Liu Taiming, Zhang Meijuan, Duot Abraham, Mukosera George, Schroeder Hobe, Power Gordon G, Blood Arlin B
Department of Pediatrics, Loma Linda University School of Medicine, Loma Linda, CA 92354, USA.
Lawrence D. Longo, MD Center for Perinatal Biology, Loma Linda University School of Medicine, Loma Linda, CA 92354, USA.
Antioxidants (Basel). 2023 Aug 25;12(9):1672. doi: 10.3390/antiox12091672.
We recently developed a combination of four chemiluminescence-based assays for selective detection of different nitric oxide (NO) metabolites, including nitrite, S-nitrosothiols (SNOs), heme-nitrosyl (heme-NO), and dinitrosyl iron complexes (DNICs). However, these NO species (NOx) may be under dynamic equilibria during sample handling, which affects the final determination made from the readout of assays. Using fetal and maternal sheep from low and high altitudes (300 and 3801 m, respectively) as models of different NOx levels and compositions, we tested the hypothesis that sample handling introduces artifacts in chemiluminescence assays of NOx. Here, we demonstrate the following: (1) room temperature placement is associated with an increase and decrease in NOx in plasma and whole blood samples, respectively; (2) snap freezing and thawing lead to the interconversion of different NOx in plasma; (3) snap freezing and homogenization in liquid nitrogen eliminate a significant fraction of NOx in the aorta of stressed animals; (4) A "stop solution" commonly used to preserve nitrite and SNOs leads to the interconversion of different NOx in blood, while deproteinization results in a significant increase in detectable NOx; (5) some reagents widely used in sample pretreatments, such as mercury chloride, acid sulfanilamide, N-ethylmaleimide, ferricyanide, and anticoagulant ethylenediaminetetraacetic acid, have unintended effects that destabilize SNO, DNICs, and/or heme-NO; (6) blood, including the residual blood clot left in the washed purge vessel, quenches the signal of nitrite when using ascorbic acid and acetic acid as the purge vessel reagent; and (7) new limitations to the four chemiluminescence-based assays. This study points out the need for re-evaluation of previous chemiluminescence measurements of NOx, and calls for special attention to be paid to sample handling, as it can introduce significant artifacts into NOx assays.
我们最近开发了一组基于化学发光的检测方法,用于选择性检测不同的一氧化氮(NO)代谢产物,包括亚硝酸盐、S-亚硝基硫醇(SNOs)、血红素亚硝基(heme-NO)和二亚硝基铁络合物(DNICs)。然而,在样品处理过程中,这些NO物种(NOx)可能处于动态平衡状态,这会影响基于检测读数的最终测定结果。我们以来自低海拔和高海拔地区(分别为300米和3801米)的胎羊和母羊作为不同NOx水平和组成的模型,测试了样品处理在NOx化学发光检测中引入假象的假设。在此,我们证明了以下几点:(1)室温放置分别与血浆和全血样品中NOx的增加和减少有关;(2)速冻和解冻导致血浆中不同NOx的相互转化;(3)在液氮中速冻并匀浆可消除应激动物主动脉中相当一部分NOx;(4)一种常用于保存亚硝酸盐和SNOs的“终止溶液”会导致血液中不同NOx的相互转化,而去蛋白作用则会导致可检测到的NOx显著增加;(5)一些在样品预处理中广泛使用的试剂,如氯化汞、酸性磺胺、N-乙基马来酰亚胺、铁氰化物和抗凝剂乙二胺四乙酸,具有使SNO、DNICs和/或heme-NO不稳定的意外作用;(6)当使用抗坏血酸和乙酸作为吹扫容器试剂时,血液(包括留在洗涤后的吹扫容器中的残留血凝块)会淬灭亚硝酸盐的信号;以及(7)基于化学发光的四种检测方法存在新的局限性。本研究指出需要重新评估先前对NOx的化学发光测量,并呼吁特别注意样品处理,因为它可能在NOx检测中引入显著的假象。