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

被引:57
作者
Mallat, Ariane
Teixeira-Clerc, Fatima
Deveaux, Vanessa
Lotersztajn, Sophie [1 ]
机构
[1] Univ Paris 12, INSERM, Unite 841, Inst Mondor Rech Biomed, F-94000 Creteil, France
[2] Grp Hosp Henri Mondor Albert Chenevier, AP HP, Serv Hepatol & Gastroenterol, F-94000 Creteil, France
关键词
cannabinoid receptor; CB1; CB2; cirrhosis; endocannabinoid; liver fibrosis; portal hypertension; steatosis;
D O I
10.1517/14728222.11.3.403
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
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.
引用
收藏
页码:403 / 409
页数:7
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