Antinori Daniele, Lucarelli Marco, Fuso Andrea
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Pasteur Institute Cenci Bolognetti Foundation, Sapienza University of Rome, Rome, Italy.
Essays Biochem. 2025 Jul 1. doi: 10.1042/EBC20253019.
Alzheimer's disease (AD) is a neurodegenerative disease, representing the seventh cause of death worldwide and the first cause of dementia. Several pathogenic mechanisms have been connected to this pathology, including protein aggregation, oxidative stress, metabolic dysfunction, mitochondrial dysfunction, neuroinflammation, synaptic dysfunction, and cell death. The etiology of AD is multifactorial, suggesting that, in addition to a genetic component, the environment may strongly influence its onset and progression. Exposure to heavy metals, such as lead, cadmium, mercury, and arsenic (As), is known to be associated with AD, with As showing one of the strongest correlations, in relation to the epigenetic changes. The World Health Organization (WHO) set a very low limit for its concentration to 10 μg/l in drinking water. The possibility that As may induce epigenetic effects is a recent hypothesis. Evidence, so far, suggests that As may induce DNA hypomethylation in the brain, by mechanisms not yet completely disclosed. This minireview aims to provide evidence to support the role of As exposure in AD, maintaining a focus on oxidative stress and ferroptosis, with a perspective on DNA methylation.
阿尔茨海默病(AD)是一种神经退行性疾病,是全球第七大死因和痴呆的首要病因。多种致病机制与这种病理状况相关,包括蛋白质聚集、氧化应激、代谢功能障碍、线粒体功能障碍、神经炎症、突触功能障碍和细胞死亡。AD的病因是多因素的,这表明除了遗传因素外,环境可能对其发病和进展有强烈影响。已知接触铅、镉、汞和砷(As)等重金属与AD有关,就表观遗传变化而言,砷显示出最强的相关性之一。世界卫生组织(WHO)将其在饮用水中的浓度下限设定为非常低的10μg/l。砷可能诱导表观遗传效应这一可能性是最近提出的假说。迄今为止的证据表明,砷可能通过尚未完全揭示的机制诱导大脑中的DNA低甲基化。本综述旨在提供证据支持砷暴露在AD中的作用,重点关注氧化应激和铁死亡,并从DNA甲基化的角度进行探讨。