Effect of phenobarbital and 3-methylcholanthrene on aldehyde dehydrogenase activity in cultures of HepG2 cells and normal human hepatocytes

dc.contributor.authorMarselos, M.en
dc.contributor.authorStrom, S. C.en
dc.contributor.authorMichalopoulos, G.en
dc.date.accessioned2015-11-24T19:22:38Z
dc.date.available2015-11-24T19:22:38Z
dc.identifier.issn0009-2797-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/22179
dc.rightsDefault Licence-
dc.subjectAldehyde Dehydrogenase/*metabolismen
dc.subjectAldehydes/metabolismen
dc.subjectBenzaldehydes/metabolismen
dc.subjectCarcinoma, Hepatocellular/enzymology/pathologyen
dc.subjectCells, Cultureden
dc.subjectLiver/cytology/*enzymologyen
dc.subjectLiver Neoplasmsen
dc.subjectMethylcholanthrene/*pharmacologyen
dc.subjectNAD/metabolismen
dc.subjectNeoplasm Proteins/metabolismen
dc.subjectPhenobarbital/*pharmacologyen
dc.subjectSubstrate Specificityen
dc.titleEffect of phenobarbital and 3-methylcholanthrene on aldehyde dehydrogenase activity in cultures of HepG2 cells and normal human hepatocytesen
heal.abstractAldehyde dehydrogenase (ALDH) activity was measured in primary cultures of normal human hepatocytes and of the human hepatoma cell line HepG2 after application of phenobarbital (PB) or 3-methylcholanthrene (MC) for 5 days. Treatment with PB alone resulted in a significant increase in both protein and DNA content at concentrations of 2 and 3 mM. Treatment with MC at a concentration as low as 5 microM led to a significant loss of cells when it lasted more than 5 days. Concentrations of 3-5 mM of PB in the media of HepG2 cell cultures caused a 2-fold enhancement of the activity of ALDH, as measured with NAD and propionaldehyde (P/NAD) or benzaldehyde (B/NAD). On the other hand, MC-treated cultures (5 microM) showed a 20-fold increase in enzyme activity measured with NADP and benzaldehyde (B/NADP), and a 2-fold increase in B/NAD activity. Combined treatment with both PB and MC led to an effect of dynamic synergism as far as B/NAD and B/NADP activities are concerned, suggesting a metabolite of MC as the mediator for the increase of ALDH activity. Normal human hepatocytes in primary cultures responded to PB (3 mM) in a similar way as HepG2 cells as far as DNA and protein content and ALDH activity are concerned. It is concluded, that HepG2 hepatoma cells behave similar to the normal hepatocytes in terms of ALDH regulation and can be used for studies on the activity of ALDH as modified by added xenobiotics.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/3034438-
heal.identifier.secondaryhttp://ac.els-cdn.com/0009279787900809/1-s2.0-0009279787900809-main.pdf?_tid=07c08820d149dedbe83eb024503b4f73&acdnat=1332744462_5e92b111800269d1eaa55671f7beabbd-
heal.journalNameChem Biol Interacten
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate1987-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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