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首页> 外文期刊>European archives of psychiatry and clinical neuroscience >Changes in neurogenesis in dementia and Alzheimer mouse models: are they functionally relevant?
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Changes in neurogenesis in dementia and Alzheimer mouse models: are they functionally relevant?

机译:痴呆和阿尔茨海默病小鼠模型中神经发生的变化:它们在功能上相关吗?

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Alzheimer's disease and related dementias are devastating disorders that lead to the progressive decline of cognitive functions. Characteristic features are severe brain atrophy, paralleled by accumulation of beta amyloid and neurofibrillary tangles. With the discovery of neurogenesis in the adult brain, the hopes have risen that these neurodegenerative conditions could be overcome, or at least ameliorated, by the generation of new neurons. The location of the adult neurogenic zones in the hippocampus and the lateral ventricle wall, close to corpus callosum and neocortex, indicates strategic positions for potential repair processes. However, we also need to consider that the generation of new neurons is possibly involved in cognitive functions and could, therefore, be influenced by disease pathology. Moreover, aberrant neurogenic mechanisms could even be a part of the pathological events of neurodegenerative diseases. It is the scope of this review to summarize and analyze the recent data from neurogenesis research with respect to Alzheimer's disease and its animal models.
机译:阿尔茨海默氏病和相关的痴呆症是破坏性疾病,导致认知功能的逐步下降。特征是严重的脑萎缩,同时伴有β淀粉样蛋白和神经原纤维缠结的积累。随着在成年大脑中神经发生的发现,人们希望通过产生新的神经元来克服或至少改善这些神经退行性疾病的希望。在海马体和侧脑室壁,成年神经源性区域的位置靠近call体和新皮层,表明潜在的修复过程的战略位置。但是,我们还需要考虑新神经元的产生可能与认知功能有关,因此可能会受到疾病病理的影响。而且,异常的神经发生机制甚至可能是神经退行性疾病的病理事件的一部分。本综述的范围是总结和分析来自神经发生研究的有关阿尔茨海默氏病及其动物模型的最新数据。

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