Chapman P F, White G L, Jones M W, Cooper-Blacketer D, Marshall V J, Irizarry M, Younkin L, Good M A, Bliss T V, Hyman B T, Younkin S G, Hsiao K K
Cardiff School of Biosciences, Cardiff University, Wales, UK.
Nat Neurosci. 1999 Mar;2(3):271-6. doi: 10.1038/6374.
We investigated synaptic communication and plasticity in hippocampal slices from mice overexpressing mutated 695-amino-acid human amyloid precursor protein (APP695SWE), which show behavioral and histopathological abnormalities simulating Alzheimer's disease. Although aged APP transgenic mice exhibit normal fast synaptic transmission and short term plasticity, they are severely impaired in in-vitro and in-vivo long-term potentiation (LTP) in both the CA1 and dentate gyrus regions of the hippocampus. The LTP deficit was correlated with impaired performance in a spatial working memory task in aged transgenics. These deficits are accompanied by minimal or no loss of presynaptic or postsynaptic elementary structural elements in the hippocampus, suggesting that impairments in functional synaptic plasticity may underlie some of the cognitive deficits in these mice and, possibly, in Alzheimer's patients.
我们研究了过度表达突变型695个氨基酸的人淀粉样前体蛋白(APP695SWE)的小鼠海马切片中的突触通讯和可塑性,这些小鼠表现出模拟阿尔茨海默病的行为和组织病理学异常。尽管老年APP转基因小鼠表现出正常的快速突触传递和短期可塑性,但它们在海马体CA1区和齿状回区的体外和体内长时程增强(LTP)均严重受损。LTP缺陷与老年转基因小鼠在空间工作记忆任务中的表现受损相关。这些缺陷伴随着海马体中突触前或突触后基本结构元件极少丢失或无丢失,这表明功能性突触可塑性受损可能是这些小鼠以及可能是阿尔茨海默病患者某些认知缺陷的基础。