Kojima S
Department of Pharmacology, Dokkyo University School of Medicine, Mibu, Japan.
Eur J Pharmacol. 1999 Jun 11;374(1):113-5. doi: 10.1016/s0014-2999(99)00336-2.
The present study was designed to determine the influence of KW-5092 ((1-[2-[[[5-(piperidinomethyl)-2-furanyl]methyl]amino]ethyl]-2- imidazolidinylidene) propanedinitrile fumarate), a novel gastroprokinetic agent on intraluminal serotonin (5-hydroxytryptamine, 5-HT) release which reflects the release of 5-HT from enterochromaffin cells, using the luminally perfused isolated guinea-pig proximal colon in vitro. 5-HT was determined by high-performance liquid chromatography with electrochemical detection. KW-5092 (1-10 microM) concentration-dependently caused an increase in the luminal 5-HT outflow. In the presence of atropine (0.2 microM) or tetrodotoxin (0.3 microM), the stimulatory action of KW-5092 (10 microM) was inhibited by 94% and 74%, respectively. These results suggest that KW-5092 stimulates intraluminal 5-HT release from luminally perfused proximal colon of the guinea-pig via the stimulation of cholinergic neurons. Because 5-HT is recognized as an important messenger substance in the control of intestinal motility, this stimulatory effect could be considered as an indirect action of KW-5092 that may contribute to its prokinetic effects.
本研究旨在利用体外经腔内灌注的豚鼠离体近端结肠,确定新型促胃肠动力药KW-5092(富马酸(1-[2-[[[5-(哌啶甲基)-2-呋喃基]甲基]氨基]乙基]-2-咪唑烷亚基)丙二腈)对腔内5-羟色胺(5-羟色胺,5-HT)释放的影响,5-HT释放反映了肠嗜铬细胞中5-HT的释放。采用高效液相色谱-电化学检测法测定5-HT。KW-5092(1-10微摩尔)浓度依赖性地导致腔内5-HT流出增加。在阿托品(0.2微摩尔)或河豚毒素(0.3微摩尔)存在的情况下,KW-5092(10微摩尔)的刺激作用分别被抑制94%和74%。这些结果表明,KW-5092通过刺激胆碱能神经元,刺激豚鼠经腔内灌注的近端结肠释放腔内5-HT。由于5-HT被认为是控制肠道运动的重要信使物质,这种刺激作用可被视为KW-5092的间接作用,可能有助于其促动力作用。