Objective, To compare the proinflammatory effects of tenidap to those
of indomethacin, and to assess the influence of lipoxygenase inhibitio
n with either a leukotriene synthesis inhibitor (L663,536) or tenidap
on platelet activating factor (PAF) induced leukocyte adhesion. Method
s. Adherent leukocytes, emigrated leukocytes, number of rolling leukoc
ytes/100 mu m venule, flux of rolling leukocytes, and leukocyte rollin
g velocity were quantitated in mesenteric venules (25-35 mu m diameter
and > 150 mu m length) of Sprague-Dawley rats using intravital micros
copy. In,some experiments, the mesentery was superfused with indometha
cin (25 mu g/ml), tenidap (30 mu g/ml), or both drugs simultaneously.
In other experiments the mesentery was superfused with PAF 100 nM and
the effects of treatment with 1,663,536 (Ip mg/kg given orally) or sup
erfusion with tenidap were determined. Results, Indomethacin significa
ntly increased leukocyte rolling and adhesion. Tenidap did not promote
leukocyte-endothelial cell adhesion and blocked the increased leukocy
te rolling and adhesion promoted by indomethacin. Both L663,536 and te
nidap significantly attenuated PAF induced leukocyte-endothelial cell
adhesion. Conclusion, Tenidap does not exhibit the proinflammatory pro
perties of indomethacin. The reduction of indomethacin or PAF induced
leukocyte-endothelial :cell adhesion by tenidap appeared to result fro
m its lipoxygenase inhibitory activity. Modulation of leukocyte-endoth
elial cell adhesion may be a never mechanism of the antiinflammatory a
ctivity of tenidap and may reduce the relative risk of gastric ulcerat
ion with tenidap.