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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Woolbright, BL; Li, F; Xie, Y; Farhood, A; Fickert, P; Trauner, M; Jaeschke, H.
Lithocholic acid feeding results in direct hepato-toxicity independent of neutrophil function in mice.
Toxicol Lett. 2014; 228(1):56-66 Doi: 10.1016/j.toxlet.2014.04.001 [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Fickert Peter
Trauner Michael
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Abstract:
Lithocholic acid (LCA) supplementation in the diet results in intrahepatic cholestasis and bile infarcts. Previously we showed that an innate immune response is critical for cholestatic liver injury in the bile duct ligated mice. Thus, the purpose of this study was to investigate the role of neutrophils in the mechanism of liver injury caused by feeding mice a diet containing LCA. C57BL/6 mice were given control or 1% LCA containing diet for 24-96 h and then examined for parameters of hepatotoxicity. Plasma ALT levels were significantly increased by 48 h after LCA feeding, which correlated with both neutrophil recruitment to the liver and upregulation of numerous pro-inflammatory genes. The injury was confirmed by histology. Deficiency in intercellular adhesion molecule-1 (ICAM-1) expression or inhibition of neutrophil function failed to protect against the injury. Bile acid levels were quantified in plasma and bile of LCA-fed mice after 48 and 96 h. Only the observed biliary levels of taurochenodeoxycholic acid and potentially tauro-LCA caused direct cytotoxicity in mouse hepatocytes. These data support the conclusion that neutrophil recruitment occurs after the onset of bile acid-induced necrosis in LCA-fed animals, and is not a primary mechanism of cell death when cholestasis occurs through accumulation of hydrophobic bile acids. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Bile - metabolism
Bile Acids and Salts - metabolism
Blotting, Western -
Caspases - metabolism
Cholestasis - chemically induced Cholestasis - pathology
Diet -
Drug-Induced Liver Injury - metabolism Drug-Induced Liver Injury - pathology
Hepatocytes - drug effects Hepatocytes - metabolism
Immunohistochemistry -
Inflammation - genetics
Lithocholic Acid - metabolism Lithocholic Acid - toxicity
Membrane Glycoproteins - genetics
Mice -
Mice, Inbred C57BL -
Mice, Knockout -
NADPH Oxidase - genetics
Necrosis -
Neutrophils - drug effects
Real-Time Polymerase Chain Reaction -
Receptors, Immunologic - genetics
Up-Regulation - drug effects

Find related publications in this database (Keywords)
Bile acid hepatotoxicity
Lithocholic acid
Cholestasis
Innate immunity
Neutrophils
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