Baumann P, Gaillard J M, Jonzier-Perey M, Gerber C, Bouras C
Psychopharmacology (Berl). 1984;84(4):489-95. doi: 10.1007/BF00431455.
This study was conducted in order to investigate the level of amitriptyline (AT) and its metabolites. Three separate experiments were carried out. In two of these experiments, rats were treated over 7 days with IP doses of AT (10 mg/kg in experiment A and 2 X 20 mg/kg in experiment C). The rats were sacrificed either 2 (experiment C) or 12 h (experiments A and C) after the last dose. In experiment B, rats were sacrificed 2 or 12 h after a single dose of 20 mg/kg AT. The results of these experiments showed the following: in experiment A only AT was measurable in the brain and in the plasma, in contrast to experiments B and C, where NT and the hydroxylated metabolites AT-OH and NT-OH reached significant levels in the plasma and in the brain. The concentrations of AT-OH, NT-OH, and NT (12-h values) that were found in the brain are probably not pharmacologically relevant. The 12-h plasma values of all compounds tested were, even with the highest dose, lower than those expected to be clinically effective in man. Our results suggest that AT, at higher doses, may induce its own metabolism. The free plasma levels of this drug and its metabolites are higher in man than in the rat. The possible implications of these results in the use of antidepressants in the treatment of depression are discussed.
本研究旨在调查阿米替林(AT)及其代谢物的水平。进行了三项独立实验。在其中两项实验中,给大鼠腹腔注射AT,连续处理7天(实验A中剂量为10mg/kg,实验C中剂量为2×20mg/kg)。在最后一剂后2小时(实验C)或12小时(实验A和C)处死大鼠。在实验B中,给大鼠单次注射20mg/kg AT后2小时或12小时处死。这些实验结果如下:与实验B和C不同,在实验A中,仅在脑和血浆中可检测到AT,而在实验B和C中,去甲替林(NT)以及羟基化代谢物AT - OH和NT - OH在血浆和脑中达到显著水平。脑中发现的AT - OH、NT - OH和NT(12小时值)的浓度可能与药理作用无关。即使使用最高剂量,所有测试化合物的12小时血浆值仍低于预期在人体中产生临床疗效的水平。我们的结果表明,较高剂量的AT可能会诱导自身代谢。该药物及其代谢物的游离血浆水平在人体中高于大鼠。讨论了这些结果在使用抗抑郁药治疗抑郁症方面可能的影响。