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Antioxidant Effect of CoQ(10) on N-nitrosodiethylamine-induced Oxidative Stress in Mice

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dc.contributor.authorSong, Ho Sun-
dc.contributor.authorKim, Hee Rae-
dc.contributor.authorPark, Tae Wook-
dc.contributor.authorCho, Bong Jae-
dc.contributor.authorChoi, Mi Young-
dc.contributor.authorKim, Chang Jong-
dc.contributor.authorSohn, Uy Dong-
dc.contributor.authorSim, Sang Soo-
dc.date.available2019-05-30T02:54:46Z-
dc.date.issued2009-08-
dc.identifier.issn1226-4512-
dc.identifier.issn2093-3827-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23053-
dc.description.abstractThe antioxidant effect of CoQ(10) on N-nitrosodiethylamine (NDEA)-induced oxidative stress was investigated in mice. Food intake and body weight were similar in both CoQ(10) and control groups during the 3-week experimental period. NDEA significantly increased the activities of typical marker enzymes of liver function (AST, ALT and ALP) both in control and CoQ(10) groups. However, the increase of plasma aminotransferase activity was significantly reduced in the CoQ(10) group. Lipid peroxidation in various tissues, such as heart, lung, liver, kidney, spleen and plasma, was significantly increased by NDEA, but this increase was significantly reduced by 100 mg/kg of CoQ(10). Superoxide dismutase activity increased significantly upon NDEA-induced oxidative stress in both the control and CoQ(10) groups with the effect being less in the CoQ(10) group. Catalase activity decreased significantly in both the control and CoQ(10) groups treated with NDEA, again with the effect being less in the CoQ(10) group. The lesser effect on superoxide dismutase and catalase in the NDEA-treated CoQ(10) group is indicative of the protective effect CoQ(10). Thus, CoQ(10) can offer useful protection against NDEA-induced oxidative stress.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.titleAntioxidant Effect of CoQ(10) on N-nitrosodiethylamine-induced Oxidative Stress in Mice-
dc.typeArticle-
dc.identifier.doi10.4196/kjpp.2009.13.4.321-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.13, no.4, pp 321 - 326-
dc.identifier.kciidART001373567-
dc.description.isOpenAccessN-
dc.identifier.wosid000269737700009-
dc.identifier.scopusid2-s2.0-70349404445-
dc.citation.endPage326-
dc.citation.number4-
dc.citation.startPage321-
dc.citation.titleKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.citation.volume13-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorCatalase-
dc.subject.keywordAuthorCoQ(10)-
dc.subject.keywordAuthorLipid peroxidation-
dc.subject.keywordAuthorReactive oxygen species-
dc.subject.keywordAuthorSuperoxide dismutase-
dc.subject.keywordPlusLIPID-PEROXIDATION-
dc.subject.keywordPlusUBIQUINONE FUNCTION-
dc.subject.keywordPlusMEDICAL ASPECTS-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusERYTHROCYTES-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusLIVER-
dc.subject.keywordPlusASSAY-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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