Lanzon-Miller S, Pounder R E, Chronos N A, Raymond F, Hamilton M R, Dalgleish D
Academic Department of Medicine, Royal Free Hospital School of Medicine, London.
Gut. 1988 Oct;29(10):1364-9. doi: 10.1136/gut.29.10.1364.
Nine healthy volunteers were studied on the seventh day of dosing at 21:00 h with nizatidine 150 mg (N 150), nizatidine 300 mg (N 300), ranitidine 300 mg (R 300), or placebo, given in a predetermined random order. The double-blind 24 hour studies, using the Royal Free Hospital standard protocol, simultaneously measured intragastric acidity and plasma gastrin concentration. Compared with placebo, subjects responded to dosing with each H2-antagonist by a significant decrease of 24 hour intragastric acidity (N 150-45%; N 300-49% R 300-56%; p less than 0.01) and a significant rise of plasma gastrin concentration (N 150 + 20%; N 300 + 27%; R 300 + 58%; p less than 0.01). All three drug regimens caused similar significant decreases of nocturnal acidity (N 150-72%; N 300-79%; R 300-85%; p less than 0.01) and increases of nocturnal plasma gastrin concentration (N 150 + 41%; N300 + 52%; R 300 + 80%; p less than 0.01). Dosing with ranitidine 300 mg at 21:00 h also caused a simultaneous significant decrease of morning acidity (-32%; p less than 0.05) with a significant increase of plasma gastrin concentration (+36%; p less than 0.05), but the antisecretory effects of nizatidine 150 or 300 mg at 21:00 h were only observed during the night, with no effect during the morning. No drug regimen had any effect on acidity or plasma gastrin in the afternoon or early evening.
9名健康志愿者于给药第7天21:00接受研究,分别给予150毫克尼扎替丁(N 150)、300毫克尼扎替丁(N 300)、300毫克雷尼替丁(R 300)或安慰剂,给药顺序预先随机确定。采用皇家自由医院标准方案进行的双盲24小时研究,同时测量胃内酸度和血浆胃泌素浓度。与安慰剂相比,每种H2拮抗剂给药后,受试者24小时胃内酸度显著降低(N 150 - 45%;N 300 - 49%;R 300 - 56%;p < 0.01),血浆胃泌素浓度显著升高(N 150 + 20%;N 300 + 27%;R 300 + 58%;p < 0.01)。所有三种药物方案均导致夜间酸度显著降低(N 150 - 72%;N 300 - 79%;R 300 - 85%;p < 0.01),夜间血浆胃泌素浓度升高(N 150 + 41%;N300 + 52%;R 300 + 80%;p < 0.01)。21:00给予300毫克雷尼替丁也导致早晨酸度同时显著降低(-32%;p < 0.05),血浆胃泌素浓度显著升高(+36%;p < 0.05),但21:00给予150毫克或300毫克尼扎替丁的抑酸作用仅在夜间观察到,早晨无作用。没有任何药物方案对下午或傍晚的酸度或血浆胃泌素产生影响。