Rodrigues, Robim M., Kollipara, Laxmikanth, Chaudhari, Umesh ORCID: 0000-0002-7743-4371, Sachinidis, Agapios, Zahedi, Rene P., Sickmann, Albert ORCID: 0000-0002-2388-5265, Kopp-Schneider, Annette, Jiang, Xiaoqi, Keun, Hector, Hengstler, Jan, Oorts, Marlies, Annaert, Pieter, Hoeben, Eef, Gijbels, Eva ORCID: 0000-0002-7366-0769, De Kock, Joery ORCID: 0000-0002-4078-4896, Vanhaecke, Tamara ORCID: 0000-0002-6685-7299, Rogiers, Vera ORCID: 0000-0003-0635-7740 and Vinken, Mathieu ORCID: 0000-0001-5115-8893 (2018). Omics-based responses induced by bosentan in human hepatoma HepaRG cell cultures. Arch. Toxicol., 92 (6). S. 1939 - 1953. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1432-0738

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Abstract

Bosentan is well known to induce cholestatic liver toxicity in humans. The present study was set up to characterize the hepatotoxic effects of this drug at the transcriptomic, proteomic, and metabolomic levels. For this purpose, human hepatoma-derived HepaRG cells were exposed to a number of concentrations of bosentan during different periods of time. Bosentan was found to functionally and transcriptionally suppress the bile salt export pump as well as to alter bile acid levels. Pathway analysis of both transcriptomics and proteomics data identified cholestasis as a major toxicological event. Transcriptomics results further showed several gene changes related to the activation of the nuclear farnesoid X receptor. Induction of oxidative stress and inflammation were also observed. Metabolomics analysis indicated changes in the abundance of specific endogenous metabolites related to mitochondrial impairment. The outcome of this study may assist in the further optimization of adverse outcome pathway constructs that mechanistically describe the processes involved in cholestatic liver injury.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Rodrigues, Robim M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kollipara, LaxmikanthUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Chaudhari, UmeshUNSPECIFIEDorcid.org/0000-0002-7743-4371UNSPECIFIED
Sachinidis, AgapiosUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zahedi, Rene P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Sickmann, AlbertUNSPECIFIEDorcid.org/0000-0002-2388-5265UNSPECIFIED
Kopp-Schneider, AnnetteUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Jiang, XiaoqiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Keun, HectorUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hengstler, JanUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Oorts, MarliesUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Annaert, PieterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hoeben, EefUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gijbels, EvaUNSPECIFIEDorcid.org/0000-0002-7366-0769UNSPECIFIED
De Kock, JoeryUNSPECIFIEDorcid.org/0000-0002-4078-4896UNSPECIFIED
Vanhaecke, TamaraUNSPECIFIEDorcid.org/0000-0002-6685-7299UNSPECIFIED
Rogiers, VeraUNSPECIFIEDorcid.org/0000-0003-0635-7740UNSPECIFIED
Vinken, MathieuUNSPECIFIEDorcid.org/0000-0001-5115-8893UNSPECIFIED
URN: urn:nbn:de:hbz:38-183211
DOI: 10.1007/s00204-018-2214-z
Journal or Publication Title: Arch. Toxicol.
Volume: 92
Number: 6
Page Range: S. 1939 - 1953
Date: 2018
Publisher: SPRINGER HEIDELBERG
Place of Publication: HEIDELBERG
ISSN: 1432-0738
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
SALT EXPORT PUMP; DRUG-INDUCED CHOLESTASIS; FARNESOID-X-RECEPTOR; SAMPLE PREPARATION; LIVER-INJURY; BILE-ACIDS; MECHANISMS; IDENTIFICATION; HEPATOCYTES; INHIBITIONMultiple languages
ToxicologyMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/18321

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