Bertaccini G, Poli E, Adami M, Coruzzi G
Agents Actions. 1983 Apr;13(2-3):157-62. doi: 10.1007/BF01967321.
Some new histamine H2-receptor antagonists were tested for their effects on gastrointestinal motility. Ranitidine was found to possess definite stimulatory effects which appeared to be connected with an interference with the cholinergic system and occurred, though in different degree, from the lower esophageal sphincter (LES) to the colon. Etintidine, on the contrary, showed a remarkable antimuscarinic effect on the LES of the rat and the guinea-pig. Cimetidine, SK&F 93479 and tiotidine were virtually ineffective whereas oxmetidine exerted a consistent inhibitory activity on both basal motility and on the contractions induced by a variety of stimulatory agents. This effect, which was completely independent of the autonomic nervous system appeared to be connected with an inhibition of the transport of calcium ions. All the above results suggest that the H2-antagonists so far available may not be absolutely selective for the H2-receptor but may be endowed with non-specific effects which could have an interest at least from a pharmacological viewpoint.
对一些新型组胺H2受体拮抗剂对胃肠动力的影响进行了测试。发现雷尼替丁具有明确的刺激作用,这似乎与对胆碱能系统的干扰有关,且从食管下括约肌(LES)到结肠均有不同程度的出现。相反,依替替丁对大鼠和豚鼠的LES表现出显著的抗毒蕈碱作用。西咪替丁、SK&F 93479和替奥替丁实际上无效,而奥美替丁对基础动力和由多种刺激剂诱导的收缩均有持续的抑制活性。这种完全独立于自主神经系统的作用似乎与钙离子转运的抑制有关。上述所有结果表明,目前可用的H2拮抗剂可能并非对H2受体绝对具有选择性,而是可能具有非特异性作用,至少从药理学角度来看可能会引起人们的兴趣。