Yoshida N, Karasawa T, Kadokawa T
Department of Pharmacology, Dainippon Pharmaceutical Co., Ltd., Suita/Osaka, Japan.
Arch Int Pharmacodyn Ther. 1988 Sep-Oct;295:245-56.
Metoclopramide and ranitidine (10(-6)-10(-4) M) enhanced the electrical field stimulation-evoked contractions of isolated rat fundus and increased the gastric emptying in conscious rats. The enhancement of the fundus contractions by metoclopramide and ranitidine was abolished by atropine, but not by yohimbine, hexamethonium, propranolol or methysergide. The electrical field stimulation-evoked [3H]outflow from rat fundus strips, which has been preincubated with [3H]choline, was reduced by tetrodotoxin (10(-6) M) or in calcium-free medium, and potentiated by 4-amino-pyridine (3 X 10(-4) M), an acetylcholine (ACh)-releasing agent. Metoclopramide and ranitidine (10(-6)-10(-4) M) did not increase the [3H]outflow from the strips, in spite of causing a significant enhancement of their contractile response. However, both agents caused an increase in the ratio of [3H]acetylcholine/[3H]choline released into the superfusate during electrical field-stimulation. In rat fundus homogenates, metoclopramide and ranitidine showed a significant cholinesterase inhibition. These results seem to cast a doubt on the generally held ACh release hypothesis for the action mechanism of metoclopramide on one hand, and suggest, on the other hand, that cholinesterase inhibition contributes to some extent to the gastrokinetic effects of metoclopramide and ranitidine.
甲氧氯普胺和雷尼替丁(10⁻⁶ - 10⁻⁴ M)增强了电场刺激诱发的离体大鼠胃底收缩,并增加了清醒大鼠的胃排空。甲氧氯普胺和雷尼替丁对胃底收缩的增强作用被阿托品消除,但不受育亨宾、六甲铵、普萘洛尔或麦角新碱的影响。预先用[³H]胆碱孵育的大鼠胃底条带在电场刺激下诱发的[³H]流出量,在河豚毒素(10⁻⁶ M)存在下或无钙培养基中减少,并被乙酰胆碱(ACh)释放剂4-氨基吡啶(3×10⁻⁴ M)增强。尽管甲氧氯普胺和雷尼替丁(10⁻⁶ - 10⁻⁴ M)显著增强了胃底条带的收缩反应,但并未增加其[³H]流出量。然而,两种药物均导致电场刺激期间释放到灌流液中的[³H]乙酰胆碱/[³H]胆碱的比率增加。在大鼠胃底匀浆中,甲氧氯普胺和雷尼替丁表现出显著的胆碱酯酶抑制作用。这些结果一方面似乎对普遍认为的甲氧氯普胺作用机制的ACh释放假说提出了质疑,另一方面表明胆碱酯酶抑制在一定程度上有助于甲氧氯普胺和雷尼替丁的胃肠动力作用。