Impact of vitamin E-blended UHMWPE wear particles on the osseous microenvironment in polyethylene particle-induced osteolysis

Int J Mol Med. 2016 Dec;38(6):1652-1660. doi: 10.3892/ijmm.2016.2780. Epub 2016 Oct 18.

Abstract

Aseptic loosening mediated by wear particle-induced osteolysis (PIO) remains the major cause of implant loosening in endoprosthetic surgery. The development of new vitamin E (α-tocopherol)-blended ultra-high molecular weight polyethylene (VE-UHMWPE) with increased oxidation resistance and improved mechanical properties has raised hopes. Furthermore, regenerative approaches may be opened, as vitamin E supplementation has shown neuroprotective characteristics mediated via calcitonin gene-related peptide (CGRP), which is known to affect bone remodeling in PIO. Therefore, the present study aimed to further clarify the impact of VE-UHMWPE wear particles on the osseous microenvironment and to identify the potential modulatory pathways involved. Using an established murine calvaria model, mice were subjected to sham operation (SHAM group), or treated with UHMWPE or VE-UHMWPE particles for different experimental durations (7, 14 and 28 days; n=6/group). Morphometric analysis by micro-computed tomography detected significant (p<0.01) and comparable signs of PIO in all particle-treated groups, whereas markers of inflammation [tumor necrosis factor (TNF)-α/tartrate resistant acid phosphatase (TRAP) staining] and bone remodeling [Dickkopf-related protein 1 (DKK-1)/osteoprotegerin (OPG)] were most affected in the early stages following surgery. Taking the present data into account, VE-UHMWPE appears to have a promising biocompatibility and increased ageing resistance. According to the α-CGRP serum levels and immunohistochemistry, the impact of vitamin E on neuropeptidergic signaling and its chance for regenerative approaches requires further investigation.

MeSH terms

  • Animals
  • Biomarkers
  • Bone Resorption / metabolism
  • Bone Resorption / pathology
  • Bone and Bones / metabolism
  • Bone and Bones / pathology
  • Calcitonin Gene-Related Peptide / metabolism
  • Granuloma / metabolism
  • Granuloma / pathology
  • Inflammation / etiology
  • Inflammation / metabolism
  • Inflammation / pathology
  • Male
  • Mice
  • Osteoclasts / metabolism
  • Osteogenesis
  • Osteolysis / diagnostic imaging
  • Osteolysis / etiology*
  • Osteolysis / metabolism
  • Osteolysis / pathology*
  • Polyethylenes* / administration & dosage
  • Skull / diagnostic imaging
  • Skull / metabolism
  • Skull / pathology
  • Vitamin E* / administration & dosage
  • X-Ray Microtomography

Substances

  • Biomarkers
  • Polyethylenes
  • ultra-high molecular weight polyethylene
  • Vitamin E
  • Calcitonin Gene-Related Peptide