Cyclosporin A inhibits production and activity of matrix metalloproteinases by gingival fibroblasts

J Periodontal Res. 2000 Feb;35(1):51-8. doi: 10.1034/j.1600-0765.2000.035001051.x.

Abstract

Cyclosporin A (CyA) is a potent immunosuppressor used in organ transplantation and in the management of various autoimmune diseases. Gingival overgrowth is one of the side-effects of the CyA-treatment, affecting the attached gingiva of 25-81% of treated patients. To investigate the production and activity of matrix metalloproteinases (MMPs) in the CyA-induced gingival overgrowth, 2 well-documented models were utilized: the in vivo CyA-induced rat gingival overgrowth and primary cultures of human gingival fibroblasts treated with CyA. Our results obtained from the Western blot assays demonstrated clearly that the production of MMP-1 and MMP-3 was significantly inhibited by CyA at similar concentrations found in the serum of patients undergoing CyA-treatment. Moreover, the gelatinolytic activity of MMP-2 was also reduced both in cultured fibroblasts and in the rat CyA-induced gingival overgrowth. Taken together, the data presented here suggest that these inhibitory effects may contribute to the extracellular matrix (ECM) components accumulation in the CyA-induced gingival overgrowth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Analysis of Variance
  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Cyclosporine / pharmacology*
  • Electrophoresis, Polyacrylamide Gel / methods
  • Extracellular Matrix / enzymology
  • Female
  • Fibroblasts / drug effects*
  • Fibroblasts / enzymology
  • Fibroblasts / metabolism
  • Gingiva / cytology
  • Gingiva / drug effects*
  • Gingiva / enzymology
  • Gingival Overgrowth / chemically induced*
  • Gingival Overgrowth / enzymology
  • Humans
  • Male
  • Matrix Metalloproteinase Inhibitors*
  • Matrix Metalloproteinases / biosynthesis
  • Rats
  • Rats, Wistar

Substances

  • Matrix Metalloproteinase Inhibitors
  • Cyclosporine
  • Matrix Metalloproteinases