Deakin M, Glenny H P, Ramage J K, Mills J G, Burland W L, Williams J G
Gut. 1987 May;28(5):566-72. doi: 10.1136/gut.28.5.566.
The effects of single doses of cimetidine 800, 1200, and 1600 mg, given at 2300 h or 800, and 1600 mg at 1800 h, have been studied in patients with duodenal ulcer disease in symptomatic remission, and compared with cimetidine 400 mg bd (0800 h and 2300 h) and ranitidine 300 mg (given at 1800 h) respectively. A dose related reduction in intragastric acidity was seen. All single nocturnal (2300 h) doses of cimetidine produced anacidity overnight. This was not achieved with dosing at 1800 h although the duration of inhibition of gastric acidity was longer. Inhibition of overnight acid and pepsin outputs were similarly dose and timing related, but inhibition of peptic activity was much less after dosing at 1800 h. Cimetidine 1600 mg and ranitidine 300 mg were similar in their effects.
对处于症状缓解期的十二指肠溃疡病患者,研究了分别于23:00服用800、1200和1600毫克西咪替丁单剂量,以及于18:00服用800和1600毫克西咪替丁单剂量的效果,并分别与每日两次(08:00和23:00)服用400毫克西咪替丁及于18:00服用300毫克雷尼替丁进行了比较。观察到胃内酸度呈剂量相关性降低。所有夜间(23:00)单剂量的西咪替丁均可使夜间无酸。虽然在18:00给药时胃酸抑制持续时间更长,但无法达到此效果。夜间胃酸和胃蛋白酶分泌的抑制同样与剂量和给药时间相关,但在18:00给药后对胃蛋白酶活性的抑制作用要小得多。1600毫克西咪替丁和300毫克雷尼替丁的效果相似。