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AMPA受体亚基在颞叶癫痫患者海马结构中的分布。

Distribution of AMPA receptor subunits in the hippocampal formation of temporal lobe epilepsy patients.

作者信息

Lynd-Balta E, Pilcher W H, Joseph S A

机构信息

Division of Neurological Surgery, University of Rochester Medical School, NY 14642, USA.

出版信息

Neuroscience. 1996 May;72(1):15-29. doi: 10.1016/0306-4522(95)00554-4.

Abstract

The immunocytochemical distribution of the AMPA-selective receptor subunits GluR1 and GluR2/3 were mapped in the human hippocampal formation obtained from surgery for medically intractable temporal lobe epilepsy. GluR2/3 immunoreactivity was detected in all principal cell types of the hippocampal formation, including hilar neurons, granule cells of the dentate gyrus, and pyramidal cells of the cornu ammonis fields and subiculum. GluR2/3 immunostaining typically filled the cell bodies and processes of neurons. A comparison of GluR2/3 immunoreactivity in a sclerotic specimen versus a non-sclerotic specimen demonstrated a profound loss of staining, specifically in the areas where neuronal dropout was occurring, including CA1, CA3 and the hilus. An analysis of GluR1 immunoreactivity in non-sclerotic specimens revealed that it was predominantly localized to cellular processes throughout the cornu ammonis fields, with a sparse staining of the dentate gyrus outer molecular layer and little to no staining of the dentate gyrus inner molecular layer. Similar to the GluR2/3-immunostained patterns, GluR1 immunoreactivity was lost in the cornu ammonis fields of sclerotic hippocampal specimens, corresponding to patterns of neuronal dropout. Our most compelling finding was a unique extensive pattern of GluR1 and Glu2/3 immunoreactivity throughout the molecular layers of the dentate gyrus of severely compromised hippocampi. The altered staining of GluR1 and GluR2/3 complements some of the patterns of axonal sprouting already described for the dentate gyrus, with a conjecture that their anatomy and distribution pattern underlies to some degree the reorganization of the sclerotic hippocampus. A combination of enhanced glutamatergic transmission and changes in neuropeptides that modulate hippocampal circuitry could greatly affect the degree of excitability in the hippocampal formation. The alterations of GluR1 and GluR2/3 immunoreactivity in the dentate gyrus add another component to the concept of reorganization in the epileptic sclerotic hippocampus.

摘要

在因药物难治性颞叶癫痫接受手术获取的人类海马结构中,绘制了AMPA选择性受体亚基GluR1和GluR2/3的免疫细胞化学分布图。在海马结构的所有主要细胞类型中均检测到GluR2/3免疫反应性,包括门区神经元、齿状回颗粒细胞以及海马角区和下托的锥体细胞。GluR2/3免疫染色通常充满神经元的细胞体和突起。对硬化标本与非硬化标本中的GluR2/3免疫反应性进行比较,结果显示染色明显减少,特别是在神经元缺失的区域,包括CA1、CA3和门区。对非硬化标本中GluR1免疫反应性的分析表明,它主要定位于整个海马角区的细胞突起,齿状回外分子层染色稀疏,齿状回内分子层几乎没有染色。与GluR2/3免疫染色模式相似,硬化海马标本的海马角区中GluR1免疫反应性丧失,与神经元缺失模式相对应。我们最引人注目的发现是,在严重受损海马的齿状回分子层中,GluR1和Glu2/3免疫反应性呈现独特的广泛模式。GluR1和GluR2/3染色的改变补充了一些已描述的齿状回轴突发芽模式,并推测它们的解剖结构和分布模式在一定程度上是硬化海马重组的基础。谷氨酸能传递增强和调节海马回路的神经肽变化相结合,可能会极大地影响海马结构的兴奋程度。齿状回中GluR1和GluR2/3免疫反应性的改变为癫痫性硬化海马重组的概念增添了另一个要素。

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