Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites

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 dynam...

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Published in:Antioxidants
Main Authors: Taiming Liu, Meijuan Zhang, Abraham Duot, George Mukosera, Hobe Schroeder, Gordon G. Power, Arlin B. Blood
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Subjects:
Online Access:https://www.mdpi.com/2076-3921/12/9/1672
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author Taiming Liu
Meijuan Zhang
Abraham Duot
George Mukosera
Hobe Schroeder
Gordon G. Power
Arlin B. Blood
author_facet Taiming Liu
Meijuan Zhang
Abraham Duot
George Mukosera
Hobe Schroeder
Gordon G. Power
Arlin B. Blood
author_sort Taiming Liu
collection DOAJ
container_title Antioxidants
description 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.
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spelling doaj-art-e5afd16478fd4063b083ca9c0581eb802025-08-19T22:52:09ZengMDPI AGAntioxidants2076-39212023-08-01129167210.3390/antiox12091672Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide MetabolitesTaiming Liu0Meijuan Zhang1Abraham Duot2George Mukosera3Hobe Schroeder4Gordon G. Power5Arlin B. Blood6Department of Pediatrics, Loma Linda University School of Medicine, Loma Linda, CA 92354, USADepartment of Pediatrics, Loma Linda University School of Medicine, Loma Linda, CA 92354, USADepartment of Pediatrics, Loma Linda University School of Medicine, Loma Linda, CA 92354, USALawrence D. Longo, MD Center for Perinatal Biology, Loma Linda University School of Medicine, Loma Linda, CA 92354, USALawrence D. Longo, MD Center for Perinatal Biology, Loma Linda University School of Medicine, Loma Linda, CA 92354, USALawrence D. Longo, MD Center for Perinatal Biology, Loma Linda University School of Medicine, Loma Linda, CA 92354, USALawrence D. Longo, MD Center for Perinatal Biology, Loma Linda University School of Medicine, Loma Linda, CA 92354, USAWe 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.https://www.mdpi.com/2076-3921/12/9/1672chemiluminescence methodologyPitfallNO metabolitesnitriteDNICheme-NO
spellingShingle Taiming Liu
Meijuan Zhang
Abraham Duot
George Mukosera
Hobe Schroeder
Gordon G. Power
Arlin B. Blood
Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites
chemiluminescence methodology
Pitfall
NO metabolites
nitrite
DNIC
heme-NO
title Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites
title_full Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites
title_fullStr Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites
title_full_unstemmed Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites
title_short Artifacts Introduced by Sample Handling in Chemiluminescence Assays of Nitric Oxide Metabolites
title_sort artifacts introduced by sample handling in chemiluminescence assays of nitric oxide metabolites
topic chemiluminescence methodology
Pitfall
NO metabolites
nitrite
DNIC
heme-NO
url https://www.mdpi.com/2076-3921/12/9/1672
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