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Remodeling dendritic spines in the rat pilocarpine model of temporal lobe epilepsy.

机译:在颞叶癫痫的大鼠毛果芸香碱模型中重塑树突棘。

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摘要

Dendritic degeneration is a common pathology in temporal lobe epilepsy and its animal models. However, little is known when and how the degeneration occurs. In the present study of the rat pilocarpine model, visualization of dendrites of the hippocampal dentate granule cells (DGCs) by biocytin revealed a generalized spine loss immediately after the acute seizure induced by pilocarpine. However, this generalized damage was followed by recovery and plastic changes in spine shape and density, which occurred 15-35 days after the initial acute seizure, i.e., during the period of establishing a chronic phase of this model with the induction of spontaneous seizures. The present finding suggests that initial acute seizures do not cause permanent damages in dendrites and spines of DGCs; instead, dendritic spines are dynamically maintained in the course of the establishment and maintenance of spontaneous seizures. Local dendritic spine degeneration, detected later in the chronic phase of epilepsy, is likely to have a separate cause from initial acute insults.
机译:树突变性是颞叶癫痫及其动物模型的常见病理。但是,很少知道何时以及如何发生变性。在目前对大鼠毛状腕果模型的研究中,生物素对海马齿状颗粒细胞(DGC)的树突进行可视化显示,在毛状腕果素引起的急性癫痫发作后立即出现了广泛的脊柱丢失。但是,这种普遍性损害之后是脊柱形状和密度的恢复和可塑性变化,这发生在最初的急性癫痫发作后15-35天,即在建立该模型的慢性阶段并诱发自发性癫痫发作期间。目前的发现表明,最初的急性癫痫发作不会对DGC的树突和棘刺造成永久性损害。而是在自发性发作的建立和维持过程中动态维持树突棘。在癫痫病的慢性阶段后期发现的局部树突棘变性可能与最初的急性损伤有不同的原因。

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