Wilder-Smith C H, Ernst T, Gennoni M, Zeyen B, Halter F, Merki H S
Department of Medicine, University of Berne, Inselspital, Switzerland.
Dig Dis Sci. 1990 Aug;35(8):976-83. doi: 10.1007/BF01537246.
The acid-inhibitory action of H2-receptor antagonists was shown to decrease after one to two weeks of dosing in healthy volunteers. This tolerance was evaluated in three randomized, placebo-controlled trials with the H2-receptor antagonists famotidine, 40 mg given after the evening meal for 28 days; ranitidine, 300 mg four times a day for seven days followed by 300 mg at night until day 28; and ranitidine, 300 mg three times a day vs 300 mg at night for 14 days. Continuous 24-hr pH monitoring with glass electrodes was performed under fed conditions. The median 24-hr pH decreased from 3.2 on day 1 with famotidine 40 mg to 1.9 on day 28 (P less than 0.0012). After seven days of dosing with ranitidine 300 mg four times a day the median 24-hr pH dropped from 5.0 on day 1 to 3.0 on day 7 (P less than 0.001) and then to 2.2 with ranitidine 300 mg at night on day 28. With ranitidine 300 mg three times a day the median 24-hr pH fell from 4.3 on day 1 to 2.4 on day 14 (P less than 0.0005). With ranitidine 300 mg at night the respective pH values were 2.5 and 1.8 (P less than 0.003). Tolerance to H2-receptor antagonists given in a single evening dose was only evident during the night, whereas tolerance occurred throughout the day and night with the three- and four-times-a-day regimens. A large increase in the interindividual variability of pH response was seen during the nighttime.
在健康志愿者中,服用H2受体拮抗剂一至两周后,其胃酸抑制作用会减弱。在三项随机、安慰剂对照试验中评估了这种耐受性,使用的H2受体拮抗剂分别为法莫替丁(晚餐后服用40毫克,持续28天);雷尼替丁(每天四次,每次300毫克,服用七天,之后每晚服用300毫克直至第28天);以及雷尼替丁(每天三次,每次300毫克与每晚300毫克对比,服用14天)。在进食条件下,使用玻璃电极进行连续24小时的pH监测。服用40毫克法莫替丁时,24小时pH中位数从第1天的3.2降至第28天的1.9(P小于0.0012)。每天四次服用300毫克雷尼替丁七天后,24小时pH中位数从第1天的5.0降至第7天的3.0(P小于0.001),然后在第28天晚上服用300毫克雷尼替丁时降至2.2。每天三次服用300毫克雷尼替丁时,24小时pH中位数从第1天的4.3降至第14天的2.4(P小于0.0005)。每晚服用300毫克雷尼替丁时,相应的pH值分别为2.5和1.8(P小于0.003)。单次夜间服用H2受体拮抗剂的耐受性仅在夜间明显,而每日三次和四次给药方案则在白天和夜间均出现耐受性。夜间pH反应的个体间变异性大幅增加。