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Dalton Trans. 2010 Mar 7;39(9):2177-87. doi: 10.1039/b919237a. Epub 2009 Dec 17.
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本文引用的文献

1
Metal trafficking: from maintaining the metal homeostasis to future drug design.金属转运:从维持金属内稳态到未来的药物设计。
Metallomics. 2009;1(4):292-311. doi: 10.1039/b904533c. Epub 2009 Jun 11.
2
Site-activated multifunctional chelator with acetylcholinesterase and neuroprotective-neurorestorative moieties for Alzheimer's therapy.用于阿尔茨海默病治疗的具有乙酰胆碱酯酶和神经保护 - 神经修复部分的位点激活多功能螯合剂。
J Med Chem. 2009 Jul 23;52(14):4095-8. doi: 10.1021/jm900504c.
3
Nanoparticle-chelator conjugates as inhibitors of amyloid-beta aggregation and neurotoxicity: a novel therapeutic approach for Alzheimer disease.纳米颗粒-螯合剂偶联物作为β-淀粉样蛋白聚集和神经毒性的抑制剂:一种治疗阿尔茨海默病的新方法。
Neurosci Lett. 2009 May 22;455(3):187-90. doi: 10.1016/j.neulet.2009.03.064. Epub 2009 Mar 25.
4
New drug delivery strategies for improved Parkinson's disease therapy.用于改善帕金森病治疗的新型药物递送策略。
Expert Opin Drug Deliv. 2009 Apr;6(4):389-404. doi: 10.1517/17425240902870405.
5
Glycosylated tetrahydrosalens as multifunctional molecules for Alzheimer's therapy.糖基化四氢萨伦作为用于阿尔茨海默病治疗的多功能分子。
Dalton Trans. 2009 Apr 28(16):3034-43. doi: 10.1039/b902545f. Epub 2009 Mar 5.
6
Bioinorganic chemistry of copper and zinc ions coordinated to amyloid-beta peptide.与β-淀粉样肽配位的铜离子和锌离子的生物无机化学
Dalton Trans. 2009 Feb 21(7):1080-94. doi: 10.1039/b813398k. Epub 2008 Nov 26.
7
Nanoparticles in cellular drug delivery.细胞药物递送中的纳米颗粒。
Bioorg Med Chem. 2009 Apr 15;17(8):2950-62. doi: 10.1016/j.bmc.2009.02.043. Epub 2009 Feb 26.
8
Design, selection, and characterization of thioflavin-based intercalation compounds with metal chelating properties for application in Alzheimer's disease.具有金属螯合特性的硫黄素基插层化合物的设计、选择及表征,用于阿尔茨海默病研究
J Am Chem Soc. 2009 Feb 4;131(4):1436-51. doi: 10.1021/ja806062g.
9
Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases.铁的不良表现:不适当的铁螯合是血管及其他进行性炎症和退行性疾病病因的主要促成因素。
BMC Med Genomics. 2009 Jan 8;2:2. doi: 10.1186/1755-8794-2-2.
10
Altering pyridinone N-substituents to optimise activity as potential prodrugs for Alzheimer's disease.改变吡啶酮N-取代基以优化作为阿尔茨海默病潜在前药的活性。
Dalton Trans. 2008 Dec 7(45):6364-7. doi: 10.1039/b815404j. Epub 2008 Oct 6.

关注金属:为神经退行性疾病定制多功能螯合剂。

Minding metals: tailoring multifunctional chelating agents for neurodegenerative disease.

机构信息

Department of Chemistry, Duke University, Durham, NC 27708-0346, USA.

出版信息

Dalton Trans. 2010 Mar 7;39(9):2177-87. doi: 10.1039/b919237a. Epub 2009 Dec 17.

DOI:10.1039/b919237a
PMID:20162187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2860397/
Abstract

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.

摘要

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。