To characterize the urinary kinetics of AVP, and the influence of regi
onal blood dow on the metabolic degradation of AVP, multiple doses of
AVP were administered to conscious rabbits. AVP systemic clearance (Cl
-T) was not influenced by changes in dose, in spite of a decrease in A
VP urinary clearance following the highest dose. Hepatic blood dow was
inversely associated with AVP concentrations, and despite a decrease
in hepatic plasma flow of 37% (p < 0.05), following the high dose of A
VP, Cl-T remained unchanged. These results indicate that AVP plasma ki
netics are first order and plasma flow independent, and urinary kineti
cs are zero order.