Anger W K
Center for Research on Occupational and Environmental Toxicology, Oregon Health Sciences University, Portland 97201.
Neurotoxicology. 1991 Fall;12(3):403-13.
The Eighth International Neurotoxicology Conference, Role of Toxicants in Neurological Disorders (1990), evaluated the evidence that chemical exposures may play a role in the development of neurodegenerative disorders. This article describes the major neurodegenerative disorders (Amyotrophic Lateral Sclerosis, Huntington disease, Parkinson disease, and Alzheimer disease) addressed at the conference, followed by a description of test systems or models developed to study behavioral aspects of these disorders in animals. However, due to the complexity of the disorders and the species in which they are found, fully-developed models in animals of neurodegenerative disorders are lacking. This suggests the need for a clear strategy for selecting behavioral tests in animals to study aspects of any neurodegenerative disorders. Such a strategy is here exemplified for Alzheimer disease (AD) as a prototypical neurodegenerative disorder. Since an animal model cannot provide the full range of effects of human neurodegenerative diseases, particularly AD which produces incompletely characterized cognitive deficits, a rodent model must at this time be drawn from multiple sources, including: (1) Tests currently used to identify in rodents deficits associated with AD; (2) tests to identify Alzheimer-related signs in patients; and, (3) tests that relate to theoretical constructs of human and animal cognition. A battery that draws from those sources could include tests of: (a) Spatial learning and memory (Morris Water Maze and Radial Arm Maze), (b) delayed recall match-to-sample; (c) serial response learning; and, (d) visual discrimination (e.g., vertical vs. horizontal stimuli). This battery will identify behavioral changes characteristic of early-, middle- and late-stage AD, afford the potential to relate the findings to theoretical constructs of cognition, and evaluate learning capabilities not previously studied in rodent models of neurodegenerative disorders.
第八届国际神经毒理学会议“毒物在神经紊乱中的作用”(1990年)评估了化学物质暴露可能在神经退行性疾病发展中起作用的证据。本文描述了会议上讨论的主要神经退行性疾病(肌萎缩侧索硬化症、亨廷顿病、帕金森病和阿尔茨海默病),随后介绍了为研究这些疾病在动物身上的行为方面而开发的测试系统或模型。然而,由于这些疾病的复杂性以及发现这些疾病的物种的复杂性,目前还缺乏动物身上完全成熟的神经退行性疾病模型。这表明需要一种明确的策略来选择动物行为测试,以研究任何神经退行性疾病的各个方面。本文以阿尔茨海默病(AD)作为典型的神经退行性疾病为例阐述了这样一种策略。由于动物模型无法提供人类神经退行性疾病的全部影响,尤其是AD会产生特征不完全明确的认知缺陷,因此目前必须从多个来源构建啮齿动物模型,包括:(1)目前用于识别啮齿动物中与AD相关缺陷的测试;(2)用于识别患者中与阿尔茨海默病相关体征的测试;以及(3)与人类和动物认知理论结构相关的测试。从这些来源选取的一组测试可能包括:(a)空间学习和记忆(莫里斯水迷宫和放射状臂迷宫),(b)延迟回忆匹配样本;(c)序列反应学习;以及(d)视觉辨别(例如,垂直与水平刺激)。这组测试将识别出AD早期、中期和晚期的特征性行为变化,有潜力将研究结果与认知理论结构联系起来,并评估以前在神经退行性疾病啮齿动物模型中未研究过的学习能力。