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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Cytochrome P450 1A1 (CYP1A1) protects against nonalcoholic fatty liver disease caused by Western diet containing benzo[a]pyrene in mice
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Cytochrome P450 1A1 (CYP1A1) protects against nonalcoholic fatty liver disease caused by Western diet containing benzo[a]pyrene in mice

机译:细胞色素P450 1A1(CYP1A1)保护由含有小鼠苯并[A]芘的西方饮食引起的非酒精性脂肪肝病

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摘要

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.
机译:西方饮食有助于非酒精性脂肪肝病(NAFLD)发病机制。苯并[a]芘(BAP),由燃烧过程产生的原型环境污染物,存在于木炭烤的肉中。细胞色素P450 1A1(CYP1A1)代谢BAP,导致以上下文依赖的方式解毒或代谢激活。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,或没有口服烘烤治疗的影响,对CYP1A1( - / - )小鼠与野生型小鼠的NAFLD的发育。西方饮食加BAP诱导CYP1A1( - / - )小鼠肝脏的脂质 - 液滴积累,但不是野生型小鼠。在CYP1A1( - / - )小鼠中观察到的肝脏脂肪变性与胆固醇,甘油三酯和胆汁酸水平增加有关。 CYP1A1( - / - )小鼠喂养Western Diet Plus Bap的表达变化胆汁酸和脂质代谢的基因表达,并且表达CYP1A2表达没有增加,但表现出增强的CYP1B1 mRNA表达,以及肝炎症。增强的BAP代谢活化,氧化应激和炎症可加剧CYP1A1( - / - )小鼠的肝脏代谢功能障碍。因此,与野生型小鼠相比,西方饮食加BAP诱导CYP1A1( - / - )小鼠中的NAFLD和肝脏炎症,表明CYP1A1对NAFLD发病机制的保护作用。

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