Hetman M, Danysz W, Kaczmarek L
Nencki Institute of Experimental Biology, Warsaw, Poland.
Exp Neurol. 1997 Oct;147(2):229-37. doi: 10.1006/exnr.1997.6603.
Single administration of a high dose of an uncompetitive NMDA receptor antagonist-dizocilpine maleate (MK-801)-results in transient neuronal vacuolization and cell death in retrosplenial cortex in rodents. In this study expression of cathepsin D (CatD), a major lysosomal aspartic protease, was investigated in brains of female rats treated with 1, 5, or 10 mg/kg of MK-801. Northern blot analysis demonstrated that the CatD mRNA level was moderately increased in retrosplenial cortex 24 h-7 days after the treatment. Concomitantly, increased CatD immunoreactivity was observed, predominantly in the degenerating neurons in layer III of retrosplenial cortex. Neuronal response was spatially distinguished from glial reactivation marked by increased mRNA and protein levels of glial fibrillary acidic protein, as demonstrated by Northern blot and immunohistochemistry in retrosplenial cortex 24 h-7 days after MK-801 treatment. These data suggest that activation of the lysosomal proteolytic system of neurons may play a role in MK-801-evoked neurodegeneration.
单次给予高剂量非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂——马来酸氯胺酮(MK-801),会导致啮齿动物脾后皮质出现短暂的神经元空泡化和细胞死亡。在本研究中,我们调查了用1、5或10mg/kg MK-801处理的雌性大鼠大脑中主要溶酶体天冬氨酸蛋白酶组织蛋白酶D(CatD)的表达情况。Northern印迹分析表明,处理后24小时至7天,脾后皮质中CatD mRNA水平适度增加。同时,观察到CatD免疫反应性增加,主要出现在脾后皮质III层的退化神经元中。通过Northern印迹和免疫组织化学检测发现,在MK-801处理后24小时至7天的脾后皮质中,神经元反应在空间上与以胶质纤维酸性蛋白mRNA和蛋白质水平增加为标志的胶质细胞再激活不同。这些数据表明,神经元溶酶体蛋白水解系统的激活可能在MK-801诱发的神经退行性变中起作用。