Matyja E, Smiałek M, Kosicka B
Department of Neuropathology, Medical Research Centre, Polish Academy of Science, Warsaw.
Folia Neuropathol. 1994;32(1):43-50.
The ultrastructural studies of QUIN-injected rat hippocampus were performed in long-term experiment in order to determine delayed neurotoxic effect of this compound. QUIN, in a single dose, was administered stereotaxically into the dorsal hippocampus. The morphological changes were characterized by marked atrophy of neuropil accompanied by remarkable glial pathology. The neuronal changes consisted in loss of many nerve cells, abnormalities of nuclear chromatin in the persisting pyramidal neurons and degeneration of postsynaptic dendrites. The glial changes were represented by electron-lucency of astrocytic cytoplasm and their processes. The mechanism of this reaction is unclear and the suggestion, that electron-lucent astrocytes represent a form of transformed glia especially sensitive to amino acids, releasing from degenerating neurons is discussed.
为了确定喹啉(QUIN)这种化合物的延迟神经毒性作用,我们对注射喹啉的大鼠海马体进行了长期的超微结构研究。将单剂量的喹啉立体定向注射到背侧海马体中。形态学变化的特征是神经纤维网明显萎缩,并伴有明显的神经胶质病变。神经元变化包括许多神经细胞的丢失、残留锥体神经元中核染色质的异常以及突触后树突的退化。神经胶质变化表现为星形胶质细胞胞质及其突起的电子透明性。这种反应的机制尚不清楚,本文还讨论了一种观点,即电子透明的星形胶质细胞代表了一种对从退化神经元释放的氨基酸特别敏感的转化神经胶质细胞形式。