Summary
March 2007, Vol. 11, No. 3, Pages 403-409 , DOI 10.1517/14728222.11.3.403

Cannabinoid receptors as new targets of antifibrosing strategies during chronic liver diseases

Ariane Mallat1,2, Fatima Teixeira-Clerc1, Vanessa Deveaux1 & Sophie Lotersztajn1,2
1INSERM, Unité 841, Institut Mondor de Recherche Biomédicale, Université Paris XII – Val de Marne, Créteil, F-94000, France.
2AP-HP, Groupe Hospitalier Henri-Mondor-Albert Chenevier, Service d’Hépatologie et de Gastroentérologie, Créteil, F-94000 France
Author for correspondence



Chronic liver injury exposes the patient to liver fibrosis and its end stage, cirrhosis, is a major public health problem worldwide. In western countries, prevailing causes of cirrhosis include chronic alcohol consumption, hepatitis C virus infection and non-alcoholic steatohepatitis. Current treatment of hepatic fibrosis is limited to withdrawal of the noxious agent. Nevertheless, suppression of the cause of hepatic injury is not always feasible and numerous efforts are directed at the development of liver-specific antifibrotic therapies. Along these lines, the authors recently demonstrated that the endocannabinoid system shows promise as a novel target for antifibrotic therapy during chronic liver injury. Indeed, cannabinoid receptors CB1 and CB2 promote dual pro- and antifibrogenic effects, respectively. Therefore, endocannabinoid-based therapies, combining CB2 agonists and CB1 antagonists may open novel therapeutic perspectives for the treatment of chronic liver diseases.

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S Lotersztajn, F Teixeira-Clerc, B Julien, V Deveaux, Y Ichigotani, S Manin, J Tran-Van-Nhieu, M Karsak, A Zimmer, A Mallat. (2008) CB2 receptors as new therapeutic targets for liver diseases. British Journal of Pharmacology 153:2, 286-289
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Matthias Banasch, Oliver Goetze, Wolfgang E. Schmidt, Juris J. Meier. (2007) Rimonabant as a novel therapeutic option for nonalcoholic steatohepatitis. Liver International 27:8, 1152-1155
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R G Pertwee. (2007) The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: Δ9-tetrahydrocannabinol, cannabidiol and Δ9-tetrahydrocannabivarin. British Journal of Pharmacology
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Authors:
Ariane Mallat
Fatima Teixeira-Clerc
Vanessa Deveaux
Sophie Lotersztajn
Keywords:
cannabinoid receptor
CB1
CB2
cirrhosis
endocannabinoid
liver fibrosis
portal hypertension
steatosis