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评估金纳米粒子对成年雄性白化大鼠结构和功能的潜在小脑毒性。

Assessment of the potential cerebellar toxicity of gold nanoparticles on the structure and function of adult male albino rats.

机构信息

Department of Medical Physiology, Faculty of Medicine in Rabigh, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

Department of Medical Physiology, Faculty of Medicine, Suez Canal University, Ismailia 41522, Egypt.

出版信息

Biosci Rep. 2023 Aug 31;43(8). doi: 10.1042/BSR20222255.

Abstract

BACKGROUND

The regular use of gold nanoparticles (Au-NPs) may increase the likelihood of human exposure to these nanoparticles (NPs) and raises concerns about toxicity.

AIM

This study investigated the short-term impact of exposure to Au-NPs on inducing cerebellar pathology in rats, and whether the dose or duration of exposure was more important.

METHODOLOGY

The study used two concentrations of Au-NPs (25 and 50 particles per million) and 18 rats were randomly assigned to three groups. Assessments of the animals were done via behavioral, gene expression, histological, and immunohistochemistry analyses.

RESULTS

Both concentrations of Au-NPs caused cerebellar pathology, as assessed through the investigation test battery. The Au-NPs50 group displayed more injury and decreased mobility compared with the control and the Au-NPs25 group. The Au-NPs25 group showed an increase in supported rearing and significant up-regulation of the Rgc32 gene compared with the control. The Trkb gene was insignificantly up-regulated in both Au-NPs groups compared with the control.

CONCLUSION

The study indicates that exposure to Au-NPs can cause cerebellar pathology in rats and that the toxicity is more dependent on dose than the duration of exposure. These findings have significant implications for the safe use of Au-NPs in various applications.

摘要

背景

金纳米粒子(Au-NPs)的常规使用可能会增加人类接触这些纳米粒子(NPs)的可能性,并引发对其毒性的担忧。

目的

本研究旨在探讨暴露于 Au-NPs 对大鼠小脑病理的短期影响,以及暴露剂量或时间的长短更为重要。

方法

本研究使用了两种浓度的 Au-NPs(25 个和 50 个/百万个),将 18 只大鼠随机分为三组。通过行为、基因表达、组织学和免疫组织化学分析对动物进行评估。

结果

两种浓度的 Au-NPs 均导致小脑病理,通过调查测试电池进行评估。与对照组和 Au-NPs25 组相比,Au-NPs50 组表现出更多的损伤和运动能力下降。与对照组相比,Au-NPs25 组的支持性饲养增加,Rgc32 基因显著上调。与对照组相比,两个 Au-NPs 组的 Trkb 基因均无显著上调。

结论

本研究表明,暴露于 Au-NPs 可导致大鼠小脑病理,其毒性更依赖于剂量而非暴露时间。这些发现对 Au-NPs 在各种应用中的安全使用具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44d8/10472208/21dd19e60e83/bsr-43-bsr20222255-g1.jpg

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