McDonald J W, Garofalo E A, Hood T, Sackellares J C, Gilman S, McKeever P E, Troncoso J C, Johnston M V
Department of Neurology, University of Michigan, Ann Arbor.
Ann Neurol. 1991 May;29(5):529-41. doi: 10.1002/ana.410290513.
We examined binding to excitatory amino acid and inhibitory amino acid receptors in frozen hippocampal sections prepared from surgical specimens resected from 8 individuals with medically refractory temporal lobe epilepsy. The excitatory receptors studied included N-methyl-D-aspartate (NMDA), strychnine-insensitive glycine, phencyclidine, and quisqualate. The inhibitory receptors studied were gamma-aminobutyric acid type A (GABAA) and benzodiazepine. Excitatory and inhibitory amino acid receptor binding were differentially altered in the patients with temporal lobe epilepsy in comparison to 8 age-comparable autopsy control subjects, and changes in receptor binding were regionally selective in four areas. Binding to phencyclidine receptors associated with the NMDA channel was reduced by 35 to 70% in all regions in the hippocampi of the patients. In contrast, binding to the NMDA recognition site and its associated glycine modulatory site was elevated by 20 to 110% in the cornu ammonis (CA) 1 area and dentate gyrus of the hippocampus of the patients. Binding to these sites was unaffected in area CA4. Binding to the quisqualate-type excitatory amino acid receptor was unchanged in all regions except the stratum lacunosum moleculare CA1, where it was increased by 63%. GABAA and benzodiazepine receptor binding was reduced by 20 to 60% in CA1 and CA4, but unchanged in dentate gyrus. The data indicate that excitatory and inhibitory amino acid receptors are altered in the hippocampus of patients with temporal lobe epilepsy.
我们检测了从8例药物难治性颞叶癫痫患者手术切除的标本制备的冷冻海马切片中与兴奋性氨基酸和抑制性氨基酸受体的结合情况。所研究的兴奋性受体包括N-甲基-D-天冬氨酸(NMDA)、士的宁不敏感型甘氨酸、苯环利定和喹啉酸。所研究的抑制性受体是A型γ-氨基丁酸(GABAA)和苯二氮䓬。与8例年龄匹配的尸检对照受试者相比,颞叶癫痫患者的兴奋性和抑制性氨基酸受体结合存在差异改变,且受体结合的变化在四个区域具有区域选择性。患者海马所有区域中与NMDA通道相关的苯环利定受体结合减少了35%至70%。相反,患者海马的海马角(CA)1区和齿状回中与NMDA识别位点及其相关甘氨酸调节位点的结合增加了20%至110%。CA4区这些位点的结合未受影响。除分子层CA1的腔隙层外,所有区域中与喹啉酸型兴奋性氨基酸受体的结合均未改变,在该区域结合增加了63%。CA1区和CA4区中GABAA和苯二氮䓬受体结合减少了20%至60%,但齿状回中未改变。数据表明,颞叶癫痫患者海马中的兴奋性和抑制性氨基酸受体发生了改变。