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人尿中亚硝酸盐和丙二醛的同时五氟苄基衍生化及气相色谱-电子捕获负化学电离质谱测定:这些不同氧化应激生物标志物之间存在密切正相关。

Simultaneous pentafluorobenzyl derivatization and GC-ECNICI-MS measurement of nitrite and malondialdehyde in human urine: Close positive correlation between these disparate oxidative stress biomarkers.

作者信息

Hanff Erik, Eisenga Michele F, Beckmann Bibiana, Bakker Stephan J L, Tsikas Dimitrios

机构信息

Centre of Pharmacology and Toxicology, Hannover Medical School, Hannover, Germany.

Department of Internal Medicine, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Feb 1;1043:167-175. doi: 10.1016/j.jchromb.2016.07.027. Epub 2016 Jul 16.

Abstract

Urinary nitrite and malondialdehyde (MDA) are biomarkers of nitrosative and oxidative stress, respectively. At physiological pH values of urine and plasma, nitrite and MDA exist almost entirely in their dissociated forms, i.e., as ONO (ONOH, pK=3.4) and CH(CHO) (CH(CHO), pK=4.5). Previously, we reported that nitrite and MDA react with pentafluorobenzyl (PFB) bromide (PFB-Br) in aqueous acetone. Here, we report on the simultaneous derivatization of nitrite and MDA and their stable-isotope labeled analogs ONO (4μM) and CH(CDO) (1μM or 10μM) with PFB-Br (10μL) to PFBNO, PFBNO, C(PFB)(CHO)), C(PFB)(CDO) by heating acetonic urine (urine-acetone, 100:400μL) for 60min at 50°C. After acetone evaporation under a stream of nitrogen, derivatives were extracted with ethyl acetate (1mL). A 1-μL aliquot of the ethyl acetate phase dried over anhydrous NaSO was injected in the splitless mode for simultaneous GC-MS analysis in the electron capture negative-ion chemical ionization mode. Quantification was performed by selected-ion monitoring (SIM) the anions [M-PFB]m/z 46 for ONO, m/z 47 for ONO, m/z 251 for C(PFB)(CHO), and m/z 253 for C(PFB)(CDO). The retention times were 3.18min for PFB-ONO/PFB-ONO, and 7.13min for C(PFB)(CHO)/C(PFB)(CDO). Use of CH(CDO) at 1μM but not at 10μM was associated with an unknown interference with the C(PFB)(CDO) peak. Endogenous MDA can be quantified using ONO (4μM) and CH(CDO) (10μM) as the internal standards. The method is also useful for the measurement of nitrate and creatinine in addition to nitrite and MDA. Nitrite and MDA were measured by this method in urine of elderly healthy subjects (10 females, 9 males; age, 60-70 years; BMI, 25-30kg/m). Creatinine-corrected excretion rates did not differ between males and females for MDA (62.6 [24-137] vs 80.2 [52-118]nmol/mmol, P=0.448) and for nitrite (102 [71-174] vs. 278 [110-721]nmol/mmol P=0.053). We report for the first time a close correlation (r=0.819, P<0.0001) between MDA and nitrite in human urine. This correlation is assumed to be due to involvement of myeloperoxidase which catalyzes the formation of hypochlorite (OCl) from chloride and hydrogen peroxide. In turn, hypochlorite reacts both with nitrite and with polyunsaturated fatty acids such as arachidonic acid, with the later reaction generating MDA. The proposed mechanisms are supported by the literature but remain to be fully explored.

摘要

尿亚硝酸盐和丙二醛(MDA)分别是亚硝化应激和氧化应激的生物标志物。在尿液和血浆的生理pH值下,亚硝酸盐和MDA几乎完全以解离形式存在,即分别为ONO⁻(ONOH,pK = 3.4)和CH(CHO)₂⁻(CH(CHO)₂,pK = 4.5)。此前,我们报道过亚硝酸盐和MDA在丙酮水溶液中与五氟苄基(PFB)溴化物(PFB - Br)发生反应。在此,我们报告通过将含丙酮的尿液(尿液 - 丙酮,100:400μL)在50°C加热60分钟,使亚硝酸盐、MDA及其稳定同位素标记类似物ONO₂⁻(4μM)和CH(CDO)₂⁻(1μM或10μM)与PFB - Br(10μL)同时衍生化为PFBNO₂、PFBNO₂、C(PFB)₂(CHO)₂、C(PFB)₂(CDO)₂。在氮气流下蒸发丙酮后,用乙酸乙酯(1mL)萃取衍生物。取1μL经无水Na₂SO₄干燥的乙酸乙酯相以不分流模式进样,在电子捕获负离子化学电离模式下进行同步气相色谱 - 质谱分析。通过选择离子监测(SIM)对阴离子进行定量,[M - PFB]⁻的m/z值分别为:ONO₂⁻为46,ONO₂⁻为47,C(PFB)₂(CHO)₂为251,C(PFB)₂(CDO)₂为253。保留时间分别为:PFB - ONO₂/PFB - ONO₂为3.18分钟,C(PFB)₂(CHO)₂/C(PFB)₂(CDO)₂为7.13分钟。使用1μM的CH(CDO)₂而非10μM的CH(CDO)₂会对C(PFB)₂(CDO)₂峰产生未知干扰。内源性MDA可以使用ONO₂⁻(4μM)和CH(CDO)₂⁻(10μM)作为内标进行定量。该方法除了可用于测量亚硝酸盐和MDA外,还可用于测量硝酸盐和肌酐。用此方法对老年健康受试者(10名女性,9名男性;年龄60 - 70岁;BMI 25 - 30kg/m²)的尿液进行了亚硝酸盐和MDA的测量。男性和女性之间经肌酐校正后的排泄率,MDA分别为62.6 [24 - 137]与80.2 [52 - 118]nmol/mmol,P = 0.448;亚硝酸盐分别为102 [71 - 174]与278 [110 - 721]nmol/mmol,P = 0.053,两者无差异。我们首次报道了人体尿液中MDA与亚硝酸盐之间存在密切相关性(r = 0.819,P < 0.0001)。这种相关性被认为是由于髓过氧化物酶参与其中,该酶催化氯离子和过氧化氢形成次氯酸盐(OCl⁻)。反过来,次氯酸盐既与亚硝酸盐反应,也与多不饱和脂肪酸如花生四烯酸反应,后一反应生成MDA。所提出的机制有文献支持,但仍有待充分探索。

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