Pasinetti G M, Morgan D G, Finch C E
Ethel Percy Andrus Gerontology Center, Department of Biological Sciences, University of Southern California, Los Angeles 90089-0191.
Exp Neurol. 1991 May;112(2):131-9. doi: 10.1016/0014-4886(91)90063-i.
Transneuronal regression in substantia nigra reticulata (SNR) and substantia nigra compacta (SNC) neurons was studied in Fischer 344 male rats by immunocytochemistry and by in situ hybridization. Three months after striatal lesioning by ibotenic acid, there was a shrinkage (30%) of the SNR region cross-sectional area and a 50% disappearance of neurons that contain glutamic acid decarboxylase (GAD)-mRNA, but only in the ventromedial portion of this nucleus. Loss of dopaminergic neurons, as recognized by tyrosine hydroxylase immunoreactivity, occurred only in caudal portions of the SNC and SNR. These findings suggest that lesions in reciprocally connected pathways, like the nigrostriatal and striatonigral systems, may produce a vicious cycle (feedforward cascade) of neurodegeneration due to interference with retrograde ana anterograde influences.
通过免疫细胞化学和原位杂交技术,在Fischer 344雄性大鼠中研究了黑质网状部(SNR)和黑质致密部(SNC)神经元的跨神经元退变。在通过鹅膏蕈氨酸损伤纹状体三个月后,SNR区域横截面积缩小了30%,且含有谷氨酸脱羧酶(GAD)-mRNA的神经元消失了50%,但仅发生在该核的腹内侧部分。酪氨酸羟化酶免疫反应所识别的多巴胺能神经元的丢失,仅发生在SNC和SNR的尾部。这些发现表明,在相互连接的通路如黑质纹状体和纹状体黑质系统中,损伤可能由于干扰逆行和顺行影响而产生神经退行性变的恶性循环(前馈级联反应)。