Department of Life Sciences, Laboratory of Pharmacology and Toxicology, University of Siena, Siena, Italy.
Nat Protoc. 2013 Sep;8(9):1660-9. doi: 10.1038/nprot.2013.095. Epub 2013 Aug 1.
This protocol describes a procedure for determining glutathione (GSH) and glutathione disulfide (GSSG) concentrations in blood and other tissues. Artifactual oxidation to GSSG of 5-15% of the GSH found in a sample can occur during deproteination of biological samples with any of the commonly used acids, with consequent marked overestimation of GSSG. This can be prevented by derivatizing GSH with the alkylating agent N-ethylmaleimide (NEM) to form GS-NEM before acid deproteination, followed by back-extraction of excess NEM from the deproteinized samples with dichloromethane. GSSG concentration is then measured by spectrophotometry with the GSH recycling method, on the basis of conversion of GSSG to GSH by glutathione reductase and NADPH and reaction with 5,5'-dithiobis-(2-nitrobenzoic acid). GSH concentration is instead measured by either of two methods: by analysis of GS-NEM conjugates by HPLC in the same sample that is used to measure GSSG or, alternatively, by analysis of GSH by spectrophotometry (GSH recycling method) on one additional sample aliquot that has not been derivatized with NEM. The procedure can assay GSH and GSSG in blood and other tissues in 30 min or less.
本方案描述了一种测定血液和其他组织中谷胱甘肽(GSH)和谷胱甘肽二硫化物(GSSG)浓度的方法。在使用任何常用酸进行生物样品脱蛋白时,样品中约 5-15%的 GSH 会发生人为氧化生成 GSSG,从而导致 GSSG 的测定值严重偏高。为避免这种情况,可在酸脱蛋白前,用烷化剂 N-乙基马来酰亚胺(NEM)对 GSH 进行衍生化,形成 GS-NEM,然后用二氯甲烷从脱蛋白样品中反萃取过量的 NEM。GSSG 浓度可通过谷胱甘肽还原酶和 NADPH 将 GSSG 转化为 GSH 以及与 5,5'-二硫代双(2-硝基苯甲酸)反应的 GSH 循环法,用分光光度法测定。GSH 浓度则可通过两种方法中的任意一种测定:在测定 GSSG 的同一样品中通过 HPLC 分析 GS-NEM 缀合物,或者在未用 NEM 衍生化的另一份样品等分试样中,用分光光度法(GSH 循环法)分析 GSH。该方法可在 30 分钟或更短时间内测定血液和其他组织中的 GSH 和 GSSG。