Bianchi Porro G, Lazzaroni M, Imbimbo B P, Sangaletti O, Ghirardosi C, Daniotti S
Gastrointestinal Unit, L. Sacco Hospital, Milan, Italy.
Eur J Clin Pharmacol. 1987;32(6):555-8. doi: 10.1007/BF02455987.
A study has been done in 10 duodenal ulcer patients of the effect of a single oral dose of 10 mg mifentidine on the acid and pepsin responses to sham feeding after 1 h 30 min and to pentagastrin after 4 h 15 min. The study followed a double-blind, randomized, placebo-controlled, cross-over design. Gastric juice was collected for 5 h 15 min after treatment. Blood was sampled for up to 3 h 30 min to determine the effects of mifentidine on serum gastrin. Mifentidine suppressed basal acid output by 77% and sham feeding-stimulated acid output by 71% vs the placebo values. Pentagastrin-stimulated acid output was inhibited by 30% throughout the pentagastrin infusion. The suppressant effect of the drug on pepsin output was not as marked as on acid secretion. Mifentidine did not affect the serum gastrin level during the basal and sham feeding phases. No untoward effects were reported by the patients. The results show that 10 mg mifentidine p.o. produced a large reduction in the acid output in response to sham feeding and pentagastrin without affecting the serum gastrin responses.
一项针对10名十二指肠溃疡患者的研究,观察了单次口服10毫克米芬替丁对1小时30分钟后假饲以及4小时15分钟后五肽胃泌素刺激引起的胃酸和胃蛋白酶反应的影响。该研究采用双盲、随机、安慰剂对照、交叉设计。治疗后收集5小时15分钟的胃液。采集血样长达3小时30分钟,以确定米芬替丁对血清胃泌素的影响。与安慰剂相比,米芬替丁使基础胃酸分泌量降低了77%,假饲刺激的胃酸分泌量降低了71%。在整个五肽胃泌素输注过程中,五肽胃泌素刺激的胃酸分泌量被抑制了30%。该药物对胃蛋白酶分泌的抑制作用不如对胃酸分泌的作用明显。在基础期和假饲期,米芬替丁不影响血清胃泌素水平。患者未报告有不良反应。结果表明,口服10毫克米芬替丁可使假饲和五肽胃泌素刺激引起的胃酸分泌大幅减少,而不影响血清胃泌素反应。