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联合铈和氧化锌纳米粒子通过氧化应激介导的炎症诱导大鼠肝肾功能损伤。

Combined cerium and zinc oxide nanoparticles induced hepato-renal damage in rats through oxidative stress mediated inflammation.

机构信息

Department of Biochemistry, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan, Ibadan, Nigeria.

Department of Biochemistry, University of Ibadan, Ibadan, Nigeria.

出版信息

Sci Rep. 2023 May 25;13(1):8513. doi: 10.1038/s41598-023-35453-5.

Abstract

The toxicity profiles of nanoparticles (NPs) used in appliances nowadays remains unknown. In this study, we investigated the toxicological consequences of exposure to cerium oxide (CeO) and zinc oxide (ZnO) nanoparticles given singly or in combination on the integrity of liver and kidney of male Wistar rats. Twenty (20) rats were allotted into four groups and treated as: Control (normal saline), CeONPs (50 μg/kg), ZnONPs (80 μg/kg) and [CeONPs (50 μg/kg) + ZnONPs (80 μg/kg)]. The nanoparticles were given to the animals through the intraperitoneal route, three times per week for four repeated weeks. Results revealed that CeO and ZnO NPs (singly) increased serum AST and ALT by 29% & 57%; 41% & 18%, and co-administration by 53% and 23%, respectively. CeO and ZnO NPs increased hepatic and renal malondialdehyde (MDA) by 33% and 30%; 38% and 67%, respectively, while co-administration increased hepatic and renal MDA by 43% and 40%, respectively. The combined NPs increased hepatic NO by 28%. Also, CeO and ZnO NPs, and combined increased BAX, interleukin-1β and TNF-α by 45, 38, 52%; 47, 23, 82% and 41, 83, 70%, respectively. Histology revealed hepatic necrosis and renal haemorrhagic parenchymal in NPs-treated rats. Summarily, CeO and ZnO NPs produced oxidative injury and induced inflammatory process in the liver and kidney of experimental animals.

摘要

目前,用于电器的纳米颗粒(NPs)的毒性特征尚不清楚。在这项研究中,我们研究了单独或联合暴露于氧化铈(CeO)和氧化锌(ZnO)纳米颗粒对雄性 Wistar 大鼠肝肾功能完整性的毒理学后果。将 20 只大鼠分配到四组并进行如下处理:对照组(生理盐水)、CeONPs(50μg/kg)、ZnONPs(80μg/kg)和[CeONPs(50μg/kg)+ZnONPs(80μg/kg)]。通过腹腔途径每周三次给予纳米颗粒,重复四次。结果表明,CeO 和 ZnO NPs(单独)分别使血清 AST 和 ALT 增加了 29%和 57%;41%和 18%,联合给药则分别增加了 53%和 23%。CeO 和 ZnO NPs 分别使肝和肾丙二醛(MDA)增加了 33%和 30%;38%和 67%,联合给药则分别使肝和肾 MDA 增加了 43%和 40%。联合 NPs 增加了肝脏中 NO 的含量 28%。此外,CeO 和 ZnO NPs 以及联合 NPs 使 BAX、白细胞介素-1β 和 TNF-α 分别增加了 45、38、52%;47、23、82%和 41、83、70%。组织学显示 NPs 处理的大鼠存在肝坏死和肾出血性实质。综上所述,CeO 和 ZnO NPs 导致实验动物的肝和肾产生氧化损伤并诱导炎症过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04f9/10212995/1a6ca9ffa179/41598_2023_35453_Fig1_HTML.jpg

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