Abstract
The present study was done to characterize a new compound, PNU-171990, 2-diisopropyl aminoethyl 1-phenylcyclopentane carboxylate hydrochloride, with functional smooth muscle selectivity at least as high as tolterodine. In vitro homogenates of guinea pig cerebral cortex, parotid gland, heart, urinary bladder, and Chinese hamster ovary (CHO) cells expressing human muscarinic m 1–m 5 receptors PNU-171990 did not show selectivity for any subtype (p K i, 7.72–8.64). PNU-171990 caused a parallel shift in the concentration–response curve for carbachol-induced contraction of smooth muscle from guinea pig bladder (p K B, 7.65), guinea pig ileum (p K B, 8.48), and human ileum (p K B, 7.10). In vivo PNU-171990 inhibited urinary bladder contraction with a significantly lower ID 50 than on the salivary secretion (206 and 706 nmol/kg, respectively, P<0.05). In conclusion, PNU-171990 is a competitive and potent muscarinic receptor antagonist in vitro with a numerically better selectivity ratio for the bladder contraction over salivation in vivo than tolterodine.
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