Ozaki Ken-ichi, Yogo Kenji, Sudo Hirokazu, Onoma Mitsu, Kamei Kenshi, Akima Michitaka, Koga Hiroshi, Itoh Zen, Omura Satoshi, Takanashi Hisanori
Fuji-Gotemba Research Laboratories, Chugai Pharmaceutical Co. Ltd., Shizuoka, Japan.
Pharmacology. 2007;79(4):223-35. doi: 10.1159/000101537. Epub 2007 Apr 5.
The effects of mitemcinal (GM-611) on the gastrointestinal contractile activity were investigated using chronically implanted force transducers in conscious dogs and were compared with the effects of porcine motilin (pMTL), EM-523 and EM-574. In the interdigestive state, intravenous and oral administration of mitemcinal, EM-523 and EM-574 induced the gastrointestinal contractile activity in a manner similar to pMTL. The contractile activity caused by mitemcinal was suppressed by continuous intravenous infusion of a motilin receptor antagonist. In the digestive state, intravenous and oral administration of mitemcinal, EM-523 and EM-574 also stimulated the gastrointestinal contractile activity. Mitemcinal, EM-523 and EM-574 given intravenously increased the gastric contractile activity in a similar dose range; however, mitemcinal was approximately 10 times more potent than EM-523 and EM-574 when administered orally in the digestive state. These results indicate that the mitemcinal-induced gastrointestinal contractile activity operates via motilin receptors and possesses a higher activity than EM-523 and EM-574 when administered orally in conscious dogs in the digestive state. Mitemcinal may therefore be useful in the treatment of several gastrointestinal disorders involving dysmotility, such as gastroparesis and functional dyspepsia, even when administered orally.
使用慢性植入的力传感器在清醒犬中研究了米替卡宁(GM - 611)对胃肠收缩活动的影响,并与猪胃动素(pMTL)、EM - 523和EM - 574的作用进行了比较。在消化间期,静脉内和口服给予米替卡宁、EM - 523和EM - 574均以类似于pMTL的方式诱导胃肠收缩活动。米替卡宁引起的收缩活动被持续静脉输注胃动素受体拮抗剂所抑制。在消化期,静脉内和口服给予米替卡宁、EM - 523和EM - 574也刺激胃肠收缩活动。静脉内给予米替卡宁、EM - 523和EM - 574在相似剂量范围内增加胃收缩活动;然而,在消化期口服给药时,米替卡宁的效力比EM - 523和EM - 574约强10倍。这些结果表明,米替卡宁诱导的胃肠收缩活动通过胃动素受体起作用,并且在清醒犬消化期口服给药时比EM - 523和EM - 574具有更高的活性。因此,即使口服给药,米替卡宁也可能对治疗几种涉及运动障碍的胃肠疾病有用,如胃轻瘫和功能性消化不良。