Iwamoto Y, Nakamura R, Akanuma Y
Gastroenterol Jpn. 1984 Feb;19(1):53-8. doi: 10.1007/BF02774646.
The effect of proglumide on cholecystokinin (CCK)-stimulated amylase release was studied in vitro and in vivo in dispersed acini from mouse pancreas. In an in vitro study, proglumide at concentrations between 0.3-10 mM inhibited CCK-stimulated amylase release dose-dependently, while proglumide did not influence the basal amylase release at concentrations between 0-3 mM. Dose-response curves to CCK for amylase release shifted to the right with increase in proglumide concentration. This inhibition by proglumide was reversible. In addition, the effect of proglumide was selective for CCK and its related peptide, and this drug did not inhibit other secretagogues such as carbachol or gastrin releasing peptide in mouse acini. In contrast to its inhibitory effect in vitro, in vivo administration of proglumide (500 mg/kg/day, i.p., for 5 days) to mice did not cause the rightward shift of the dose-response curve to CCK for amylase release from dispersed acini.
在体外和体内对小鼠胰腺分散腺泡进行了研究,以探讨丙谷胺对胆囊收缩素(CCK)刺激的淀粉酶释放的影响。在一项体外研究中,浓度为0.3 - 10 mM的丙谷胺剂量依赖性地抑制CCK刺激的淀粉酶释放,而浓度在0 - 3 mM之间的丙谷胺对基础淀粉酶释放无影响。随着丙谷胺浓度增加,淀粉酶释放对CCK的剂量反应曲线向右移动。丙谷胺的这种抑制作用是可逆的。此外,丙谷胺对CCK及其相关肽具有选择性作用,该药物不抑制小鼠腺泡中的其他促分泌剂,如卡巴胆碱或胃泌素释放肽。与其在体外的抑制作用相反,对小鼠体内给予丙谷胺(500 mg/kg/天,腹腔注射,共5天)并未导致分散腺泡淀粉酶释放对CCK的剂量反应曲线右移。