Koons J C, Long J P, Koble D L, Cannon J G, Fischer L J
J Pharmacol Exp Ther. 1985 Apr;233(1):51-7.
Possible metabolic activation of the dopamine receptor agonist DK-118 (5-hydroxy-6-methyl-N,N-di-n-propyl-2-aminotetralin) was investigated in cats. Metyrapone, an inhibitor of oxidative drug metabolism, was given to cats before DK-118 and the pharmacologic effects of the dopamine agonist were compared to those observed in nonpretreated animals. A sensitive high-performance liquid chromatography assay using electrochemical detection was developed to monitor urine and plasma concentrations of DK-118 in metyrapone-pretreated and control animals. The DK-118-mediated inhibition of cardioaccelerator nerve stimulation-induced tachycardia was reduced markedly in cats pretreated with metyrapone but the pretreatment had no effect on the hypotension or bradycardia produced by DK-118. In a separate group of cats, the tachycardia inhibitory effect of a nonbioactivated dopamine agonist, dipropyldopamine, was unaffected by metyrapone pretreatment, confirming that the inhibitor of drug metabolism does not interfere with this dopamine receptor-mediated effect. Pretreatment with metyrapone before a 0.14-mumol/kg i.v. dose of DK-118 increased the half-life, reduced total drug clearance and increased urinary excretion of unchanged DK-118. All of the changes are consistent with a metyrapone-related inhibition of DK-118 metabolism. The results of this study show that inhibition of DK-118 metabolism reduces certain of its pharmacologic actions, indicating that one or more of the metabolites of the drug may contribute to its effects.
在猫身上研究了多巴胺受体激动剂DK - 118(5 - 羟基 - 6 - 甲基 - N,N - 二正丙基 - 2 - 氨基四氢萘)可能的代谢活化作用。在给猫注射DK - 118之前,先给予其氧化药物代谢抑制剂美替拉酮,然后将多巴胺激动剂的药理作用与未预处理动物中观察到的作用进行比较。开发了一种使用电化学检测的灵敏高效液相色谱法,以监测美替拉酮预处理动物和对照动物尿液及血浆中DK - 118的浓度。在用美替拉酮预处理的猫中,DK - 118介导的对心脏加速神经刺激诱导的心动过速的抑制作用明显降低,但预处理对DK - 118产生的低血压或心动过缓没有影响。在另一组猫中,非生物活化的多巴胺激动剂二丙基多巴胺的心动过速抑制作用不受美替拉酮预处理的影响,证实药物代谢抑制剂不会干扰这种多巴胺受体介导的作用。在静脉注射0.14 μmol/kg剂量的DK - 118之前用美替拉酮预处理,可增加半衰期、降低总药物清除率并增加未改变的DK - 118的尿排泄。所有这些变化都与美替拉酮相关的DK - 118代谢抑制作用一致。本研究结果表明,抑制DK - 118代谢会降低其某些药理作用,表明该药物的一种或多种代谢产物可能对其作用有贡献。