Sayer Rachel, Robertson Deborah, Balfour David J K, Breen Kieran C, Stewart Caroline A
Alzheimer's Disease Research Centre, Section of Psychiatry and Behavioural Sciences, Division of Pathology and Neuroscience, University of Dundee, Ninewells Hospital & Medical School, Dundee DD1 9SY, UK.
Neurosci Lett. 2008 Feb 6;431(3):197-200. doi: 10.1016/j.neulet.2007.11.032. Epub 2007 Dec 3.
The abnormal processing of the amyloid precursor protein (APP) is a pivotal event in the development of the unique pathology that defines Alzheimer's disease (AD). Stress, and the associated increase in corticosteroids, appear to accelerate brain ageing and may increase vulnerability to Alzheimer's disease via altered APP processing. In this study, rats were repeatedly exposed to an unavoidable stressor, an open elevated platform. Previous studies in this laboratory have shown that a single exposure produces a marked increase in plasma corticosterone levels but animals develop tolerance to this effect between 10 and 20 daily sessions. Twenty-four hours after stress, there was an increase in the ratio of the deglycosylated form of APP in the particulate fraction of the brain, which subsequently habituated after 20 days. The levels of soluble APP (APPs) tended to be lower in the stress groups compared to controls except for a significant increase in the hippocampus after 20 days of platform exposure. Since APPs is reported to have neurotrophic properties, this increased release may represent a neuroprotective response to repeated stress. It is possible that the ability to mount this response decreases with age thus increasing the vulnerability to stress-induced AD-related pathology.
淀粉样前体蛋白(APP)的异常加工是定义阿尔茨海默病(AD)的独特病理学发展中的关键事件。应激以及随之而来的皮质类固醇增加似乎会加速大脑衰老,并可能通过改变APP加工过程而增加患阿尔茨海默病的易感性。在本研究中,大鼠反复暴露于不可避免的应激源——开放的高架平台。该实验室之前的研究表明,单次暴露会使血浆皮质酮水平显著升高,但动物在每日10至20次暴露之间会对此效应产生耐受性。应激24小时后,大脑颗粒部分中APP去糖基化形式的比例增加,随后在20天后逐渐适应。与对照组相比,应激组中可溶性APP(APPs)的水平往往较低,但在平台暴露20天后海马体中的APPs水平显著增加。由于据报道APPs具有神经营养特性,这种增加的释放可能代表对反复应激的一种神经保护反应。随着年龄增长,产生这种反应的能力可能会下降,从而增加对应激诱导的AD相关病理学的易感性。