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Fragrance chemicals lyral and lilial decrease viability of HaCat cells' by increasing free radical production and lowering intracellular ATP level: protection by antioxidants.

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dc.contributor.author Usta J.
dc.contributor.author Hachem Y.
dc.contributor.author El-Rifai O.
dc.contributor.author Bou-Moughlabey Y.
dc.contributor.author Echtay K.
dc.contributor.author Griffiths D.
dc.contributor.author Nakkash-Chmaisse H.
dc.contributor.author Makki R.F.
dc.contributor.editor
dc.date 2013
dc.date.accessioned 2017-10-05T15:30:58Z
dc.date.available 2017-10-05T15:30:58Z
dc.date.issued 2013
dc.identifier
dc.identifier.isbn
dc.identifier.issn 18793177
dc.identifier.uri http://hdl.handle.net/10938/15303
dc.description.abstract We investigate in this study the biochemical effects on cells in culture of two commonly used fragrance chemicals: lyral and lilial. Whereas both chemicals exerted a significant effect on primary keratinocyte(s), HaCat cells, no effect was obtained with any of HepG2, Hek293, Caco2, NIH3T3, and MCF7 cells. Lyral and lilial: (a) decreased the viability of HaCat cells with a 50percent cell death at 100 and 60 nM respectively; (b) decreased significantly in a dose dependant manner the intracellular ATP level following 12-h of treatment; (c) inhibited complexes I and II of electron transport chain in liver sub-mitochondrial particles; and (d) increased reactive oxygen species generation that was reversed by N-acetyl cysteine and trolox and the natural antioxidant lipoic acid, without influencing the level of free and-or oxidized glutathione. Lipoic acid protected HaCat cells against the decrease in viability induced by either compound. Dehydrogenation of lyral and lilial produce α,β-unsaturated aldehydes, that reacts with lipoic acid requiring proteins resulting in their inhibition. We propose lyral and lilial as toxic to mitochondria that have a direct effect on electron transport chain, increase ROS production, derange mitochondrial membrane potential, and decrease cellular ATP level, leading thus to cell death. Copyright © 2012 Elsevier Ltd. All rights reserved.
dc.format.extent
dc.format.extent Pages: (339-348)
dc.language English
dc.relation.ispartof Publication Name: Toxicology in vitro : an international journal published in association with BIBRA; Publication Year: 2013; Volume: 27; no. 1; Pages: (339-348);
dc.relation.ispartofseries
dc.relation.uri
dc.source Scopus
dc.subject.other
dc.title Fragrance chemicals lyral and lilial decrease viability of HaCat cells' by increasing free radical production and lowering intracellular ATP level: protection by antioxidants.
dc.type Article
dc.contributor.affiliation Usta, J., Department of Biochemistry and Molecular Genetics, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.
dc.contributor.affiliation Hachem, Y.
dc.contributor.affiliation El-Rifai, O.
dc.contributor.affiliation Bou-Moughlabey, Y.
dc.contributor.affiliation Echtay, K.
dc.contributor.affiliation Griffiths, D.
dc.contributor.affiliation Nakkash-Chmaisse, H.
dc.contributor.affiliation Makki, R.F.
dc.contributor.authorAddress Usta, J.email: justa@aub.edu.lb
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Biochemistry and Molecular Genetics;
dc.contributor.authorDepartment Biochemistry and Molecular Genetics
dc.contributor.authorDivision
dc.contributor.authorEmail
dc.contributor.faculty Faculty of Medicine
dc.contributor.authorInitials
dc.contributor.authorOrcidID
dc.contributor.authorReprintAddress
dc.contributor.authorResearcherID
dc.contributor.authorUniversity American University of Beirut Medical Center
dc.description.cited
dc.description.citedCount 3
dc.description.citedTotWOSCount
dc.description.citedWOSCount
dc.format.extentCount 10
dc.identifier.articleNo
dc.identifier.coden
dc.identifier.pubmedID 22940465
dc.identifier.scopusID 84874283341
dc.identifier.url
dc.publisher.address
dc.relation.ispartofConference
dc.relation.ispartofConferenceCode
dc.relation.ispartofConferenceDate
dc.relation.ispartofConferenceHosting
dc.relation.ispartofConferenceLoc
dc.relation.ispartofConferenceSponsor
dc.relation.ispartofConferenceTitle
dc.relation.ispartofFundingAgency
dc.relation.ispartOfISOAbbr
dc.relation.ispartOfIssue 1
dc.relation.ispartOfPart
dc.relation.ispartofPubTitle Toxicology in vitro : an international journal published in association with BIBRA
dc.relation.ispartofPubTitleAbbr Toxicol In Vitro
dc.relation.ispartOfSpecialIssue
dc.relation.ispartOfSuppl
dc.relation.ispartOfVolume 27
dc.source.ID
dc.type.publication Journal
dc.subject.otherAuthKeyword
dc.subject.otherChemCAS acetylcysteine, 616-91-1
dc.subject.otherChemCAS adenosine triphosphate, 15237-44-2, 56-65-5, 987-65-5
dc.subject.otherChemCAS beta (4 tert butylphenyl) alpha methylpropionaldehyde, 80-54-6
dc.subject.otherChemCAS glutathione, 70-18-8
dc.subject.otherChemCAS lactate dehydrogenase, 9001-60-9
dc.subject.otherChemCAS thioctic acid, 1077-29-8, 1200-22-2, 2319-84-8, 62-46-4
dc.subject.otherChemCAS trolox C, 56305-04-5
dc.subject.otherChemCAS 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid, 56305-04-5
dc.subject.otherChemCAS Acetylcysteine, 616-91-1
dc.subject.otherChemCAS Adenosine Triphosphate, 56-65-5
dc.subject.otherChemCAS Aldehydes
dc.subject.otherChemCAS Antioxidants
dc.subject.otherChemCAS Chromans
dc.subject.otherChemCAS Cyclohexenes
dc.subject.otherChemCAS Electron Transport Chain Complex Proteins
dc.subject.otherChemCAS Glutathione, 70-18-8
dc.subject.otherChemCAS L-Lactate Dehydrogenase, 1.1.1.27
dc.subject.otherChemCAS Perfume
dc.subject.otherChemCAS Reactive Oxygen Species
dc.subject.otherChemCAS Thioctic Acid, 62-46-4
dc.subject.otherChemCAS hydroxyisohexyl 3-cyclohexene carboxaldehyde, QUE43B9Z2Q
dc.subject.otherChemCAS lilial, T7540GJV69
dc.subject.otherIndex 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid
dc.subject.otherIndex acetylcysteine
dc.subject.otherIndex adenosine triphosphate
dc.subject.otherIndex aldehyde
dc.subject.otherIndex antioxidant
dc.subject.otherIndex beta (4 tert butylphenyl) alpha methylpropionaldehyde
dc.subject.otherIndex chroman derivative
dc.subject.otherIndex cyclohexene derivative
dc.subject.otherIndex glutathione
dc.subject.otherIndex hydroxyisohexyl 3 cyclohexene carboxaldehyde
dc.subject.otherIndex hydroxyisohexyl 3-cyclohexene carboxaldehyde
dc.subject.otherIndex lactate dehydrogenase
dc.subject.otherIndex multienzyme complex
dc.subject.otherIndex perfume
dc.subject.otherIndex reactive oxygen metabolite
dc.subject.otherIndex thioctic acid
dc.subject.otherIndex trolox C
dc.subject.otherIndex animal
dc.subject.otherIndex article
dc.subject.otherIndex cell strain 3T3
dc.subject.otherIndex cell survival
dc.subject.otherIndex drug effect
dc.subject.otherIndex human
dc.subject.otherIndex metabolism
dc.subject.otherIndex mitochondrial membrane
dc.subject.otherIndex mouse
dc.subject.otherIndex tumor cell line
dc.subject.otherIndex Acetylcysteine
dc.subject.otherIndex Adenosine Triphosphate
dc.subject.otherIndex Aldehydes
dc.subject.otherIndex Animals
dc.subject.otherIndex Antioxidants
dc.subject.otherIndex Cell Line, Tumor
dc.subject.otherIndex Cell Survival
dc.subject.otherIndex Chromans
dc.subject.otherIndex Cyclohexenes
dc.subject.otherIndex Electron Transport Chain Complex Proteins
dc.subject.otherIndex Glutathione
dc.subject.otherIndex Humans
dc.subject.otherIndex L-Lactate Dehydrogenase
dc.subject.otherIndex Mice
dc.subject.otherIndex Mitochondrial Membranes
dc.subject.otherIndex NIH 3T3 Cells
dc.subject.otherIndex Perfume
dc.subject.otherIndex Reactive Oxygen Species
dc.subject.otherIndex Thioctic Acid
dc.subject.otherKeywordPlus
dc.subject.otherWOS


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