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Microzonal decreases in the immunostaining for non-NMDA ionotropic excitatory amino acid receptor subunits GluR 2/3 and GluR 5/6/7 in the human epileptogenic neocortex

机译:人类癫痫新皮层中非NMDA离子型兴奋性氨基酸受体亚基GluR 2/3和GluR 5/6/7的免疫染色微区减少

摘要

Potential alterations in glutamate-utilizing excitatory circuits in resected human epileptogenic frontal and temporal neocortex were investigated by using immunocytochemical methods to visualize receptor subunits which comprise the AMPA/kainate (GluR2/3) and kainate (GluR5/6/7) receptor subtypes. Examination of the patterns of immunostaining in regions of neocortex that were identified as spiking and non-spiking based on intraoperative electrocorticography revealed dramatic, microzonal decreases in immunoreactivity for the receptor subunits examined. The patches of decreased immunostaining for GluR2/3 and for GluR5/6/7 were often coincident with respect to each other. However, such abnormal regions were not necessarily correlated with any particular electrocorticographically defined regions nor any overtly abnormal cytoarchitectural features in adjacent Nissl-stained sections. Moreover in many but not all cases, the focal regions of decreased receptor subunit immunoreactivity coincided with small patches of decreased parvalbumin immunoreactivity, a calcium-binding protein which labels a subpopulation of powerful inhibitory GABAergic interneurons. These results indicate that in the human epileptogenic neocortex there may be alterations in particular excitatory and/or inhibitory synaptic systems at small, multiple neocortical foci, and that these alterations are found mostly in the same regions. We suggest that these alterations may contribute to the initiation and/or propagation of seizure activity.
机译:通过使用免疫细胞化学方法观察包括AMPA /海藻酸酯(GluR2 / 3)和海藻酸酯(GluR5 / 6/7)受体亚型的受体亚基,研究了切除的人类癫痫发生前额叶和颞叶新皮层中利用谷氨酸的兴奋性回路的潜在变化。根据术中脑电图检查,对新皮层区域中被识别为加标和不加标的区域的免疫染色模式进行了检查,发现所检查受体亚单位的免疫反应性显着降低。 GluR2 / 3和GluR5 / 6/7免疫染色降低的斑块通常彼此重合。但是,这种异常区域不一定与相邻的Nissl染色切片中任何特定的皮层电图定义区域或任何明显异常的细胞结构特征相关。此外,在许多但不是全部情况下,受体亚单位免疫反应性降低的病灶区域与小白蛋白免疫反应性降低的小斑块相吻合,小钙蛋白结合蛋白是一种钙结合蛋白,标记了强大的抑制性GABA能中间神经元。这些结果表明在人类致癫痫性新皮层中,在小的,多个新皮层病灶处,特别是兴奋性和/或抑制性突触系统可能发生改变,并且这些改变主要存在于相同区域。我们建议这些改变可能有助于癫痫发作活动的开始和/或传播。

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