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可卡因及其某些代谢物和类似物的神经元内多巴胺能作用。

Intraneuronal dopaminergic action of cocaine and some of its metabolites and analogs.

作者信息

Bagchi S P, Reilly M A

出版信息

Neuropharmacology. 1983 Nov;22(11):1289-95. doi: 10.1016/0028-3908(83)90202-2.

Abstract

The present study investigated the actions of cocaine and some of its metabolites and analogs upon the synaptosomal (P2) synthesis and release of dopamine appearing from [14C]phenylalanine. Also examined was the influence of reserpine upon these actions of cocaine. The P2 preparations from the rat caudate nucleus were incubated with the drugs for [14C]phenylalanine and, after filtration, the particulates and medium fractions were analyzed for [14C]dopamine and [14C]phenylalanine. Labelled dopamine in the medium was taken as a measure of its release by any addition of drug. Cocaine, norcocaine and the synthetic cocaine analogs WIN 35428 and WIN 35-065(2) each stimulated both the total (medium plus particulates) formation and the release of dopamine, while benzoylecgonine and ecgonine were without effect. Reserpine inhibited the synthesis and enhanced the release of dopamine. An addition of reserpine blocked the stimulating effect of cocaine, norcocaine, WIN 35428 and WIN 35-065(2) on synthesis and furthermore, these drugs had, in the same experiments, inhibitory effects on the synthesis, additive to the reserpine-induced inhibition. Benzoylecgonine and ecgonine were only weakly inhibitory in the presence of reserpine. Stimulation, rather than additive inhibition, by cocaine was observed in the presence of exogenous dopamine, and amphetamine increased the synthesis in the presence of either reserpine or added dopamine. Pretreatment of rats with reserpine also blocked the stimulation of synthesis by cocaine and WIN 35428. The uptake of labelled substrate was not affected by addition of drug, or by the pretreatment.

摘要

本研究调查了可卡因及其一些代谢产物和类似物对突触体(P2)从[14C]苯丙氨酸合成和释放多巴胺的作用。同时还研究了利血平对可卡因这些作用的影响。将来自大鼠尾状核的P2制剂与药物一起孵育[14C]苯丙氨酸,过滤后,分析颗粒部分和培养基部分中的[14C]多巴胺和[14C]苯丙氨酸。培养基中标记的多巴胺被用作药物添加后其释放量的指标。可卡因、去甲可卡因以及合成可卡因类似物WIN 35428和WIN 35 - 065(2)均能刺激多巴胺的总合成(培养基加颗粒部分)和释放,而苯甲酰芽子碱和芽子碱则无此作用。利血平抑制多巴胺的合成并增强其释放。添加利血平可阻断可卡因、去甲可卡因、WIN 35428和WIN 35 - 065(2)对合成的刺激作用,此外,在相同实验中,这些药物对合成具有抑制作用,且与利血平诱导的抑制作用相加。在利血平存在的情况下,苯甲酰芽子碱和芽子碱的抑制作用较弱。在外源性多巴胺存在时观察到可卡因的刺激作用而非相加抑制作用,并且苯丙胺在利血平或添加多巴胺存在时会增加合成。用利血平预处理大鼠也可阻断可卡因和WIN 35428对合成的刺激作用。添加药物或进行预处理均不影响标记底物的摄取。

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