Silvestrini B, Palmery M, Basta F, Valeri P
Institute of Pharmacology and Pharmacognosy, University of Rome La Sapienza, Italy.
J Neural Transm Gen Sect. 1991;86(1):51-9. doi: 10.1007/BF01250375.
Amphetamine increased the response of rabbit aortic strips to adrenaline, dopamine and serotonin at consistently lower doses than those exerting a direct contracting effect. The amphetamine-facilitated contraction had the same shape as that produced by biogenic amines alone, whereas the contraction produced by amphetamine alone was more delayed and flatter. Serotonin and dopamine facilitated each other, but less markedly and with a narrower interval between facilitating and contracting doses than amphetamine. Pargyline exerted no facilitating effect on biogenic amines. Phentolamine and prazosin inhibited the direct response to adrenaline, dopamine and amphetamine, and the amphetamine-facilitated response to adrenaline and dopamine; they were inactive against serotonin alone and combined with a facilitating dose of amphetamine or dopamine. Cyproheptadine inhibited the direct response to serotonin and amphetamine, and the amphetamine-facilitated response to serotonin; it was inactive against dopamine and adrenaline both alone and combined with a facilitating dose of amphetamine or serotonin.
苯丙胺以始终低于产生直接收缩作用的剂量增强了兔主动脉条对肾上腺素、多巴胺和5-羟色胺的反应。苯丙胺促进的收缩与仅由生物胺产生的收缩形状相同,而仅由苯丙胺产生的收缩更延迟且更平缓。5-羟色胺和多巴胺相互促进,但不如苯丙胺明显,且促进和收缩剂量之间的间隔更窄。帕吉林对生物胺没有促进作用。酚妥拉明和哌唑嗪抑制对肾上腺素、多巴胺和苯丙胺的直接反应,以及苯丙胺促进的对肾上腺素和多巴胺的反应;它们单独对5-羟色胺无活性,与促进剂量的苯丙胺或多巴胺联合使用时也无活性。赛庚啶抑制对5-羟色胺和苯丙胺的直接反应,以及苯丙胺促进的对5-羟色胺的反应;它单独对多巴胺和肾上腺素无活性,与促进剂量的苯丙胺或5-羟色胺联合使用时也无活性。