首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Particle Size and Biological Fate of ZnO Do Not Cause Acute Toxicity but Affect Toxicokinetics and Gene Expression Profiles in the Rat Livers after Oral Administration
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Particle Size and Biological Fate of ZnO Do Not Cause Acute Toxicity but Affect Toxicokinetics and Gene Expression Profiles in the Rat Livers after Oral Administration

机译:ZnO的粒度和生物命运不会引起急性毒性但在口服给药后大鼠肝脏的毒性动力学和基因表达谱

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摘要

Zinc oxide (ZnO) particles have been used as dietary supplements because zinc is an essential trace element for humans. Along with the rapid development of nanotechnology, the use of ZnO nanoparticles (NPs) is increasing in the food industry, but their oral toxicity potential still remains to be answered. In this study, the effects of particle size and biological fate of ZnO on acute toxicity, toxicokinetics, and gene expression profiles in the livers were investigated after oral administration of ZnO NPs (N-ZnO), bulk-sized ZnO (B-ZnO) or Zn ions in rats. The plasma concentration-time profiles after a single-dose oral administration of ZnOs differed depending on particle/ionic forms and particle size, showing high absorption of Zn ions, followed by N-ZnO and B-ZnO, although in vivo solubility did not differ from particle size. No significant acute toxicity was found after oral administration of ZnOs for 14 days in rats. However, transcriptomic responses in the livers were differently affected, showing that metabolic process and metal biding were up-regulated by Zn ions and N-ZnO, respectively, which were not pronounced in the liver treated with B-ZnO. These findings will be useful to predict the potential oral toxicity of ZnO NPs and further mechanistic and long-term exposure studies are required to assume their safety.
机译:氧化锌(ZnO)颗粒已被用作膳食补充剂,因为锌是人类的必需痕量元素。随着纳米技术的快速发展,在食品工业中使用ZnO纳米粒子(NPS)的使用,但它们的口腔毒性潜力仍有待解答。在本研究中,在口服ZnO NPS(N- ZnO),散装ZnO(B-ZnO)中,研究了ZnO粒度和生物命运对肝脏中急性毒性,毒物学和基因表达谱的影响,散装ZnO(B-ZnO)或大鼠的Zn离子。单剂量口服施用后的血浆浓度 - 时间曲线根据颗粒/离子形式和粒度不同,显示出高吸收Zn离子,其次是N- ZnO和B- ZnO,但体内溶解度没有不同从粒径。在大鼠口服ZnOS 14天后发现了在大鼠口服14天后没有显着的急性毒性。然而,肝脏中的转录组反应受到不同的影响,表明代谢过程和金属凸片分别由Zn离子和N-ZnO上调,其在用B-ZnO处理的肝脏中并不明显。这些发现将有助于预测ZnO NP的潜在口腔毒性,并且需要进一步的机械和长期暴露研究来承担其安全性。

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