Retz K C, Coyle J T
J Neurochem. 1982 Jan;38(1):196-203. doi: 10.1111/j.1471-4159.1982.tb10872.x.
Intrastriatal injection of either kainic acid (0.35 micrograms) or ibotenic acid (7.0 micrograms) in the mouse causes a profound and selective degeneration of striatal neurons accompanied by a secondary astrocytic response. The kainate injection (0.35 micrograms) resulted in significant decrements in the striatal levels of phosphocreatine and ATP by 30 min. a progressive reduction in adenosine phosphates between 30 min and 48 h, and a decrease in energy charge; whereas lactate levels increased by 44% at 2 h, glucose levels fell by 56%. Two hours after intrastriatal injection of ibotenic acid (7.0 micrograms) similar alternations in striatal high-energy phosphates and glucose disposition were found. Prior decortication protected against the neurotoxic effects of kainate in the mouse striatum and prevented the alterations in high-energy phosphates at 2 h although lactate levels increased by 212%. These findings in vivo are consistent with the hypothesis that the neurotoxic effects of acidic excitatory amino acids involve a profound activation of energy consumption by affected neurons.
给小鼠纹状体内注射海藻酸(0.35微克)或鹅膏蕈氨酸(7.0微克)会导致纹状体神经元发生严重的选择性退化,并伴有继发性星形细胞反应。注射海藻酸(0.35微克)30分钟后,纹状体内磷酸肌酸和三磷酸腺苷水平显著下降。在30分钟至48小时之间,腺苷磷酸逐渐减少,能量电荷降低;而乳酸水平在2小时时增加了44%,葡萄糖水平下降了56%。纹状体内注射鹅膏蕈氨酸(7.0微克)2小时后,发现纹状体高能磷酸盐和葡萄糖代谢有类似变化。预先进行去皮质手术可保护小鼠纹状体免受海藻酸的神经毒性作用,并防止2小时时高能磷酸盐的改变,尽管乳酸水平增加了212%。这些体内研究结果与酸性兴奋性氨基酸的神经毒性作用涉及受影响神经元能量消耗的深度激活这一假说一致。