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年龄相关的胰岛素降解酶增加与 APPswe/PS1dE9 小鼠的认知功能呈负相关。

Age-Related Increase of Insulin-Degrading Enzyme Is Inversely Correlated with Cognitive Function in APPswe/PS1dE9 Mice.

机构信息

Department of Clinical Laboratory, Xuanwu Hospital, Capital Medical University, Beijing, China (mainland).

出版信息

Med Sci Monit. 2018 Apr 22;24:2446-2455. doi: 10.12659/msm.909596.

DOI:10.12659/msm.909596
PMID:29680859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5935016/
Abstract

BACKGROUND Insulin-degrading enzyme (IDE) is an important regulator for Ab clearance and diabetes. Although it is indispensable in removing plaques related to onset Alzheimer's disease (AD) and in degrading insulin related to diabetes, there have been few studies on the dynamic level of IDE in different stages of AD. MATERIAL AND METHODS The present study explored the level IDE protein in different stages of APPswe/PS1dE9 mice and their correlations with cognitive decline. The 4-month-old, 10-month-old, and 18-month-old mice were used as the different age stages of mice. Cognitive function was evaluated using the Morris water maze test. We also observed the level of Ab plaques in brain regions of different stages. RESULTS The data revealed that the expression of IDE was dramatically higher than in age-matched wild mice at the age of 10 months and 18 months. In terms of distribution, Aβ plaques were deposited mostly in the cortex and hippocampus, especially in 10-month-old and 18-month-old APPswe/PS1dE9 mice. The cognitive function of 4-month-old APPswe/PS1dE9 mice was not significantly differ in spatial learning. However, the cognitive function, both spatial learning and spatial memory, was dramatically lower in 10-month-old and 18-month-old groups. CONCLUSIONS There was a positive correlation between the expression of IDE and spatial memory in 10-month-old and 18-month-old APPswe/PS1dE9 mice. The study of this protein may provide reference values for the further study of IDE in Alzheimer's disease.

摘要

背景

胰岛素降解酶(IDE)是清除 Ab 并治疗糖尿病的重要调节剂。尽管它在去除与阿尔茨海默病(AD)相关的斑块和降解与糖尿病相关的胰岛素方面不可或缺,但对 AD 不同阶段 IDE 的动态水平的研究较少。

材料和方法

本研究探讨了 APPswe/PS1dE9 小鼠不同阶段 IDE 蛋白的水平及其与认知能力下降的关系。将 4 月龄、10 月龄和 18 月龄的小鼠分别作为不同年龄阶段的小鼠。使用 Morris 水迷宫测试评估认知功能。我们还观察了不同阶段大脑区域中 Ab 斑块的水平。

结果

数据显示,10 月龄和 18 月龄时,IDE 的表达明显高于同龄野生型小鼠。在分布方面,Aβ斑块主要沉积在皮质和海马区,尤其是 10 月龄和 18 月龄的 APPswe/PS1dE9 小鼠。4 月龄 APPswe/PS1dE9 小鼠的空间学习认知功能没有明显差异。然而,10 月龄和 18 月龄组的认知功能,包括空间学习和空间记忆,显著降低。

结论

在 10 月龄和 18 月龄的 APPswe/PS1dE9 小鼠中,IDE 的表达与空间记忆呈正相关。对该蛋白的研究可能为进一步研究阿尔茨海默病中的 IDE 提供参考值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/7b036f8d53d1/medscimonit-24-2446-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/29019e40517d/medscimonit-24-2446-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/fc906f86cc4b/medscimonit-24-2446-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/7b036f8d53d1/medscimonit-24-2446-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/29019e40517d/medscimonit-24-2446-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/6ea284864b35/medscimonit-24-2446-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/208eabf96eaf/medscimonit-24-2446-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/fc906f86cc4b/medscimonit-24-2446-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234f/5935016/7b036f8d53d1/medscimonit-24-2446-g005.jpg

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