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dc.creatorVeskoukis A.S., Margaritelis N.V., Kyparos A., Paschalis V., Nikolaidis M.G.en
dc.date.accessioned2023-01-31T10:32:41Z
dc.date.available2023-01-31T10:32:41Z
dc.date.issued2018
dc.identifier10.1080/13510002.2017.1392695
dc.identifier.issn13510002
dc.identifier.urihttp://hdl.handle.net/11615/80601
dc.description.abstractNicotinamide 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. © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.en
dc.language.isoenen
dc.sourceRedox Reporten
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85032812138&doi=10.1080%2f13510002.2017.1392695&partnerID=40&md5=37bd4cbb8d1da3e045ac01dd25eef858
dc.subjectnitric oxide synthaseen
dc.subjectperoxiredoxinen
dc.subjectreduced nicotinamide adenine dinucleotideen
dc.subjectreduced nicotinamide adenine dinucleotide phosphateen
dc.subjectreduced nicotinamide adenine dinucleotide phosphate oxidaseen
dc.subjectthioredoxinen
dc.subjectthioredoxin reductaseen
dc.subjectbiological markeren
dc.subjectnicotinamide adenine dinucleotideen
dc.subjectnicotinamide adenine dinucleotide kinaseen
dc.subjectnicotinamide adenine dinucleotide phosphateen
dc.subjectnitric oxide synthaseen
dc.subjectperoxiredoxinen
dc.subjectphosphotransferaseen
dc.subjectreduced nicotinamide adenine dinucleotide phosphate oxidaseen
dc.subjectthioredoxinen
dc.subjectthioredoxin reductaseen
dc.subjectTXN protein, humanen
dc.subjectenergy metabolismen
dc.subjectenzyme phosphorylationen
dc.subjecthumanen
dc.subjectoxidative stressen
dc.subjectpentose phosphate cycleen
dc.subjectphagocyteen
dc.subjectpriority journalen
dc.subjectprotein processingen
dc.subjectredox stressen
dc.subjectReviewen
dc.subjectsignal transductionen
dc.subjectspectrophotometryen
dc.subjecttissue homogenateen
dc.subjectblooden
dc.subjectmetabolismen
dc.subjectoxidation reduction reactionen
dc.subjectproceduresen
dc.subjectspectrophotometryen
dc.subjectBiomarkersen
dc.subjectHumansen
dc.subjectNADen
dc.subjectNADPen
dc.subjectNADPH Oxidasesen
dc.subjectNitric Oxide Synthaseen
dc.subjectOxidation-Reductionen
dc.subjectPeroxiredoxinsen
dc.subjectPhosphotransferases (Alcohol Group Acceptor)en
dc.subjectSpectrophotometryen
dc.subjectThioredoxin-Disulfide Reductaseen
dc.subjectThioredoxinsen
dc.subjectTaylor and Francis Ltd.en
dc.titleSpectrophotometric assays for measuring redox biomarkers in blood and tissues: the NADPH networken
dc.typeotheren


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