Meoni P, Mugnaini M, Bunnemann B H, Trist D G, Bowery N G
Department of Pharmacology, Medical School, University of Birmingham, UK.
Brain Res Mol Brain Res. 1998 Feb;54(1):13-23. doi: 10.1016/s0169-328x(97)00289-1.
The distributions of [3H]MK-801 binding and the NMDA NR1 subunit mRNA were studied using receptor autoradiography and in-situ hybridization in rat and human brain whole-hemisphere coronal sections. Receptor protein detected by radioligand autoradiography and the mRNA for the key subunit of the receptor presented similar distributions in the forebrain, with a few areas showing an imbalance between the levels of mRNA and receptor protein. Human frontal cortex showed a relative abundance of NMDAR1 mRNA as compared to [3H]MK-801 binding. The same area in rat brain did not show any difference in the two distributions. In comparison, the rat claustrum presented a relative excess of NMDAR1 mRNA which was not detected in human sections. Human caudate nucleus exhibited relatively high levels of [3H]MK-801 binding that were unmatched in rat caudate. The hippocampi of either species presented similar levels of [3H]MK-801 binding and NMDAR1 mRNA, but when the two signals were measured in specific subfields of the hippocampal formation, the differential distribution of the two signals reflected the anatomy of hippocampal connections assuming a preferential dendritic distribution for MK-801 binding. Interestingly, rat and human hippocampi also showed some important species-dependent difference in the relative distribution of the receptor protein and mRNA. The data presented show an overall good correlation between the mRNA for the key subunit of the NMDA receptor and the functional receptor detected with radioligand binding and highlight the presence of local differences in their ratio. This may reflect different splicing of the mRNA for the NMDAR1 subunit in specific brain areas of rat and human. The species-dependent differences in the relative distribution of the mRNA for the key subunit of the NMDA receptor and that of a marker of functional receptors also highlights important differences in the NMDA function in rat and human brain.
使用受体放射自显影术和原位杂交技术,在大鼠和人类大脑全脑冠状切片中研究了[3H]MK-801结合及NMDA NR1亚基mRNA的分布情况。通过放射性配体放射自显影术检测到的受体蛋白与受体关键亚基的mRNA在前脑中呈现出相似的分布,不过有一些区域显示出mRNA水平与受体蛋白水平之间存在失衡。与[3H]MK-801结合相比,人类额叶皮质显示出NMDAR1 mRNA相对丰富。大鼠脑的同一区域在这两种分布上未显示出任何差异。相比之下,大鼠屏状核呈现出相对过量的NMDAR1 mRNA,而在人类切片中未检测到。人类尾状核表现出相对较高水平的[3H]MK-801结合,这在大鼠尾状核中并不匹配。两种物种的海马体呈现出相似水平的[3H]MK-801结合和NMDAR1 mRNA,但当在海马结构的特定亚区测量这两种信号时,两种信号的差异分布反映了海马连接的解剖结构,假设MK-801结合具有优先的树突分布。有趣的是,大鼠和人类海马体在受体蛋白和mRNA的相对分布上也显示出一些重要的物种依赖性差异。所呈现的数据显示,NMDA受体关键亚基的mRNA与通过放射性配体结合检测到的功能性受体之间总体上具有良好的相关性,并突出了它们比例中存在局部差异。这可能反映了大鼠和人类特定脑区中NMDAR1亚基mRNA的不同剪接。NMDA受体关键亚基的mRNA与功能性受体标志物相对分布的物种依赖性差异也突出了大鼠和人类大脑中NMDA功能的重要差异。