Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/11642
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dc.contributor.authorRolo, Anabela P.-
dc.contributor.authorPalmeira, Carlos M.-
dc.contributor.authorHoly, Jon M.-
dc.contributor.authorWallace, Kendall B.-
dc.date.accessioned2009-10-09T12:53:37Z-
dc.date.available2009-10-09T12:53:37Z-
dc.date.issued2004-05-
dc.identifier.citationToxicological Sciences. 79:1 (2004) 196-204en_US
dc.identifier.issn1096-6080-
dc.identifier.urihttp://hdl.handle.net/10316/11642-
dc.description.abstractThe goal of this investigation was to determine whether chenodeoxycholic acid (CDCA)-induced apoptosis is prevented by ursodeoxycholic acid (UDCA) or tauroursodeoxycholic acid (TUDC) and to characterize the involvement of mitochondria in the process. Cultured human HepG2 cells were treated in a dose- and time-dependent protocol in order to establish a sufficiently low exposure to CDCA that causes apoptosis but not necrosis. Low-dose CDCA induced an S-phase block and G2 arrest of the cell cycle, as determined by flow cytometry. As a result, cell proliferation was inhibited. CDCA-induced apoptosis, as determined by fluorescence microscopy of Hoechst 33342-stained nuclei, was evident upon coincubation with TUDC. Additionally, after exposure to UDCA plus CDCA, the cell membrane was permeable to fluorescent dyes. Caspase-9-like activity, poly(ADP-ribose) polymerase (PARP) cleavage, and extensive DNA fragmentation were detected in CDCA-exposed cells and in cells coincubated with TUDC, but not UDCA. CDCA caused a decrease in mitochondrial membrane potential and depletion of ATP, both of which were potentiated by UDCA but not TUDC. The results suggest that UDCA potentiates CDCA cytotoxicity, probably at the level of induction of the mitochondrial permeability transition (MPT). Consequently, as suggested by the lack of the main hallmarks of the apoptotic pathway, in the presence of UDCA, CDCA-induced apoptosis is not properly executed but degenerates into necrosis.en_US
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.rightsopenAccessen_US
dc.subjectChenodeoxycholic acid;en_US
dc.subjectUrsodeoxycholic aciden_US
dc.subjectCombinationen_US
dc.subjectApoptosisen_US
dc.subjectNecrosisen_US
dc.subjectMitochondriaen_US
dc.titleRole of mitochondrial dysfunction in combined bile acid-induced cytotoxicity: the switch between apoptosis and necrosisen_US
dc.typearticleen_US
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
Appears in Collections:FCTUC Ciências da Vida - Artigos em Revistas Internacionais
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