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在经肠胃外和腔内刺激后,对灌注大鼠胃制备物进行胃酸的胃内滴定。

Intragastric titration of acid in the perfused rat stomach preparation following parenteral and intraluminal stimulation.

作者信息

Halter F, Galeazzi R, Leuenberger J, Smith G M

出版信息

Eur J Pharmacol. 1977 Jun 1;43(3):247-52. doi: 10.1016/0014-2999(77)90024-3.

Abstract

The anaesthetised rat stomach preparation was adapted to assay intraluminally administered stimulants and inhibitors of acid secretion by continuously recirculating the perfusate (15 ml of 5% glucose) and measuring acid by the pH-stat technique. The responses obtained were linear. Continuous artificial neutralisation of the stomach to pH 5.5 as well as variation of the pH between 6.5 and 4.0 did not significantly alter the sensitivity of the preparation to intravenously administered human gastrin-heptadecapeptide I (HG I). Basal acid secretion however significantly declined following stepwise lowering of the intragastric pH between 6.5 and 4.0. The threshold values for responses to i.v. HG I were below 16 ng. 6 doses could be given per rat without tachyphylaxis. Acetylcholine, 1.3, 2.5, 5.2 and 10.4 micron g/ml in the perfusate, induced a dose-dependent linear (r=0.902) acid secretion. Metiamide 1.66 mg/ml in the perfusate, produced a parallel shift to the right of the HG I dose--response curve producing an agonist dose ratio of 3.66. The data suggest that intragastrically applied stimulants and inhibitors of acid secretion can be studied precisely in this relatively simple preparation.

摘要

将麻醉大鼠的胃制备物进行改良,通过使灌注液(15毫升5%葡萄糖)持续循环,并采用pH计技术测量胃酸,来测定腔内给予的胃酸分泌刺激剂和抑制剂。所获得的反应呈线性。将胃持续人工中和至pH 5.5以及将pH在6.5至4.0之间变化,均未显著改变该制备物对静脉注射人胃泌素十七肽I(HG I)的敏感性。然而,在胃内pH从6.5逐步降至4.0后,基础胃酸分泌显著下降。静脉注射HG I的反应阈值低于16纳克。每只大鼠可给予6剂而不产生快速耐受性。灌注液中乙酰胆碱浓度为1.3、2.5、5.2和10.4微克/毫升时,可诱导剂量依赖性线性(r = 0.902)胃酸分泌。灌注液中甲硫咪胺浓度为1.66毫克/毫升时,使HG I剂量 - 反应曲线平行右移,激动剂剂量比为3.66。数据表明,在这种相对简单的制备物中,可以精确研究胃内给予的胃酸分泌刺激剂和抑制剂。

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