Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/23101
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dc.date.accessioned2021-12-09T06:05:04Z-
dc.date.available2021-12-09T06:05:04Z-
dc.date.issued2006-03-01-
dc.identifier.citationSürmen-Gür, E. vd. (2006). ''Chronic black tea administration protects plasma proteins, plasma, liver and kidney lipids against oxidation''. Medical Science Monitor, 12(3), BR102-BR105.en_US
dc.identifier.issn1643-3750-
dc.identifier.urihttps://www.medscimonit.com/abstract/index/idArt/447103/act/2-
dc.identifier.urihttp://hdl.handle.net/11452/23101-
dc.description.abstractBackground: Black tea is known to have protective effects against plasma lipid and lipoprotein oxidation, but its influence on lipid peroxidation in tissue has been less studied. The effect of oral black tea consumption on protein oxidation has also not been demonstrated. The present study investigated the antioxidant effects of oral black tea consumption. Material/Methods: Male Sprague-Dawley rats were fed a regular murine chow diet. The controls were supplied With water ad libitum, while the black tea group received aqueous black tea extract as the sole source of liquids. At the end of the ten-week experimental period, intestinal brush border, liver and kidney reduced-glutathione concentrations were evaluated as an index of cellular antioxidant defence. Plasma and tissue malondialdehyde concentrations and plasma protein carbonyl content were measured to evaluate lipid peroxidation and protein oxidation, respectively. Results: The plasma malondialclehyde and protein carbonyl contents of rats consuming the black tea were significantly less than in controls. Similarly, liver and kidney malondialdehyde concentrations were significantly lower in the experimental group, while jejunoileal mucosa were not affected. Ten weeks of black tea administration caused significantly higher reduced-glutathione levels in the kidneys of black tea-administered rats, and a significant negative correlation was observed between kidney malondialdehyde and glutathione concentrations. Conclusions: These findings provide evidence that long term black tea supplementation is capable of protecting both plasma proteins and plasma lipids from oxidative injury, and demonstrate that chronic black tea administration protects both liver and kidney tissues - but not the jejunoileal mucosa against oxidation.en_US
dc.language.isoenen_US
dc.publisherInt Scientific Informationen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectResearch & experimental medicineen_US
dc.subjectTissue lipid peroxidationen_US
dc.subjectProtein oxidationen_US
dc.subjectPlasma lipid peroxidationen_US
dc.subjectGlutathioneen_US
dc.subjectAntioxidantsen_US
dc.subjectTheaflavinsen_US
dc.subjectGreenen_US
dc.subjectDNA-damageen_US
dc.subject.meshThiobarbituric acid reactive substancesen_US
dc.subject.meshTeaen_US
dc.subject.meshReference standardsen_US
dc.subject.meshSprague-dawleyen_US
dc.subject.meshRatsen_US
dc.subject.meshRandom allocationen_US
dc.subject.meshPlant extractsen_US
dc.subject.meshMalondialdehydeen_US
dc.subject.meshAdministration, oralen_US
dc.subject.meshMaleen_US
dc.subject.meshLiveren_US
dc.subject.meshLipidsen_US
dc.subject.meshLipid peroxidationen_US
dc.subject.meshKidneyen_US
dc.subject.meshGlutathioneen_US
dc.subject.meshBlood proteinsen_US
dc.subject.meshAntioxidantsen_US
dc.subject.meshAnimalsen_US
dc.titleChronic black tea administration protects plasma proteins, plasma, liver and kidney lipids against oxidationen_US
dc.typeArticleen_US
dc.identifier.wos000236071000004tr_TR
dc.identifier.scopus2-s2.0-33644679659tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji ve Genetik Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0001-7377-9682tr_TR
dc.contributor.orcid0000-0002-0909-618Xtr_TR
dc.identifier.startpageBR102tr_TR
dc.identifier.endpageBR105tr_TR
dc.identifier.volume12tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalMedical Science Monitoren_US
dc.contributor.buuauthorSürmen-Gür, Esma-
dc.contributor.buuauthorGülten, Tuna-
dc.contributor.buuauthorSerdar, Zehra-
dc.contributor.buuauthorÇolakoğulları, Mukaddes-
dc.contributor.researcheridAAG-7327-2021tr_TR
dc.contributor.researcheridAAH-6200-2021tr_TR
dc.identifier.pubmed16501415tr_TR
dc.subject.wosMedicine, research & experimentalen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid7801407302tr_TR
dc.contributor.scopusid6505944216tr_TR
dc.contributor.scopusid57222002284tr_TR
dc.contributor.scopusid14423975800tr_TR
dc.subject.scopusFlavanols; White Tea; Epigallocatechin Gallateen_US
dc.subject.emtreeWateren_US
dc.subject.emtreePlasma proteinen_US
dc.subject.emtreeMalonaldehydeen_US
dc.subject.emtreeGlutathioneen_US
dc.subject.emtreeCarbonyl derivativeen_US
dc.subject.emtreeBlack tea extracten_US
dc.subject.emtreeTissue levelen_US
dc.subject.emtreeSupplementationen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeProtein metabolismen_US
dc.subject.emtreePlasmaen_US
dc.subject.emtreeOxidationen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAnimal tissueen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeLiveren_US
dc.subject.emtreeLipid peroxidationen_US
dc.subject.emtreeLipid oxidationen_US
dc.subject.emtreeAntioxidant activityen_US
dc.subject.emtreeLipid liver levelen_US
dc.subject.emtreekidney;en_US
dc.subject.emtreeJejunum mucosaen_US
dc.subject.emtreeIntestine brush borderen_US
dc.subject.emtreeIleum mucosaen_US
dc.subject.emtreeCorrelation analysisen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeChronic drug administrationen_US
dc.subject.emtreeCellular immunityen_US
dc.subject.emtreeBlood levelen_US
dc.subject.emtreeArticleen_US
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