Dring L G, Franklin R B, Williams R T
West Afr J Pharmacol Drug Res. 1975 Jun;2(1):26-30.
When [14C] (+/-)-amphetamine sulphate (0.3 mg/kg) was injected into Tamarin monkeys, some 70-80% of the 14C was excreted in the urine in 24 hours. Some 75% of the 24-hour excretion was unchanged drug, 7% was free and conjugated benzoic acid and 7% was hydroxylated in the aromatic ring to give mainly 4-hydroxyamphetamine (Paredrine). With similar doses of [14C] norephedrine hydrochloride nearly 90% of the 14C was excreted in 24 hours, most of this being unchanged drug. Only 3-4% was metabolized at the side chain and there was no aromatic hydroxylation. The results were compared with those obtained earlier in man, rat, rabbit and guinea pig. Quantitatively the metabolites of amphetamine, norephedrine and preludin in the tamarin were more like those in man than in the other three species.
当将[14C](±)-硫酸苯丙胺(0.3毫克/千克)注射到绢毛猴体内时,24小时内约70 - 80%的14C通过尿液排出。24小时排泄物中约75%为未变化的药物,7%为游离及结合的苯甲酸,7%在芳环上发生羟基化,主要生成4-羟基苯丙胺(对羟麻黄碱)。使用相似剂量的[14C]盐酸去甲麻黄碱时,24小时内约90%的14C排出,其中大部分为未变化的药物。仅3 - 4%在侧链发生代谢,且无芳环羟基化。将这些结果与早前在人、大鼠、兔子和豚鼠身上获得的结果进行了比较。从数量上看,绢毛猴体内苯丙胺、去甲麻黄碱和普律定的代谢产物与人的更相似,而非与其他三个物种的相似。