Oxidative stress, inflammation, and DNA damage in multiple organs of mice acutely exposed to amorphous silica nanoparticles

Abderrahim Nemmar, Priya Yuvaraju, Sumaya Beegam, Javed Yasin, Elsadig E. Kazzam, Badreldin H. Ali

Research output: Contribution to journalArticle

40 Citations (Scopus)

Abstract

The use of amorphous silica (SiO2) in biopharmaceutical and industrial fields can lead to human exposure by injection, skin penetration, ingestion, or inhalation. However, the in vivo acute toxicity of amorphous SiO2nanoparticles (SiNPs) on multiple organs and the mechanisms underlying these effects are not well understood. Presently, we investigated the acute (24 hours) effects of intraperitoneally administered 50 nm SiNPs (0.25 mg/kg) on systemic toxicity, oxidative stress, inflammation, and DNA damage in the lung, heart, liver, kidney, and brain of mice. Lipid peroxidation was significantly increased by SiNPs in the lung, liver, kidney, and brain, but was not changed in the heart. Similarly, superoxide dismutase and catalase activities were significantly affected by SiNPs in all organs studied. While the concentration of tumor necrosis factor α was insignificantly increased in the liver and brain, its increase was statistically significant in the lung, heart, and kidney. SiNPs induced a significant elevation in pulmonary and renal interleukin 6 and interleukin-1 beta in the lung, liver, and brain. Moreover, SiNPs caused a significant increase in DNA damage, assessed by comet assay, in all the organs studied. SiNPs caused leukocytosis and increased the plasma activities of lactate dehydrogenase, creatine kinase, alanine aminotranferase, and aspartate aminotransferase. These results indicate that acute systemic exposure to SiNPs causes oxidative stress, inflammation, and DNA damage in several major organs, and highlight the need for thorough evaluation of SiNPs before they can be safely used in human beings.

Original languageEnglish
Pages (from-to)919-928
Number of pages10
JournalInternational Journal of Nanomedicine
Volume11
DOIs
Publication statusPublished - Mar 7 2016

Fingerprint

Oxidative stress
Silicon Dioxide
Liver
Nanoparticles
DNA Damage
Brain
Oxidative Stress
DNA
Silica
Inflammation
Lung
Kidney
Toxicity
Creatine Kinase
Aspartate Aminotransferases
Alanine Transaminase
Interleukin-1beta
L-Lactate Dehydrogenase
Comet Assay
Catalase

Keywords

  • Amorphous silica nanoparticles
  • DNA damage
  • Inflammation
  • Organ toxicity
  • Oxidative stress

ASJC Scopus subject areas

  • Biophysics
  • Bioengineering
  • Biomaterials
  • Organic Chemistry
  • Drug Discovery

Cite this

Oxidative stress, inflammation, and DNA damage in multiple organs of mice acutely exposed to amorphous silica nanoparticles. / Nemmar, Abderrahim; Yuvaraju, Priya; Beegam, Sumaya; Yasin, Javed; Kazzam, Elsadig E.; Ali, Badreldin H.

In: International Journal of Nanomedicine, Vol. 11, 07.03.2016, p. 919-928.

Research output: Contribution to journalArticle

Nemmar, Abderrahim ; Yuvaraju, Priya ; Beegam, Sumaya ; Yasin, Javed ; Kazzam, Elsadig E. ; Ali, Badreldin H. / Oxidative stress, inflammation, and DNA damage in multiple organs of mice acutely exposed to amorphous silica nanoparticles. In: International Journal of Nanomedicine. 2016 ; Vol. 11. pp. 919-928.
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