Mori M, Fujita M, Kozuka H
J Pharm Pharmacol. 1985 Nov;37(11):819-20. doi: 10.1111/j.2042-7158.1985.tb04976.x.
There was marked variation between p-hydroxylation and N-demethylation of methamphetamine in rats. Within 24 h, 10.4, 24-7 and 4.1% of the administered methamphetamine was excreted in urine unchanged, p-hydroxymethamphetamine (p-OH-MP, free plus conjugated) and also as amphetamine, respectively. Treatment by imipramine, desipramine, chlorpromazine, perphenazine and propericiazine 8 h before the administration with methamphetamine completely inhibited the urinary excretion of p-OH-MP whereas the excretion of amphetamine was enhanced by about 700 to 800%. This effect was also observed in rats treated with imipramine 16 and 24 h before methamphetamine. Phenothiazine and dibenzazepine derivatives reverse the degree of p-hydroxylation and N-demethylation of methamphetamine in-vivo in rats.
大鼠体内甲基苯丙胺的对羟基化和N-去甲基化存在显著差异。在24小时内,分别有10.4%、24 - 7%和4.1%的给药甲基苯丙胺以原形、对羟基甲基苯丙胺(p-OH-MP,游离加结合型)以及苯丙胺的形式经尿液排出。在给予甲基苯丙胺前8小时用丙咪嗪、地昔帕明、氯丙嗪、奋乃静和丙酰奋乃静进行处理,完全抑制了p-OH-MP的尿排泄,而苯丙胺的排泄增加了约700%至800%。在用甲基苯丙胺前16小时和24小时用丙咪嗪处理的大鼠中也观察到了这种效应。吩噻嗪和二苯氮䓬衍生物在体内可逆转大鼠体内甲基苯丙胺的对羟基化和N-去甲基化程度。