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不同促动力药物及一种新型肠动力药物对大鼠术后肠梗阻的影响。

Effect of different prokinetic agents and a novel enterokinetic agent on postoperative ileus in rats.

作者信息

De Winter B Y, Boeckxstaens G E, De Man J G, Moreels T G, Schuurkes J A, Peeters T L, Herman A G, Pelckmans P A

机构信息

Division of Gastroenterology and Pharmacology, Faculty of Medical and Pharmaceutical Sciences, University of Antwerp, Wilrijk, Belgium.

出版信息

Gut. 1999 Nov;45(5):713-8. doi: 10.1136/gut.45.5.713.

Abstract

BACKGROUND/AIM: The effects of different prokinetic agents, the motilide erythromycin and the substituted benzamides metoclopramide and cisapride, were investigated in a rat model of postoperative ileus. These effects were compared with that of granisetron, a 5-hydroxytryptamine (5-HT(3)) receptor antagonist, and a novel enterokinetic agent, prucalopride, a 5-HT(4) receptor agonist.

METHODS

Different degrees of inhibition of gastrointestinal transit, measured by the migration of Evans blue, were achieved by skin incision, laparotomy, or laparotomy plus mechanical stimulation of the gut.

RESULTS

Metoclopramide decreased the transit after laparotomy with or without mechanical stimulation, whereas cisapride increased it after all three operations. Granisetron had no effect on the transit after the three operations when given alone. Prucalopride tended to increase the transit after laparotomy with or without mechanical stimulation when given alone. However, statistical significance was only reached when prucalopride was combined with granisetron. Erythromycin, a motilin receptor agonist, did not improve postoperative ileus in the rat.

CONCLUSIONS

Cisapride, but not metoclopramide or erythromycin, is able to improve postoperative ileus in the rat. The results suggest that a combination of 5-HT(3) receptor antagonist and 5-HT(4) receptor agonist properties may be required to obtain a beneficial effect on surgery induced ileus in the rat. Furthermore, they indirectly indicate that stimulation of the excitatory mechanisms is not able to overcome the inhibitory influence of the neural reflex pathways activated during abdominal surgery.

摘要

背景/目的:在大鼠术后肠梗阻模型中研究了不同促动力剂、胃动素类药物红霉素以及取代苯甲酰胺类药物甲氧氯普胺和顺阿曲库铵的作用。将这些作用与5-羟色胺(5-HT(3))受体拮抗剂格拉司琼以及新型肠动力剂、5-HT(4)受体激动剂普芦卡必利的作用进行比较。

方法

通过皮肤切口、剖腹术或剖腹术加肠道机械刺激,利用伊文思蓝迁移来测定不同程度的胃肠运输抑制。

结果

甲氧氯普胺在有或无机械刺激的剖腹术后均降低了运输速度,而顺阿曲库铵在所有三种手术后均增加了运输速度。单独给予格拉司琼时,对三种手术后的运输速度均无影响。单独给予普芦卡必利时,在有或无机械刺激的剖腹术后倾向于增加运输速度。然而,仅在普芦卡必利与格拉司琼联合使用时才达到统计学显著性。胃动素受体激动剂红霉素并未改善大鼠术后肠梗阻。

结论

顺阿曲库铵而非甲氧氯普胺或红霉素能够改善大鼠术后肠梗阻。结果表明,可能需要5-HT(3)受体拮抗剂和5-HT(4)受体激动剂特性的联合才能对大鼠手术引起的肠梗阻产生有益作用。此外,它们间接表明,刺激兴奋性机制无法克服腹部手术期间激活的神经反射途径的抑制性影响。

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