大鼠胃十二指肠碱性反应的测定

Koji Takeuchi, Hiromichi Niida, Koji Ueshima, Susumu Okabe
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引用次数: 9

摘要

我们建立了一种新的系统,通过pH变化和电位差(PD)来测量麻醉大鼠胃十二指肠HCO3−的反应。以0.7 mL/min的流速向胃或十二指肠近端灌注生理盐水(pH值为4.5),连续监测灌注液和PD的pH值,并通过反滴定灌注液和测量pH变化面积来测定HCO3−的输出。在胃的情况下,奥美拉唑(60 mg/kg, i.p)抑制胃酸分泌。静脉给药前列腺素(PGE2)、16,16 -二甲基PGE2、碳醇和YM-14673(促甲状腺激素释放激素(TRH)类似物)显著增加了这些组织中的pH和HCO3−的输出,而PD对这些药物的反应是十二指肠显著升高,胃显著降低。这些参数也响应生理刺激,如粘膜酸化。当将各种药剂引起的pH变化面积与反滴定测定的HCO3−净输出量进行对比时,发现这两个因素之间存在显著关系(r = 0.98)。这些结果表明,这种利用pH变化的系统可能有助于定量测定胃十二指肠黏膜的HCO3−反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of gastroduodenal alkaline responses in the rat

We set up a new system for measuring the gastroduodenal HCO3 responses using pH change and potential difference (PD) in the anesthetized rat. The stomach or the proximal duodenum was perfused at the flow rate of 0.7 mL/min with saline (pH 4.5), the pH of the perfusate and PD were continuously monitored, and HCO3 output was determined by back-titrating the perfusate and by measuring the area of pH change. In the case of the stomach, acid secretion was inhibited by omeprazole (60 mg/kg, i.p.). Output of both pH and HCO3 in these tissues was significantly increased by intravenous administration of prostaglandin (PGE2), 16, 16-dimethyl PGE2, carbachol, and YM-14673 (a thyrotropin-releasing hormone (TRH) analog), whereas the PD responded to these agents by a significant rise in the duodenum and decrease in the stomach. These parameters also responded to physiological stimulation such as mucosal acidification. When the area of pH change caused by various agents was plotted against the net amount of HCO3 output determined from back-titration, a significant relationship was found between these two factors (r = 0.98). These results indicate that this system using pH change may be useful for quantitative determination of HCO3 response in the gastroduodenal mucosa.

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