Inhibition of bone formation in rats by aluminum exposure via Wnt/β-catenin pathway

Chemosphere. 2017 Jun:176:1-7. doi: 10.1016/j.chemosphere.2017.02.086. Epub 2017 Feb 20.

Abstract

The previous research found that aluminum trichloride (AlCl3) inhibited rat osteoblastic differentiation through inactivation of Wnt/β-catenin signaling pathway in vitro. On that basis, the experiment in vivo was conducted in this study. Rats were orally exposed to 0 (control group) and 0.4 g/L AlCl3 (AlCl3-treated group) for 30, 60, 90 or 120 days, respectively. We found that mRNA expressions of type I collagen and insulin-like growth factor-1, mRNA and protein expressions of Runx2 and survivin, ratio of p-GSK3β/GSK3β and protein expression of β-catenin were all decreased, whereas the mRNA and protein expressions Dkk1 and sFRP1 and the mRNA expressions and activity of Caspase-3 were increased in the AlCl3-treated group compared with the control group with time prolonged. These results suggest that AlCl3 inhibits bone formation and induces bone impairment by inhibiting the Wnt/β-catenin signaling pathway in young growing rats.

Keywords: Aluminum trichloride; Bone formation; Rat; Wnt/β-catenin signaling pathway.

MeSH terms

  • Aluminum Chloride
  • Aluminum Compounds / toxicity*
  • Animals
  • Caspase 3 / metabolism
  • Chlorides / toxicity*
  • Collagen Type I / metabolism
  • Femur / drug effects*
  • Femur / growth & development
  • Femur / metabolism
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Osteogenesis / drug effects*
  • Rats
  • Rats, Wistar
  • Wnt Signaling Pathway / drug effects*

Substances

  • Aluminum Compounds
  • Chlorides
  • Collagen Type I
  • insulin-like growth factor-1, rat
  • Aluminum Chloride
  • Insulin-Like Growth Factor I
  • Caspase 3