Couturier D, Chaussade S, Grandjouan S
Service d'Hépato-Gastro-Entérologie, Hôpital Cochin, Paris.
Presse Med. 1989 Feb 15;18(6):303-7.
Trimebutine maleate induces a specific motor response in the human proximal small bowel: except for the few minutes lapse following the occurrence of a spontaneous phase 3, an intravenous injection of 100 mg trimebutine systematically produces, in fed or fasted state, a systemic propagated activity analogous to the spontaneous phase 3 of the migrating motor complex. In lower doses, this effect is not observed. The intraduodenal administration of a high dose (600 mg) induces a similar response to that observed after intravenous injection. Trimebutine possibly acts as a stimulator of peripheral receptors of the enkephalinergic nervous system. Theoretically, these results may result in recommending the therapeutic use of trimebutine in intestinal motility disorders where disappearance or depletion of phase 3 are observed. However, information is still lacking about the relationship between therapeutic activity and the effects on intestinal motility in pathological states.
除了自发的第3相出现后的几分钟间隔外,静脉注射100mg曲美布汀在进食或禁食状态下均会系统性地产生一种类似于移行运动复合波自发第3相的全身性传播活动。在较低剂量下,未观察到这种效应。十二指肠内给予高剂量(600mg)会诱导出与静脉注射后观察到的类似反应。曲美布汀可能作为脑啡肽能神经系统外周受体的刺激剂。从理论上讲,这些结果可能会促使推荐在观察到第3相消失或耗竭的肠道动力障碍中使用曲美布汀进行治疗。然而,关于治疗活性与病理状态下对肠道动力影响之间的关系仍缺乏相关信息。