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 |
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dc.contributor.faculty |
Faculty of Medicine |
dc.contributor.authorInitials |
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dc.contributor.authorOrcidID |
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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 |
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dc.relation.ispartofConference |
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dc.relation.ispartofConferenceCode |
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dc.relation.ispartofConferenceDate |
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dc.relation.ispartofConferenceHosting |
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dc.relation.ispartofConferenceLoc |
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dc.relation.ispartofConferenceSponsor |
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dc.relation.ispartofConferenceTitle |
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dc.relation.ispartofFundingAgency |
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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 |
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dc.relation.ispartOfSuppl |
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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 |
|