Bons N, Rieger F, Prudhomme D, Fisher A, Krause K-H
Institut BioPARK, Domaine de Chosal, Archamps, INSERM U 488, Hôpital du Kremlin-Bicêtre, Paris, France.
Genes Brain Behav. 2006 Mar;5(2):120-30. doi: 10.1111/j.1601-183X.2005.00149.x.
Age-associated dementia, in particular Alzheimer's disease (AD), will be a major concern of the 21st century. Research into normal brain aging and AD will therefore become increasingly important. As for other areas of medicine, the availability of good animal models will be a limiting factor for progress. Given the complexity of the human brain, the identification of appropriate primate models will be essential to further knowledge of the disease. In this review, we describe the features of brain aging and age-associated neurodegeneration in a small lemurian primate, the Microcebus murinus, also referred to as the mouse lemur. The mouse lemur has a relatively short life expectancy, and animals over 5 years of age are considered to be elderly. Among elderly mouse lemurs, the majority show normal brain aging, whereas approximately 20% develop neurodegeneration. This Microcebus age-associated neurodegeneration is characterized by a massive brain atrophy, abundant amyloid plaques, a cytoskeletal Tau pathology and a loss of cholinergic neurons. While elderly mouse lemurs with normal brain aging maintain memory function and social interaction, animals with age-associated neurodegeneration lose their cognitive and social capacities and demonstrate certain similarities with age-associated human AD. We conclude that M. murinus is an interesting primate model for the study of normal brain aging and the biochemical dysfunctions occurring in age-associated neurodegeneration. Mouse lemurs might also become an increasingly important model for the development of novel treatments in this domain.
与年龄相关的痴呆,尤其是阿尔茨海默病(AD),将成为21世纪的一个主要关注点。因此,对正常脑老化和AD的研究将变得越来越重要。与医学的其他领域一样,良好动物模型的可用性将是进展的限制因素。鉴于人类大脑的复杂性,确定合适的灵长类动物模型对于进一步了解该疾病至关重要。在这篇综述中,我们描述了一种小型狐猴灵长类动物——小鼠狐猴(Microcebus murinus)脑老化和与年龄相关的神经退行性变的特征。小鼠狐猴的预期寿命相对较短,5岁以上的动物被认为是老年动物。在老年小鼠狐猴中,大多数表现出正常的脑老化,而大约20%会发生神经退行性变。这种小鼠狐猴与年龄相关的神经退行性变的特征是大脑大量萎缩、丰富的淀粉样斑块、细胞骨架Tau病理学改变以及胆碱能神经元丧失。虽然脑老化正常的老年小鼠狐猴保持记忆功能和社交互动,但患有与年龄相关神经退行性变的动物会丧失其认知和社交能力,并表现出与人类年龄相关AD的某些相似之处。我们得出结论,小鼠狐猴是研究正常脑老化以及与年龄相关神经退行性变中发生的生化功能障碍的一个有趣的灵长类动物模型。小鼠狐猴也可能成为该领域新型治疗方法开发中越来越重要的模型。