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阿米替林氮氧化物的中枢作用。

Central action of amitriptyline N-oxide.

作者信息

Maj J, Vetulani J, Michaluk J, Rogóz Z, Skuza G

出版信息

Pharmacopsychiatria. 1982 Nov;15(6):187-91. doi: 10.1055/s-2007-1019536.

Abstract

The central action of amitriptyline N-oxide (AMINO) has been compared with amitriptyline (AMI) in biochemical and pharmacological studies in rats and mice. It has been found in rats that both drugs prevent 6-OH-dopamine-induced depletion of brain noradrenaline (NA). At the same time AMINO increases and AMI lowers the NA level, both being without effect on 3-methoxy-4-hydroxyphenylglycol concentrations in the brain. AMINO and AMI potentiate the depletion of 5-hydroxytryptamine (5-HT) induced by p-chloroamphetamine in the rat brain and it may be considered as evidence that both drugs do not inhibit 5-HT uptake in vivo. Neither AMINO nor AMI affects the rat brain level of 5-HT but at higher doses they elevate the 5-hydroxy-indoleacetic acid concentrations. AMINO antagonizes the head twitch reaction induced by 5-hydroxytryptophan in mice and tryptamine convulsions in rats. The hyperthermia induced by fenfluramine (in rats at a high ambient temperature) as well as the stimulation of the hind limb flexor reflex in spinal rats, induced by fenfluramine or LSD, are also inhibited. AMINO antagonizes the 5-HT-induced increase in blood pressure in pithed rats. All the above effects are similar to those induced by AMI, only the active doses of AMINO are higher. The results presented indicate that AMINO, like AMI, inhibits NA uptake and is a 5-HT antagonist.

摘要

在对大鼠和小鼠进行的生化及药理学研究中,已将阿米替林N-氧化物(AMINO)的中枢作用与阿米替林(AMI)进行了比较。在大鼠中发现,两种药物均可预防6-羟基多巴胺诱导的脑去甲肾上腺素(NA)耗竭。同时,AMINO可升高而AMI可降低NA水平,两者对脑中3-甲氧基-4-羟基苯乙二醇浓度均无影响。AMINO和AMI可增强对氯苯丙胺诱导的大鼠脑内5-羟色胺(5-HT)耗竭,这可被视为两种药物在体内均不抑制5-HT摄取的证据。AMINO和AMI均不影响大鼠脑内5-HT水平,但在较高剂量时它们会升高5-羟基吲哚乙酸浓度。AMINO可拮抗小鼠中5-羟色氨酸诱导的头部抽搐反应以及大鼠中色胺惊厥。(在大鼠处于高环境温度时)芬氟拉明诱导的体温过高以及芬氟拉明或麦角酸二乙胺诱导的脊髓大鼠后肢屈肌反射的刺激也受到抑制。AMINO可拮抗脊髓大鼠中5-HT诱导的血压升高。上述所有作用均与AMI诱导的作用相似,只是AMINO的有效剂量更高。所呈现的结果表明,AMINO与AMI一样,可抑制NA摄取且是一种5-HT拮抗剂。

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