Nishiwaki H, Saitoh N, Nishio H, Takeuchi T, Hata F
Department of Veterinary Pharmacology, College of Agriculture, Osaka Prefecture University, Sakai, Japan.
Jpn J Pharmacol. 1998 Sep;78(1):83-6. doi: 10.1254/jjp.78.83.
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.
内吗啡肽-1和-2是μ-阿片受体的假定内源性配体,在豚鼠回肠的含肌间神经丛的纵行肌(LMMP)标本中,它们抑制1Hz电场刺激(EFS)诱发的乙酰胆碱(ACh)释放,1Hz的EFS可部分激活毒蕈碱型自身受体,但不抑制10Hz EFS诱发的ACh释放,10Hz的EFS可完全激活毒蕈碱型自身受体。用阿托品阻断自身抑制后,这些肽也抑制10Hz EFS诱发的ACh释放。μ-阿片拮抗剂环丙二甲基吗啡可消除对ACh释放的抑制作用。这些结果表明,内吗啡肽-1和-2抑制豚鼠回肠LMMP标本中ACh的释放,且这种抑制机制必定有与毒蕈碱型自身抑制相同的成分。