Pharmacological properties of pteleprenine, a quinoline alkaloid from Orixa japonica (Rutaceae), in guinea pig ileum and canine left atrium.

Kiyoshi Murata, Yoshiteru Oshima, Kazuhiko Seya, Izumi Miki, Hisae Junke, Shigeru Motomura

研究成果: Article

抜粋

We investigated the pharmacological properties of pteleprenine, a quinoline alkaloid contained in the Rutaceous plant, Orixa japonica, on the contractile responses of the guinea pig ileum and on the inotropic responses of the canine left atrium. Contractile responses of the ileum to acetylcholine and histamine were not inhibited by less than 10-6 M of pteleprenine. Meanwhile, the nicotine induced-contraction of the ileum was dose-dependently diminished by pteleprenine, but the contractile response to nicotine did not reach the maximum value in the presence of 10-5M of pteleprenine. The pA2value of pteleprenine was 6.6 as determined from the Schild plot, which slope was nearly unity. Furthermore, the contraction of the ileum by 10-5M of 1,1 -dimethyi-4-phenylpiperazinium (DMPP), a specific agonist of nicotinic acetylcholine receptors, was also dose-dependently suppressed by pteleprenine. On the other hand, 10-5M of pteleprenine did not have consider ble inhibitory effects on acetylcholine- and nicotine-induced negative inotropic effects in the canine left atrium. From these results, it is suggested that pteleprenine has a specific inhibitory effect on nicotinic acetylcholine receptors in the guinea pig ileum.

元の言語English
ページ(範囲)148-152
ページ数5
ジャーナルFolia Pharmacologica Japonica
110
DOI
出版物ステータスPublished - 1997 1 1

ASJC Scopus subject areas

  • Pharmacology

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