Journal article

Pharmacologic Antagonization of Cannabinoid Receptor 1 Improves Cholestasis in Abcb4-/- Mice


Authors listHelmrich, Nora; Roderfeld, Martin; Baier, Anne; Windhorst, Anita; Herebian, Diran; Mayatepek, Ertan; Dierkes, Christian; Ocker, Matthias; Glebe, Dieter; Christ, Bruno; Churin, Yuri; Irungbam, Karuna; Roeb, Elke

Publication year2022

Pages1041-1055

JournalCellular and Molecular Gastroenterology and Hepatology

Volume number13

Issue number4

ISSN2352-345X

Open access statusGreen

DOI Linkhttps://doi.org/10.1016/j.jcmgh.2021.12.013

PublisherElsevier


Abstract
BACKGROUND & AIMS: The endocannabinoid system is involved in the modulation of inflammatory, fibrotic, metabolic, and carcinogenesis-associated signaling pathways via cannabinoid receptor (CB)1 and CB2. We hypothesized that the pharmacologic antagonization of CB1 receptor improves cholestasis in Abcb4(-/-& nbsp;)mice.& nbsp;METHODS: After weaning, male Abcb4(-/-& nbsp;)mice were treated orally with rimonabant (a specific antagonist of CB1) or ACEA (an agonist of CB1) until up to 16 weeks of age. Liver tissue and serum were isolated and examined by means of serum analysis, quantitative real time polymerase chain reaction, Western blot, immunohistochemistry, and enzyme function. Untreated Abcb4(-/-& nbsp;)and Bagg Albino Mouse/c wild-type mice served as controls.& nbsp;RESULTS: Cholestasis-induced symptoms such as liver damage, bile duct proliferation, and enhanced circulating bile acids were improved by CB1 antagonization. Rimonabant treatment also improved Phosphoenolpyruvat-Carboxykinase expression and reduced inflammation and the acute-phase response. The carcinogenesis-associated cellular-Jun N-terminal kinase/cellular-JUN and signal transducer and activator of transcription 3 signaling pathways activated in Abcb4(-/-& nbsp;)mice were reduced to wild-type level by CB1 antagonization.& nbsp;CONCLUSIONS: We showed a protective effect of oral CB1 antagonization in chronic cholestasis using the established Abcb4(-/-)model. Our results suggest that pharmacologic antagonization of the CB1 receptor could have a therapeutic benefit in cholestasis-associated metabolic changes, liver damage, inflammation, and carcinogenesis.& nbsp;



Citation Styles

Harvard Citation styleHelmrich, N., Roderfeld, M., Baier, A., Windhorst, A., Herebian, D., Mayatepek, E., et al. (2022) Pharmacologic Antagonization of Cannabinoid Receptor 1 Improves Cholestasis in Abcb4-/- Mice, Cellular and Molecular Gastroenterology and Hepatology, 13(4), pp. 1041-1055. https://doi.org/10.1016/j.jcmgh.2021.12.013

APA Citation styleHelmrich, N., Roderfeld, M., Baier, A., Windhorst, A., Herebian, D., Mayatepek, E., Dierkes, C., Ocker, M., Glebe, D., Christ, B., Churin, Y., Irungbam, K., & Roeb, E. (2022). Pharmacologic Antagonization of Cannabinoid Receptor 1 Improves Cholestasis in Abcb4-/- Mice. Cellular and Molecular Gastroenterology and Hepatology. 13(4), 1041-1055. https://doi.org/10.1016/j.jcmgh.2021.12.013



Keywords


Acute PhaseC-JUNFIBROSISHEPATIC CB1 RECEPTORSLIPID-ACCUMULATIONLIVER FIBROSISRimonabant

Last updated on 2025-10-06 at 11:38