细胞色素 P450 1A1(CYP1A1)可预防含苯并[a]芘的西方饮食引起的小鼠非酒精性脂肪性肝病。
Cytochrome P450 1A1 (CYP1A1) protects against nonalcoholic fatty liver disease caused by Western diet containing benzo[a]pyrene in mice.
机构信息
Division of Biochemistry, Department of Biomedical Sciences, Nihon University School of Medicine, 30-1 Oyaguchi-kamicho, Itabashi-ku, Tokyo 173-8610, Japan.
Department of Environmental Health, Center for Environmental Genetics, University of Cincinnati Medical Center, P.O. Box 670056, Cincinnati, OH 45267, USA.
出版信息
Food Chem Toxicol. 2018 Mar;113:73-82. doi: 10.1016/j.fct.2018.01.029. Epub 2018 Jan 31.
The Western diet contributes to nonalcoholic fatty liver disease (NAFLD) pathogenesis. Benzo[a]pyrene (BaP), a prototypical environmental pollutant produced by combustion processes, is present in charcoal-grilled meat. Cytochrome P450 1A1 (CYP1A1) metabolizes BaP, resulting in either detoxication or metabolic activation in a context-dependent manner. To elucidate a role of CYP1A1-BaP in NAFLD pathogenesis, we compared the effects of a Western diet, with or without oral BaP treatment, on the development of NAFLD in Cyp1a1(-/-) mice versus wild-type mice. A Western diet plus BaP induced lipid-droplet accumulation in liver of Cyp1a1(-/-) mice, but not wild-type mice. The hepatic steatosis observed in Cyp1a1(-/-) mice was associated with increased cholesterol, triglyceride and bile acid levels. Cyp1a1(-/-) mice fed Western diet plus BaP had changes in expression of genes involved in bile acid and lipid metabolism, and showed no increase in Cyp1a2 expression but did exhibit enhanced Cyp1b1 mRNA expression, as well as hepatic inflammation. Enhanced BaP metabolic activation, oxidative stress and inflammation may exacerbate metabolic dysfunction in liver of Cyp1a1(-/-) mice. Thus, Western diet plus BaP induces NAFLD and hepatic inflammation in Cyp1a1(-/-) mice in comparison to wild-type mice, indicating a protective role of CYP1A1 against NAFLD pathogenesis.
西方饮食促进非酒精性脂肪性肝病(NAFLD)的发病机制。苯并[a]芘(BaP),一种由燃烧过程产生的典型环境污染物,存在于木炭烤肉类中。细胞色素 P450 1A1(CYP1A1)代谢 BaP,导致解毒或代谢激活的方式依赖于上下文。为了阐明 CYP1A1-BaP 在 NAFLD 发病机制中的作用,我们比较了西方饮食,加或不加口服 BaP 处理,对 Cyp1a1(-/-)小鼠与野生型小鼠 NAFLD 发展的影响。西方饮食加 BaP 诱导 Cyp1a1(-/-)小鼠肝脏中脂滴积累,但野生型小鼠没有。在 Cyp1a1(-/-)小鼠中观察到的肝脂肪变性与胆固醇、甘油三酯和胆汁酸水平升高有关。用西方饮食加 BaP 喂养的 Cyp1a1(-/-)小鼠参与胆汁酸和脂质代谢的基因表达发生变化,Cyp1a2 表达没有增加,但 Cyp1b1 mRNA 表达增强,同时伴有肝炎症。增强的 BaP 代谢激活、氧化应激和炎症可能会加剧 Cyp1a1(-/-)小鼠肝脏的代谢功能障碍。因此,与野生型小鼠相比,西方饮食加 BaP 诱导 Cyp1a1(-/-)小鼠发生 NAFLD 和肝炎症,表明 CYP1A1 对 NAFLD 发病机制具有保护作用。