Hasbani M J, Hyrc K L, Faddis B T, Romano C, Goldberg M P
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Exp Neurol. 1998 Nov;154(1):241-58. doi: 10.1006/exnr.1998.6929.
The postsynaptic neuronal dendrite is selectively vulnerable to hypoxic-ischemic brain injury and glutamate receptor overactivation. We explored the glutamate receptor pharmacology and ionic basis of rapid, reversible alterations in dendritic shape which occur in cultured neurons exposed to glutamate. Dendrite morphology was assessed with the fluorescent membrane tracer, DiI, or immunofluorescence labeling of the somatodendritic protein, MAP2. Cortical cultures derived from 15-day-old mouse embryos underwent segmental dendritic beading when exposed to NMDA, AMPA, or kainate, but not to metabotropic glutamate receptor agonists. Varicosity formation in response to NMDA or kainate application was substantially attenuated in reduced sodium buffer (substituted with N-methyl-D-glucamine). Furthermore, veratridine-induced sodium entry mimicked excitotoxic alterations in dendrites and additionally caused varicosity formation in axons. Solutions deficient in chloride (substituted with Na methylsulfate) and antagonists of chloride-permeable GABA/glycine receptors reduced NMDA- or kainate-induced varicosity formation. An increase in dendrite volume was observed as varicosities formed, and varicosity formation was attenuated in sucrose-supplemented hypertonic media. Despite marked structural changes affecting virtually all neurons, dendrite shape returned to normal within 2 h of terminating glutamate receptor agonist application. Neurons exposed to kainate recovered more rapidly than those exposed to NMDA, and neurons exposed to NMDA in calcium-free buffer recovered more rapidly than cells treated with NMDA in normal buffer. While sodium, chloride, and water entry contribute to excitotoxic dendritic injury acutely, calcium entry through NMDA receptors results in lasting structural changes in damaged dendrites.
突触后神经元树突对缺氧缺血性脑损伤和谷氨酸受体过度激活具有选择性易损性。我们探讨了谷氨酸受体药理学以及在暴露于谷氨酸的培养神经元中发生的树突形状快速、可逆改变的离子基础。用荧光膜示踪剂DiI或树突体蛋白MAP2的免疫荧光标记来评估树突形态。来自15日龄小鼠胚胎的皮质培养物在暴露于NMDA、AMPA或海人酸时会发生节段性树突串珠化,但暴露于代谢型谷氨酸受体激动剂时则不会。在低钠缓冲液(用N-甲基-D-葡糖胺替代)中,对NMDA或海人酸应用的曲张形成明显减弱。此外,藜芦碱诱导的钠内流模拟了树突中的兴奋毒性改变,并额外导致轴突中曲张形成。缺乏氯离子的溶液(用甲磺酸钠替代)和氯离子通透的GABA/甘氨酸受体拮抗剂减少了NMDA或海人酸诱导的曲张形成。随着曲张的形成,观察到树突体积增加,并且在补充蔗糖的高渗培养基中曲张形成减弱。尽管几乎所有神经元都出现了明显的结构变化,但在终止谷氨酸受体激动剂应用后2小时内,树突形状恢复正常。暴露于海人酸的神经元比暴露于NMDA的神经元恢复得更快,并且在无钙缓冲液中暴露于NMDA的神经元比在正常缓冲液中用NMDA处理的细胞恢复得更快。虽然钠、氯和水的内流急性促成兴奋毒性树突损伤,但通过NMDA受体的钙内流导致受损树突发生持久的结构变化。