Hatanaka S, Kawarabayashi K, Iseri M, Tsubokura K, Furuhama K, Nijima A
Exploratory Research Laboratories III, Daiichi Pharmaceutical Co. Ltd, Tokyo, Japan.
Neurogastroenterol Motil. 1996 Sep;8(3):227-33. doi: 10.1111/j.1365-2982.1996.tb00261.x.
We compared the main pharmacological effect of DQ-2511 (3-[[[2-(3,4-dimethoxyphenyl)- ethyl]carbamoyl]methyl]amino-N-methylbenzamide), a novel gastroprokinetic agent, with that of cisapride. Single oral administration of DQ-2511 (3-10 mg kg-1) caused similar significant improvements to delays in gastric emptying of semi-solid meals evoked by cholecystokinin-octapeptide (CCK8: 5 micrograms kg-1, i.v.) in monkeys, to that with cisapride (3 mg kg-1). A 2-week oral treatment of unilaterally vagotomized rats with DQ-2511 (1-10 mg kg-1) lessened delays in gastric emptying, whereas cisapride (0.3-10 mg kg-1) had no effect under the same experimental protocols. In anesthetized rats, bolus intravenous injection of either compound (60 micrograms kg-1) enhanced gastric motility determined by means of strain gauge force transducers. Electrophysiological investigations revealed that bolus injection of DQ-2511 (6-60 micrograms kg-1) depressed the afferent discharge rate of the ventral gastric branch of the vagus nerve, while cisapride showed no effect. These results suggest that the mechanism of ameliorative action of DQ-2511 on delayed gastric emptying may differ from that of cisapride.
我们将新型促胃动力药DQ-2511(3-[[[2-(3,4-二甲氧基苯基)-乙基]氨基甲酰基]甲基]氨基-N-甲基苯甲酰胺)的主要药理作用与西沙必利进行了比较。在猴子中,单次口服DQ-2511(3-10毫克/千克)对由八肽胆囊收缩素(CCK8:5微克/千克,静脉注射)诱发的半固体食物胃排空延迟产生的改善作用与西沙必利(3毫克/千克)相似。用DQ-2511(1-10毫克/千克)对单侧迷走神经切断的大鼠进行为期2周的口服治疗,可减轻胃排空延迟,而在相同实验方案下,西沙必利(0.3-10毫克/千克)则无此作用。在麻醉大鼠中,静脉推注任一化合物(60微克/千克)均可通过应变片式力传感器测定增强胃动力。电生理研究表明,推注DQ-2511(6-60微克/千克)可降低迷走神经腹侧胃支的传入放电率,而西沙必利则无此作用。这些结果表明,DQ-2511改善胃排空延迟的作用机制可能与西沙必利不同。