Transient pulmonary fibrogenic effect induced by intratracheal instillation of ultrafine amorphous silica in A/J mice

Toxicol Lett. 2008 Nov 10;182(1-3):97-101. doi: 10.1016/j.toxlet.2008.08.019. Epub 2008 Sep 13.

Abstract

In order to evaluate the degree of pulmonary fibrosis and to identify the fibrogenic mechanisms induced by ultrafine amorphous silica (UFAS), UFAS suspensions ( approximately 50microl) were instilled intratracheally into A/J mice at doses of 0, 2, 10 and 50mg/kg (n=5 per group). Mice were sacrificed at 24h, 1, 4 and 14 weeks after exposure. Gomori's trichrome staining revealed that UFAS induced severe alveolar epithelial thickening and pulmonary fibrosis at 1 week, though animals almost recovered at 4 and 14 weeks. The mRNA and protein levels of cytokines (IL-4, IL-10, IL-13 and IFN-gamma), matrix metalloproteinases (MMP-2, MMP-9 and MMP-10) and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) in lung tissues were significantly elevated at 24h and 1week post-treatment, though these levels decreased to near the control range at 4 and 14 weeks except IFN-gamma and MMP-2. These results demonstrate that UFAS can induce pulmonary fibrosis in the same way as crystalline silica. However, the degree of fibrosis observed was transient. This study shows that cytokines (IL-4, IL-10, IL-13 and IFN-gamma), MMPs (MMP-2, MMP-9 and MMP-10) and TIMP-1 play important roles in the fibrosis induced by the intratracheal instillation of UFAS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Inhalation
  • Animals
  • Coloring Agents
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • DNA, Complementary / biosynthesis
  • DNA, Complementary / genetics
  • Image Processing, Computer-Assisted
  • Immunohistochemistry
  • Male
  • Matrix Metalloproteinases / biosynthesis
  • Matrix Metalloproteinases / genetics
  • Mice
  • Mice, Inbred A
  • Nanoparticles / administration & dosage
  • Nanoparticles / toxicity*
  • Pulmonary Fibrosis / chemically induced*
  • Pulmonary Fibrosis / pathology*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Silicon Dioxide / administration & dosage
  • Silicon Dioxide / toxicity*

Substances

  • Coloring Agents
  • Cytokines
  • DNA, Complementary
  • RNA, Messenger
  • Silicon Dioxide
  • Matrix Metalloproteinases