Silicon dioxide nanoparticles induce insulin resistance through endoplasmic reticulum stress and generation of reactive oxygen species.
Clicks: 329
ID: 64898
2019
Article Quality & Performance Metrics
Overall Quality
Improving Quality
0.0
/100
Combines engagement data with AI-assessed academic quality
Reader Engagement
Steady Performance
77.7
/100
321 views
262 readers
Trending
AI Quality Assessment
Not analyzed
Abstract
Silicon dioxide nanoparticles (SiO NPs) are one of the most widely utilized NPs in various food sectors. However, the potential endocrine toxicity of SiO NPs has not been characterized.In the present study, mice were orally administered a series of doses of SiO NPs. All doses of SiO NPs were absorbed into the blood, liver, and pancreas of the mice. Administration of 100 mg/kg bw (body weight) of SiO NPs significantly increased blood glucose levels in mice. However, the same dose of SiO fine-particles (FPs) did not result in altered blood glucose. Whole-genome analysis showed that SiO NPs affected the expression of genes associated with reactive oxygen species (ROS) production and endoplasmic reticulum (ER) stress. In addition, we showed that SiO NPs activated xenobiotic metabolism, resulting in ER stress. Endoplasmic reticulum stress resulted in increased ROS production, which activated the NF-κB pathway leading to expression of inflammatory cytokines. Increased inflammatory cytokine expression resulted in serine phosphorylation of IRS1, which induced insulin resistance (IR). Furthermore these inflammatory cytokines activated the MAPK pathway, which further promoted the serine phosphorylation of IRS1. Insulin resistance resulted in elevated blood glucose. The ER stress inhibitor 4-phenylbutyric acid (4-PBA) inhibited SiO NP-induced ROS production. The ROS scavenger N-acetylcysteine (NAC) did not affect SiO NP-induced ER stress, but inhibited SiO NP-induced activation of the NF-κB and MAPK pathways, expression of inflammatory cytokines, SiO NP-induced serine phosphorylation of IRS1, and SiO2 NP-induced elevations of blood glucose.Silicon dioxide NPs induced IR through ER stress and generation of ROS, but SiO FPs did not. Therefore, lifelong exposure of humans to SiO NPs may result in detrimental effects on blood glucose. The results of this study strongly suggested that non-nanoformed SiO should be used as food additives.
| Reference Key |
hu2019siliconparticle
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Hu, Hailong;Fan, Xingpei;Guo, Qian;Wei, Xiangjuan;Yang, Daqian;Zhang, Boya;Liu, Jing;Wu, Qiong;Oh, Yuri;Feng, Yujie;Chen, Kun;Hou, Liping;Gu, Ning; |
| Journal | particle and fibre toxicology |
| Year | 2019 |
| DOI |
10.1186/s12989-019-0327-z
|
| URL | |
| Keywords |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.