Department of Chemistry, Duke University, Durham, NC 27708-0346, USA.
Dalton Trans. 2010 Mar 7;39(9):2177-87. doi: 10.1039/b919237a. Epub 2009 Dec 17.
Neurodegenerative diseases like Alzheimer's and Parkinson's disease are associated with elevated levels of iron, copper, and zinc and consequentially high levels of oxidative stress. Given the multifactorial nature of these diseases, it is becoming evident that the next generation of therapies must have multiple functions to combat multiple mechanisms of disease progression. Metal-chelating agents provide one such function as an intervention for ameliorating metal-associated damage in degenerative diseases. Targeting chelators to adjust localized metal imbalances in the brain, however, presents significant challenges. In this perspective, we focus on some noteworthy advances in the area of multifunctional metal chelators as potential therapeutic agents for neurodegenerative diseases. In addition to metal chelating ability, these agents also contain features designed to improve their uptake across the blood-brain barrier, increase their selectivity for metals in damage-prone environments, increase antioxidant capabilities, lower Abeta peptide aggregation, or inhibit disease-associated enzymes such as monoamine oxidase and acetylcholinesterase.
神经退行性疾病,如阿尔茨海默病和帕金森病,与铁、铜和锌水平升高有关,进而导致氧化应激水平升高。鉴于这些疾病的多因素性质,很明显,下一代疗法必须具有多种功能,以对抗疾病进展的多种机制。金属螯合剂提供了一种干预措施,可减轻退行性疾病中与金属相关的损伤。然而,将螯合剂靶向到大脑中局部的金属失衡部位存在重大挑战。在这篇观点文章中,我们重点介绍了多功能金属螯合剂在神经退行性疾病潜在治疗中的一些显著进展。除了金属螯合能力外,这些试剂还包含了旨在提高其透过血脑屏障摄取的特性,增加其在易受损环境中对金属的选择性,提高抗氧化能力,降低 Abeta 肽聚集,或抑制疾病相关酶,如单胺氧化酶和乙酰胆碱酯酶。