使用OPA和n -乙酰半胱氨酸乙酯对人红细胞谷胱甘肽形式的高效液相色谱分析:亚硝酸盐诱导谷胱甘肽氧化为GSSG的证据。

Jan Thomas Michaelsen, Sabine Dehnert, Daniela Giustarini, Bibiana Beckmann, Dimitrios Tsikas
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引用次数: 51

摘要

谷胱甘肽以还原形式(GSH)、二硫化物(GSSG)和与硫醇(RSH)混合的二硫化物(GSSR)存在于生物样品中。谷胱甘肽是最丰富的低分子质量硫醇,作为细胞内氧化还原状态的辅助因子和主要成分起着重要作用。由于其自身的巯基(SH), GSH很容易与邻苯二醛(OPA)反应,形成高度稳定和荧光的异吲哚衍生物(GSH-OPA),这使得用荧光(FL)检测高效液相色谱法(HPLC)对生物系统中的GSH进行敏感和特异的定量测定成为可能。本文报道了一种新型的强二硫键还原巯基n -乙酰半胱氨酸乙酯(NACET)作为GSH- opa衍生物,利用FL(激发/发射338/458nm)或UV吸收(338nm)检测,用于红细胞胞浆中GSH和GSSG的特异性定量分析。与在水溶液中不同,在不含NACET的情况下,红细胞胞浆中GSH的衍生化产生两个密切相关的衍生物,而在有NACET的情况下,GSH- opa衍生物仅产生一个。对HPLC法进行了优化和验证,并应用于健康人红细胞中GSH和GSSG的测定。测定12名健康青年志愿者(23-38岁)红细胞中GSH和GSSG的基础浓度分别为2340+/-350微米和11.4+/-3.2微米。该方法还应用于研究亚硝酸盐对完整和裂解的人红细胞中谷胱甘肽状态的影响。亚硝酸盐在mm浓度下可在裂解的红细胞中立即形成大量的GSSG,但在完整的红细胞中则不太明显。外添加谷胱甘肽到裂解红细胞抑制亚硝酸盐诱导的高铁血红蛋白的形成。我们的研究结果表明,一氧化氮/亚硝酸盐相关的GSH消耗率,以及NADH和NADPH的消耗率,可能在健康受试者的红细胞中约为600微摩尔/天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HPLC analysis of human erythrocytic glutathione forms using OPA and N-acetyl-cysteine ethyl ester: evidence for nitrite-induced GSH oxidation to GSSG.

Glutathione exists in biological samples in the reduced form (GSH), as its disulfide (GSSG) and as a mixed disulfide (GSSR) with thiols (RSH). GSH is the most abundant low-molecular-mass thiol and plays important roles as a cofactor and as a main constituent of the intracellular redox status. Due to its own sulfhydryl (SH) group, GSH reacts readily with o-phthaldialdehyde (OPA) to form a highly stable and fluorescent isoindole derivative (GSH-OPA), which allows for sensitive and specific quantitative determination of GSH in biological systems by HPLC with fluorescence (FL) detection. In the present article we report on the utility of the novel, strongly disulfide bond-reducing thiol N-acetyl-cysteine ethyl ester (NACET) for the specific quantitative analysis of GSH and GSSG in the cytosol of red blood cells (RBC) as GSH-OPA derivative with FL (excitation/emission 338/458nm) or UV absorbance (338nm) detection. Unlike in aqueous solution, the derivatization of GSH in RBC cytosol yielded two closely related derivatives in the absence of NACET and only the GSH-OPA derivative in the presence of NACET. The HPLC method was optimized and validated for human RBC and applied to measure GSH and GSSG in RBC of healthy subjects. Basal GSH and GSSG concentrations were determined to be 2340+/-350microM and 11.4+/-3.2microM, respectively, in RBC of 12 healthy young volunteers (aged 23-38 years). The method was also applied to study the effects of nitrite on the glutathione status in intact and lysed human RBC. Nitrite at mM-concentrations caused instantaneous and considerable GSSG formation in lysed but much less pronounced in intact RBC. GSH externally added to lysed RBC inhibited nitrite-induced methemoglobin formation. Our findings suggest that nitric oxide/nitrite-related consumption rate of GSH, and presumably that of NADH and NADPH, could be of the order of 600micromol/day in RBC of healthy subjects.

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