Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, KM | - |
dc.contributor.author | Jung, BH | - |
dc.contributor.author | Paeng, KJ | - |
dc.contributor.author | Kim, I | - |
dc.contributor.author | Chung, BC | - |
dc.date.accessioned | 2024-01-21T06:39:53Z | - |
dc.date.available | 2024-01-21T06:39:53Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2004-07-30 | - |
dc.identifier.issn | 0361-9230 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/137390 | - |
dc.description.abstract | Isoprostanes, 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'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.language | English | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.subject | LIPID-PEROXIDATION | - |
dc.subject | OXIDATIVE STRESS | - |
dc.subject | DIETARY-INTAKE | - |
dc.subject | IN-VIVO | - |
dc.subject | RISK | - |
dc.title | Increased urinary F-2-isoprostanes levels in the patients with Alzheimer's disease | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.brainresbull.2004.04.016 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | BRAIN RESEARCH BULLETIN, v.64, no.1, pp.47 - 51 | - |
dc.citation.title | BRAIN RESEARCH BULLETIN | - |
dc.citation.volume | 64 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 47 | - |
dc.citation.endPage | 51 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000223282700007 | - |
dc.identifier.scopusid | 2-s2.0-3242690571 | - |
dc.relation.journalWebOfScienceCategory | Neurosciences | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | LIPID-PEROXIDATION | - |
dc.subject.keywordPlus | OXIDATIVE STRESS | - |
dc.subject.keywordPlus | DIETARY-INTAKE | - |
dc.subject.keywordPlus | IN-VIVO | - |
dc.subject.keywordPlus | RISK | - |
dc.subject.keywordAuthor | F-2-isoprostanes | - |
dc.subject.keywordAuthor | Alzheimer&apos | - |
dc.subject.keywordAuthor | s disease | - |
dc.subject.keywordAuthor | oxidative stress | - |
dc.subject.keywordAuthor | gas chromatography-mass spectrometry | - |
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