Wong Bruce X, Hung Ya Hui, Bush Ashley I, Duce James A
Oxidation Biology Unit, The Florey Institute of Neuroscience and Mental Health, The University of Melbourne Parkville, VIC, Australia.
Oxidation Biology Unit, The Florey Institute of Neuroscience and Mental Health, The University of Melbourne Parkville, VIC, Australia ; School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds Leeds, North Yorkshire, UK.
Front Aging Neurosci. 2014 May 15;6:91. doi: 10.3389/fnagi.2014.00091. eCollection 2014.
Alzheimer's disease (AD) is a multifactorial neurodegenerative disease. It begins years prior to the onset of clinical symptoms, such as memory loss and cognitive decline. Pathological hallmarks of AD include the accumulation of β-amyloid in plaques and hyperphosphorylated tau in neurofibrillary tangles. Copper, iron, and zinc are abnormally accumulated and distributed in the aging brain. These metal ions can adversely contribute to the progression of AD. Dysregulation of cholesterol metabolism has also been implicated in the development of AD pathology. To date, large bodies of research have been carried out independently to elucidate the role of metals or cholesterol on AD pathology. Interestingly, metals and cholesterol affect parallel molecular and biochemical pathways involved in AD pathology. The possible links between metal dyshomeostasis and altered brain cholesterol metabolism in AD are reviewed.
阿尔茨海默病(AD)是一种多因素神经退行性疾病。它在临床症状如记忆丧失和认知衰退出现前数年就已开始。AD的病理特征包括β-淀粉样蛋白在斑块中的积累以及神经原纤维缠结中过度磷酸化的tau蛋白。铜、铁和锌在衰老大脑中异常积累和分布。这些金属离子会对AD的进展产生不利影响。胆固醇代谢失调也与AD病理的发展有关。迄今为止,已经独立开展了大量研究来阐明金属或胆固醇在AD病理中的作用。有趣的是,金属和胆固醇影响与AD病理相关的平行分子和生化途径。本文综述了AD中金属稳态失衡与脑胆固醇代谢改变之间的可能联系。