Seil F J, Blank N K, Leiman A L
Brain Res. 1979 Feb 2;161(2):253-65. doi: 10.1016/0006-8993(79)90067-2.
Cultures of mouse cerebellum were exposed for various intervals after explantation to kainic acid, a glutamic acid analog. Purkinje cells and intracerebellar nucleus neurons were destroyed and cortical laminar formation was inhibited by exposure to kainic acid, while granule cells were relatively spared. Prolonged kainate treatment also reduced the granule cell population. The destructive effects of kainic acid were evident upon exposure of Purkinje cells prior to the development of parallel fiber-Purkinje cell synapses, the neurotransmitter for which is believed to be glutamic acid. Glutamate application to intracerebellar nucleus neurons in vitro did not evoke extracellularly recorded excitatory effects, suggesting that these kainate-sensitive neurons do not have significant numbers of glutamate receptors. The combination of these observations suggests that neuronal toxic effects of kainic acid are not exclusively mediated by action on glutamate receptors, but involve other, less specific mechanisms as well.
将小鼠小脑培养物在移出后暴露于谷氨酸类似物 kainic 酸不同时间。暴露于 kainic 酸会破坏浦肯野细胞和小脑核神经元,并抑制皮质层状形成,而颗粒细胞相对未受影响。长时间的 kainate 处理也会减少颗粒细胞数量。在平行纤维 - 浦肯野细胞突触发育之前暴露浦肯野细胞时,kainic 酸的破坏作用就很明显,据信其神经递质为谷氨酸。在体外将谷氨酸应用于小脑核神经元并未引起细胞外记录到的兴奋作用,这表明这些对 kainate 敏感的神经元没有大量的谷氨酸受体。这些观察结果共同表明,kainic 酸的神经元毒性作用并非仅由对谷氨酸受体的作用介导,还涉及其他不太特异的机制。