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SC - 49518通过5 - 羟色胺4受体机制增强犬固体和液体食物的胃排空并刺激胃肠蠕动。

SC-49518 enhances gastric emptying of solid and liquid meals and stimulates gastrointestinal motility in dogs by a 5-hydroxytryptamine4 receptor mechanism.

作者信息

Gullikson G W, Virina M A, Loeffler R F, Yang D C, Goldstin B, Wang S X, Moummi C, Flynn D L, Zabrowski D L

机构信息

Gastrointestinal Diseases Research Department, G.D. Searle and Co., Skokie, Illinois.

出版信息

J Pharmacol Exp Ther. 1993 Jan;264(1):240-8.

PMID:8380862
Abstract

SC-49518 (N-[exo-(hexahydro-1H-pyrrolizine-1-yl)methyl]-2-methoxy-4- amino-5-chlorobenzamide HCl), a new benzamide gastrointestinal prokinetic compound, was investigated to determine its ability to stimulate gastrointestinal motility in vivo and whether these actions could be mediated by agonist activity at the putative 5-hydroxytryptamine (5-HT)4 receptor. In conscious fasted dogs with strain gauge transducers and myoelectrodes, SC-49518 disrupted gastric and small intestinal migrating motility complex cycling for more than 3.5 hr. It stimulated gastric antral contractile and intestinal myoelectric spike burst activities during the normally quiescent Phase I of the migrating motility complex at doses as low as 0.01 and 0.03 mg/kg i.v., respectively. In a canine model of gastroparesis, SC-49518 reversed completely alpha-2 adrenergically delayed gastric emptying of a solid meal with an ED50 value of 0.1 mg/kg intragastrically and partially reversed delayed emptying of a liquid meal. SC-49518, like 5-HT, cisapride and renzapride, acted as an agonist (EC50 = 6.6 +/- 1.1 x 10(-8) M) at the putative 5-HT4 receptor in rat esophageal tunica muscularis mucosae by relaxing carbachol-induced contractions. SC-49518 was a partial agonist at 5-HT4 receptors, but also blocked high affinity (5-HT4-mediated) responses to 5-HT (10(-9) M to 3 x 10(-7) M) in guinea pig ileum with a pA2 value of 8.39.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

SC - 49518(N - [外 - (六氢 - 1H - 吡咯嗪 - 1 - 基)甲基] - 2 - 甲氧基 - 4 - 氨基 - 5 - 氯苯甲酰胺盐酸盐)是一种新型苯甲酰胺类胃肠促动力化合物,对其在体内刺激胃肠蠕动的能力以及这些作用是否可由假定的5 - 羟色胺(5 - HT)4受体激动剂活性介导进行了研究。在装有应变片传感器和肌电电极的清醒禁食犬中,SC - 49518使胃和小肠移行性运动复合波循环中断超过3.5小时。在移行性运动复合波正常静止的I期,分别以低至0.01和0.03 mg/kg静脉注射剂量时,它刺激胃窦收缩和肠肌电尖峰爆发活动。在胃轻瘫犬模型中,SC - 49518完全逆转了α - 2肾上腺素能介导的固体餐胃排空延迟,胃内给药的ED50值为0.1 mg/kg,并部分逆转了液体餐排空延迟。与5 - HT、西沙必利和雷尼替丁一样,SC - 49518通过松弛卡巴胆碱诱导的收缩,在大鼠食管肌层黏膜中作为假定的5 - HT4受体的激动剂(EC50 = 6.6 +/- 1.1 x 10(-8)M)。SC - 49518是5 - HT4受体的部分激动剂,但在豚鼠回肠中也能阻断对5 - HT(10(-9)M至3 x 10(-7)M)的高亲和力(5 - HT4介导)反应,pA2值为8.39。(摘要截短至250字)

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