Bertaccini G, Coruzzi G, Vizi E S
Int J Tissue React. 1983;5(3):257-62.
Some new H2-receptor antagonists were tested for their motor effects on the rat lower oesophageal sphincter, on the guinea pig ileum and on the guinea pig gall bladder. Two of these compounds, SKF93479 and DA4577, were found to be virtually inactive despite the fact that they are the most potent antagonists of the H2-receptors so far described. Ranitidine possessed a stimulatory effect on all the preparations examined and its mechanism of action was shown to involve the cholinergic system. Conversely oxmetidine exerted an inhibitory effect on the contractions produced by a variety of spasmogenic compounds. All of these observations, together with other data from our laboratory, seem to suggest that H2-receptors do not play an important role in the regulation of the motility of the digestive system. Moreover our data emphasize the fact that the motor effects of the H2-antagonists are connected with single molecules rather than with the entire class, and therefore represent side-effects of these compounds independent of the H2-receptor blockade.
对一些新型H2受体拮抗剂进行了测试,观察它们对大鼠下食管括约肌、豚鼠回肠和豚鼠胆囊的运动效应。尽管SKF93479和DA4577这两种化合物是迄今为止所描述的最有效的H2受体拮抗剂,但发现它们实际上没有活性。雷尼替丁对所有检测的标本都有刺激作用,其作用机制表明涉及胆碱能系统。相反,奥美替丁对多种致痉化合物所引起的收缩有抑制作用。所有这些观察结果,连同我们实验室的其他数据,似乎表明H2受体在消化系统运动调节中不发挥重要作用。此外,我们的数据强调了这样一个事实,即H2拮抗剂的运动效应与单个分子有关,而不是与整个类别有关,因此代表了这些化合物独立于H2受体阻断作用的副作用。