Sohn S, Kim E Y, Gwag B J
Laboratory of Cell Biology, Institute for Medical Sciences, Kyungkido, South Korea.
Neurosci Lett. 1998 Jan 16;240(3):147-50. doi: 10.1016/s0304-3940(97)00936-1.
The possibility that glutamate may induce neuronal apoptosis was examined in cultured cortical neurons. Neurons underwent widespread death 24 h following exposure to 50 microM glutamate. The glutamate neurotoxicity was blocked by inclusion of the glutamate antagonists, 10 microM MK-801 and 50 microM CNQX. The death was characterized by swelling cell body and bursting cytoplasmic membrane in the early phase of degeneration, suggesting that glutamate produces receptor-mediated excitotoxic necrosis. With blockade of excitotoxicity by addition of 10 microM MK-801 and 50 microM CNQX, cortical neurons exposed to 2 mM glutamate underwent necrosis morphologically identical to excitotoxicity but sensitive to 100 microM trolox, an antioxidant, suggesting that high doses of glutamate produce oxidative neuronal necrosis via non-receptor-mediated mechanisms. Interestingly, internucleosomal DNA fragmentation and chromatin condensation were observed in the course of glutamate-induced neuronal necrosis.
在培养的皮层神经元中研究了谷氨酸可能诱导神经元凋亡的可能性。暴露于50微摩尔谷氨酸后24小时,神经元发生广泛死亡。谷氨酸拮抗剂10微摩尔MK-801和50微摩尔CNQX可阻断谷氨酸神经毒性。死亡的特征是在变性早期细胞体肿胀和细胞质膜破裂,表明谷氨酸产生受体介导的兴奋性毒性坏死。通过添加10微摩尔MK-801和50微摩尔CNQX阻断兴奋性毒性后,暴露于2毫摩尔谷氨酸的皮层神经元发生形态上与兴奋性毒性相同但对100微摩尔抗氧化剂曲洛克斯敏感的坏死,表明高剂量谷氨酸通过非受体介导的机制产生氧化性神经元坏死。有趣的是,在谷氨酸诱导的神经元坏死过程中观察到核小体间DNA片段化和染色质浓缩。