Pandey Rupal, Hegde Venkatesh L, Singh Narendra P, Hofseth Lorne, Singh Uday, Ray Swapan, Nagarkatti Mitzi, Nagarkatti Prakash S
Department of Pathology, University of South Carolina School of Medicine, Columbia, South Carolina, USA.
Vitam Horm. 2009;81:487-504. doi: 10.1016/S0083-6729(09)81019-4.
Autoimmune hepatitis is a severe immune mediated chronic liver disease with a prevalence range between 50 and 200 cases per million in Western Europe and North America and mortality rates of up to 80% in untreated patients. The induction of CB1 and CB2 cannabinoid receptors during liver injury and the potential involvement of endocannabinoids in the regulation of this process have sparked significant interest in further evaluating the role of cannabinoid systems during hepatic disease. Cannabinoids have been shown to possess significant immunosuppressive and anti-inflammatory properties. Cannabinoid abuse has been shown to exacerbate liver fibrogenesis in patients with chronic hepatitis C infection involving CB1 receptor. Nonetheless, CB2 receptor activation may play a protective role during chronic liver diseases. Thus, differential targeting of cannabinoid receptors may provide novel therapeutic modality against autoimmune hepatitis. In this review, we summarize current knowledge on the role of endocannabinoids and exocannabinoids in the regulation of autoimmune hepatitis.
自身免疫性肝炎是一种严重的免疫介导的慢性肝病,在西欧和北美,其患病率为每百万人口中有50至200例,未经治疗的患者死亡率高达80%。肝脏损伤期间CB1和CB2大麻素受体的诱导以及内源性大麻素在这一过程调节中的潜在作用,引发了人们对进一步评估大麻素系统在肝病中的作用的浓厚兴趣。大麻素已被证明具有显著的免疫抑制和抗炎特性。在涉及CB1受体的慢性丙型肝炎感染患者中,滥用大麻素会加剧肝脏纤维化。然而,CB2受体激活在慢性肝病中可能发挥保护作用。因此,对大麻素受体的差异化靶向可能为自身免疫性肝炎提供新的治疗方式。在本综述中,我们总结了目前关于内源性大麻素和外源性大麻素在自身免疫性肝炎调节中作用的知识。