Inhibitory effect of endomorphin-1 and -2 on acetylcholine release from myenteric plexus of guinea pig ileum

被引:26
|
作者
Nishiwaki, H
Saitoh, N
Nishio, H
Takeuchi, T
Hata, F [1 ]
机构
[1] Univ Osaka Prefecture, Coll Agr, Dept Vet Pharmacol, Sakai, Osaka 5998531, Japan
[2] Univ Osaka Prefecture, Adv Sci & Technol Res Inst, Dept Mol Physiol & Biochem, Sakai, Osaka 5998531, Japan
[3] Nippon Boehringer Ingelheim Co Ltd, Kawanishi Pharma Res Inst, Kawanishi 6660131, Japan
来源
JAPANESE JOURNAL OF PHARMACOLOGY | 1998年 / 78卷 / 01期
关键词
endomorphin; acetylcholine release; autoinhibition;
D O I
10.1254/jjp.78.83
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Endomorphin-1 and -2, putative endogenous ligands for the mu-opioid receptor, inhibited acetylcholine (ACh) release evoked by electrical field stimulation (EFS) at 1 Hz, which partially activates muscarinic autoreceptors, but not at 10 Hz, which fully activates muscarinic autoreceptors, in longitudinal muscle with the myenteric plexus (LMMP) preparations of guinea pig ileum. After blockade of autoinhibition by atropine, the peptides also inhibited EFS-evoked ACh release at 10 Hz. The inhibitory effects on ACh release were abolished by the mu-opioid antagonist cyprodime. These results suggest that endomorphin-1 and -2 inhibit ACh release from LMMP preparations of guinea pig ileum and that the mechanism of the inhibition must have a component in common with muscarinic autoinhibition.
引用
收藏
页码:83 / 86
页数:4
相关论文
共 50 条