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癫痫大脑受损齿状回中的神经可塑性。

Neuroplasticity in the damaged dentate gyrus of the epileptic brain.

作者信息

Ribak Charles E, Dashtipour Khashayar

机构信息

Department of Anatomy and Neurobiology, University of California at Irvine, College of Medicine, Irvine, CA 92697-1275, USA.

出版信息

Prog Brain Res. 2002;136:319-28. doi: 10.1016/s0079-6123(02)36027-8.

Abstract

Using Golgi preparations, Cajal described many cell types and connections of the dentate gyrus. He described granule cells as having a round or elliptical cell body with their long axis perpendicular to the granule cell layer, dendrites arising from one pole and an axon arising from the other. Cajal apparently never studied the brains from epileptic animals or humans, and thus did not report on changes in granule cell morphology after epilepsy. Several neuroplastic changes have been described in the dentate gyrus of epileptic mammals in the past decade or so using modern methods. Two changes involving their processes include mossy fiber sprouting of granule cell axons into the inner molecular layer of the dentate gyrus and the formation of hilar basal dendrites. Two changes associated with increased neurogenesis of granule cells in the epileptic brain include hilar ectopic granule cells and the dispersion of the granule cell layer. The significance of the first two changes is that granule cell axon collaterals establish additional synapses with apical and basal dendrites of granule cells, and these connections contribute to new recurrent excitatory circuitry. The significance of increased neurogenesis is that granule cells are migrating into inappropriate areas (deep hilus) or excessive numbers of granule cells accumulate in the layer (dispersion). These data on the epileptic dentate gyrus show that granule cells may change their axonal and dendritic arbors as well as their numbers and position to respond to altered activity possibly caused by decreased inhibition. These findings indicate that the dentate gyrus shows several neuroplastic changes following temporal lobe epilepsy.

摘要

通过高尔基染色法,卡哈尔描述了齿状回的多种细胞类型和连接。他描述颗粒细胞具有圆形或椭圆形的细胞体,其长轴垂直于颗粒细胞层,树突从一极发出,轴突从另一极发出。卡哈尔显然从未研究过癫痫动物或人类的大脑,因此也没有报告癫痫后颗粒细胞形态的变化。在过去十年左右的时间里,使用现代方法在癫痫哺乳动物的齿状回中描述了几种神经可塑性变化。涉及它们突起的两种变化包括颗粒细胞轴突的苔藓纤维向齿状回内分子层的发芽以及门区基底树突的形成。与癫痫大脑中颗粒细胞神经发生增加相关的两种变化包括门区异位颗粒细胞和颗粒细胞层的分散。前两种变化的意义在于颗粒细胞轴突侧支与颗粒细胞的顶树突和基底树突建立了额外的突触,这些连接有助于形成新的反复性兴奋性回路。神经发生增加的意义在于颗粒细胞迁移到不适当的区域(深部门区)或该层中积累了过多数量的颗粒细胞(分散)。这些关于癫痫齿状回的数据表明,颗粒细胞可能会改变其轴突和树突分支以及它们的数量和位置,以应对可能由抑制减少引起的活动改变。这些发现表明,颞叶癫痫后齿状回会出现几种神经可塑性变化。

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