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dc.contributor.authorKim, KM-
dc.contributor.authorJung, BH-
dc.contributor.authorPaeng, KJ-
dc.contributor.authorKim, I-
dc.contributor.authorChung, BC-
dc.date.accessioned2024-01-21T06:39:53Z-
dc.date.available2024-01-21T06:39:53Z-
dc.date.created2021-09-05-
dc.date.issued2004-07-30-
dc.identifier.issn0361-9230-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137390-
dc.description.abstractIsoprostanes, novel markers of oxidative injury, are generated by the free radical-mediated peroxidation of arachidonic acid (AA). They are thought to be important in the pathogenesis of neurodegenerative diseases such as Alzheimer&apos;s disease (AD). Using gas chromatography-mass spectrometry (GC-MS), we investigated the alteration of urinary F-2-isoprostanes in AD patients compared to that of healthy subjects. Our results show that the levels of urinary F-2-isoprostanes, sum of the prostaglandin F-2alpha isomer; prostaglandin F-2alpha (PGF(2alpha)), prostaglandin F-2beta (PGF(2beta)), and 8-isoprostaglandin F-2alpha (8-isoPGF(2alpha)), significantly increased in AD patients (P < 0.05). The concentration of urinary 8-isoPGF(2alpha), one of the biomarkers of oxidative stress, was not significantly different between 34 AD patients and 20 age-matched controls (P > 0.05). The PGF(2alpha), formed by endoperoxide reductase from PGH(2), was significantly increased in AD patients, when compared with the levels of the normal controls (P < 0.05). The PGF(2alpha), an enzymatic product of arachidonic acid, may affect the pathogenesis of AD. In addition, urinary F-2-isoprostanes can play an important role as a biomarker in AD. (C) 2004 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectLIPID-PEROXIDATION-
dc.subjectOXIDATIVE STRESS-
dc.subjectDIETARY-INTAKE-
dc.subjectIN-VIVO-
dc.subjectRISK-
dc.titleIncreased urinary F-2-isoprostanes levels in the patients with Alzheimer&apos;s disease-
dc.typeArticle-
dc.identifier.doi10.1016/j.brainresbull.2004.04.016-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBRAIN RESEARCH BULLETIN, v.64, no.1, pp.47 - 51-
dc.citation.titleBRAIN RESEARCH BULLETIN-
dc.citation.volume64-
dc.citation.number1-
dc.citation.startPage47-
dc.citation.endPage51-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000223282700007-
dc.identifier.scopusid2-s2.0-3242690571-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.type.docTypeArticle-
dc.subject.keywordPlusLIPID-PEROXIDATION-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusDIETARY-INTAKE-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusRISK-
dc.subject.keywordAuthorF-2-isoprostanes-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthoroxidative stress-
dc.subject.keywordAuthorgas chromatography-mass spectrometry-
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KIST Article > 2004
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