Immunization of rats with cholinergic neurons induces behavioral deficits.

J Chapman, J Feldon, G Alroy, D M Michaelson
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引用次数: 10

Abstract

We have previously shown that sera from patients with Alzheimer's disease (AD) contain a significantly high level of antibodies to the cell bodies (Perikarya; PK) but not to the nerve terminals (synaptosomes) of purely cholinergic neurons from the electric fish Torpedo. In the present study we examined the effect of repeated immunization of rats with either of these antigens for one year. Immunoblot studies revealed that sera of cholinergic PK immunized rats contained a high level of antibodies to cholinergic PK proteins, in particular to a 200 kilodalton protein, to which there are specifically high levels of antibodies in AD. Sera from rats immunized with cholinergic synaptosomes and from control rats contained very low levels of these antibodies. Behavioral studies performed one year after the initial immunization revealed that the cholinergic PK immunized rats were impaired in spatial learning and memory tasks (Morris swim test and T-maze alternation) when compared to control rats and that the synaptosome-immunized rats showed no such deficit. In contrast, the three groups performed similarly in general activity, active avoidance and conditioned emotional response tests. Further experiments revealed that the cholinergic PK immunized rats displayed a significant deficit in short term memory. The association of antibodies to cholinergic neurons with cognitive deficits in this rat model suggests that such antibodies may be involved in the pathogenesis of AD.

免疫胆碱能神经元大鼠可引起行为缺陷。
我们之前的研究表明,阿尔茨海默病(AD)患者的血清中含有明显高水平的细胞体抗体(Perikarya;PK),而不是来自电鱼鱼雷的纯胆碱能神经元的神经末梢(突触体)。在本研究中,我们检查了用这两种抗原中的任何一种重复免疫大鼠一年的效果。免疫印迹研究显示,经胆碱能PK免疫的大鼠血清中含有高水平的胆碱能PK蛋白抗体,特别是对一种200千道尔顿蛋白的抗体,这种蛋白在AD中有特异性的高水平抗体。用胆碱能突触体免疫的大鼠和对照大鼠的血清中含有极低水平的这些抗体。初始免疫一年后进行的行为学研究显示,与对照大鼠相比,胆碱能PK免疫大鼠在空间学习和记忆任务(Morris游泳测试和T-maze交替)中受到损害,而突触体免疫大鼠则没有这种缺陷。相比之下,三组在一般活动、主动回避和条件情绪反应测试中的表现相似。进一步实验发现,经胆碱能PK免疫的大鼠在短期记忆方面表现出明显的缺陷。在这种大鼠模型中,胆碱能神经元抗体与认知缺陷的关联表明这种抗体可能参与了AD的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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