Itoh Z, Aizawa I, Nakamura T
Nihon Heikatsukin Gakkai Zasshi. 1980 Jun;16(2):99-107.
Effect of dopamine and its antagonists, domperidone and metoclopramide (MCP), on contractile activity of the lower esophageal sphincter (LES) and the stomach was studied in 5 healthy conscious dogs. Contractile activity was measured by means of chronically implanted force transducers. Contractile activity of the LES and the stomach was completely inhibited by an intravenous infusion of dopamine (10, 20 and 40 micrograms/kg-min) during the digestive and interdigestive state. Domperidone, when administered alone (0.5, 1.0 and 2.0 mg/kg), had no effect on contractile activity of the LES and the stomach during the both periods. Though deprived of any noticeable effect on the digestive contractions, MCP (0.25, 0.5 and 1.0 mg/kg) abolished the interdigestive contractions and produced characteristic contractions. Domperidone restored postprandial and interdigestive contractions to their initial stage before dopamine administration in a dose-related fashion. Dopamine-induced inhibition was antagonized by MCP during the digestive state, however, MCP had no effect on the interdigestive contractions that had been inhibited by dopamine. Since domperidone has no activity upon normal contractions of the gastrointestinal tract, it may be assumed that if domperidone alone has some influence upon gut motor activity or any improvement in clinical symptoms is seen after domperidone, a disorder of the dopaminergic system could be strongly suggested.
在5只清醒健康犬中研究了多巴胺及其拮抗剂多潘立酮和甲氧氯普胺(MCP)对食管下括约肌(LES)和胃收缩活动的影响。收缩活动通过长期植入的力传感器进行测量。在消化期和消化间期,静脉输注多巴胺(10、20和40微克/千克·分钟)可完全抑制LES和胃的收缩活动。单独给予多潘立酮(0.5、1.0和2.0毫克/千克)时,在这两个时期对LES和胃的收缩活动均无影响。尽管MCP(0.25、0.5和1.0毫克/千克)对消化期收缩无明显影响,但可消除消化间期收缩并产生特征性收缩。多潘立酮以剂量相关的方式使餐后和消化间期收缩恢复到多巴胺给药前的初始阶段。在消化期,MCP可拮抗多巴胺诱导的抑制作用,然而,MCP对已被多巴胺抑制的消化间期收缩无影响。由于多潘立酮对胃肠道正常收缩无作用,因此可以推测,如果单独使用多潘立酮对肠道运动活动有某种影响或在使用多潘立酮后临床症状有任何改善,则强烈提示多巴胺能系统存在紊乱。