的显微镜网格下进行的,在不同的丘脑前后水平。癫痫组的几个丘脑核,特别是中央内侧核、中央外侧核、中央旁核、中背核、后背核和后背核,表现出强烈的细胞丢失、病理性钙化和铁组织沉积。我们的结果与支持丘脑在癫痫发病机制中的重要性有关。
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Thalamic neuropathology in the chronic pilocarpine and picrotoxin model of epilepsy

Adult male Wistar rats were injected with 150/0.5, 75/1.5 and 50/2.0 mg/kg of pilocarpine (Pilo) and picrotoxin (PTX) (Pilo/PTX mg/kg). The vast majority of the animals developed status epilepticus (SE), after which they were observed for a period of 120–131 days for the occurrence of spontaneous recurrent seizures (SRS). After the experiments, animals were deeply anesthetized, perfused with a 10% formaldehyde fixative solution and their brains were processed with cresyl violet, Perls and Von Kossa techniques. Cell counts were performed under a regular microscopic grid in diverse anteroposterior levels of the thalamus. Several thalamic nuclei in the epileptic groups, particularly the central medial, central lateral, paracentral, mediodorsal, laterodorsal and lateroposterior, showed intense cell loss, pathologic calcification and iron tissue deposits. Our results are relevant to support the importance of the thalamus in the pathogenesis of the epilepsies.

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