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Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network

Nicotinamide adenine dinucleotide (NAD(+)/NADH) along with its phosphorylated form (NADP(+)/NADPH) are two molecules ubiquitously present in all organisms, and they play key roles as cofactors in fundamental catabolic and anabolic processes, respectively. The oxidation of NADPH to NADP(+) initiates...

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Autores principales: Veskoukis, Aristidis S., Margaritelis, Nikos V., Kyparos, Antonios, Paschalis, Vassilis, Nikolaidis, Michalis G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748689/
https://www.ncbi.nlm.nih.gov/pubmed/29088980
http://dx.doi.org/10.1080/13510002.2017.1392695
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author Veskoukis, Aristidis S.
Margaritelis, Nikos V.
Kyparos, Antonios
Paschalis, Vassilis
Nikolaidis, Michalis G.
author_facet Veskoukis, Aristidis S.
Margaritelis, Nikos V.
Kyparos, Antonios
Paschalis, Vassilis
Nikolaidis, Michalis G.
author_sort Veskoukis, Aristidis S.
collection PubMed
description Nicotinamide adenine dinucleotide (NAD(+)/NADH) along with its phosphorylated form (NADP(+)/NADPH) are two molecules ubiquitously present in all organisms, and they play key roles as cofactors in fundamental catabolic and anabolic processes, respectively. The oxidation of NADPH to NADP(+) initiates a cascade of reactions, where a network of molecules is implicated. The molecules of this cascade form a network with eminent translational potential in redox metabolism. A special point of interest is that spectrophotometric assays have been developed both for NADH/NADPH and the molecules directly regulated by them. Therefore, crucial molecules of the NADPH-dependent redox network can be measured, and the results can be used to assess the bioenergetic and/or oxidative stress status. The main aim of this review is to collectively present the NADPH-related molecules, namely NADPH, NADH, NAD(+) kinase, NADPH oxidase, peroxiredoxin, thioredoxin, thioredoxin reductase, and nitric oxide synthase, that can be measured in blood and tissues with the use of a spectrophotometer, which is probably the most simple, inexpensive and widely used tool in biochemistry. We are providing the researchers with reliable and valid spectrophotometric assays for the measurement of the most important biomarkers of the NADPH network in blood and other tissues, thus allowing the opportunity to follow the redox changes in response to a stimulus.
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spelling pubmed-67486892020-04-15 Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network Veskoukis, Aristidis S. Margaritelis, Nikos V. Kyparos, Antonios Paschalis, Vassilis Nikolaidis, Michalis G. Redox Rep Review Article Nicotinamide adenine dinucleotide (NAD(+)/NADH) along with its phosphorylated form (NADP(+)/NADPH) are two molecules ubiquitously present in all organisms, and they play key roles as cofactors in fundamental catabolic and anabolic processes, respectively. The oxidation of NADPH to NADP(+) initiates a cascade of reactions, where a network of molecules is implicated. The molecules of this cascade form a network with eminent translational potential in redox metabolism. A special point of interest is that spectrophotometric assays have been developed both for NADH/NADPH and the molecules directly regulated by them. Therefore, crucial molecules of the NADPH-dependent redox network can be measured, and the results can be used to assess the bioenergetic and/or oxidative stress status. The main aim of this review is to collectively present the NADPH-related molecules, namely NADPH, NADH, NAD(+) kinase, NADPH oxidase, peroxiredoxin, thioredoxin, thioredoxin reductase, and nitric oxide synthase, that can be measured in blood and tissues with the use of a spectrophotometer, which is probably the most simple, inexpensive and widely used tool in biochemistry. We are providing the researchers with reliable and valid spectrophotometric assays for the measurement of the most important biomarkers of the NADPH network in blood and other tissues, thus allowing the opportunity to follow the redox changes in response to a stimulus. Taylor & Francis 2017-10-31 /pmc/articles/PMC6748689/ /pubmed/29088980 http://dx.doi.org/10.1080/13510002.2017.1392695 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review Article
Veskoukis, Aristidis S.
Margaritelis, Nikos V.
Kyparos, Antonios
Paschalis, Vassilis
Nikolaidis, Michalis G.
Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network
title Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network
title_full Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network
title_fullStr Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network
title_full_unstemmed Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network
title_short Spectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH network
title_sort spectrophotometric assays for measuring redox biomarkers in blood and tissues: the nadph network
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748689/
https://www.ncbi.nlm.nih.gov/pubmed/29088980
http://dx.doi.org/10.1080/13510002.2017.1392695
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