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首页> 外文期刊>Toxicology Research >A metabolomic-based study on disturbance of bile acids metabolism induced by intratracheal instillation of nickel oxide nanoparticles in rats
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A metabolomic-based study on disturbance of bile acids metabolism induced by intratracheal instillation of nickel oxide nanoparticles in rats

机译:基于代谢物的脂肪酸性代谢紊乱研究大鼠镍氧化镍纳米粒子瘤瘤诱导的紊乱

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摘要

Nickel oxide nanoparticles (Nano NiO) evoke hepatotoxicity, while whether it affects the hepatic metabolism remains unclear. The aim of this study was to explore the differential metabolites and their metabolic pathways in rat serum and to further verify the potential mechanism of bile acids' (BAs) metabolism dysregulation after Nano NiO exposure. Sixteen male Wistar rats were intratracheally instilled with Nano NiO (0.24 mg/kg body weight) twice a week for 9 weeks. Liquid chromatography/mass spectrometry was applied to filter the differentially expressed metabolites in rat serum. Western blot was employed to detect the protein contents. TWenty-one differential metabolites that associated with BAs, lipid and phospholipid metabolism pathways were identified in rat serum after Nano NiO exposure. Decreased cholic acid and deoxycholic acid implied that the BAs metabolism was disturbed. The nickel content increased in liver after Nano NiO exposure. The protein expression of cholesterol 7 alpha-hydroxylase (CYP7A1) was down-regulated, and the bile salt export pump was up-regulated after Nano NiO administration in rat liver. Moreover, dehydroepiandrosterone sulphotransferase (SULT2A1) and cytochrome P450 (CYP) 3A4 were elevated in the exposure group. In conclusion, Nano NiO might trigger the disturbances of BAs, lipid and phospholipid metabolism pathways in rats. The diminished serum BAs induced by Nano NiO might be related to the down-regulation of synthetase and to the overexpression of transmembrane protein and detoxification enzymes in BAs metabolism.
机译:氧化镍纳米颗粒(Nano-NiO)引起肝毒性,但其是否影响肝脏代谢尚不清楚。本研究旨在探索大鼠血清中的差异代谢物及其代谢途径,并进一步验证纳米氧化镍暴露后胆汁酸(BAs)代谢失调的潜在机制。16只雄性Wistar大鼠气管内注入纳米NiO(0.24 mg/kg体重),每周两次,共9周。应用液相色谱/质谱法筛选大鼠血清中差异表达的代谢物。采用westernblot检测蛋白质含量。纳米氧化镍暴露后,在大鼠血清中鉴定出21种与BAs、脂质和磷脂代谢途径相关的差异代谢物。胆酸和脱氧胆酸的降低意味着BAs代谢受到干扰。纳米NiO暴露后,肝脏中的镍含量增加。在大鼠肝脏中服用纳米NiO后,胆固醇7α羟化酶(CYP7A1)的蛋白表达下调,胆盐输出泵上调。此外,暴露组的脱氢表雄酮硫转移酶(SULT2A1)和细胞色素P450(CYP)3A4升高。总之,纳米NiO可能会引起大鼠BAs、脂质和磷脂代谢途径的紊乱。纳米NiO诱导的血清BAs减少可能与合成酶的下调以及BAs代谢中跨膜蛋白和解毒酶的过度表达有关。

著录项

  • 来源
    《Toxicology Research》 |2021年第3期|共13页
  • 作者单位

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

    First Peoples Hosp Lanzhou City Lanzhou 730050 Peoples R China;

    Lanzhou Univ Sch Publ Hlth Dept Toxicol 199 Donggang West Rd Lanzhou 730000 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

    nickel oxide nanoparticles; metabolomics; metabolic pathway; bile acids;

    机译:氧化镍纳米颗粒;代谢组学;代谢途径;胆汁酸;

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