Hill D R, Suman-Chauhan N, Woodruff G N
Parke-Davis Neuroscience Research Centre, Addenbrookes Hospital Site, Cambridge, UK.
Eur J Pharmacol. 1993 Feb 15;244(3):303-9. doi: 10.1016/0922-4106(93)90156-4.
The autoradiographical distribution of [3H]gabapentin, the tritiated analogue of the novel anticonvulsant gabapentin (1-(aminomethyl)cyclohexaneacetic acid) was measured in rat brain. Binding to sections was uniformly inhibited by non-radioactive gabapentin and 3-isobutyl-gamma-aminobutyric acid (3-isobutyl-GABA). Specific gabapentin binding sites were unevenly distributed throughout the brain with the highest level being found in the outer layers of the cerebral cortex (38 +/- 7 fmol/mm2; n = 3) and the lowest amounts in the white matter. In the hippocampus, the distribution of the binding site paralleled the excitatory neuronal input with the highest levels of binding being measured in the outer layers of the dentate gyrus and in the dendritic regions of the CA1 pyramidal cell layer. The binding site appeared absent from the cell body region of granule and pyramidal cells. Lesions performed unilaterally in the striatum using quinolinic acid resulted in a marked loss of [3H]gabapentin binding sites as compared with sham-lesioned animals, suggesting the binding site was localized on neuronal cell bodies. These data complement and extend the results of experiments using [3H]gabapentin with homogenates of rat brain and show the discrete localization of this novel binding site in regions associated with excitatory amino acid input. The data do not support previous indications of an association of the gabapentin binding site and NMDA/glycine receptor complex.
在大鼠脑中测量了新型抗惊厥药加巴喷丁(1-(氨甲基)环己烷乙酸)的氚化类似物[3H]加巴喷丁的放射自显影分布。与切片的结合被非放射性加巴喷丁和3-异丁基-γ-氨基丁酸(3-异丁基-GABA)均匀抑制。加巴喷丁特异性结合位点在整个脑中分布不均,在大脑皮质外层水平最高(38±7 fmol/mm2;n = 3),在白质中含量最低。在海马体中,结合位点的分布与兴奋性神经元输入平行,在齿状回外层和CA1锥体细胞层的树突区域测量到最高水平的结合。在颗粒细胞和锥体细胞的胞体区域似乎没有结合位点。与假损伤动物相比,使用喹啉酸单侧损伤纹状体导致[3H]加巴喷丁结合位点明显丧失,表明结合位点定位于神经元细胞体上。这些数据补充并扩展了使用[3H]加巴喷丁与大鼠脑匀浆进行实验的结果,并显示了这个新结合位点在与兴奋性氨基酸输入相关区域的离散定位。这些数据不支持先前关于加巴喷丁结合位点与NMDA/甘氨酸受体复合物相关联的迹象。