» Articles » PMID: 24283474

Lung Alterations Following Single or Multiple Low-dose Carbon Black Nanoparticle Aspirations in Mice

Overview
Date 2013 Nov 29
PMID 24283474
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Carbon black nanoparticle (CBNP) applications in high doses have been shown to be harmful to the lung. It is postulated that even small, environmentally relevant concentrations induce changes on lung homeostasis. The present study determined the impact of low-dose single and multiple CBNP (Printex 90) applications on mouse alveolar cell metabolism, especially inflammatory and oxidative stress parameters. Nanoparticles were administered to mice by a single or 8 oropharyngeal aspirations at wk 1, 2, 3, 5, 7, 9, 11, and 12 using 7 μg Printex 90, 7 μg DQ12 quartz (positive control), with water vehicle and saline as negative controls. After 2 d or 3 mo lung function was analyzed. Further lung histology, bronchoalveolar lavage fluid (BALF) parameters, and mRNA expression of cytokines and antioxidants enzymes in type II pneumocytes were measured on d 3 or after 3 mo. Single low-dose Printex 90 application induced no marked alterations in lung functions or BALF phospholipid levels but significant decrease in superoxide dismutase 2 and numerically elevated glutathione peroxidase 3 mRNA expression levels in type II pneumocytes. Multiple CBNP applications produced reduced lung function, collagen accumulation, elevated phospholipid levels in BALF, and a massive infiltration of macrophages. Type II pneumocyte mRNA expression of antioxidative enzymes remained unchanged throughout the subchronic experiment, but showed a significant decrease in interleukin (IL)-6Rα mRNA expression. This study demonstrates that an environmentally relevant CBNP concentration induced an acute inflammatory response, an effect that is exacerbated throughout the subchronic duration.

Citing Articles

Comparative and mechanistic toxicity assessment of structure-dependent toxicity of carbon-based nanomaterials.

Jiang T, Lin Y, Amadei C, Gou N, Rahman S, Lan J J Hazard Mater. 2021; 418:126282.

PMID: 34111749 PMC: 10631494. DOI: 10.1016/j.jhazmat.2021.126282.


Resveratrol prevents nanoparticles-induced inflammation and oxidative stress via downregulation of PKC-α and NADPH oxidase in lung epithelial A549 cells.

Hsu H, Tseng Y, Wong W, Liu C, Lo Y BMC Complement Altern Med. 2018; 18(1):211.

PMID: 29986680 PMC: 6038342. DOI: 10.1186/s12906-018-2278-6.


Pulmonary challenge with carbon nanoparticles induces a dose-dependent increase in circulating leukocytes in healthy males.

Berger M, de Boer J, Lutter R, Makkee M, Sterk P, Kemper E BMC Pulm Med. 2017; 17(1):121.

PMID: 28877711 PMC: 5588713. DOI: 10.1186/s12890-017-0463-x.


Biological effects of carbon black nanoparticles are changed by surface coating with polycyclic aromatic hydrocarbons.

Lindner K, Strobele M, Schlick S, Webering S, Jenckel A, Kopf J Part Fibre Toxicol. 2017; 14(1):8.

PMID: 28327162 PMC: 5361723. DOI: 10.1186/s12989-017-0189-1.


Incomplete lung recovery following sub-acute inhalation of combustion-derived ultrafine particles in mice.

Noel A, Xiao R, Perveen Z, Zaman H, Rouse R, Paulsen D Part Fibre Toxicol. 2016; 13:10.

PMID: 26911867 PMC: 4766714. DOI: 10.1186/s12989-016-0122-z.