Taniwaki Y, Kato M, Araki T, Kobayashi T
Department of Clinical Neurophysiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Neurosci Lett. 1996 Oct 11;217(1):29-32. doi: 10.1016/0304-3940(96)13062-7.
We studied the distribution of activated microglia in the brain during kainic acid-induced acute hippocampal seizures in rats. Although no microglial activation was observed 4 h after seizure induction, activation was detected in the primary focus and also in other selected structures in the limbic and non-limbic structures after 8 and 24 h, in the absence of any obvious morphological changes in the neurons. The structures with activated microglia were highly consistent with those included in the propagation pathways of the hippocampal seizures. These findings thus suggest that the microglial cells are activated through the propagation pathways by the seizure activities that propagate transynaptically from the primary focus, even without any apparent neuronal injury.
我们研究了大鼠在 kainic 酸诱导的急性海马癫痫发作期间大脑中活化小胶质细胞的分布。尽管在癫痫发作诱导后 4 小时未观察到小胶质细胞活化,但在 8 小时和 24 小时后,在原发性病灶以及边缘和非边缘结构的其他选定结构中检测到了活化,此时神经元没有任何明显的形态变化。具有活化小胶质细胞的结构与海马癫痫发作传播途径中所包含的结构高度一致。因此,这些发现表明,即使没有任何明显的神经元损伤,小胶质细胞也会通过癫痫活动从原发性病灶经突触传递传播的途径而被激活。