Lu Yujiao, Dong Yan, Tucker Donovan, Wang Ruimin, Ahmed Mohammad Ejaz, Brann Darrell, Zhang Quanguang
J Alzheimers Dis. 2017;56(4):1469-1484. doi: 10.3233/JAD-160869.
Recent work has suggested that exercise may be beneficial in preventing or ameliorating symptoms of several neurological disorders, although the mechanism is not entirely understood. The current study was designed to examine the potential beneficial effect of treadmill exercise upon cognitive function in a streptozotocin (STZ)-induced rat model of Alzheimer's disease (AD). Animals underwent treadmill exercise (30 min/day, 5 days/week) for 4 weeks after bilateral STZ intracerebroventricular injection (2.4 mg/kg). We demonstrated that treadmill exercise significantly attenuated STZ-induced neurodegeneration in the rat hippocampal CA1 region and strongly preserved hippocampal-dependent cognitive functioning. Further mechanistic investigation displayed a marked suppression of STZ-induced amyloid-β accumulation and tau phosphorylation. Intriguingly, treadmill exercise remarkably inhibited reactive gliosis following STZ insult and effectively shifted activated microglia from a pro-inflammatory M1 to an anti-inflammatory M2 phenotype, which was correlated with a significantly reduced expression of pro-inflammatory mediators and a corresponding enhancement of anti-inflammatory cytokine expression in the hippocampus. Furthermore, treadmill exercise caused a robust suppression of oxidative damage as evidenced by significantly reduced peroxynitrite production, lipid peroxidation, and oxidized DNA damage. Finally, treadmill exercise strongly attenuated STZ-induced mitochondrial dysfunction manifested by a dramatically elevated intra-mitochondrial cytochrome c oxidase activity and ATP synthesis, and markedly inhibited neuronal apoptosis in the hippocampus. These findings demonstrate that treadmill exercise has a multifactorial effect to attenuate many of the pathological processes that play a key role in AD, and provide further support for the beneficial role of exercise as a potential therapeutic option in AD treatment.
最近的研究表明,运动可能有助于预防或改善几种神经疾病的症状,尽管其机制尚未完全明确。本研究旨在探讨跑步机运动对链脲佐菌素(STZ)诱导的阿尔茨海默病(AD)大鼠模型认知功能的潜在有益作用。双侧脑室内注射STZ(2.4mg/kg)后,动物进行4周的跑步机运动(每天30分钟,每周5天)。我们发现跑步机运动显著减轻了STZ诱导的大鼠海马CA1区神经退行性变,并有力地保留了海马依赖性认知功能。进一步的机制研究显示,STZ诱导的淀粉样β蛋白积累和tau蛋白磷酸化受到明显抑制。有趣的是,跑步机运动显著抑制了STZ损伤后的反应性胶质增生,并有效地将活化的小胶质细胞从促炎的M1表型转变为抗炎的M2表型,这与海马中促炎介质表达的显著降低和抗炎细胞因子表达的相应增强相关。此外,跑步机运动导致氧化损伤受到强烈抑制,表现为过氧亚硝酸盐生成、脂质过氧化和氧化DNA损伤显著减少。最后,跑步机运动强烈减轻了STZ诱导的线粒体功能障碍,表现为线粒体内细胞色素c氧化酶活性和ATP合成显著升高,并显著抑制海马神经元凋亡。这些发现表明,跑步机运动具有多因素作用,可减轻许多在AD中起关键作用的病理过程,并为运动作为AD治疗潜在治疗选择的有益作用提供了进一步支持。