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dc.contributor.author이경은*
dc.date.accessioned2018-06-02T08:14:58Z-
dc.date.available2018-06-02T08:14:58Z-
dc.date.issued1999*
dc.identifier.issn1226-4512*
dc.identifier.otherOAK-17143*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/244341-
dc.description.abstractIntracellular accumulation of bile acids in the hepatocytes during cholestasis is thought to be pathogenic in cholestatic liver injury. Due to the detergent-like effect of the hydrophobic bile acids, hepatocellular injury has been attributed to direct membrane damage. However histological findings of cholestatic liver diseases suggest apoptosis can be a mechanism of cell death during cholestatic liver diseases instead of necrosis. To determine the pattern of hepatocellular toxicity induced by bile acid, we incubated primary cultured rat hepatocytes with a hydrophobic bile acid, Glycochenodeoxycholate (GCDC), up to 5 hours. After 5 hours incubation with 400 μM GCDC, lactate dehydrogenase released significantly. Cell viability, quantitated in propidium iodide stained cells concomitant with fluoresceindiacetate was decreased time- and dose-dependently. Most nuclei with condensed chromatin and shrunk cytoplasm were heavily labelled time- and dose-dependently by a positive TUNEL reaction. These findings suggest that both apoptosis and necrosis are involved in hepatocytes injury caused by GCDC.*
dc.languageEnglish*
dc.titleGlycochenodeoxycholic acid induces cell death in primary cultured rat hepatocyte: Apoptosis and necrosis*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume3*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage565*
dc.relation.lastpage570*
dc.relation.journaltitleKorean Journal of Physiology and Pharmacology*
dc.identifier.scopusid2-s2.0-0033368047*
dc.author.googleSang Hui Chu*
dc.author.googleWol Mi Park*
dc.author.googleKyung Eun Lee*
dc.author.googleYoung Sook Pae*
dc.contributor.scopusid이경은(7409769243)*
dc.date.modifydate20231116115921*
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의과대학 > 의학과 > Journal papers
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