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莫沙必利对豚鼠胃、回肠和结肠运动影响的研究。

Investigation into the effects of mosapride on motility of Guinea pig stomach, ileum, and colon.

作者信息

Ji Sang-Won, Park Hyo Jin, Cho Jun-Sik, Lim Jung-Hyun, Lee Sang-In

机构信息

Department of Internal Medicine, Yongdong Severance Hospital, Yonsei University College of Medicine, 146-92 Dogok-dong, Kangnam-gu, Seoul 135-720, Korea.

出版信息

Yonsei Med J. 2003 Aug 30;44(4):653-64. doi: 10.3349/ymj.2003.44.4.653.

Abstract

Mosapride citrate (Mosapride) is a new prokinetic agent that enhances the gastrointestinal (GI) motility by stimulation of 5-HT4 receptors. This agent stimulates acetylcholine release from enteric cholinergic neurons in the GI wall. It was reported in several studies that mosapride selectively enhanced the upper, but not lower, GI motor activity. However, in these studies other 5-HT4 receptor agonists exerted stimulating effects on the motility of the colon. Moreover, it is well known that the receptors of 5-HT4 are also located in the colon. The purpose of this study was to estimate the effect of mosapride on the motility of the stomach, ileum and colon in the guinea pig and to investigate whether or not mosapride influenced the colonic motility. Mosapride significantly increased the amplitude of the contraction waves in the guinea pig stomach by electrical stimulation. In addition, it significantly increased the number of peaks, the area under the curve and the propagation velocity of the peristaltic contraction of the guinea pig ileum in a concentration dependent fashion. Mosapride also significantly shortened the transit time of the guinea pig colon. Accordingly, we concluded that mosapride exerted prokinetic effect on the entire GI tract of the guinea pig. Based on the possibility of similar results in humans, we suggest the potential use of mosapride for lower GI motor disorders such as constipation and upper GI motor disorders such as gastroesophageal reflex disease or gastroparesis.

摘要

枸橼酸莫沙必利(莫沙必利)是一种新型促动力药物,通过刺激5-羟色胺4(5-HT4)受体增强胃肠(GI)动力。该药物刺激胃肠壁内肠胆碱能神经元释放乙酰胆碱。多项研究报道,莫沙必利选择性增强上消化道而非下消化道的运动活性。然而,在这些研究中,其他5-HT4受体激动剂对结肠动力有刺激作用。此外,众所周知,5-HT4受体也存在于结肠中。本研究的目的是评估莫沙必利对豚鼠胃、回肠和结肠动力的影响,并研究莫沙必利是否影响结肠动力。通过电刺激,莫沙必利显著增加了豚鼠胃收缩波的幅度。此外,它以浓度依赖的方式显著增加了豚鼠回肠蠕动收缩的峰值数量、曲线下面积和传播速度。莫沙必利还显著缩短了豚鼠结肠的传输时间。因此,我们得出结论,莫沙必利对豚鼠整个胃肠道发挥促动力作用。基于在人类中可能得到类似结果的可能性,我们建议莫沙必利可能用于治疗诸如便秘等下消化道运动障碍以及诸如胃食管反流病或胃轻瘫等上消化道运动障碍。

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