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Antioxidant and mitochondrial protective effects of oxidized metabolites of oltipraz

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dc.contributor.authorChoi, Song Hwa-
dc.contributor.authorKim, Young Mi-
dc.contributor.authorLee, Jung Min-
dc.contributor.authorKim, Sang Geon-
dc.date.accessioned2021-06-23T13:39:03Z-
dc.date.available2021-06-23T13:39:03Z-
dc.date.created2021-01-21-
dc.date.issued2010-02-
dc.identifier.issn1742-5255-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/40000-
dc.description.abstractImportance of the field. Comprehensive studies indicate that oltipraz exerts cancer chemopreventive effects. Oltipraz has other therapeutic potentials, which include anti-fibrotic effect, inhibition of insulin resistance, mitochondrial protection and cytoprotective effect against oxidative stress. Although antioxidant mechanisms may account for its cancer chemopreventive effect, details on the molecular mechanism still remain to be clarified. Areas covered in this review. Two major metabolic pathways of oltipraz include oxidative desulfuration of the thione to yield 4-methyl-5-(pyrazin-2-yl)-3H-1,2-dithiol-3-one and molecular rearrangement to 7-methyl-6,8-bis (methylthio)H-pyrrolo[1,2-a]pyrazine. In addition to the diverse pharmacological effects of oltipraz, the oxidized metabolites may have distinct biological effects on cell survival. The AMP-activated protein kinase pathway has been recognized as a key cascade for mitochondrial protection and cell survival events, which can be activated by the oxidized metabolites of oltipraz. What the reader will gain: in this review, the metabolic activation of oltipraz and the role of the cell signaling pathways in regulating the expression of Phase II genes and antioxidant activity are discussed with particular reference to their effects on mitochondrial protection and cell survival. Take home message: In terms of therapeutic potential, the findings reviewed here demonstrate a therapeutic potential for oxidized metabolite of oltipraz and offer comparison of antioxidant capacity between metabolites and parent compound.-
dc.language영어-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.titleAntioxidant and mitochondrial protective effects of oxidized metabolites of oltipraz-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Young Mi-
dc.identifier.doi10.1517/17425250903427972-
dc.identifier.scopusid2-s2.0-76749172145-
dc.identifier.wosid000274559300007-
dc.identifier.bibliographicCitationEXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, v.6, no.2, pp.213 - 224-
dc.relation.isPartOfEXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY-
dc.citation.titleEXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY-
dc.citation.volume6-
dc.citation.number2-
dc.citation.startPage213-
dc.citation.endPage224-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusACTIVATED PROTEIN-KINASE-
dc.subject.keywordPlusPERMEABILITY TRANSITION PORE-
dc.subject.keywordPlusNRF2 TRANSCRIPTION FACTOR-
dc.subject.keywordPlusCANCER CHEMOPREVENTIVE OLTIPRAZ-
dc.subject.keywordPlusAFLATOXIN-INDUCED TUMORIGENESIS-
dc.subject.keywordPlusADENINE-NUCLEOTIDE TRANSLOCASE-
dc.subject.keywordPlusHEPATIC INSULIN-RESISTANCE-
dc.subject.keywordPlusRETICULUM STRESS-RESPONSE-
dc.subject.keywordPlusGLUTATHIONE-S-TRANSFERASE-
dc.subject.keywordPlusPHASE-2 ENZYME-INDUCTION-
dc.subject.keywordAuthorAMPK-
dc.subject.keywordAuthorantioxidant effect-
dc.subject.keywordAuthorcell survival-
dc.subject.keywordAuthormitochondrial protection-
dc.subject.keywordAuthoroxidized metabolites of oltipraz-
dc.subject.keywordAuthorPhase II enzyme-
dc.identifier.urlhttps://www.tandfonline.com/doi/full/10.1517/17425250903427972-
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