Cognitive deficits precede motor deficits in a slowly progressing model of parkinsonism in the monkey

J.S Schneider, A Pope-Coleman
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引用次数: 109

Abstract

Five adult Macaca fascicularis monkeys were trained to perform tests of cognitive and motor functioning that included a complex visual pattern discrimination task, an object retrieval task, a test of task persistence, and a timed motor task. Once stable baseline performance was achieved, monkeys were administered 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) at doses of 0.05 to 0.075 mg/kg, 2 to 3 times per week for a total of 24 weeks. Animals were assessed weekly for performance on the previously learned tasks. All monkeys developed performance deficits in a predictable pattern with behavioural and cognitive deficits (i.e. deficits in task persistence and the cognitive component of object retrieval) appearing in advance of measurable motor deficits. Deficits in visual pattern discrimination never appeared. These results show that specific cognitive dysfunction pre-dates motor dysfunction in a chronic, slowly progressing parkinson model in monkeys and support the contention that cognitive deficits in Parkinson's disease may precede the motor signs of the disorder and may not be caused by them.

认知缺陷先于运动缺陷在缓慢发展的猴子帕金森模型中
研究人员训练五只成年束状猕猴进行认知和运动功能测试,包括复杂的视觉模式识别任务、物体检索任务、任务持久性测试和定时运动任务。一旦达到稳定的基线性能,猴子被给予1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP),剂量为0.05至0.075 mg/kg,每周2至3次,共24周。每周对动物进行评估,看它们在先前学习的任务中的表现。所有的猴子都以一种可预测的模式出现了表现缺陷,行为和认知缺陷(即任务持久性和物体检索的认知成分的缺陷)出现在可测量的运动缺陷之前。视觉模式辨别的缺陷从未出现过。这些结果表明,在慢性、缓慢进展的猴子帕金森模型中,特定的认知功能障碍早于运动功能障碍,并支持帕金森病的认知缺陷可能早于该疾病的运动症状,而可能不是由运动症状引起的论点。
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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