The antagonistic activities of compound N-3389 (endo-3,9-dimethyl-3,9-diazabicyclo[3,3,1]non-7-yl 1H-indazole-3- carboxamide dihydrochlo ride) at 5-HT3and 5-HT4receptors were examined using in vitro and in vivo assays. N-3389 showed potent 5-HT3receptor antagonistic activities in a radioligand binding assay (pKi= 8.77), against 2-methyl-5-HT (2-Me-5-HT)-induced bradycardia in rats (ED50= 0.73 μg/kg i.v., 38 μg/kg p.o.) and against 2-Me-5-HT-induced contraction in longitudinal muscle myenteric plexus preparations of guinea-pig ileum (IC50= 3.2 × 10-8M). As preliminary to investigating the effect of N-3389 on 5-HT4receptors, we examined the contraction induced by 5-HT in guinea-pig ileum preparations. We confirmed that 5-HT (10-8- 10-5M) induced biphasic contractions in the preparations.Furthermore, 5-HT3receptor antagonism inhibited the late phase of the contraction induced by high concentrations of 5-HT (3 × 10-6- 10-5M), whereas 5-HT4receptor antagonism inhibited the early phase of the contraction induced by low concentrations of 5-HT (10-8- 10-6M). N-3389 (10-7- 10-5M) inhibited both phases of contraction induced by 5-HT. In addition, N-3389 (3 × 10-7-3 × 10-6M) was found to inhibit the increase of electrically stimulated twitch responses induced by 5-HT (10-8M) in longitudinal muscle myenteric plexus preparation of the guinea-pig ileum. These results suggest that N-3389 acts as a 5-HT3and 5-HT4receptor antagonist. © 1994.
Hagihara, K., Hayakawa, T., Arai, T., Eguchi, H., Mino, S., & Kawase, S. (1994). Antagonistic activities of N-3389, a newly synthetized diazabicyclo derivative, at 5-HT3and 5-HT4receptors. European Journal of Pharmacology, 271(1), 159–166. https://doi.org/10.1016/0014-2999(94)90276-3