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年轻和老年淀粉样前体蛋白转基因小鼠的体内突触传递

In vivo synaptic transmission in young and aged amyloid precursor protein transgenic mice.

作者信息

Giacchino J, Criado J R, Games D, Henriksen S

机构信息

Department of Neuropharmacology (CVN-13), The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA 92037, USA.

出版信息

Brain Res. 2000 Sep 8;876(1-2):185-90. doi: 10.1016/s0006-8993(00)02615-9.

Abstract

Alzheimer's disease (AD) is characterized by progressive neurodegeneration and cognitive impairment. We examined in vivo alterations in hippocampal neurotransmission in both young and aged PDAPP transgenic mice and nontransgenic littermates. We now report that in vivo abnormal neurotransmission in hippocampal circuits of PDAPP mice precedes beta deposition and neurodegeneration. These in vivo data provide the first evidence that dysfunction in hippocampal neuronal circuits may not be correlated with age-related extracellular beta plaque deposition.

摘要

阿尔茨海默病(AD)的特征是进行性神经退行性变和认知障碍。我们研究了年轻和老年PDAPP转基因小鼠以及非转基因同窝小鼠海马神经传递的体内变化。我们现在报告,PDAPP小鼠海马回路中的体内异常神经传递先于β淀粉样蛋白沉积和神经退行性变。这些体内数据首次证明,海马神经元回路功能障碍可能与年龄相关的细胞外β淀粉样斑块沉积无关。

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