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SHR Neuro Cancer Cardio Lipid Metab Microb

Fuchs, CD; Paumgartner, G; Wahlström, A; Schwabl, P; Reiberger, T; Leditznig, N; Stojakovic, T; Rohr-Udilova, N; Chiba, P; Marschall, HU; Trauner, M.
Metabolic preconditioning protects BSEP/ABCB11^-/- mice against cholestatic liver injury.
J Hepatol. 2017; 66(1):95-101 Doi: 10.1016/j.jhep.2016.08.017 [OPEN ACCESS]
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Leading authors Med Uni Graz: Trauner Michael
Co-authors Med Uni Graz: Stojakovic Tatjana
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Abstract:: Cholestasis is characterized by intrahepatic accumulation of potentially cytotoxic bile acids (BAs) subsequently leading to liver injury with disruption of hepatocellular integrity, inflammation, fibrosis and ultimately liver cirrhosis. Bile salt export pump (BSEP/ABCB11) is the main canalicular BA transporter and therefore the rate limiting step for hepatobiliary BA excretion. In this study we aimed to investigate the role of BSEP/ABCB11 in the development of acquired cholestatic liver and bile duct injury. Wild-type (WT) and BSEP knockout (BSEP^-/-) mice were subjected to common bile duct ligation (CBDL) or 3.5-diethoxycarbonyl-1.4-dihydrocollidine (DDC) feeding as models for cholestasis with biliary obstruction and bile duct injury. mRNA expression profile, serum biochemistry, liver histology, immunohistochemistry, hepatic hydroxyproline levels and BA composition as well as biliary pressure were assessed. BSEP^-/- mice were protected against acquired cholestatic liver injury induced by 7days of CBDL or 4weeks of DDC feeding, as reflected by unchanged serum levels of liver transaminases, alkaline phosphatase and BAs. Notably, BSEP^-/- mice were also protected from cholestasis-induced hepatic inflammation and biliary fibrosis. In line with induced BA detoxification/hydroxylation pathways in BSEP^-/- mice, polyhydroxylated BAs were increased 4-fold after CBDL and 6-fold after DDC feeding in comparison with cholestatic WT mice. Finally, following CBDL, biliary pressure in WT mice increased up to 47mmH₂O but remained below 11mmH₂O in BSEP^-/- mice. Metabolic preconditioning with subsequent changes in BA metabolism favors detoxification of potentially toxic BAs and thereby protects BSEP^-/- mice from cholestatic liver and bile duct injury. Reduced hepatobiliary bile acid transport due to loss of BSEP function leads to increased hydroxylation of bile acids in the liver. Metabolic preconditioning with a hydrophilic bile pool protects the BSEP^-/- mice from acquired cholestatic liver disease. Copyright Â© 2016 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
Find related publications in this database (using NLM MeSH Indexing): ATP Binding Cassette Transporter, Subfamily B, Member 11 - metabolism; Animals -; Bile Acids and Salts - metabolism; Bile Canaliculi -; Bile Ducts - physiopathology; Bile Ducts - surgery; Cholestasis, Intrahepatic - metabolism; Cholestasis, Intrahepatic - prevention & control; Hepatocytes - metabolism; Ligation - methods; Mice -; Therapeutic Occlusion - methods
Find related publications in this database (Keywords): Bile salt export pump; Polyhydroxylated bile acids; Intrahepatic cholestasis