The Florey Institute of Neuroscience and Mental Health, Kenneth Myer Building, The University of Melbourne, Parkville, VIC, Australia.
J Alzheimers Dis. 2018;62(3):1369-1379. doi: 10.3233/JAD-170662.
It is estimated that by the year 2050 there will be more than 1.5 billion people globally over the age of 65 years. Aging is associated with changes to a number of different cellular processes which are driven by a variety of factors that contribute to the characteristic decline in function that is seen across multiple physiological domains/tissues in the elderly (including the brain). Importantly, aging is also the primary risk factor for the development of neurodegenerative disorders such as Alzheimer's disease. As such, there is an urgent need to provide a greater understanding of both the pathogenesis and treatment of these devastating neurodegenerative disorders. One of the key cellular processes that becomes dysregulated with age and participates both directly and indirectly in age-related dysfunction, is metal homeostasis and the neurochemistry of metalloproteins, the basic science of which has been extensively reviewed in the past. In this review, we will focus on the human clinical intervention trials that have been conducted over approximately the last four decades that have attempted to establish the efficacy of targeting metal ions in the treatment of AD.
据估计,到 2050 年,全球将有超过 15 亿 65 岁以上的人口。衰老与许多不同的细胞过程的变化有关,这些变化是由多种因素驱动的,这些因素导致了老年人在多个生理领域/组织中出现的功能特征性下降(包括大脑)。重要的是,衰老也是神经退行性疾病如阿尔茨海默病发展的主要危险因素。因此,迫切需要更深入地了解这些破坏性神经退行性疾病的发病机制和治疗方法。随着年龄的增长而失调的一个关键细胞过程是金属稳态和金属蛋白的神经化学,过去已经对其基础科学进行了广泛的综述。在这篇综述中,我们将重点介绍过去四十年左右进行的人类临床干预试验,这些试验试图确定靶向 AD 治疗中金属离子的疗效。