Cannabinoid receptor type I modulates alcohol-induced liver fibrosis

The cannabinoid system (CS) is implicated in the regulation of hepatic fibrosis, steatosis and inflammation, with cannabinoid receptors 1 and 2 (CB1 and CB2) being involved in regulation of pro- and antifibrogenic effects. Daily cannabis smoking is an independent risk factor for the progression of f...

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Hauptverfasser: Patsenker, Eleonora (VerfasserIn) , Stoll, Matthias (VerfasserIn) , Millonig, Gunda (VerfasserIn) , Agaimy, Abbas (VerfasserIn) , Wissniowski, Till (VerfasserIn) , Schneider, Vreni (VerfasserIn) , Mueller, Sebastian (VerfasserIn) , Brenneisen, Rudolf (VerfasserIn) , Seitz, Helmut K. (VerfasserIn) , Ocker, Matthias (VerfasserIn) , Stickel, Felix (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 19 August 2011
In: Molecular medicine
Year: 2011, Jahrgang: 17, Heft: 11/12, Pages: 1285-1294
ISSN:1528-3658
DOI:10.2119/molmed.2011.00149
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.2119/molmed.2011.00149
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Verfasserangaben:Eleonora Patsenker, Matthias Stoll, Gunda Millonig, Abbas Agaimy, Till Wissniowski, Vreni Schneider, Sebastian Mueller, Rudolf Brenneisen, Helmut K. Seitz, Matthias Ocker, and Felix Stickel

MARC

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245 1 0 |a Cannabinoid receptor type I modulates alcohol-induced liver fibrosis  |c Eleonora Patsenker, Matthias Stoll, Gunda Millonig, Abbas Agaimy, Till Wissniowski, Vreni Schneider, Sebastian Mueller, Rudolf Brenneisen, Helmut K. Seitz, Matthias Ocker, and Felix Stickel 
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520 |a The cannabinoid system (CS) is implicated in the regulation of hepatic fibrosis, steatosis and inflammation, with cannabinoid receptors 1 and 2 (CB1 and CB2) being involved in regulation of pro- and antifibrogenic effects. Daily cannabis smoking is an independent risk factor for the progression of fibrosis in chronic hepatitis C and a mediator of experimental alcoholic steatosis. However, the role and function of CS in alcoholic liver fibrosis (ALF) is unknown so far. Thus, human liver samples from patients with alcoholic liver disease (ALD) were collected for analysis of CB1 expression. In vitro, hepatic stellate cells (HSC) underwent treatment with acetaldehyde, Δ9-tetrahydrocannabinol H₂O₂, endo- and exocannabinoids (2-arachidonoylglycerol (2-AG) and [THC]), and CB1 antagonist SR141716 (rimonabant). In vivo, CB1 knockout (KO) mice received thioacetamide (TAA)/ethanol (EtOH) to induce fibrosis. As a result, in human ALD, CB1 expression was restricted to areas with advanced fibrosis only. In vitro, acetaldehyde, H₂O₂, as well as 2-AG and THC, alone or in combination with acetaldehyde, induced CB1 mRNA expression, whereas CB1 blockage with SR141716 dose-dependently inhibited HSC proliferation and downregulated mRNA expression of fibrosis-mediated genes PCα1(I), TIMP-1 and MMP-13. This was paralleled by marked cytotoxicity of SR141716 at high doses (5-10 μmol/L). In vivo, CB1 knockout mice showed marked resistance to alcoholic liver fibrosis. In conclusion, CB1 expression is upregulated in human ALF, which is at least in part triggered by acetaldehyde (AA) and oxidative stress. Inhibition of CB1 by SR141716, or via genetic knock-out protects against alcoholic-induced fibrosis in vitro and in vivo. 
650 4 |a Acetaldehyde 
650 4 |a Animals 
650 4 |a Apoptosis 
650 4 |a Cannabinoids 
650 4 |a Cell Hypoxia 
650 4 |a Cell Proliferation 
650 4 |a Collagen 
650 4 |a Female 
650 4 |a Hepatic Stellate Cells 
650 4 |a Humans 
650 4 |a Hydrogen Peroxide 
650 4 |a Inflammation 
650 4 |a Liver 
650 4 |a Liver Cirrhosis, Alcoholic 
650 4 |a Male 
650 4 |a Matrix Metalloproteinases 
650 4 |a Mice 
650 4 |a Middle Aged 
650 4 |a Piperidines 
650 4 |a Pyrazoles 
650 4 |a Receptor, Cannabinoid, CB1 
650 4 |a Receptor, Cannabinoid, CB2 
650 4 |a Rimonabant 
650 4 |a RNA, Messenger 
650 4 |a Up-Regulation 
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700 1 |a Stickel, Felix  |e VerfasserIn  |4 aut 
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