Baker R A, Saccone G T, Toouli J
Department of Surgery, Flinders University, Bedford Park, South Australia.
Dig Dis Sci. 1990 Jun;35(6):711-5. doi: 10.1007/BF01540172.
Cisapride has been shown in a number of recent studies to have prokinetic effects on the gastrointestinal tract. Studies of its action on the biliary tract have been limited. In this study we determined the effect of cisapride on sphincter of Oddi motility of the Australian brush tailed possum in vivo, and evaluated possible mechanisms for its effect. Cisapride produced a dose-dependent inhibition of sphincter of Oddi phasic contractions. The inhibitory effect was not blocked by atropine, phentolamine, propranolol, methysergide, or hexamethonium administration, or after cervical truncal vagotomy. Tetrodotoxin, however, abolished the sphincter response to cisapride. We conclude that cisapride has an inhibitory effect on the possum sphincter of Oddi. This inhibitory effect is mediated via nonadrenergic, noncholinergic inhibitory neurons and is similar to the inhibitory effect of cholecystokinin on the sphincter of Oddi.
西沙必利在最近的一些研究中已显示出对胃肠道有促动力作用。对其在胆道作用的研究有限。在本研究中,我们确定了西沙必利对澳大利亚帚尾袋貂体内奥迪括约肌运动的影响,并评估了其作用的可能机制。西沙必利对奥迪括约肌的相性收缩产生剂量依赖性抑制。给予阿托品、酚妥拉明、普萘洛尔、甲基麦角新碱或六甲铵后,或在颈胸段迷走神经切断术后,这种抑制作用并未被阻断。然而,河豚毒素消除了括约肌对西沙必利的反应。我们得出结论,西沙必利对袋貂奥迪括约肌有抑制作用。这种抑制作用是通过非肾上腺素能、非胆碱能抑制性神经元介导的,并且类似于胆囊收缩素对奥迪括约肌的抑制作用。