Stratégie de recherche translationnelle sur la maladie d'Alzheimer : modèles animaux et biomarqueurs

M. Dhenain
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引用次数: 1

Abstract

Alzheimer's disease is leading to severe cognitive alterations in humans and is associated to two main neuropathologic lesions: amyloid plaques and neurofibrillary tangles. It also leads to functional alterations of cholinergic neurons. Imaging biomarkers can reveal the natural history of the disease and show an alteration of glucose metabolism and an evolving cerebral atrophy process. The development of new therapies against this disease relies on early stages involving animals and specific animal models have been developed to validate therapies modulating cholinergic alterations or amyloid load. Using biomarkers in these models can reveal animal endophenotypes that can be compared to human endophenotypes. Comparative studies of the effects of validated or candidate medicines on the endophenotypes of animal models and humans allow rationalizing decision-making on the basis of animal studies during the development of new therapies
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阿尔茨海默病转化研究策略:动物模型和生物标志物
阿尔茨海默病导致人类严重的认知改变,并与两种主要的神经病理病变有关:淀粉样斑块和神经原纤维缠结。它还会导致胆碱能神经元的功能改变。成像生物标志物可以揭示疾病的自然历史,显示糖代谢的改变和脑萎缩的演变过程。针对这种疾病的新疗法的开发依赖于涉及动物的早期阶段,并且已经开发了特定的动物模型来验证调节胆碱能改变或淀粉样蛋白负荷的疗法。在这些模型中使用生物标志物可以揭示动物的内表型,并与人类的内表型进行比较。对已验证或候选药物对动物模型和人类的内表型的影响进行比较研究,可以在开发新疗法期间基于动物研究使决策合理化
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
>12 weeks
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