Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/8186
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dc.contributor.authorTselepis, A. D.en
dc.contributor.authorChapman, M. J.en
dc.date.accessioned2015-11-24T16:39:42Z-
dc.date.available2015-11-24T16:39:42Z-
dc.identifier.issn1567-5688-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8186-
dc.rightsDefault Licence-
dc.subjectlow density lipoproteinen
dc.subjecthigh density lipoproteinen
dc.subjectlipoprotein subspeciesen
dc.subjectpaf-acetylhydrolaseen
dc.subjectmacrophageen
dc.subjectoxidised phospholipidsen
dc.subjectsmall dense ldlen
dc.subjectcoronary heart diseaseen
dc.subjectlow-density-lipoproteinen
dc.subjectcoronary-artery diseaseen
dc.subjectlecithin-cholesterol acyltransferaseen
dc.subjecthuman decidual macrophagesen
dc.subjectpaf-degrading acetylhydrolaseen
dc.subjectacute myocardial-infarctionen
dc.subjecthuman-plasmaen
dc.subjectoxidized phospholipidsen
dc.subjectoxidative modificationen
dc.subjectrisk factoren
dc.titleInflammation, bioactive lipids and atherosclerosis: potential roles of a lipoprotein-associated phospholipase A2, platelet activating factor-acetylhydrolaseen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondary<Go to ISI>://000181359500008-
heal.identifier.secondaryhttp://ac.els-cdn.com/S1567568802000454/1-s2.0-S1567568802000454-main.pdf?_tid=519a5657e274d248d511db55bac3b8ab&acdnat=1333111933_afcd5604bed058d6af46ab4b7e339fd3-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2002-
heal.abstractIt is well established that inflammation is an integral feature of atherosclerosis and of the cardiovascular diseases which it underlies. Oxidative stress is also recognized as a key actor in atherogenesis, in which it is closely associated with the inflammatory response and bioactive lipid formation. Several bioactive lipids have been identified in the atherosclerotic plaque, including the potent inflammatory mediator platelet activating factor (PAF), PAF-like lipids, oxidised phospholipids (oxPL) and lysophosphatidylcholine (lyso-PC). Recent evidence has established a central role of two phospholipases (PL) in atherogenesis, the nonpancreatic Type II secretory phospholipase A(2) (sPLA(2)) and the lipoprotein-associated. PLA(2)-alternatively termed as PAF-acetylhydrolase (PAF-AH). sPLA(2) is calcium-dependent and hydrolyses the sn-2 acyl group of glycerophospholipids of lipoproteins and cell membranes to produce lyso-PC and free fatty acids. It is also implicated in isoprostane production from oxPL. sPLA2 is an acute phase reactant, which is upregulated by inflammatory cytokines and may represent a new independent risk factor for coronary heart disease. In contrast to sPLA2, PAF-AH is calcium-independent and is specific for short acyl groups at the sn-2 position of the phospholipid substrate and with the exception of PAF, can equally hydrolyze oxPL to generate lyso-PC and oxidized fatty acids. Thus PAF-AH plays a key role in the degradation of proinflammatory oxPL and in the generation of lyso-PC and oxidized fatty acids. PAF-AH equally can also hydrolyze short-chain diacylglycerols, triacylglycerols, and acetylated alkanols, and displays a PLA(1) activity. Whereas sPLA(2) may represent a new independent risk factor for coronary artery disease, the potential relevance of PAF-AH to atherosclerosis remains the subject of debate, and recent results suggest that the potential role of the LDL-associated PAF-AH in atherogenesis may be distinct to that of the HDL-associated enzyme. This review is focused on the main structural and catalytic features of plasma PAF-AH, on the association of the enzyme with distinct lipoprotein particle subspecies, on its cellular sources, and finally on the potential significance of this lipoprotein-associated PLA(2) in cardiovascular disease. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.en
heal.publisherElsevier Irelanden
heal.journalNameAtherosclerosis Supplementsen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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