Tayo F M
Arch Int Pharmacodyn Ther. 1979 Oct;241(2):190-6.
Pimozide (5--10 ng/ml), haloperidol (0.5--5 ng/ml) and yohimbine (2--5 ng/ml) selectively potentiated dopamine-induced and methoxamine-induced contractions of the rat vas deferens. The concentration-response curves were significantly shifted to the left and the maximal responses were significantly increased. Responses of the vas deferens to noradrenaline were not so influenced. Concentrations of the antagonists in excess of 50 ng/ml produced concentrations-related parallel shifts of dopamine concentration-response curve to the right. These antagonists behaved in a similar manner towards methoxamine, a directly acting sympathomimetic amine which has a low affinity for neuronal uptake, suggesting that the mechanism of this potentiation may be independent of neuronal uptake inhibition.
匹莫齐特(5 - 10纳克/毫升)、氟哌啶醇(0.5 - 5纳克/毫升)和育亨宾(2 - 5纳克/毫升)可选择性增强多巴胺诱导和甲氧明诱导的大鼠输精管收缩。浓度-反应曲线显著左移,最大反应显著增加。输精管对去甲肾上腺素的反应未受如此影响。拮抗剂浓度超过50纳克/毫升时,多巴胺浓度-反应曲线会出现与浓度相关的平行右移。这些拮抗剂对甲氧明(一种对神经元摄取亲和力低的直接作用拟交感胺)的作用方式相似,这表明这种增强作用的机制可能与抑制神经元摄取无关。