Stables R, Daly M J, Humphray J M
Agents Actions. 1983 Apr;13(2-3):166-9. doi: 10.1007/BF01967323.
The antisecretory potency and duration of action of the new histamine H2-receptor antagonist AH 22216 have been compared with those of cimetidine, ranitidine and SK & F 93479 against histamine-induced gastric acid secretion in the conscious Heidenhain pouch dog. Ranitidine was 4-6 times more potent than cimetidine, with a similar duration of action. SK & F 93479 was approximately twice as potent as ranitidine and had a slightly longer duration of action. AH 22216 was most potent of the four H2-antagonists, some 20-30 times more active than cimetidine, and had an extremely prolonged duration of action.
在清醒的海登海因小胃犬中,将新型组胺H2受体拮抗剂AH 22216与西咪替丁、雷尼替丁和SK&F 93479针对组胺诱导的胃酸分泌的抗分泌效力和作用持续时间进行了比较。雷尼替丁的效力比西咪替丁强4至6倍,作用持续时间相似。SK&F 93479的效力约为雷尼替丁的两倍,作用持续时间略长。AH 22216是四种H2拮抗剂中效力最强的,比西咪替丁活性高约20至30倍,且作用持续时间极长。