Fozard J R, Mobarok ALI A T
Eur J Pharmacol. 1978 May 1;49(1):109-12. doi: 10.1016/0014-2999(78)90228-5.
Metoclopramide (0.13, 0.51, 2.0 and 8.1 X 10(-6) M) caused parallel, rightward, shifts in the dose response curves to 5-HT on the isolated rabbit heart. A significant straight line relationship was found between log (5-HT dr--1) and log [metoclopramide] (molar) with a slope of 1.08 +/- 0.13 and giving a pA2 value of 7.20. Metoclopramide did not significantly alter responses to noradrenaline and was 575 times less effective as an inhibitor of DMPP than of 5-HT. The results indicate that metoclopramide is a potent, surmountable and selective antagonist of tryptamine receptors on rabbit cardiac sympathetic nerves.
甲氧氯普胺(0.13、0.51、2.0和8.1×10⁻⁶ M)使离体兔心脏上5-羟色胺(5-HT)的剂量反应曲线平行右移。在log(5-HT dr⁻¹)与log [甲氧氯普胺](摩尔浓度)之间发现显著的直线关系,斜率为1.08±0.13,pA2值为7.20。甲氧氯普胺对去甲肾上腺素的反应无显著影响,作为二甲基苯基哌嗪(DMPP)抑制剂的效力比对5-HT的效力低575倍。结果表明,甲氧氯普胺是兔心脏交感神经上色胺受体的强效、可克服且选择性的拮抗剂。