The effects of platelet activating factor (PAF) on haemodynamics in th
e absence and presence of the potent PAF receptor antagonist TCV-309 y
l]carbonamoyl]ethyl]carbamoyl]-1-propylpyridinium nitrate) were studie
d by the microsphere technique in pentobarbitone-anaesthetized rats. I
.v. infusion of the low dose PAF (0.05 mu g kg(-1) min(-1)) did not si
gnificantly alter mean arterial pressure, cardiac output or total peri
pheral resistance but increased arterial conductances in the stomach,
intestine, caecum and colon and reduced conductance in the spleen. I.v
. infusion of the high dose of PAF (0.3 mu g kg(-1) min(-1)) markedly
reduced mean arterial pressure (-53 mm Hg) and cardiac output (-62%) a
nd insignificantly increased total peripheral resistance. Arterial con
ductances in the lungs, stomach, intestine, caecum and colon, kidneys
and spleen were reduced and those in the heart and muscle were increas
ed. TCV-309 (10 mu g kg(-1)) abolished all changes in arterial pressur
e, cardiac output and total peripheral resistance and arterial conduct
ances elicited by either the low or the high dose of PAF. The results
show that a non-hypotensive dose of PAF caused vasodilatation of the g
astrointestinal organs and vasoconstriction of the spleen. A high dose
of PAF which markedly decreased arterial pressure and cardiac output
caused vasodilatation of the heart and muscle and vasoconstriction of
the lungs (bronchial), gastrointestinal organs, kidneys and spleen. Al
l haemodynamic changes were blocked by TCV-309 indicating the involvem
ent of PAF receptors.