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丙谷胺和CR - 1409对豚鼠胆囊收缩素诱导的胆道压力抑制作用的体内比较。

In vivo comparison of inhibition with proglumide and CR-1409 of cholecystokinin-induced pressure in the biliary tract of the guinea pig.

作者信息

Poston G J, MacLellan D G, Hashimoto T, Upp J R, Townsend C M, Thompson J C

机构信息

Department of Surgery, University of Texas Medical Branch, Galveston 77550.

出版信息

Surg Gynecol Obstet. 1990 Mar;170(3):217-22.

PMID:2305348
Abstract

This study was done to compare the effects of two cholecystokinin antagonists, proglumide and CR-1409, on cholecystokinin-induced changes in intrabiliary pressure in vivo. We have substantially modified the constant infusion biliary manometry model, successfully used in large animals, to measure contractility of the gallbladder in guinea pigs. A silicone catheter for manometry was placed in the fundus of the gallbladder of an anesthetized guinea pig, and the biliary tree was constantly infused at 0.1 milliliter per minute with normal saline solution. The intraluminal pressure of the system was continuously recorded. The model was used to demonstrate a dose-response curve to bolus administration of exogenous cholecystokinin (0.01 to 1.0 nanomole per kilogram) and also to study the actions of proglumide, an antagonist to gastrin and cholecystokinin, and CR-1409, a newer, specific cholecystokinin antagonist, on cholecystokinin-induced contraction of the gallbladder of the guinea pig in vivo. Proglumide, at a dose of 5 millimoles per kilogram, completely abolished increases in intrabiliary pressure caused by cholecystokinin (0.5 nanomole per kilogram), whereas this effect was achieved by only 5 micromoles per kilogram of CR-1409. In both, there was full recovery from cholecystokinin antagonism within one hour. CR-1409 is one thousand times more potent than proglumide against cholecystokinin-induced changes in intrabiliary pressure in vivo and appears to be a useful pharmacologic reagent to study cholecystokinin-mediated components of physiologic contraction of the gallbladder.

摘要

本研究旨在比较两种胆囊收缩素拮抗剂丙谷胺和CR - 1409对胆囊收缩素诱导的体内胆管内压力变化的影响。我们对已成功应用于大型动物的恒速输注胆道测压模型进行了大幅改进,以测量豚鼠胆囊的收缩性。将用于测压的硅胶导管置于麻醉豚鼠的胆囊底部,以每分钟0.1毫升的速度向胆道系统持续输注生理盐水。持续记录系统的腔内压力。该模型用于展示对外源性胆囊收缩素(每千克0.01至1.0纳摩尔)推注给药的剂量反应曲线,还用于研究胃泌素和胆囊收缩素的拮抗剂丙谷胺以及一种更新的、特异性胆囊收缩素拮抗剂CR - 1409对胆囊收缩素诱导的豚鼠胆囊在体内收缩的作用。每千克5毫摩尔的丙谷胺完全消除了由每千克0.5纳摩尔胆囊收缩素引起的胆管内压力升高,而每千克仅5微摩尔的CR - 1409就能达到这种效果。在这两种情况下,胆囊收缩素拮抗作用在一小时内完全恢复。在对抗胆囊收缩素诱导的体内胆管内压力变化方面,CR - 1409的效力比丙谷胺强一千倍,似乎是研究胆囊收缩素介导的胆囊生理收缩成分的一种有用的药理试剂。

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