Division of Liver Diseases, Department of Medicine, Mount Sinai School of Medicine, New York, NY 10029, USA.
J Hepatol. 2013 Feb;58(2):395-8. doi: 10.1016/j.jhep.2012.08.018. Epub 2012 Aug 28.
Alcoholic (ALD) and non-alcoholic fatty liver diseases (NAFLD) are clinical conditions leading to hepatocellular injury and inflammation resulting from alcohol consumption, high fat diet, obesity and diabetes, among others. Oxidant stress is a major contributing factor to the pathogenesis of ALD and NAFLD. Multiple studies have shown that generation of reactive oxygen species (ROS) is key for the progression of fatty liver to steatohepatitis. Cytochrome P450 2E1 (CYP2E1) plays a critical role in ROS generation and CYP2E1 is also induced by alcohol itself. This review summarizes the role of CYP2E1 in ALD and NAFLD.
酒精性(ALD)和非酒精性脂肪性肝病(NAFLD)是临床病症,可导致肝细胞损伤和炎症,其病因包括饮酒、高脂饮食、肥胖和糖尿病等。氧化应激是 ALD 和 NAFLD 发病机制的主要因素之一。多项研究表明,活性氧(ROS)的产生是导致脂肪肝向脂肪性肝炎进展的关键。细胞色素 P450 2E1(CYP2E1)在 ROS 的产生中起着关键作用,而 CYP2E1 本身也可被酒精诱导。本文综述了 CYP2E1 在 ALD 和 NAFLD 中的作用。