Department of Neurology, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA, 71103, USA.
Department of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, 1120 15th Street, Augusta, GA, 30912, USA.
Geroscience. 2022 Jun;44(3):1457-1477. doi: 10.1007/s11357-022-00534-2. Epub 2022 Feb 28.
Alzheimer's disease (AD) is the most common form of dementia. Despite enormous efforts around the world, there remains no effective cure for AD. This study was performed to investigate the effects of long-term exercise pretreatment on the typical pathology of AD in a novel transgenic AD rat model. Male 2-month-old animals were divided into the following groups: wild-type (WT) rats, AD rats, and AD rats with treadmill exercise pretreatment (AD-Exe). After exercise pretreatment, the Barnes maze task, passive avoidance task, and cued fear conditioning test were performed to test learning and memory function. The elevated plus maze, open field test, sucrose preference test, and forced swim test were conducted to measure anxious-depressive-like behavior. Immunofluorescence staining, Golgi staining, transmission electron microscopy, Western blot analysis, F-Jade C staining, TUNEL staining, and related assay kits were conducted to measure Aβ plaques, tau hyperphosphorylation, neuronal damage, neuronal degeneration, dendritic spine density, synapses, synaptic vesicles, mitochondrial morphology, mitochondrial dynamic, oxidative stress, and neuroinflammation. Behavioral tests revealed that long-term exercise pretreatment significantly alleviated learning and memory dysfunction and anxious-depressive-like behaviors in AD animals. In addition, exercise pretreatment attenuated amyloid-β deposition and tau hyperphosphorylation and preserved spine density, synapses, and presynaptic vesicles. Exercise also inhibited neuronal damage, neuronal apoptosis, and neuronal degeneration. Additional studies revealed the imbalance of mitochondrial dynamics was significantly inhibited by exercise pretreatment accompanied by a remarkable suppression of oxidative stress and neuroinflammation. Our findings suggest that long-term exercise pretreatment alleviated behavioral deficits and typical pathologies of the AD rat model, supporting long-term exercise pretreatment as a potential approach to delay the progression of AD.
阿尔茨海默病(AD)是最常见的痴呆症形式。尽管全世界都在努力,但仍然没有有效的 AD 治疗方法。本研究旨在探讨长期运动预处理对新型转基因 AD 大鼠模型中 AD 典型病理学的影响。将雄性 2 月龄动物分为以下几组:野生型(WT)大鼠、AD 大鼠和 AD 大鼠经跑台运动预处理(AD-Exe)。运动预处理后,进行 Barnes 迷宫任务、被动回避任务和条件恐惧测试,以测试学习和记忆功能。高架十字迷宫、旷场试验、蔗糖偏好试验和强迫游泳试验用于测量焦虑抑郁样行为。免疫荧光染色、Golgi 染色、透射电镜、Western blot 分析、F-Jade C 染色、TUNEL 染色和相关试剂盒用于测量 Aβ 斑块、tau 过度磷酸化、神经元损伤、神经元变性、树突棘密度、突触、突触小泡、线粒体形态、线粒体动力学、氧化应激和神经炎症。行为学测试表明,长期运动预处理可显著缓解 AD 动物的学习记忆功能障碍和焦虑抑郁样行为。此外,运动预处理可减轻淀粉样蛋白-β沉积和 tau 过度磷酸化,维持树突棘密度、突触和突触小泡。运动还抑制神经元损伤、神经元凋亡和神经元变性。进一步的研究表明,运动预处理可显著抑制线粒体动力学失衡,同时显著抑制氧化应激和神经炎症。我们的研究结果表明,长期运动预处理可缓解 AD 大鼠模型的行为缺陷和典型病理学,支持长期运动预处理作为延缓 AD 进展的潜在方法。