An involvement of granulocyte medullasin in phenytoin-induced gingival overgrowth in rats

Jpn J Pharmacol. 2002 Jul;89(3):235-41. doi: 10.1254/jjp.89.235.

Abstract

To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in phenytoin-induced gingival overgrowth, we established a rat model of gingival overgrowth. Thirty-two, 20-day-old male Fischer 344 rats were fed a diet containing phenytoin and sacrificed at 1, 2, 4 and 8 weeks. Control rats (n = 40) were fed the same diet, but without the drug and killed at the same weeks as experimental rats (n = 32) and 0 week (n = 8). The mandible specimens were resected and sectioned bucco-lingually between the first and second molars. A marked inflammatory-cell infiltration and elongated rete pegs were seen in the phenytoin-treated group. The extent of the overgrowth assessed by computer image analysis and the density of medullasin-positive cells by immunohistochemistry in the approximal gingiva showed a significant increase in the phenytoin-treated group compared to the control group. A marked infiltration of the positive cells in experimental rats was observed as early as 2 weeks when gingival overgrowth was not fully established. Medullasin-positive cells were mostly neutrophils and partly macrophage-like cells. These findings suggest that medullasin may be involved in mainly host defense and secondarily collagen metabolism in the phenytoin-induced rat model of gingival overgrowth.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Gingiva / chemistry
  • Gingiva / drug effects*
  • Gingiva / metabolism
  • Gingival Hyperplasia / chemically induced*
  • Gingival Hyperplasia / metabolism
  • Granulocytes / chemistry
  • Granulocytes / drug effects*
  • Granulocytes / metabolism
  • Male
  • Phenytoin / pharmacology*
  • Rats
  • Rats, Inbred F344
  • Serine Endopeptidases / analysis
  • Serine Endopeptidases / biosynthesis*

Substances

  • Phenytoin
  • Serine Endopeptidases
  • medullasin