Running exercise protects spinophilin‐immunoreactive puncta and neurons in the medial prefrontal cortex of APP/PS1 transgenic mice

前额叶皮质 转基因小鼠 神经科学 转基因 生物 认知 生物化学 基因
作者
Lin Zhu,Jinhua Fan,Feng‐lei Chao,Chunni Zhou,Lin Jiang,Yi Zhang,Yanmin Luo,Lei Zhang,Qian Xiao,Hao Yang,Shan‐shan Zhang,Hong Wu,Yong Tang
出处
期刊:Journal of comparative neurology [Wiley]
卷期号:530 (6): 858-870 被引量:8
标识
DOI:10.1002/cne.25252
摘要

The medial prefrontal cortex (mPFC) is thought to be closely associated with emotional processes, decision making, and memory. Previous studies have identified the prefrontal cortex as one of the most vulnerable brain regions in Alzheimer's disease (AD). Running exercise has widely been recognized as a simple and effective method of physical activity that enhances brain function and slows the progression of AD. However, the effect of exercise on the mPFC of AD is unclear. To address these issues, we investigated the effects of 4 months of exercise on the numbers of spinophilin-immunoreactive puncta and neurons in the mPFC of 12-month-old APPswe/PSEN1dE9 (APP/PS1) transgenic AD model mice using stereological methods. The spatial learning and memory abilities of mice were tested using the Morris water maze. Four months of running exercise delayed declines in spatial learning and memory abilities. The stereological results showed significantly lower numbers of spinophilin-immunoreactive puncta and neurons in the mPFC of APP/PS1 mice than in the wild-type control group. The numbers of spinophilin-immunoreactive puncta and neurons in the mPFC of running APP/PS1 mice were significantly greater than those in the APP/PS1 control mice. In addition, running-induced improvements in spatial learning and memory were significantly associated with running-induced increases in spinophilin-immunoreactive puncta and neurons numbers in the mPFC. Running exercise could delay the loss of spinophilin-immunoreactive puncta and neurons in the mPFC of APP/PS1 mice. This finding might provide an important structural basis for exercise-induced improvements in the spatial learning and memory abilities of individuals with AD.
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