Utilizing VIP and five VIP analogues, concentration-response curves fo
r relaxation of rat mesenteric artery and rat gastric longitudinal mus
cle were determined for comparison with our previously published radio
ligand binding data on rat smooth muscle and other tissues. The biolog
ical potency of the VIP analogues in the present study compared more c
losely with their potency for VIP receptor binding in smooth muscle ti
ssue (arteries) vs. other tissues (pituitary, brain, liver).