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生物样本中 S-亚硝基硫醇的测定——程序、问题和注意事项。

The determination of S-nitrosothiols in biological samples--procedures, problems and precautions.

机构信息

Institute for Chemico-Physical Processes, National Research Council-CNR, Pisa, Italy.

出版信息

Life Sci. 2011 Jan 17;88(3-4):126-9. doi: 10.1016/j.lfs.2010.10.024. Epub 2010 Nov 1.

DOI:10.1016/j.lfs.2010.10.024
PMID:21047520
Abstract

Despite the considerable number of published studies in the field of S-nitrosothiols (RSNO), the determination of these compounds in biological samples still represents an analytical challenge, due to several technical obstacles and often long sample preparation procedures. Other problems derive from the intrinsic lability of RSNO and the absence of certified reference material, analytically validated methods or suitable internal standards. Also, thiols and nitrites are usually present at high concentrations in biological matrices, and all precautions must be adopted in order to prevent artifactual formation of RSNO. Preanalytical steps (sampling, preservation and pre-treatment of samples) are particularly critical for the obtainment of reliable measurements. Three main mechanisms have been identified capable of compromising the assays: metal-catalyzed RSNO decomposition, reduction of the S-NO bond by thiols (transnitrosylation reactions) and enzymatic degradation of S-nitroso-glutathione (GSNO) by endogenous γ-glutamyltransferase (GGT) activity possibly present in the sample. If not adequately controlled, these factors likely contribute to the wide dispersion of values reported in the literature for RSNO and GSNO concentration in biological fluids, blood in the first place. The use of metal chelators, thiol reagents and GGT inhibitors appears therefore mandatory.

摘要

尽管在 S-亚硝基硫醇 (RSNO) 领域已经发表了相当数量的研究,但由于存在几个技术障碍,而且通常需要较长的样品制备程序,这些化合物在生物样品中的测定仍然是一个分析挑战。其他问题源于 RSNO 的固有不稳定性以及缺乏经过分析验证的方法、认证参考物质或合适的内标。此外,硫醇和亚硝酸盐通常在生物基质中以高浓度存在,因此必须采取所有预防措施以防止 RSNO 的人为形成。分析前步骤(采样、样品保存和预处理)对于获得可靠的测量结果尤为关键。已经确定了三种能够破坏测定的主要机制:金属催化的 RSNO 分解、硫醇还原 S-NO 键(transnitrosylation 反应)以及内源性 γ-谷氨酰转移酶 (GGT) 活性可能存在于样品中的 S-亚硝基谷胱甘肽 (GSNO) 酶促降解。如果不能得到充分控制,这些因素可能导致文献中报告的生物体液(尤其是血液)中 RSNO 和 GSNO 浓度值的广泛分散。因此,使用金属螯合剂、硫醇试剂和 GGT 抑制剂似乎是必要的。

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