Six-week inhalation of CdO nanoparticles in mice: The effects on immune response, oxidative stress, antioxidative defense, fibrotic response, and bones

Food Chem Toxicol. 2020 Feb:136:110954. doi: 10.1016/j.fct.2019.110954. Epub 2019 Nov 9.

Abstract

Due to the growing number of applications of cadmium oxide nanoparticles (CdO NPs), there is a concern about their potential deleterious effects. The objective of our study was to investigate the effect of CdO NPs on the immune response, renal and intestine oxidative stress, blood antioxidant defence, renal fibrotic response, bone density and mineral content. Six-week-old female ICR mice were exposed to CdO NPs for 6 weeks by inhalation (particle size: 9.82 nm, mass concentration: 31.7 μg CdO/m3, total deposited dose: 0.195 μg CdO/g body weight). CdO NPs increased percentage of thymus CD3e+CD8a+ cells and moderately enhanced splenocyte proliferation and production of cytokines and chemokines. CdO NPs elevated pro-fibrotic factors (TGF-β2, α-SMA and collagen I) in the kidney, and concentrations of AGEs in the intestine. The ratio of GSH and GSSG in blood was slightly reduced. Exposure to CdO NPs resulted in 10-fold higher Cd concentration in tibia bones. No differences were found in bone mass density, mineral content, bone area values, bone concentrations of Ca, P, Mg and Ca/P ratio. Our findings indicate stimulation of immune/inflammatory response, oxidative stress in the intestine, starting fibrotic response in kidneys and accumulation of CdO NPs in bones of mice.

Keywords: Cadmium oxide nanoparticles; Inhalation; Mice; Nanotoxicology.

MeSH terms

  • Administration, Inhalation
  • Animals
  • Cadmium Compounds / administration & dosage
  • Cadmium Compounds / toxicity*
  • Cytokines / metabolism
  • Female
  • Fibrosis / chemically induced*
  • Immunity, Cellular / drug effects*
  • Intestines / drug effects
  • Kidney / drug effects
  • Kidney / pathology
  • Lymph Nodes / drug effects
  • Metal Nanoparticles / administration & dosage
  • Metal Nanoparticles / toxicity*
  • Mice, Inbred ICR
  • Oxidative Stress / drug effects*
  • Oxides / administration & dosage
  • Oxides / toxicity*
  • Spleen / drug effects
  • Thymus Gland / drug effects
  • Tibia / drug effects*

Substances

  • Cadmium Compounds
  • Cytokines
  • Oxides
  • cadmium oxide