Golko D S, Paton D M
Can J Physiol Pharmacol. 1976 Apr;54(2):93-100. doi: 10.1139/y76-016.
The characteristics of uptake of (not equal to)-(beta-14C)ephedrine were studied in isolated rabbit atria. Ephedrine was rapidly accumulated against the concentration gradient. From 5 X 10-7 to 10-2 M, uptake occurred at a uniform initial rate. Uptake was slightly inhibited by high concentrations of ouabain, cocaine, desipramine, lidocaine and phenethylamines, and by a reduction in the external Na+ concentration. Uptake was not, however, reduced by omission of K+ from the medium, by metabolic inhibitors or by a variety of drugs known to inhibit the extraneuronal uptake and binding of noradrenaline. Pretreatment of animals with 6-hydroxydopamine very significantly reduced the uptake of (not equal to)-(3H)metaraminol, but did not alter the uptake of ephedrine. It was concluded that the uptake of ephedrine in rabbit atria occurred predominantly in extraneuronal tissues possibly as a result of passive diffusion followed by binding.
在离体兔心房中研究了(非对映体)-(β-14C)麻黄碱的摄取特性。麻黄碱能逆浓度梯度快速蓄积。在5×10-7至10-2M范围内,摄取以均匀的初始速率发生。高浓度的哇巴因、可卡因、地昔帕明、利多卡因和苯乙胺以及细胞外钠离子浓度降低会轻微抑制摄取。然而,培养基中省略钾离子、使用代谢抑制剂或多种已知抑制去甲肾上腺素非神经元摄取和结合的药物并不会降低摄取。用6-羟基多巴胺预处理动物可非常显著地降低(非对映体)-(3H)间羟胺的摄取,但不会改变麻黄碱的摄取。得出的结论是,兔心房中麻黄碱的摄取主要发生在非神经元组织中,可能是被动扩散后结合的结果。