Division of Neurosciences, CIMA, University of Navarra, Pamplona, Spain.
J Alzheimers Dis. 2012;28(3):567-78. doi: 10.3233/JAD-2011-110572.
The etiology of the more common (sporadic) forms of Alzheimer's disease (AD) remains unknown, although age is the most important risk factor. Nevertheless, interactions between environmental risk factors and genetic background may also influence the onset and progression of sporadic AD. Chronic stress, associated with altered memory and other neurological processes, is thought to influence the pathogenesis of AD. Hence, we evaluated the effect of unpredictable and consecutive chronic mild stressors on the onset of an AD-related pathology in the Tg2576 mouse line that overexpresses the human amyloid-β protein precursor with the Swedish mutation (hAβPP(Swe)). Two months after exposure to chronic mild stress, 4 month-old animals that normally display no pathological features of AD, not only expressed pathological markers but also experienced cognitive dysfunction in the Morris water maze test. These findings suggest that chronic mild stress accelerates the onset of cognitive impairment and produces an increase in hippocampal amyloid-β and phospho-tau levels on a background of AD susceptibility.
阿尔茨海默病(AD)更常见(散发性)形式的病因仍然未知,尽管年龄是最重要的危险因素。然而,环境危险因素和遗传背景之间的相互作用也可能影响散发性 AD 的发病和进展。慢性应激与记忆和其他神经过程的改变有关,被认为会影响 AD 的发病机制。因此,我们评估了不可预测和连续的慢性轻度应激源对 Tg2576 小鼠系(过度表达具有瑞典突变的人淀粉样蛋白-β前体蛋白(hAβPP(Swe)))发生 AD 相关病理的影响。在暴露于慢性轻度应激 2 个月后,正常情况下没有 AD 病理特征的 4 月龄动物不仅表达了病理标志物,而且在 Morris 水迷宫测试中还表现出认知功能障碍。这些发现表明,慢性轻度应激加速了认知障碍的发生,并在 AD 易感性的背景下增加了海马淀粉样蛋白-β和磷酸化 tau 水平。