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首页> 外文期刊>Human and Experimental Toxicology >Dynamics of oxidativeitrosative stress in mice with methionine-choline- deficient diet-induced nonalcoholic fatty liver disease
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Dynamics of oxidativeitrosative stress in mice with methionine-choline- deficient diet-induced nonalcoholic fatty liver disease

机译:蛋氨酸-胆碱缺乏饮食引起的非酒精性脂肪肝小鼠的氧化/亚硝基应激动力学

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Insulin resistance, oxidative stress, and proinflammatory cytokines play a key role in pathogenesis of nonalcoholic fatty liver disease (NAFLD). The aim of our study was to investigate the dynamics of oxidativeitrosative stress in methionine-choline-deficient (MCD) diet -induced NAFLD in mice. Male C57BL/6 mice were divided into following groups: group 1: control group on standard diet; group 2: MCD diet for 2, 4, and 6 weeks (MCD2, MCD4, and MCD6, respectively). After treatment, liver and blood samples were taken for histopathology, alanine- and aspartate aminotransferase, acute phase reactants, and oxidativeitrosative stress parameters. Liver malondialdehyde level was higher in all MCD-fed groups versus control group (p < 0.01), while nitrites + nitrates level showed a progressive increase. The activity of total superoxide dismutase and its isoenzymes was significantly lower in all MCD-fed groups (p < 0.01). Although catalase activity was significantly lower in MCD-fed animals at all intervals (p < 0.01), the lowest activity of this enzyme was evident in MCD4 group. Liver content of glutathione was lower in MCD4 (p < 0.05) and MCD6 group (p < 0.01) versus control.Ferritin and C-reactive protein serum concentration were significantly higher only in MCD6 group. Our study suggests that MCD diet induces a progressive rise in nitrosative stress in the liver. Additionally, the most prominent decrease in liver antioxidative capacity is in the fourth week, which implies that application of antioxidants would be most suitable in this period, in order to prevent nonalcoholic steatohepatitis but not the initial NAFLD phase.
机译:胰岛素抵抗,氧化应激和促炎细胞因子在非酒精性脂肪肝疾病(NAFLD)的发病机理中起着关键作用。我们研究的目的是研究小鼠蛋氨酸-胆碱缺乏(MCD)饮食诱导的NAFLD中氧化/亚硝化应激的动力学。将雄性C57BL / 6小鼠分为以下几组:第1组:标准饮食的对照组;第2组。第2组:2、4和6周的MCD饮食(分别为MCD2,MCD4和MCD6)。治疗后,采集肝脏和血液样品的组织病理学,丙氨酸和天冬氨酸转氨酶,急性期反应物以及氧化/亚硝化应激参数。在所有由MCD喂养的组中,肝脏丙二醛水平均高于对照组(p <0.01),而亚硝酸盐+硝酸盐水平则逐渐升高。在所有由MCD喂养的组中,总超氧化物歧化酶及其同工酶的活性均显着降低(p <0.01)。尽管过氧化氢酶活性在所有间隔的MCD喂养动物中均显着降低(p <0.01),但该酶的最低活性在MCD4组中明显。 MCD4组(p <0.05)和MCD6组(p <0.01)的谷胱甘肽肝含量较对照组低。仅MCD6组的铁蛋白和C反应蛋白血清浓度显着升高。我们的研究表明,MCD饮食会引起肝脏中亚硝化应激的逐步升高。此外,肝脏抗氧化能力最显着的下降是在第四周,这意味着在此期间应最适合使用抗氧化剂,以预防非酒精性脂肪性肝炎,但不能预防最初的NAFLD阶段。

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