A comparative study of lung toxicity in rats induced by three types of nanomaterials.

Nanoscale Res Lett

Institute of Health and Environmental Medicine, Academy of Military Medical Sciences, Tianjin 300050, People's Republic of China.

Published: December 2013

AI Article Synopsis

  • The study examines the toxicity of various engineered nanomaterials, particularly their effects on lung health through oxidative stress and inflammation.
  • Researchers utilized techniques like transmission electron microscopy (TEM) and proteomics to assess damage in rats exposed to nano-ferroso-ferric oxide, nano-silicon dioxide, and single-walled carbon nanotubes.
  • Findings indicated that all three nanomaterials could lead to lung damage, evidenced by changes in specific biomarkers related to oxidative stress and inflammation in the lung tissue and fluid.

Article Abstract

The public is increasingly exposed to various engineered nanomaterials because of their mass production and wide application. Even when the biological effects of nanomaterials have been assessed, the underlying mechanisms of action in vivo are poorly understood. The present study was designed to seek a simple, effective, and oxidative stress-based biomarker system used for screening toxicity of nanomaterials. Nano-ferroso-ferric oxide (nano-Fe3O4), nano-silicon dioxide (nano-SiO2), and single-walled carbon nanotubes (SWCNTs) were dispersed in corn oil and characterized using transmission electron microscopy (TEM). Rats were exposed to the three nanomaterials by intratracheal instillation once every 2 days for 5 weeks. We investigated their lung oxidative and inflammatory damage by bronchoalveolar lavage fluid (BALF) detection and comparative proteomics by lung tissue. Two-dimensional electrophoresis (2-DE) of proteins isolated from the lung tissue, followed by matrix-assisted laser desorption-ionization time-of-flight mass spectrometry, was performed. In the present study, we chose to detect lactate dehydrogenase, total antioxidant capacity, superoxide dismutase, and malondialdehyde as the biomarker system for screening the oxidative stress of nanomaterials and IL-6 as the inflammatory biomarker in BALF. Proteomics analysis revealed 17 differentially expressed proteins compared with the control group: nine were upregulated and eight were downregulated. Our results indicated that exposure by intratracheal instillation to any of the three typical nanomaterials may cause lung damage through oxidative damage and/or an inflammatory reaction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879061PMC
http://dx.doi.org/10.1186/1556-276X-8-521DOI Listing

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