Sato F, Sekiguchi M, Marui S, Inatomi N, Shino A, Itoh Z, Omura S
Pharmaceutical Research Laboratories III, Takeda Chemical Industries, Ltd., Osaka, Japan.
Eur J Pharmacol. 1997 Mar 12;322(1):63-71. doi: 10.1016/s0014-2999(96)00983-1.
This study was performed to examine whether an erythromycin derivative, de(N-methyl)-N-isopropyl-8,9-anhydroerythromycin A 6,9-hemiacetal (EM574) is a motilin receptor agonist in the rabbit gastrointestinal tract. EM574 and porcine motilin induced contractions in segments of isolated rabbit intestine with pEC50 values of 8.26 +/- 0.04 and 8.69 +/- 0.07, respectively, but not in rat or guinea pig preparations. The sensitivity and efficacy of the response to both compounds in rabbits decreased aborally and was insensitive to pretreatment with atropine or tetrodotoxin, but was markedly suppressed under Ca(2+)-free conditions. EM574 and porcine motilin specifically displaced [125I-Tyr23]canine motilin bound to gastric antral smooth muscle homogenates with plC50 values of 8.21 +/- 0.13 and 9.20 +/- 0.11, respectively. The pEC50 value for the contractile response and plC50 value for the receptor binding for motilin, EM574, erythromycin A and three other derivatives correlated well (r = 0.94, P < 0.01). Tissue section autoradiography in the antrum revealed that specific labeled motilin binding sites were localized in the circular muscle layer and myenteric plexus, and could be reduced in the presence of an excess of EM574. These results indicate that EM574 is a potent motilin receptor agonist in the rabbit gastrointestinal tract.
本研究旨在检测一种红霉素衍生物,去(N-甲基)-N-异丙基-8,9-脱水红霉素A 6,9-半缩醛(EM574)在兔胃肠道中是否为胃动素受体激动剂。EM574和猪胃动素均可引起离体兔肠段收缩,其pEC50值分别为8.26±0.04和8.69±0.07,但对大鼠或豚鼠制剂无此作用。兔对这两种化合物反应的敏感性和效能沿口向肛向降低,且对阿托品或河豚毒素预处理不敏感,但在无Ca(2+)条件下明显受到抑制。EM574和猪胃动素能特异性地置换与胃窦平滑肌匀浆结合的[125I-Tyr23]犬胃动素,其plC50值分别为8.21±0.13和9.20±0.11。胃动素、EM574、红霉素A及其他三种衍生物的收缩反应pEC50值与受体结合plC50值相关性良好(r = 0.94,P < 0.01)。胃窦组织切片放射自显影显示,特异性标记的胃动素结合位点定位于环行肌层和肌间神经丛,且在过量EM574存在时可减少。这些结果表明,EM574是兔胃肠道中一种有效的胃动素受体激动剂。