Acute exposure to silica nanoparticles aggravate airway inflammation: different effects according to surface characteristics.
- Author:
Hye Jung PARK
1
;
Jung Ho SOHN
;
Yoon Ju KIM
;
Yoon Hee PARK
;
Heejae HAN
;
Kyung Hee PARK
;
Kangtaek LEE
;
Hoon CHOI
;
Kiju UM
;
In Hong CHOI
;
Jung Won PARK
;
Jae Hyun LEE
Author Information
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- MeSH: Animals; Asthma/*chemically induced/pathology; Female; Inflammation/*chemically induced/pathology; Interferon-gamma/analysis; Interleukins/analysis; Lung/drug effects/*pathology; Mice, Inbred BALB C; Nanoparticles/*adverse effects/chemistry; Ovalbumin/adverse effects; Polyethylene Glycols/adverse effects/chemistry; Silicon Dioxide/*adverse effects/chemistry; Surface Properties
- From:Experimental & Molecular Medicine 2015;47(7):e173-
- CountryRepublic of Korea
- Language:English
- Abstract: Silica nanoparticles (SNPs) are widely used in many scientific and industrial fields despite the lack of proper evaluation of their potential toxicity. This study examined the effects of acute exposure to SNPs, either alone or in conjunction with ovalbumin (OVA), by studying the respiratory systems in exposed mouse models. Three types of SNPs were used: spherical SNPs (S-SNPs), mesoporous SNPs (M-SNPs), and PEGylated SNPs (P-SNPs). In the acute SNP exposure model performed, 6-week-old BALB/c female mice were intranasally inoculated with SNPs for 3 consecutive days. In the OVA/SNPs asthma model, the mice were sensitized two times via the peritoneal route with OVA. Additionally, the mice endured OVA with or without SNP challenges intranasally. Acute SNP exposure induced significant airway inflammation and airway hyper-responsiveness, particularly in the S-SNP group. In OVA/SNPs asthma models, OVA with SNP-treated group showed significant airway inflammation, more than those treated with only OVA and without SNPs. In these models, the P-SNP group induced lower levels of inflammation on airways than both the S-SNP or M-SNP groups. Interleukin (IL)-5, IL-13, IL-1beta and interferon-gamma levels correlated with airway inflammation in the tested models, without statistical significance. In the mouse models studied, increased airway inflammation was associated with acute SNPs exposure, whether exposed solely to SNPs or SNPs in conjunction with OVA. P-SNPs appear to be relatively safer for clinical use than S-SNPs and M-SNPs, as determined by lower observed toxicity and airway system inflammation.
