Binding activities by propiverine and its N-oxide metabolites of L-type calcium channel antagonist receptors in the rat bladder and brain

Abstract

The present study was undertaken to characterize the binding activities of propiverine and its N-oxide metabolites (1-methyl-4-piperidyl diphenylpropoxyacetate N-oxide: P-4(N → O), 1-methyl-4-piperidyl benzilate N-oxide: DPr-P-4(N → O)) toward L-type calcium channel antagonist receptors in the rat bladder and brain. Propiverine and P-4(N → O) inhibited specific (+)-[ 3H]PN 200–110 binding in the rat bladder in a concentration-dependent manner. Compared with that for propiverine, the K i value for P-4(N → O) in the bladder was significantly greater. Scatchard analysis has revealed that propiverine increased significantly K d values for bladder (+)-[ 3H]PN 200–110 binding. DPr-P-4(N → O) had little inhibitory effects on the bladder (+)-[ 3H]PN 200–110 binding. Oxybutynin and N-desethyl-oxybutynin (DEOB) also inhibited specific (+)-[ 3H]PN 200–110 binding in the rat bladder. Propiverine, oxybutynin and their metabolites inhibited specific [ N-methyl- 3H]scopolamine methyl chloride ([ 3H]NMS) binding in the rat bladder. The ratios of K i values for (+)-[ 3H]PN 200–110 to [ 3H]NMS were markedly smaller for propiverine and P-4(N → O) than oxybutynin and DEOB. Propiverine and P-4(N → O) inhibited specific binding of (+)-[ 3H]PN 200–110, [ 3H]diltiazem and [ 3H]verapamil in the rat cerebral cortex in a concentration-dependent manner. The K i values of propiverine and P-4(N → O) for [ 3H]diltiazem were significantly smaller than those for (+)-[ 3H]PN 200–110 and [ 3H]verapamil. Further, their K i values for [ 3H]verapamil were significantly smaller than those for (+)-[ 3H]PN 200–110. The K i values of propiverine for each radioligand in the cerebral cortex were significantly ( P < 0.05) smaller than those of P-4(N → O). In conclusion, the present study has shown that propiverine and P-4(N → O) exert a significant binding activity of L-type calcium channel antagonist receptors in the bladder and these effects may be pharmacologically relevant in the treatment of overactive bladder after oral administration of propiverine.