RT Journal Article SR Electronic T1 Mechanism of Gallbladder Relaxation in the Cat: Role of Norepinephrine , JF Journal of Pharmacology and Experimental Therapeutics JO J Pharmacol Exp Ther FD American Society for Pharmacology and Experimental Therapeutics SP 475 OP 479 VO 285 IS 2 A1 Qian Chen A1 Kwang Lee A1 Zuoliang Xiao A1 Piero Biancani A1 Jose Behar YR 1998 UL http://jpet.aspetjournals.org/content/285/2/475.abstract AB We investigated the mechanisms of neurally mediated relaxation of cat gallbladder muscle. Muscle strips from the gallbladder corpus placed in the muscle bath with oxygenated Krebs’ solution developed spontaneous active tension. Tension was measured with isometric force transducers, and muscle relaxation was expressed as percent decrease of active basal tension. Electrical field stimulation (EFS) evoked a tetrodotoxin-sensitive and hexamethonium-insensitive frequency-dependent relaxation with a maximal relaxation at 20 Hz. Gallbladder muscle strips also relaxed in response to increasing concentrations of vasoactive intestinal peptide (VIP), isoproterenol and, after pretreatment with phentolamine, norepinephrine. Nitric oxide synthase inhibitors Nω-nitro-l-arginine and Nω-nitro-l-arginine methyl ester at a concentration of 100 μM, which blocked EFS-induced relaxation in the lower esophageal sphincter, had no significant effect on EFS-induced gallbladder muscle relaxation. The VIP antagonists VIP10–28 and [4Cl-d-Phe6,Leu17]VIP at a concentration of 10 μM that blocked exogenous VIP-induced gallbladder relaxation also had no effect on the relaxation caused by EFS. In contrast, either propranolol or guanethidine at concentrations of ≥1 μM significantly reduced EFS-evoked gallbladder relaxation (P < .01, analysis of variance). It is concluded that norepinephrine utilizing beta adrenergic receptors mediates EFS-stimulating postganglionic intramural neurons in the cat gallbladder. The American Society for Pharmacology and Experimental Therapeutics