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Age-related cognitive decline in baboons: modeling the prodromal phase of Alzheimers disease and related dementias

机译:狒狒与年龄相关的认知衰退:模拟阿尔茨海默氏病和相关痴呆的前驱期

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摘要

The aging of brain cells and synaptic loss are the major underlying pathophysiological processes contributing to the progressive decline in cognitive functions and Alzheimer’s disease. The difference in cognitive performances observed between adult and aged subjects across species highlights the decline of brain systems with age. The inflection point in age-related cognitive decline is important for our understanding of the pathophysiology of neurodegenerative diseases and for timing therapeutic interventions. Humans and nonhuman primates share many similarities including age-dependent changes in gene expression and decline in neural and immune functions. Given these evolutionary conserved organ systems, complex human-like behavioral and age-dependent changes may be modeled and monitored longitudinally in nonhuman primates. We integrated three clinically relevant outcome measures to investigate the effect of age on cognition, motor function and diurnal activity in aged baboons. We provide evidence of a naturally-occurring age-dependent precipitous decline in movement planning, in learning novel tasks, in simple discrimination and in motivation. These results suggest that baboons aged ~20 years (equivalent to ~60 year old humans) may offer a relevant model for the prodromal phase of Alzheimer’s disease and related dementias to investigate mechanisms involved in the precipitous decline in cognitive functions and to develop early therapeutic interventions
机译:脑细胞的衰老和突触丧失是导致认知功能和阿尔茨海默氏病逐渐下降的主要病理生理过程。不同物种的成年和老年受试者之间观察到的认知表现差异突出了大脑系统随年龄的增长而下降。与年龄有关的认知能力下降的拐点对于我们了解神经退行性疾病的病理生理学和确定治疗干预的时间很重要。人类和非人类的灵长类动物有许多相似之处,包括基因表达随年龄的变化以及神经和免疫功能的下降。鉴于这些进化保守的器官系统,可以在非人类灵长类动物中对复杂的类似于人类的行为和年龄相关的变化进行建模和纵向监测。我们整合了三种临床相关的结局指标,以调查年龄对老年狒狒认知,运动功能和昼夜活动的影响。我们提供了运动计划,学习新任务,简单的歧视和动机方面自然而然的年龄相关性急剧下降的证据。这些结果表明,年龄约20岁的狒狒(相当于60岁左右的人类)可能为阿尔茨海默氏病和相关痴呆的前驱期提供了一个相关模型,以研究与认知功能急剧下降有关的机制并制定早期治疗性干预措施

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