A specific COX-2 inhibitor attenuates cell infiltration but does not prolong graft survival in murine cardiac transplantation

Transplant Proc. 2005 Jan-Feb;37(1):121-2. doi: 10.1016/j.transproceed.2004.11.050.

Abstract

COX-2 is a key factor in the progression of inflammation, the effects of a specific COX-2 inhibitor in cardiac transplantation have not yet been elucidated. To test the hypothesis that a COX-2 inhibitor can alter cardiac rejection, we analyzed graft survival using totally allomismatched grafts. Although the COX-2 inhibitor attenuated myocardial cell infiltration, the inhibitor did not prolong survival. We conclude that the COX-2 inhibition may have potential for the suppression of inflammation in cardiac allografts.

MeSH terms

  • Animals
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / therapeutic use*
  • Graft Survival / drug effects
  • Graft Survival / immunology*
  • Heart / drug effects
  • Heart Transplantation / immunology
  • Heart Transplantation / pathology*
  • Male
  • Meloxicam
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Myocardium / pathology
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Thiazines / therapeutic use*
  • Thiazoles / therapeutic use*
  • Time Factors
  • Transplantation, Homologous / immunology

Substances

  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Thiazines
  • Thiazoles
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Meloxicam