Wang Qing, Hu Feng-Rui, Gou Xing-Chun, Wang Shan, Ji Nai-Chun
Shaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, 710021 Xi'an, Shaanxi, China.
Engineering Research Center of Brain Diseases Drug Development, Universities of Shaanxi Province, Xi'an Medical University, 710021 Xi'an, Shaanxi, China.
Front Biosci (Landmark Ed). 2025 Apr 22;30(4):36597. doi: 10.31083/FBL36597.
Alzheimer's disease (AD) is a neurodegenerative disease which significantly and negatively affects families and society. Aerobic exercise serves as a non-pharmacological strategy, potentially safeguarding against cognitive decline and lowering the risk of AD. However, how aerobic exercise ameliorates AD remains unknown. This study investigated the effects of two types of aerobic exercise, including aerobic interval training (AIT) and aerobic continuous training (ACT), on cognitive and exploratory function, brain histopathology, and hepatic amyloid beta (Aβ) clearance in amyloid precursor protein/presenilin-1 double transgenic (APP/PS1) transgenic mice.
Twenty-four six-month-old male APP/PS1 transgenic mice (body weight: 20-22 g) were used to establish the AD model. APP/PS1 transgenic mice were randomly assigned to one of the three groups: rest (AD group, n = 8), aerobic interval training (AIT group, n = 8), and aerobic continuous training (ACT group, n = 8). The exploration ability and anxiety of AD mice were measured using the open-field test. Learning and memory of AD mice were detected using the novel object recognition test, Y-maze test, and Morris water maze test. Neuronal damage was analyzed using hematoxylin and eosin staining and Nissl staining. Aβ deposition in the brain was detected using a thioflavin-S fluorescence assay and immunofluorescence. The mechanisms underlying hepatic Aβ clearance were investigated using an immunofluorescence assay and western blotting. Data were analyzed using one-way ANOVA with Tukey's post hoc test, and < 0.05 was deemed statistically significant.
The results revealed that both AIT and ACT improved the recognition memory and exploration ability of mice after 8 weeks of intervention. Additionally, both forms of aerobic exercise significantly mitigated neuronal damage and Aβ deposition in the brain and improved the hepatic clearance of Aβ.
Our findings indicated that AIT and ACT can improve cognitive deficits in APP/PS1 mice, potentially by increasing the hepatic phagocytic capacity of Aβ. Hepatic clearance of Aβ may serve as a supplementary mechanism by which aerobic exercise can improve AD.
阿尔茨海默病(AD)是一种神经退行性疾病,对家庭和社会产生重大负面影响。有氧运动作为一种非药物策略,可能预防认知能力下降并降低患AD的风险。然而,有氧运动如何改善AD尚不清楚。本研究调查了两种有氧运动类型,即有氧间歇训练(AIT)和有氧持续训练(ACT),对淀粉样前体蛋白/早老素-1双转基因(APP/PS1)转基因小鼠的认知和探索功能、脑组织病理学以及肝脏淀粉样β蛋白(Aβ)清除的影响。
使用24只6个月大的雄性APP/PS1转基因小鼠(体重:20 - 22克)建立AD模型。将APP/PS1转基因小鼠随机分为三组之一:休息组(AD组,n = 8)、有氧间歇训练组(AIT组,n = 8)和有氧持续训练组(ACT组,n = 8)。使用旷场试验测量AD小鼠的探索能力和焦虑水平。使用新物体识别试验、Y迷宫试验和莫里斯水迷宫试验检测AD小鼠的学习和记忆能力。使用苏木精-伊红染色和尼氏染色分析神经元损伤。使用硫黄素-S荧光测定法和免疫荧光检测脑中的Aβ沉积。使用免疫荧光测定法和蛋白质印迹法研究肝脏Aβ清除的潜在机制。数据采用单因素方差分析和Tukey事后检验进行分析,P < 0.05被认为具有统计学意义。
结果显示,干预8周后,AIT和ACT均改善了小鼠的识别记忆和探索能力。此外,两种形式的有氧运动均显著减轻了脑中的神经元损伤和Aβ沉积,并改善了肝脏对Aβ的清除。
我们的研究结果表明,AIT和ACT可以改善APP/PS1小鼠的认知缺陷,可能是通过增加肝脏对Aβ的吞噬能力。肝脏对Aβ的清除可能是有氧运动改善AD的一种补充机制。