持续性淋巴细胞性脉络丛脑膜炎病毒感染对小鼠行为的影响

Lisa H. Gold, Michelle D. Brot, Ilham Polis, Richard Schroeder, Antoinette Tishon, Juan-Carlos de la Torre, Michael B.A. Oldstone, George F. Koob
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引用次数: 33

摘要

淋巴细胞性脉络丛脑膜炎病毒(LCMV)是一种非溶性小鼠病毒,为研究中枢神经系统病毒感染的行为相关性提供了有价值的模型系统。新生儿或免疫抑制小鼠感染LCMV后会出现持续的耐受性感染,其特征是持续产生病毒。病毒可以在肺、肝、肾和脑等身体器官中发现。在大脑中,神经元是受感染的主要中枢神经系统细胞,持续感染的神经元数量最多的是大脑皮层、海马、其他边缘结构和下丘脑部分。尽管在动物的一生中持续感染,但神经元没有出现结构性损伤或脱落。DBA/2J菌株小鼠在出生后18小时内感染LCMV(1000斑块形成单位),并测试成年后的行为功能。空斑试验表明在注射病毒的小鼠中持续感染。测试小鼠学习y形迷宫空间辨别的能力以避免轻度足震(0.43 mA)的发生。在训练期间做出的正确回避反应的数量被作为习得绩效的衡量标准。与注射和未注射病毒的对照组相比,感染病毒的小鼠在获得y迷宫辨别能力方面表现出缺陷。经过额外的训练以达到控制水平的表现,感染小鼠和对照组注射了胆碱能拮抗剂东莨菪碱。东莨菪碱(2.0 mg/kg)对受感染小鼠的影响明显大于对照组,这表明胆碱能功能障碍是部分学习障碍的原因。另一组感染病毒的小鼠在第一次接触运动测试装置时表现出活动不足。与生理盐水相比,东莨菪碱(2.0 mg/kg)在所有三组小鼠中都产生了运动多动,而较低剂量的东莨菪碱(0.3 mg/kg)在病毒感染小鼠中选择性地产生了运动多动。总之,我们的研究结果表明,LCMV感染引起明显的行为影响和对胆碱能拮抗剂的敏感性增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behavioral effects of persistent lymphocytic choriomeningitis virus infection in mice

Lymphocytic choriomeningitis virus (LCMV) is a nonlytic murine virus that provides a valuable model system for studying the behavioral correlates of CNS viral infection. Newborn or immunosuppressed mice infected with LCMV develop a persistent tolerant infection characterized by continuous viral production. Virus can be found in various body organs including lung, liver, kidney, and brain. In brain, neurons are the predominant CNS cells infected and the greatest number of persistently infected neurons are found in the cerebral cortex, hippocampus, other limbic structures and parts of the hypothalamus. Despite continuous infection throughout the animal's life, neurons show no structural injury or dropout. Mice from the DBA/2J strain were infected with LCMV (1000 plaque-forming units) within 18 h of birth and tested for behavioral function as adults. Plaque assays indicated persistent infection in virus-injected mice. Mice were tested for their ability to learn a Y-maze spatial discrimination to avoid the onset of a mild footshock (0.43 mA). The number of correct avoidance responses made during training was taken as a measure of acquisition performance. The virus-infected mice showed a deficit in acquisition of the Y-maze discrimination compared to that seen in vehicle-injected and noninjected controls. Following additional training to reach control levels of performance, the infected mice and the controls were injected with the cholinergic antagonist scopolamine. Scopolamine (2.0 mg/kg) disrupted the performance of the infected mice significantly more than control performance, suggesting that a cholinergic dysfunction accounted for some of the learning deficit. A separate group of virus-infected mice exhibited hypoactivity during the first exposure to a locomotor testing apparatus. Scopolamine (2.0 mg/kg) produced locomotor hyperactivity in all three groups compared to saline, whereas a lower scopolamine dose, 0.3 mg/kg, produced hyperactivity selectively in the virus-infected mice. Overall, our results indicate that LCMV infection causes pronounced behavioral effects and an increased sensitivity to cholinergic antagonists.

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