Bertaccini G, Coruzzi G, Poli E
Pharmacol Res Commun. 1985 Mar;17(3):241-54. doi: 10.1016/0031-6989(85)90099-2.
Various histamine H2 receptor antagonists were tested for their possible effects on intestinal motility of the dog both "in vivo" and "in vitro". They were found to behave quite differently from one another: ranitidine exerted a small atropine-sensitive stimulatory effect by itself and strongly potentiated the stimulatory action of compounds which interfere with the cholinergic system thus confirming its cholinomimetic direct and/or indirect activities. Cimetidine and mifentidine were ineffective even at very high doses. Oxmetidine exerted an inhibitory effect independently of the kind of the stimulant agent and this suggested a direct effect on the smooth muscle. The different effects elicited by the above H2 antagonists indicate that their action on the intestinal motility is completely independent of the H2 blockade. This was furtherly confirmed by the lack of effect shown by the H2 receptor selective agonists, dimaprit and impromidine. The motor effects of ranitidine were, so far, the only ones which have been encountered, in different conditions, also in humans.
对多种组胺H2受体拮抗剂进行了测试,以观察它们在“体内”和“体外”对犬肠道运动的可能影响。发现它们彼此的表现差异很大:雷尼替丁本身具有轻微的对阿托品敏感的刺激作用,并强烈增强干扰胆碱能系统的化合物的刺激作用,从而证实了其拟胆碱直接和/或间接活性。西咪替丁和米芬替丁即使在非常高的剂量下也无效。奥美替丁无论刺激剂类型如何均发挥抑制作用,这表明其对平滑肌有直接作用。上述H2拮抗剂引起的不同作用表明它们对肠道运动的作用完全独立于H2阻断。H2受体选择性激动剂二甲普利和英普咪定无作用进一步证实了这一点。雷尼替丁的运动效应是迄今为止在不同条件下在人类中也观察到的唯一效应。