Taylor D, Ho B T
Res Commun Chem Pathol Pharmacol. 1978 Jul;21(1):67-75.
Amphetamine and methylphenidate both inhibited the uptake of 3H-norepinephrine (NE) and 3H-dopamine (DA) although the activity (as measured by I50 and Ki values) of d-amphetamine was lower with respect to uptake of the two catecholamines in synaptosomes from thalamus-hypothalamus and and striatum. Cocaine was a much stonger inhibitor of 3H-5-hydroxytryptamine (5-HT) uptake in septum-caudate synaptosomes than amphetamine or methylphenidate. The I50 values were 70, 118 and 570 micron for cocaine, methylphenidate and d-amphetamine, respectively. The results of the present study suggested that a serotonergic system may be involved in the stimulant properties of cocaine. It may also explain certain differences in pharmacological activities between cocaine and the other two stimulants as described in the literature.
苯丙胺和哌醋甲酯均抑制3H-去甲肾上腺素(NE)和3H-多巴胺(DA)的摄取,尽管d-苯丙胺的活性(以I50和Ki值衡量)在丘脑-下丘脑和纹状体突触体中对两种儿茶酚胺摄取方面较低。可卡因对隔区-尾状核突触体中3H-5-羟色胺(5-HT)摄取的抑制作用比苯丙胺或哌醋甲酯强得多。可卡因、哌醋甲酯和d-苯丙胺的I50值分别为70、118和570微摩尔。本研究结果提示,5-羟色胺能系统可能参与可卡因的兴奋特性。这也可能解释文献中所描述的可卡因与其他两种兴奋剂在药理活性上的某些差异。