Nickel B, Niebch G, Peter G, von Schlichtegroll A, Tibes U
Drug Alcohol Depend. 1986 Jun;17(2-3):235-57. doi: 10.1016/0376-8716(86)90011-6.
In the fenetylline molecule, theophylline is covalently linked with amphetamine via an alkyl chain. The inclusion of amphetamine and results from early metabolic studies have led to speculation that fenetylline may be merely a prodrug for amphetamine and/or theophylline. Although previous studies are not consistent with this hypothesis, additional studies were conducted to comparatively evaluate the profiles of activity exhibited by fenetylline and its two postulated primary metabolites, (+/-)-amphetamine and theophylline. Investigations were also initiated using newly developed high pressure liquid chromatography (HPLC) techniques to further characterize the metabolic pattern that fenetylline undergoes and to examine the relationship between plasma pharmacokinetics and the pharmacodynamic actions of the drug. Fenetylline inhibits activity associated with amphetamine in certain test systems, an effect similar to that previously observed with fenfluramine. Only small amounts of the amphetamine theoretically available in the fenetylline molecule are released. Pharmacodynamic activity associated with fenetylline administration is more closely tied to plasma levels of the parent compound than to any (+/-)-amphetamine produced.
在芬乙茶碱分子中,茶碱通过一条烷基链与苯丙胺共价连接。苯丙胺的存在以及早期代谢研究结果引发了一种推测,即芬乙茶碱可能仅仅是苯丙胺和/或茶碱的前体药物。尽管先前的研究与这一假设不一致,但还是进行了额外的研究,以比较评估芬乙茶碱及其两种假定的主要代谢产物(±)-苯丙胺和茶碱所表现出的活性特征。还开始使用新开发的高压液相色谱(HPLC)技术进行研究,以进一步表征芬乙茶碱所经历的代谢模式,并研究血浆药代动力学与该药物药效学作用之间的关系。在某些测试系统中,芬乙茶碱会抑制与苯丙胺相关的活性,这一效果与先前观察到的氟苯丙胺类似。理论上芬乙茶碱分子中可利用的苯丙胺只有少量会释放出来。与芬乙茶碱给药相关的药效学活性与母体化合物的血浆水平关系更为密切,而非与所产生的任何(±)-苯丙胺的关系。