The objective of the present study was to evaluate the effects of a selecti
ve beta(3)-adrenoceptor agonist, (R,R)-5-[2-[[2-(3-chlorophenyl)- 2- hydrox
yethyl]- amino] propyl]-1,3-benzodioxole-2,2-dicarboxylate (CL 316243), on
the acutely obstructed ureter in anesthetized dogs. After a complete ureter
al obstruction produced by the inflation of a balloon catheter placed withi
n the left lower ureter, the intraluminal ureteral pressure gradually rose
to reach a plateau of similar to 52.5 mm Hg. Intravenous administration of
isoproterenol (a nonselective beta-adrenoceptor agonist; 10 mu g/kg) and CL
316243 (1 mu g/kg) significantly decreased this elevated ureteral pressure
(by 74.1 and 77.2%, respectively), with the reduction more sustained with
CL 316243 than with isoproterenol. In addition, under both isoproterenol an
d CL 316243, urine flow (which had been interrupted by the balloon) was res
umed, resulting in further sustained decreases in ureteral pressure. The me
an blood pressure decreased and heart rate increased after the administrati
on of both drugs, but these changes were greater in the isoproterenol group
than in the CL 316243 group. In contrast, i.v. administration of butylscop
olamine (an anticholinergic agent; 1000 mu g/kg) had no evident effects on
ureteral pressure or on urine flow. The increase in left kidney weight seen
after ureteral obstruction was suppressed by CL 316243. We conclude that t
he selective beta(3)-adrenoceptor agonist tested appears to be more useful
than isoproterenol for reducing ureteral pressure above the obstructed site
and for promoting ureteral relaxation and increasing urine flow around the
point of obstruction in dogs.