首页> 外文期刊>Journal of Neurocytology: A Journal of Cellular Neurobiology >Chronological changes of N-methyl-D-aspartate receptors and excitatory amino acid carrier 1 immunoreactivities in CA1 area and subiculum after transient forebrain ischemia.
【24h】

Chronological changes of N-methyl-D-aspartate receptors and excitatory amino acid carrier 1 immunoreactivities in CA1 area and subiculum after transient forebrain ischemia.

机译:短暂性前脑缺血后CA1区和下丘脑N-甲基-D-天冬氨酸受体和兴奋性氨基酸载体1免疫反应性的时间变化。

获取原文
获取原文并翻译 | 示例
       

摘要

We investigated changes of immunoreactivities of N-methyl-D-aspartate receptor (NR) and of excitatory amino acid carrier 1 (EAAC-1), the neuronal glutamate transporter, in the vulnerable CA1 area and the less vulnerable subiculum of the gerbil hippocampus at various times following transient forebrain ischemia. At 30 min after ischemia-reperfusion, the intensity of NR immunoreactivity increased markedly in neurons of CA1 and subiculum, particularly NR2A/B, while EAAC-1 immunoreactivity was reduced in CA1. At 3 hr after reperfusion, the density of NR1 immunoreactivity markedly decreased in CA1. In contrast EAAC-1 immunoreactivity increased in CA1 and in the subiculum. At 12 hr after reperfusion, the decrease of NR1 immunoreactivity was not detected whereas EAAC-1 immunoreactivities in the CA1 area were intensified. In the subiculum, both NR subunits immunoreactivities decreased significantly, in contrast to the maintenance of EAAC-1 immunoreactivity. At 24 hr after reperfusion, both NR2A/B and EAAC-1 immunoreactivities decreased markedly in CA1 and subiculum. We tentatively suggest that the increase of NR immunoreactivity in CA1 at early times after ischemia-reperfusion may increase the delayed neuronal death, and that the increase or maintenance of EAAC-1 immunoreactivity at early times after ischemia-reperfusion may be an important factor in survival of neurons.
机译:我们调查了在脆弱的CA1区和沙土海马的较弱脆弱亚支的N-甲基-D-天冬氨酸受体(NR)和兴奋性氨基酸载体1(EAAC-1),神经元谷氨酸转运蛋白的免疫反应性在短暂性前脑缺血后的不同时间。缺血再灌注后30分钟,CA1和下丘脑神经元,尤其是NR2A / B的神经元中NR免疫反应强度显着增加,而CA1中EAAC-1免疫反应性降低。再灌注后3小时,CA1中NR1免疫反应性的密度显着降低。相反,CA1和下丘脑中的EAAC-1免疫反应性增加。再灌注后12小时,未检测到NR1免疫反应性降低,而CA1区域中的EAAC-1免疫反应性增强。与EAEA-1免疫反应性维持相反,在亚下丘脑中,两个NR亚基的免疫反应性均显着降低。再灌注后24小时,CA1和下丘脑中的NR2A / B和EAAC-1免疫反应性均显着降低。我们初步建议缺血再灌注后早期CA1的NR免疫反应性增加可能会增加延迟性神经元死亡,而缺血再灌注后早期EAAC-1免疫反应性的增加或维持可能是存活的重要因素神经元。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号