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兰索拉唑对健康志愿者胃内24小时pH值、进餐刺激的胃酸分泌以及血清和胃液中胃肠激素及酶浓度的影响。

Influence of lansoprazole on intragastric 24-hour pH, meal-stimulated gastric acid secretion, and concentrations of gastrointestinal hormones and enzymes in serum and gastric juice in healthy volunteers.

作者信息

Brunner G, Hell M, Hengels K J, Hennig U, Fuchs W

机构信息

Medizinische Hochschule Hannover, Krankenhaus Oststadt, Germany.

出版信息

Digestion. 1995;56(2):137-44. doi: 10.1159/000201233.

Abstract

Twelve healthy volunteers (6 females, 6 males) between 26 and 36 years of age were enroled in this double-blind, randomized, placebo-controlled, three-way cross-over study. The objective was to determine the influence of lansoprazole (Agopton, Takeda Pharma GmbH, Aachen), a novel proton pump inhibitor, in doses of 30 and 60 mg, on the intragastric pH, on meal-stimulated gastric acid secretion and on the concentration of gastrointestinal hormones and enzymes in serum and gastric juice. Active drug or placebo had to be taken as single daily morning doses on an empty stomach for 7 days. Each wash-out period between drug application periods was 2 weeks long. Lansoprazole induced a dose-related increase in intragastric pH as well as a relevant reduction of basal acid output, meal-stimulated acid output and meal-stimulated secretion volume. 60 mg lansoprazole was significantly superior to 30 mg in increasing intragastric pH. The basal secretion volume in volunteers on 30 and 60 mg lansoprazole were lower than in volunteers on placebo. Serum gastrin and serum pepsinogen concentrations increased in a dose-dependent manner. Pepsin output and pepsin activity in gastric juice were slightly decreased in volunteers on 30 mg lansoprazole and markedly suppressed in volunteers on 60 mg lansoprazole 2 h after meal stimulation. Intrinsic factor concentration increased in volunteers on lansoprazole with a clear dose relationship. The evaluation of laboratory data and reported nonserious adverse events proved the relative safety of this new antiulcer agent.

摘要

12名年龄在26至36岁之间的健康志愿者(6名女性,6名男性)参与了这项双盲、随机、安慰剂对照、三向交叉研究。目的是确定新型质子泵抑制剂兰索拉唑(商品名Agopton,武田制药有限公司,亚琛)30毫克和60毫克剂量对胃内pH值、进餐刺激的胃酸分泌以及血清和胃液中胃肠激素及酶浓度的影响。活性药物或安慰剂必须每天早晨空腹单剂量服用7天。每个用药周期之间的洗脱期为2周。兰索拉唑使胃内pH值呈剂量相关升高,同时基础酸分泌量、进餐刺激的酸分泌量和进餐刺激的分泌量显著降低。60毫克兰索拉唑在提高胃内pH值方面明显优于30毫克。服用30毫克和60毫克兰索拉唑的志愿者的基础分泌量低于服用安慰剂的志愿者。血清胃泌素和血清胃蛋白酶原浓度呈剂量依赖性增加。进餐刺激2小时后,服用30毫克兰索拉唑的志愿者胃液中的胃蛋白酶分泌量和胃蛋白酶活性略有下降,而服用60毫克兰索拉唑的志愿者则受到明显抑制。服用兰索拉唑的志愿者体内内因子浓度升高,且有明显的剂量关系。实验室数据评估和报告的非严重不良事件证明了这种新型抗溃疡药物的相对安全性。

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