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脑脊液中金属形态分析的研究进展:方法与结果述评。

Review on metal speciation analysis in cerebrospinal fluid-current methods and results: a review.

机构信息

Helmholtz Zentrum München, Institute of Ecological Chemistry, 85764 Neuherberg, Germany.

出版信息

Anal Chim Acta. 2010 Dec 3;682(1-2):23-36. doi: 10.1016/j.aca.2010.09.054. Epub 2010 Oct 8.

Abstract

The large number of patients suffering from neurodegenerative diseases like Alzheimer's disease and Parkinson's disease motivates many research groups worldwide to investigate pathogenic factors and molecular mechanisms of these diseases. Recent studies and reviews indicate that metals are involved in these neurodegenerative processes in case their homeostasis in the brain is disturbed. Important is that the focus of these recent studies is on essential metals like Fe, Cu, Zn and Mn, but not on the well-known neurotoxic metals like Hg and Pb. Key issues for understanding metal induced neurotoxic effects are the transport processes across the neural barriers, the metal binding forms (species) and their interactions with neuronal structures. Total metal concentrations in cerebrospinal fluid were published in several studies for controls and patients, but the amount of reliable data sets is not yet sufficient for clear definition of normal and elevated levels. The need for more detailed information on metal species in CSF is highlighted in this review. However, studies on element speciation analysis, that means identification and quantification of the various binding forms of metals in cerebrospinal fluid, are rare. The major reasons therefore are difficulties in accessing cerebrospinal fluid samples, the non-covalent nature of many metal species of interest and their rather low concentrations. In spite of this, several applications demonstrate the potential of hyphenated techniques as additional diagnostic tools for cerebrospinal fluid analysis. This review shows the importance of trace element analysis and more specifically of element speciation in cerebrospinal fluid for an improved understanding of pathologic mechanisms promoting neuro-degeneration. Respective analytical techniques are also highlighted. Additionally, biochemical assays for selected high molecular mass metal species are summarized and critically discussed. Moreover additional potential techniques like direct non-invasive methods as well as mathematical modelling approaches are considered. Data on total concentrations of numerous elements in CSF as well as speciation information of elements such as Al, As, Ca, Cd, Cu, Fe, Mg, Mn, Hg, Pb, Se and Zn in CSF are summarized.

摘要

大量患有神经退行性疾病(如阿尔茨海默病和帕金森病)的患者促使全球许多研究小组研究这些疾病的发病因素和分子机制。最近的研究和综述表明,在大脑内环境平衡被打破的情况下,金属会参与这些神经退行性过程。重要的是,这些最近的研究的重点是铁、铜、锌和锰等必需金属,而不是汞和铅等众所周知的神经毒性金属。理解金属诱导的神经毒性作用的关键问题是金属穿过神经屏障的转运过程、金属的结合形式(物种)及其与神经元结构的相互作用。几项研究发表了脑脊液中总金属浓度的结果,这些结果既有对照组也有患者组,但可靠数据组的数量还不足以明确界定正常和升高的水平。本综述强调了 CSF 中金属物种更详细信息的需求。然而,有关 CSF 中元素形态分析的研究(即鉴定和量化脑脊液中各种金属的结合形式)却很少。因此,主要原因是难以获取脑脊液样本、许多感兴趣的金属物种具有非共价性质以及它们的浓度相当低。尽管如此,一些应用表明,联用技术作为脑脊液分析的附加诊断工具具有潜力。本综述表明,痕量元素分析,特别是脑脊液中元素形态分析,对于更好地理解促进神经退化的病理机制非常重要。相应的分析技术也得到了强调。此外,还总结和批判性地讨论了选定高分子质量金属物种的生化测定法。此外,还考虑了其他潜在技术,如直接非侵入性方法和数学建模方法。综述总结了 CSF 中许多元素的总浓度数据以及 Al、As、Ca、Cd、Cu、Fe、Mg、Mn、Hg、Pb、Se 和 Zn 等元素的形态信息。

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