van Wijk M, Korf J
Psychopharmacology (Berl). 1982;76(1):48-51. doi: 10.1007/BF00430754.
Serum and brain levels of the tricyclic antidepressant drug imipramine (IMI) were studied in the rat under a variety of conditions. IV doses (range 1 nmol kg-1 to 15 mumol kg-1, 350 ng--5 mg kg-1) and administered 5 min before death, were linearly correlated with IMI levels in serum, frontal cortex, and cerebellum. In this experiment, the highest levels of IMI were achieved in the frontal and occipital cortex and the lowest levels were found in the brain stem. The regional distribution was more even in rats pretreated with thiopental or gamma-hydroxybutyric acid, drugs that alter cerebral blood flow. After 20 min or more, tracer amounts of IMI injected IV to IMI-pretreated rats [1 or 17 days, daily dose 2 x 36 mumol kg-1 (10 mg kg-1), last dose 89 mumol kg-1 (25 mg kg-1), 2--3 h before death] exhibited a distribution pattern in serum and various brain regions similar to that of the unlabeled drug. In the latter experiments, content (per volume) of the tracer or unlabeled IMI was more than 25-fold higher in various brain areas than in serum. It is concluded that despite large differences in drug levels in serum or brain, a close relationship is maintained under the conditions studied.
在多种条件下对大鼠体内三环类抗抑郁药丙咪嗪(IMI)的血清和脑内水平进行了研究。静脉注射剂量(范围为1 nmol kg-1至15 μmol kg-1,350 ng - 5 mg kg-1),并在死亡前5分钟给药,与血清、额叶皮质和小脑中的IMI水平呈线性相关。在本实验中,额叶和枕叶皮质中IMI水平最高,脑干中最低。在用硫喷妥钠或γ-羟基丁酸预处理的大鼠中,区域分布更为均匀,这两种药物可改变脑血流量。20分钟或更长时间后,向预先用IMI处理的大鼠静脉注射微量示踪剂IMI(1或17天,每日剂量2×36 μmol kg-1(10 mg kg-1),最后一剂89 μmol kg-1(25 mg kg-1),在死亡前2 - 3小时),血清和各个脑区的分布模式与未标记药物相似。在后者的实验中,示踪剂或未标记的IMI在各个脑区的含量(每体积)比血清中高25倍以上。结论是,尽管血清或脑内药物水平存在很大差异,但在所研究的条件下仍保持密切关系。