Mallat A, Lotersztajn S
INSERM, U 841, Institut Mondor de recherche Biomédicale Hôpital Henri Mondor 94010 Créteil, France.
Am J Physiol Gastrointest Liver Physiol. 2008 Jan;294(1):G9-G12. doi: 10.1152/ajpgi.00467.2007. Epub 2007 Nov 1.
Cannabinoid receptors (CB1 and CB2) and their endogenous ligands (endocannabinoids) have recently emerged as novel mediators of liver diseases. Endogenous activation of CB1 receptors promotes nonalcoholic fatty liver disease (NAFLD) and progression of liver fibrosis associated with chronic liver injury; in addition, CB1 receptors contribute to the pathogenesis of portal hypertension and cirrhotic cardiomyopathy. CB2 receptor-dependent effects are also increasingly characterized, including antifibrogenic effects and regulation of liver inflammation during ischemia-reperfusion and NAFLD. It is likely that the next few years will allow us to delineate whether molecules targeting CB1 and CB2 receptors are useful therapeutic agents for the treatment of chronic liver diseases.
大麻素受体(CB1和CB2)及其内源性配体(内源性大麻素)最近已成为肝脏疾病的新型介质。CB1受体的内源性激活促进非酒精性脂肪性肝病(NAFLD)以及与慢性肝损伤相关的肝纤维化进展;此外,CB1受体还参与门静脉高压症和肝硬化性心肌病的发病机制。CB2受体依赖性效应也越来越多地得到阐明,包括抗纤维化作用以及在缺血再灌注和NAFLD期间对肝脏炎症的调节。未来几年很可能会让我们明确靶向CB1和CB2受体的分子是否是治疗慢性肝病的有效治疗药物。