Early Memory Impairment is Accompanied by Changes in GluA1/ p-GluA1 in APP/PS1 Mice

Author:

Xu Lin1,Zhou Qi-Xin2,Zhao Ya-Bo1,Hou Xue-Fei2,Li Xin2,Zhu Li-Su2,zhu Jing2,Ma Guo-Rui2,Liu Yu-Xuan2,Miao Yu-Can2,Zhou Qian-Yu2

Affiliation:

1. Laboratory of Learning and Memory, Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Kunming, Yunnan 650223, China

2. Yunnan Key Laboratory of Stem Cell and Regenerative Medicine, Biomedical Engineering Research Institute, Kunming Medical University, Kunming, Yunnan 650500, China

Abstract

Aims: Exploring the neurobiological mechanisms of early AD damage. Background: The early diagnosis of Alzheimer's disease (AD) has a very important impact on the prognosis of AD. However, the early symptoms of AD are not obvious and difficult to diagnose. Existing studies have rarely explored the mechanism of early AD. AMPARs are early important learning memory-related receptors. However, it is not clear how the expression levels of AMPARs change in early AD. Objective: We explored learning memory abilities and AMPAR expression changes in APP/PS1 mice at 4 months, 8 months, and 12 months. Method: We used the classic Morris water maze to explore the learning and memory impairment of APP/PS1 mice and used western blotting to explore the changes in AMPARs in APP/PS1 mice. Result: We found that memory impairment occurred in APP/PS1 mice as early as 4 months of age, and the impairment of learning and memory gradually became serious with age. The changes in GluA1 and p-GluA1 were most pronounced in the early stages of AD in APP/PS1 mice. Conclusion: Our study found that memory impairment in APP/PS1 mice could be detected as early as 4 months of age, and this early injury may be related to GluA1.

Funder

National Natural Science Foundation of China

Strategic Priority Research Program of the Chinese Academy of Sciences

Publisher

Bentham Science Publishers Ltd.

Subject

Neurology (clinical),Neurology

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