Mathern G W, Pretorius J K, Kornblum H I, Mendoza D, Lozada A, Leite J P, Chimelli L M, Fried I, Sakamoto A C, Assirati J A, Lévesque M F, Adelson P D, Peacock W J
Department of Neurology, University of California, USA.
Brain. 1997 Nov;120 ( Pt 11):1937-59. doi: 10.1093/brain/120.11.1937.
This study was designed to determine whether hippocampal neuronal AMPA (alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid) and NMDA (N-methyl-D-aspartate) mRNA levels were differentially increased in temporal lobe epilepsy patients compared with those measured in control tissue from non-seizure autopsies. Hippocampi from hippocampal sclerosis patients (n = 28) and temporal mass lesion cases (n = 12) were compared with those from the autopsies (n = 4), and studied for AMPA GluR1-3 and NMDAR1-2 mRNAs using semi-quantitative in situ hybridization, along with fascia dentata and Ammon's horn neuron densities. Compared with the autopsies, and without correction for neuron counts, the mass lesion cases with neuron densities similar to autopsies showed: (i) significantly increased NMDAR2 hybridization densities for fascia dentata granule cells; (ii) increased AMPA GluR3 mRNA densities for Ammon's horn pyramids; and (iii) similar or numerically increased mRNAs for all other subunits and hippocampal subfields. Compared with the autopsies, hippocampal sclerosis cases with decreased neuron densities showed: (i) significantly decreased AMPA GluR1-2 and NMDAR1-2 hybridization densities for Ammon's horn pyramids and (ii) similar or numerically decreased mRNAs for all other subunits and subfields. However, correcting for changes in neuron densities showed that hippocampal sclerosis patients had increased AMPA and NMDA mRNA levels per neuron compared with autopsies, and in the CA2 resistant sector GluR2 mRNA levels were numerically greater than autopsies and mass lesion cases. Furthermore, relative to autopsies both sclerosis and mass lesion hippocampi showed that, in the stratum granulosum, the greatest mRNA increases were in AMPA GluR1 and NMDAR2 compared with the other mRNAs. In chronic temporal lobe seizure patients these results indicate that mass lesion and sclerosis cases show differential increases in hippocampal AMPA and NMDA mRNA levels per neuron compared with autopsies, especially for AMPA GluR1 and NMDAR2 in fascia dentata granule cells. These findings support the hypothesis that temporal lobe seizures are associated with increased ionotropic glutamate receptor mRNA levels and alterations in receptor subunit composition that probably contribute to neuronal hyperexcitability, synchronization and seizure generation.
本研究旨在确定与非癫痫尸检对照组织相比,颞叶癫痫患者海马神经元的α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)和N-甲基-D-天冬氨酸(NMDA)mRNA水平是否有差异增加。将海马硬化患者(n = 28)和颞叶占位性病变患者(n = 12)的海马与尸检者(n = 4)的海马进行比较,采用半定量原位杂交技术研究AMPA GluR1-3和NMDAR1-2 mRNA,并检测齿状回和海马角神经元密度。与尸检者相比,在未校正神经元计数的情况下,神经元密度与尸检者相似的占位性病变患者表现为:(i)齿状回颗粒细胞的NMDAR2杂交密度显著增加;(ii)海马角锥体的AMPA GluR3 mRNA密度增加;(iii)所有其他亚基和海马亚区的mRNA相似或在数值上增加。与尸检者相比,神经元密度降低的海马硬化患者表现为:(i)海马角锥体的AMPA GluR1-2和NMDAR1-2杂交密度显著降低;(ii)所有其他亚基和亚区的mRNA相似或在数值上降低。然而,校正神经元密度变化后发现,与尸检者相比,海马硬化患者每个神经元的AMPA和NMDA mRNA水平增加,并且在CA2抗性区,GluR2 mRNA水平在数值上高于尸检者和占位性病变患者。此外,相对于尸检者,硬化和占位性病变的海马均显示,在颗粒层中,与其他mRNA相比,AMPA GluR1和NMDAR2的mRNA增加最为显著。在慢性颞叶癫痫患者中,这些结果表明,与尸检者相比,占位性病变和硬化病例每个神经元的海马AMPA和NMDA mRNA水平有差异增加,尤其是齿状回颗粒细胞中的AMPA GluR1和NMDAR2。这些发现支持了以下假设:颞叶癫痫与离子型谷氨酸受体mRNA水平增加以及受体亚基组成改变有关,这可能导致神经元兴奋性过高、同步化和癫痫发作。