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EM574和西沙必利对正常犬及药物诱导性胃轻瘫犬胃收缩和排空活性的影响。

Effects of EM574 and cisapride on gastric contractile and emptying activity in normal and drug-induced gastroparesis in dogs.

作者信息

Tanaka T, Mizumoto A, Mochiki E, Suzuki H, Itoh Z, Omura S

机构信息

Gastrointestinal Research Laboratory, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Japan.

出版信息

J Pharmacol Exp Ther. 1998 Nov;287(2):712-9.

PMID:9808701
Abstract

EM574, an erythromycin derivative and potent motilin receptor agonist, is now undergoing clinical trials as a gastroprokinetic drug. The aim of this study was to compare the effect of EM574 with that of cisapride on gastric motility and emptying in normal and gastroparesis dogs. Six dogs were each implanted with two duodenal cannulas for infusion of phenolsulfonphthalein into the proximal duodenum and for aspiration of luminal samples from the distal duodenum. Both solid and liquid gastric emptying were determined by a novel freeze-drying method developed in our laboratory. A freeze-dried standard meal (100 g, 400 kcal) was given with 100 ml normal saline containing 15 g of polyethylene glycol as a liquid marker. Gastric muscle contractility was measured by means of a force transducer implanted on the gastric antrum. EM574 (3-30 microgram/kg) and cisapride (0.3-3.0 mg/kg) were administered intraduodenally at the start of feeding. Clonidine (3-30 microgram/kg) was injected subcutaneously 15 min before feeding to induce gastroparesis. EM574 and cisapride both enhanced gastric muscle contractility in a dose-dependent manner. EM574 (30 microgram/kg and 10 microgram/kg) significantly accelerated gastric emptying of solids and liquids, respectively. Cisapride (1 mg/kg) significantly accelerated solid gastric emptying, but 3.0 mg/kg significantly delayed liquid gastric emptying. Clonidine (10 and 30 microgram/kg) significantly delayed solid and liquid gastric emptying and reduced gastric muscle contractility. EM574, at a dose of 30 microgram/kg, completely restored solid and liquid gastric emptying and muscle contractility to the normal range in dogs with clonidine-induced gastroparesis. Cisapride (1 mg/kg) restored liquid gastric emptying in dogs with gastroparesis to the normal range and partially restored solid emptying. EM574 accelerated gastric muscle contractility and emptying of solids and liquids in normal dogs. The stimulating activity of EM574 on gastric muscle contractility and emptying was comparable to that of cisapride, but EM574 was as effective as cisapride in normalizing gastric muscle contractility and emptying in dogs with clonidine-induced gastroparesis.

摘要

EM574是一种红霉素衍生物,也是一种强效胃动素受体激动剂,目前正在作为一种胃肠促动力药物进行临床试验。本研究的目的是比较EM574与西沙必利对正常犬和胃轻瘫犬胃动力和排空的影响。六只犬每只均植入两根十二指肠插管,一根用于向十二指肠近端输注酚磺酞,另一根用于从十二指肠远端抽吸肠腔样本。固体和液体胃排空均通过我们实验室开发的一种新型冷冻干燥方法来测定。给予一份冷冻干燥的标准餐(100克,400千卡),同时给予100毫升含15克聚乙二醇的生理盐水作为液体标记物。通过植入胃窦的力传感器来测量胃肌收缩力。在喂食开始时经十二指肠给予EM574(3 - 30微克/千克)和西沙必利(0.3 - 3.0毫克/千克)。在喂食前15分钟皮下注射可乐定(3 - 30微克/千克)以诱导胃轻瘫。EM574和西沙必利均以剂量依赖性方式增强胃肌收缩力。EM574(30微克/千克和10微克/千克)分别显著加速了固体和液体的胃排空。西沙必利(1毫克/千克)显著加速了固体胃排空,但3.0毫克/千克显著延迟了液体胃排空。可乐定(10和30微克/千克)显著延迟了固体和液体胃排空并降低了胃肌收缩力。在可乐定诱导的胃轻瘫犬中,30微克/千克剂量的EM574完全将固体和液体胃排空以及肌肉收缩力恢复到正常范围。西沙必利(1毫克/千克)将胃轻瘫犬的液体胃排空恢复到正常范围,并部分恢复了固体排空。EM574加速了正常犬的胃肌收缩力以及固体和液体的排空。EM574对胃肌收缩力和排空的刺激活性与西沙必利相当,但在使可乐定诱导的胃轻瘫犬的胃肌收缩力和排空正常化方面,EM574与西沙必利效果相当。

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