Evaluation of a new laboratory model for pulp healing: preliminary study

Int Endod J. 2008 Sep;41(9):781-90. doi: 10.1111/j.1365-2591.2008.01433.x.

Abstract

Aim: To assess the feasibility of using the mouse as an in vivo model for studying pulpal healing in response to restorative procedures.

Methodology: Direct pulp capping on maxillary first molar teeth with mineral trioxide aggregate (MTA), overlaid with light-cured composite resin, was performed on nineteen 3-month-old mice. For control teeth, the composite resin was placed in direct contact with the pulp. Animals were killed at 3 days, 1 week, 2 weeks, 5 weeks and 11 weeks postoperatively. Extracted dental tissues were subsequently analysed by haematoxylin and eosin staining, immunohistochemistry for dentine sialophosphoprotein (DSPP) expression, scanning electronic microscopy and X-ray analysis to determine both pulpal response and dentine bridge formation.

Results: Of the 19 mice initially used, 16 were subsequently studied. Histological analyses of pulps directly exposed to MTA for up to 2 weeks demonstrated a distinct structural change in the extracellular matrix. By weeks 5 and 11, a dentine bridge was present in all MTA-treated specimens in which DSPP immunoreactivity was clearly apparent. Scanning electronic microscopy and X-ray analysis enabled confirmation of calcification of the dentine bridge, and demonstrated that it had a globular surface morphology as opposed to the tubular appearance associated with orthodentine.

Conclusions: This is the first description of the utilization of a murine model for study of in vivo pulpal repair. This approach provides a novel opportunity to enable the use of genetically modified animals to explore cellular and molecular processes during reparative events.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aluminum Compounds / pharmacology
  • Animals
  • Calcium Compounds / pharmacology
  • Dental Pulp / cytology
  • Dental Pulp / drug effects
  • Dental Pulp / physiology*
  • Dental Pulp Capping / methods*
  • Dental Pulp Exposure / therapy
  • Dentin, Secondary / metabolism*
  • Drug Combinations
  • Extracellular Matrix Proteins
  • Feasibility Studies
  • Immunoenzyme Techniques
  • Mice
  • Models, Animal*
  • Odontoblasts / metabolism
  • Oxides / pharmacology
  • Phosphoproteins
  • Protein Precursors / biosynthesis
  • Root Canal Filling Materials / pharmacology
  • Sialoglycoproteins
  • Silicates / pharmacology
  • Wound Healing / drug effects
  • Wound Healing / physiology*

Substances

  • Aluminum Compounds
  • Calcium Compounds
  • Drug Combinations
  • Extracellular Matrix Proteins
  • Oxides
  • Phosphoproteins
  • Protein Precursors
  • Root Canal Filling Materials
  • Sialoglycoproteins
  • Silicates
  • dentin sialophosphoprotein
  • mineral trioxide aggregate