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Copper imbalance in Alzheimer's disease: Overview of the exchangeable copper component in plasma and the intriguing role albumin plays

机译:阿尔茨海默氏病中的铜失衡:血浆中可交换铜成分的概述和白蛋白的有趣作用

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Essential metals are vital elements for human biology. Iron, copper, and zinc are all essential for life. Trace metal dyshomeostasis has been linked to cognitive deterioration and in particular to a disturbance in the regulation of copper (Cu), characterized by an increase in serum Cu not bound to ceruloplasmin (nCp-Cu also known as "free" copper). It is thought to play a role in the development of Alzheimer's disease (AD), the most common form of dementia. Copper homeostasis is finely regulated in our bodies and the expansion of exchangeable nCp-Cu is symptom of the breakdown of this homeostasis, which affects myriad biological pathways. If not structurally bound to enzymes or coordinated by proteins, copper generates free radicals via Haber-Weiss and Fenton reactions. Human Serum Albumin (HSA) is the most abundant serum protein and the main protein exchanging copper in the nCp-Cu pool. Copper coordinated by HSA is in equilibrium with copper coordinated by other small copper chelators circulating in the blood stream in a dynamic and exchangeable manner dependent on environmental osmolarity, oxidation state, pH and compounds' functions. Albumin is susceptible to glycation starting from Maillard reaction, carbohydrates, in particular glucose, form advanced glycation end-products (AGEs). AGE-albumin is one of this products. Free radicals and free metals in circulation accelerate this cross-linking of protein with carbohydrates. Modified albumins are also significantly less effective than native forms in avoiding the aggregation of A beta, the main component of the amyloid plaques in the AD brain.The current review aims to provide insight into the coordination chemistry of copper in plasma with a special glance toward the exchangeable copper coordinated by albumin, to explore how aberrant regulations of this interaction are linked to the aetiology of AD. (C) 2018 Elsevier B.V. All rights reserved.
机译:必需金属是人类生物学的重要元素。铁,铜和锌都是生命必不可少的。痕量金属异稳态与认知能力下降有关,尤其与铜(Cu)调节紊乱有关,其特征是血清铜不与铜蓝蛋白结合(nCp-Cu也称为“游离”铜)。人们认为它在痴呆的最常见形式阿尔茨海默氏病(AD)的发展中起作用。铜体内平衡在我们体内得到很好的调节,而可交换nCp-Cu的膨胀是这种体内平衡破坏的征兆,它影响着无数的生物途径。如果不是在结构上与酶结合或不受蛋白质配位,铜将通过Haber-Weiss和Fenton反应生成自由基。人血清白蛋白(HSA)是nCp-Cu库中最丰富的血清蛋白和主要的蛋白质交换铜。 HSA配比的铜与血液中循环的其他小铜螯合剂配比的铜处于平衡状态,取决于环境的摩尔渗透压浓度,氧化态,pH和化合物的功能,其动态且可交换。从美拉德反应开始,白蛋白易于糖基化,碳水化合物,特别是葡萄糖,形成高级糖基化终产物(AGEs)。 AGE-白蛋白是该产品之一。循环中的自由基和自由金属加速了蛋白质与碳水化合物的这种交联。修饰的白蛋白在避免Aβ聚集(AD淀粉样斑块在AD脑中的主要成分)方面也远不如天然形式有效。当前的综述旨在特别关注铜在血浆中的配位化学由白蛋白协调的可交换铜,以探讨这种相互作用的异常规定如何与AD的病因联系起来。 (C)2018 Elsevier B.V.保留所有权利。

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